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Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

Job Description Job Description: Direct Support Professional (Day Habilitation) Report to: Day Habilitation Program Supervisor The Direct Support Professional (DSP) is responsible for a variety of duties related to the overall care of individuals with developmental disabilities receiving services from APluscare Behavioral Health programs. This includes but not limited to caring of individuals and maintaining daily level of support, assisting them with their goals and strategies, implementing of individual support plans (ISP) and behavior plans (BP) in addition to promoting individual independence and helping with total integration and inclusion into the community. Direct Support Professionals are required to perform all duties in accordance with the Division of Developmental Disabilities (DDD) regulations and APluscare Behavioral Health policies and procedures. JOB RESPONSIBILITIES • Administer medications to individuals as prescribed, • Contact the pharmacist for medication refills and script follow ups, • Assist individuals with medical appointments, • Ensures individuals are dressed neatly and appropriately and are always groomed, • Prepares nutritional meals based on individual dietary needs, • Provides transportation to and from activities, as well as the day habilitation program, • Implementation of individual support plan and behavioral support plan goals, • Promotes participation and involvement in community outings, • Ensures all individuals rights are protected, • Treats individuals with dignity and respect, • Report any noted problems to the Program Supervisor immediately and complete an inhouse (APluscare) incident report form, • Ensures that all documentation is completed accurately and in a timely manner, • Ensures Medication Administration Record (MAR) entries are completed as required, • Completes communication logbooks during shift and all other duties as assigned, • Attend all required staff meetings and trainings scheduled, • All other duties as assigned by APluscare Shift: Monday - Friday 7:30am - 3:30pm Qualifications: • A minimum of a High school diploma, or GED required, • 6months-1year of experience working with people with developmental disabilities, • Push, pull, and lift up to 50lbs, • Ability to work on holidays, weekends and during inclement weather, • Valid Driver's License, clear driving record and driving Company's vehicle, • Must be at least 18 years of age Trainings: All must successfully complete the mandatory DDD trainings: Overview of Developmental Disabilities, Abuse and Neglect, Medication Administration, CPR & First Aid, Agency New Hire Orientation, Agency's approved training on handling Life-Threatening Emergencies/ Danielle's Law and other professionally based training deemed necessary.

Job Description • Receive and review all referrals for day Habilitation services at Folak healthcare, LLC., • Participate in the admission ,suspension and discharge processes for individuals., • Serve as the secondary contact for individuals,families, and Dsp receiving services through day Habilitation., • Review and approve schedules and any schedule changes, • Oversee and manage transportation routes for individuals receiving transportation inside and outside of the day program., • Supervise and manage the daily operations of services and support provided by the agency. Review and approve daily services logs for services rendered by employees. • Serve as a member of the agency's Quality management committee to support ongoing growth and compliance,, • Assume 24hrs on-call responsibilities as required., • Oversee the administration and safeguarding of medication., • Document , report and follow up on all agency Unusual incident reports., • Cooperate with any internal or external inspections or investigations , including those conducted by federal or Local government investigators., • Respect the confidentiality of all information related to individuals served and their families., • Protect the dignity of the individuals served., • Perform other tasks as assigned. Company DescriptionFolak is a Day Habilitation program for individuals with developmental and intellectual disabilities.Folak is a Day Habilitation program for individuals with developmental and intellectual disabilities.

Job DescriptionSalary: $30 - $36 per hour, DOE Founded in 1986 and located in Middlesex NJ, BAMCO inc. is an award-winning industry leader in the design, manufacture and erection of building envelope systems servicing the architectural, developer and general contracting communities. We specialize in engineering, custom fabrication, bending, routing, welding and finishing in all types of metals from aluminum, galvanized and stainless to the exotics with a focus on safety, green initiatives and Lean Kaizen principles throughout. Our primary markets are pharmaceutical, health care, industrial, institutional and high-rise office and residential in the northeast corridor for installation and we service all 48 states with design and fabrication offerings as well. BAMCO is a 100% employee-owned company (ESOP) that prides itself with an unparalleled commitment to excellence for our customers, our company and all our stakeholders. We are currently seeking a hands-on leader with sheet metal fabrication experience to join our growing team. This Sheet Metal Fabrication Lead position helps oversee daily operations and has a key role in maintaining production flow, ensuring quality standards, and supporting a team of skilled operators. Key Responsibilities: • Oversee and support a team of sheet metal operators, including:, • 1 Shear Operator, • 1 Laser Operator, • 3 Folding Operators, • Follow and execute production schedules as directed by supervisors., • Approve and inspect finished parts to ensure they meet drawing specifications., • Assist operators with production needs and troubleshooting., • Operate machinery (e.g., press brake) as needed to support production., • Handle materials and operate a forklift for movement and staging., • Maintain a clean, organized, and safe work area., • Communicate effectively with the Fabrication Supervisor regarding equipment, part quality, and personnel issues., • Maintain Hour-by-Hour production charts., • Assist in training and mentoring machine operators., • Cooperate in safety programs, initiatives and investigations. Comply with all safety procedures., • Participate in clean-up responsibilities and maintain daily good housekeeping practices according to 5S procedures., • Perform other duties and tasks assigned. Requirements/Qualifications: • High School Diploma or GED Equivalent., • 3-5+ years of experience in a Sheet Metal or Fabrication environment., • 3-5+ years of blueprint reading experience., • 3-10 years of hands-on experience operating sheet metal equipment, including:, • Mechanical or Hydraulic Shear, • Press Brake (ideal), • Punch Press, • CO or Fiber Laser, • Forklift, • Strong organizational and communication skills., • Proficiency with email and Microsoft Office applications., • Ability to use measurement tools (squares, tape measure, protractor, calipers). Desired Qualifications: • Bilingual in Spanish., • Experience with CNC programming (offline and online)., • Strong time management and leadership skills., • Experience with machine maintenance and troubleshooting., • Familiarity with various sheet materials (aluminum, stainless steel, galvanized)., • Experience working in a collaborative environment promoting a teamwork mentality., • Strong sense of personal accountability. Benefits: • 401(k), • 401(k) matching, • ESOP - Employee Stock Ownership Plan, • Health insurance, • Dental insurance, • Vision insurance, • Life insurance, • Paid time off (Holidays/Vacation), • Professional Development BAMCO inc. is not accepting unsolicited assistance from search firms. All resumes submitted by search firms to any employee of BAMCO inc. in any fashion without a valid written search agreement in place will be deemed the sole property of BAMCO inc. No fee will be paid if a candidate is hired by BAMCO inc. based upon an unsolicited referral. BAMCO inc. is an Equal Opportunity Employer. BAMCO inc. participates with E-Verify.

Job Description Underground Construction Supervisor - Utilities CARIAN is growing! We are a proud, woman-owned management consulting firm providing program/project management, capital project delivery, consulting, and technology solutions to our customers in the renewable energy, power utilities, infrastructure, and transit/transportation sectors. We are searching for an Underground Construction Supervisor to support our client in the New Jersey area. Positions at CARIAN offer comprehensive and competitive benefits (medical, dental, and vision), 401(k) matching, and the opportunity to work with a growing company. Summary: The UG Construction Supervisor will supervise the installation and maintenance of underground transmission and Construction facilities in accordance with manufacture and company standards to maintain Client’s Safety Standards. The supervisor will coordinate, inspect, monitor, and document the performance of outside contractors performing Underground construction and maintenance on the client’s facilities. Responsibilities: * Monitor project progress and contractor performance through field inspections covering the quantity and quality of work performed. * Supervise UG contractors and vendor crews. * Prepares reports such as work schedules, pending work, unusual field or operating conditions, or performance of equipment. * On a rotating basis, perform stand-by duty in accordance with UG Department requirements. * Support storm restoration functions when required. * Perform safety inspections, effective operations inspections, accident investigations, etc. for the area of responsibility. * Evaluate tools and equipment used to perform job functions. * Assist with the preparation of monthly project forecast, accruals, and detailed construction and payment schedules. Assist the Field Manager as required in the development and implementation of the regional work plan for major capital projects. Qualifications Required: * High School Diploma or GED and 15 or more years’ experience in the operation, design, maintenance, and construction of electric transmission and Construction facilities. * Knowledge of work rules, work methods, safety rules, and line procedures associated with overhead and underground work. * Supervisory experience and/or to be able to direct contractor’s crew operations. * Must be able to evaluate the performance of all assigned personnel as well as evaluate tools and equipment. * Ability to work off-hours which may include working nights and/or weekends. * This position requires driving to company locations and off-site assignments and events, applicants must possess and maintain a valid US driver’s license with a safe and satisfactory driver history. Minimum Years of Experience: 15 years of experience Education: High School Certifications: None CARIAN takes pride in being an Equal Opportunity Employer. We do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, citizenship, gender expression or identity, status as a veteran, and basis of disability or any other federal, state, or local legally protected class. As a Woman-Owned Business Enterprise, CARIAN is committed to providing employment opportunities to women, veterans, and underrepresented minorities.

Job Description Downstream Manufacturing Specialist Downstream Manufacturing Associate or Scientist to oversee the purification of 50L to 2000L volumes for engineering, clinical, and commercial batches in a cGMP environment. This role requires advanced technical expertise in downstream processes, including AKTA purification skids (or similar), tangential flow filtration (TFF), and comprehensive knowledge of batch records, protocols, investigations, and technical documentation. Essential Duties & Responsibilities • Execute downstream purification processes at various scales (50L to 2000L) within a cGMP environment, including column packing, troubleshooting, and data analysis., • Provide technical leadership in the development and execution of downstream purification processes., • Utilize software systems to collect, monitor, and evaluate operational data, making real-time adjustments to downstream processes, instruments, or equipment., • Ensure the timely and efficient execution of engineering and clinical batches., • Establish specifications for downstream equipment and improve manufacturing techniques to enhance process efficiency., • Collaborate with cross-functional teams and external vendors to address technical challenges and maintain downstream production equipment., • Adhere to and enforce strict GMP and environmental health and safety (EHS) policies in the manufacturing environment., • Lead investigations and implement corrective actions for downstream process deviations encountered during batch execution., • Perform additional responsibilities as required, ensuring alignment with company policies and quality standards.Qualifications & Requirements, • A Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences, with 4–5 years of relevant experience in the biopharmaceutical industry., • Proven expertise in downstream purification within a cGMP and aseptic manufacturing environment., • Hands-on experience with AKTA Process skids or equivalent systems, as well as familiarity with single-use manufacturing consumables (e.g., bags, tube sets, columns, and process manifolds)., • Comprehensive knowledge of GMP documentation and the ability to execute engineering and clinical batches., • Strong troubleshooting and problem-solving skills specific to downstream processes and purification.

Job Description Job description Quality Assurance Information Specialist I Everas Community Services, Inc. has been providing community-based services to people with intellectual and developmental disabilities for more than 40 years. Our extensive experience includes services for people across a spectrum of abilities and specialized needs including people who are deaf-blind, deaf, or blind, people with intensive medical and behavioral support needs, and people with autism spectrum disorder. Through our work to help people thrive and be empowered to contribute to their greatest capacity, we are making a positive difference in the lives of our clients, our employees, and the greater community. Join our team of professional staff committed to providing support services with care, quality, and respect throughout nine counties in NJ. Summary As a member of our Quality Assurance Team, the QAIS I ensures program quality standards are implemented in all departments through review of program data. The QAIS I supports program services integrity and compliance with all regulatory bodies and Everas policies and procedures, as well as makes specific recommendations to abate issues and continuously benchmark standards. QA Team members support program supervisors by providing direct guidance to staff, identifying agency trends, and implementing proactive and creative solutions in areas that require attention. Your commitment to excellence in disability services, collaborative mindset, professionalism, and high-level organizational skills are needed to achieve the best possible outcomes for the people in our programs. Quality Assurance Information Specialist Duties include but are not limited to: • Conduct all required investigations and inquiries within required timeframes, • File all Unusual Incident Reports in a timely, thorough, and accurate manner, • Participate in staff training to support employee development and performance, and ensure quality service provision, • Evaluate agency wide incident data to make proactive recommendations to prevent accidents and injury, • Rewarding, mission-based work, supporting an improved quality of life for people with disabilities, • Paid training/professional development opportunities, • Paid time off, • Medical Insurance Plan, • Retirement Plan, • Referral Incentive Program, • Flexible Schedule, • Bachelor’s Degree with minimum 1 year of related work experience OR HS Diploma with minimum 5 years related experience, • Experience in the I/DD field is required, • Experience in information synthesis and analysis, • Detail oriented with strong written and verbal communication skills, • Flexible schedule to include evenings/weekends, • Criminal Background Check, • Valid NJ Driver’s license Through our work to help people thrive and be empowered to contribute to their greatest capacity, we are making a positive difference in the lives of our clients, our employees, and the greater community.Everas provides comprehensive services advocating for the best possible outcome in all areas of a person’s life. We believe in lifelong, incidental learning and strive to assist each person to stretch beyond their own and others’ expectations of what can be achieved.\r\n\r\nThrough our work to help people thrive and be empowered to contribute to their greatest capacity, we are making a positive difference in the lives of our clients, our employees, and the greater community.

Job Description Job Description: The Temporary Microbiology LaboratoryTechnician is responsible for performing general microbiological laboratoryduties as outlined below: Prepare microbiological media including QC sterilitychecks and media growth promotion testing Prepare specimens and materials, including cleaning theworkspace Perform microbiological testing of water in accordancewith standard procedures, using aseptic technique. Maintain accurate, up-to-date and concise laboratoryrecords General housekeeping/upkeep/cleaning of laboratory Monitor, clean, and perform calibration checks forlaboratory equipment and machinery Dish washing of laboratory glassware Autoclave waste Stock laboratory supplies and maintain laboratoryinventory Back up for Lab Analyst with respect to generalmicrobiological duties Work in a team environment under minimal supervision Participate in laboratory investigations Additional responsibilities as needed Skills/Experience/Education Bachelors degree or equivalent in Microbiology/Biologyor working towards said degree, with Microbiology related coursework Minimum of 6-12 months experience in a Microbiologylaboratory, preferred Knowledge of GMP and aseptic techniques preferred Strong interpersonal skills Works well in a team environment Ability to work with minimal supervision Strong multi-tasking skills Precise, accurate and detail oriented

Job Description JOB DESCRIPTION We are seeking a dynamic and experienced engineer to support and lead our Mechanical Integrity, Quality Assurance (MIQA), and Reliability Program. This role is essential to ensuring compliance with Process Safety Management (PSM) standards, regulatory requirements, and driving continuous improvement in reliability and safety across our operations. Key Responsibilities • Lead MIQA and Reliability initiatives aligned with PSM standards • Maintain and train teams on the Site MIQA Manual • Integrate MIQA requirements into CMMS tools and workflows • Manage MIQA Heat Map and Action Plans to address gaps and drive improvements • Track and report MIQA performance metrics across site and business levels • Participate in incident investigations, PHAs, PSSRs, and MOC-T changes • Ensure QA and MI compliance in project management and inspection plans • Serve as a member of the Site PSM Committee, leading MI and QA elements Collaborate cross-functionally to support real-time problem-solving and reliability assessments REQUIRED SKILLS AND EXPERIENCE 3-5 years experience with Reliability, Process or Quality Engineering within manufacturing industry Experience with Root Cause Analysis, CAPAs and risk management Background with mechanical integrity, quality assurance, reliability assessments and continuous improvement Bachelors Degree in Mechanical Engineering or related field NICE TO HAVE SKILLS AND EXPERIENCE Mechanical Integrity Quality Assurance (MIQA) Experience Reliability Program/Project Management experience

Job Description We are excited to announce that due to our continued growth, APluscare is expanding our team. As we take on new opportunities and projects, we are looking for passionate and talented individuals to join us!! Job Title: Compliance Specialist Job Duties: ● Ensures quality of life of the client served and protected by minimizing risk to the entire Agency and surrounding community ● Conducts spontaneous and scheduled visits and inspections ● Creates and revises systems and procedures by analyzing compliance policies and practices. ● Identifies potential weaknesses and risks in operations, documenting needs for improvement, creating corrective plans, and ensuring correction ● Review Practices on an ongoing basis to ensure prevention of incidents or violations ● Audits and corrects employee documentation at the residential or individual/ client level ● Reviews and updates internal policies; recommends and formulates policies, procedures and guidelines ● Responds to internal and external inquiries related to licensing and compliance issues. ● Creates and maintains compliance and audit documents ● Resolves compliance and risk problems by analyzing regulations and identifying solutions ● Facilitates Agency governance filings, licensing, registrations and corporate records for oversight entities ● Assists in the development and implementation of corporate governance policies, guidelines and templates ● Responsible for compliance activities to include reporting, risk assessments, training and follow up reviews of compliance investigations and notifications ● Responsible for ensuring that all employees receive all required trainings upon hire and annually thereafter ● Responsible for ensuring that additional employee development opportunities are available on an ongoing basis to all staff ● Is available for after hours on-call duties for urgent facility matters ● Cooperation with all agency, state (DHS/DDD), and federal investigations and inspections ● All other duties as requested or assigned by APluscare Requirements: · Criminal background checks · Central registry checks · Child abuse registry checks · Drug testing Skills/Qualifications: ● Bachelor's Degree is required ● 3 to 5 years progressive and comprehensive experience or training in internal auditing and regulatory compliance in healthcare ● Certified in Healthcare Compliance (CHC) by the Health Care Compliance Association preferred ● 1-3 years of experience working in the field with individuals with developmental disabilities ● 2+ years of experience in health care administration ● Valid Driver's License ● Excellent verbal and written communications ● Employee must cooperate with the licensee and DHS department staff in any inspection or investigation ● Employee must successfully complete and demonstrate proficiency in all areas of required training ● All other duties as required or assigned by APluscare Physical Demands/Working Conditions: · Handles detailed work and highly complex problems, balancing multiple tasks simultaneously · The ability to effectively communicate (orally and written) and interact with others, including diverse, inter-disciplinary, cross-functional teams · The ability to read, concentrate and learn · Sitting, standing, and computer work for long periods of time · Push, pull, and lift up to 50lbs · The ability to write concisely and convey meaning in a manner appropriate to different readers, presenting a persuasive argument · Duties and responsibilities may be added, deleted or changed to meet the needs of the organization

Job Description Upstream Processing Manufacturing Scientist To support our next growth phase, we are hiring seven Upstream Manufacturing Scientists/Associates at various experience levels to meet the increasing demands of our Upstream and Downstream Manufacturing teams. These teams are gearing up to scale from pilot manufacturing to full-scale commercial production at our new NJ facility. Positions Available: • Execute mammalian cell culture processes to produce recombinant proteins for biologics, managing cell culture batches up to 2000L., • Operate bioreactors, establish equipment specifications, and enhance manufacturing techniques., • Collaborate with manufacturing associates and engineers, providing clear instructions and guidance., • Initiate batch records, protocols, and oversee investigations in a cGMP environment to ensure compliance., • Review and document manufacturing and packaging batch records, ensuring adherence to safety standards and GMP guidelines. Experience/Qualifications: Upstream: • At least 1-2 years of experience in cell culture and bioreactor operations, including GMP and aseptic manufacturing experience., • Proficiency with single-use manufacturing consumables (e.g., bags, tube sets, columns) and experience in scale-up manufacturing activities.

Job Description 8LOCATIONS INCLUSIVE OF: HOWELL, MONMOUTH COUNTY, JACKSON, OCEAN COUNTY, BLOOMINGDALE, PASSAIC COUNTY, BERGEN COUNTY, FLANDERS, MORRIS COUNTY, PRINCETON, MERCER COUNTY, NEW JERSEY MUST BE WILLING TO DRIVE TO EAST BRUNSWICK FOR THE INTERVIEW. Behaviorist (BCBA) Responsibilities and Duties • Development and implementation of new support services to meet the changing needs of persons receiving services., • Provide training in implementing formal comprehensive behavior support plans., • Develops, monitors and trains staff on Behavior Support Plans., • Develop behavior intervention strategies with the Interdisciplinary Team (IDT) in accordance with APluscare policies and procedures., • Intervene during a behavioral crisis, • Understand and implement current DHS rules and regulations, policies and procedures, • Assist & cooperate in inspections and investigations of any sort, including investigations by APluscare and/or DHS Consulting with direct care and supervisory staff to ensure that daily activity schedules are adequate to meet the needs of the individuals., • Act as a liaison with parents, staff and DHS staff to ensure the continuum of care and support for members, • Participate in after- hour on-call rotation in cooperation with other APluscare staff (Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) • BCBA required Master's degree in Psychology or related field required., • A Master's Degree in Social Work, ABA, Psychology, Special Education or other disciplines as may be approved by the Executive Director., • Extremely strong organizational, writing, verbal, and interpersonal skills., • Creativity and flexibility are essential in assuming significant responsibility., • Experience working in racially, ethnically, and socioeconomically diverse communities working with developmental disabilities preferred., • The Behaviorist may be required to complete mandatory DHS training. Training is provided at no charge., • Employee must cooperate with the licensee and department staff in any inspection or investigation., • Employee must successfully complete and demonstrate proficiency in all areas of required training., • Valid Driver's License, • Must be at least 18 years of age

Job Description Job Title: Human Resources Business Partner - TEMP Department: Human Resources Reports to: CHRO FLSA Status: Non-Exempt This is a remote position. Company Overview ProSmile is the fastest growing dental organization on the East Coast and has the largest network of affiliated multi-specialty dental practices in New Jersey, with an expanding footprint in Pennsylvania and Maryland. Our premier DSO is led by world class dentists who understand what highly skilled dentists and dental professionals need to grow a practice while focusing on delivering the best-in-class clinical care to their patients. Position Summary The HR Business partner Temp role will provide strategic HR advice and solutions to drive business growth and success. This position will be responsible for working on a full range of HR functions. Duties and Responsibilities The duties include, but are not limited to: • Partner with business leaders to develop and implement HR strategies that support the organization's goals and objectives., • Manages and resolves complex employee relations issues. Conducts effective, thorough, and objective investigations and provides guidance on disciplinary actions and performance improvement plans as needed., • Provide guidance and support to managers and employees on HR policies and procedures, performance management, and compliance matters., • Ensure FLSA compliance by accurately determining and classifying hourly and salary roles, including exempt and non-exempt positions., • Develop and implement succession planning strategies to identify and develop talent for key roles., • Develop workforce plans that align with business needs and talent requirements., • Collaborate with cross-functional teams to identify opportunities for process improvements and efficiency gains., • Edit and maintain the employee handbook, ensuring that it reflects current policies and legal requirements., • Draft and implement HR policies and procedures that align with the organization's culture and values., • Interpret, and apply the appropriate sections of applicable laws, guidelines, regulations, ordinances, and policies., • Develop and implement onboarding programs to ensure new hires are set up for success., • Bachelor’s degree in human resources, Business Administration, or related field., • 5+ years of experience in an HR Business Partner role, preferably in a DSO/MSO environment., • SHRM Certified Professional (SHRM-CP) or SHRM Senior Certified Professional (SHRM-SCP) a plus but not required., • Strong understanding of FLSA compliance and experience classifying hourly and salary roles., • Experience developing and implementing succession planning and workforce planning strategies., • Excellent communication, interpersonal, and analytical skills., • Expert problem-solving skills and the ability to work independently., • Experience with complex HR investigations and employee relations issues, supporting employees in a multi-state worksite organization, • Outstanding organization, prioritization, follow up, analytical and time management skills. Equal Employment Our culture encourages individual development, embraces an inclusive environment, rewards innovative excellence, and leads in provider and patient satisfaction. ProSmile values diversity, inclusion, and equity as matters of fairness and effectiveness. We are committed to hiring and retaining staff that reflects the diversity of the communities we serve, fostering an inclusive working environment where staff of all backgrounds feel welcomed and engaged. ProSmile is an Equal Opportunity Employer and encourages applications from individuals underrepresented in the medical sector, including people of color, and persons with non-traditional work and educational experience. All who believe they meet the stated qualifications are invited to apply. Company Safety We believe that the best care for our patients starts with the best care for our employees. ProSmile is committed to proactively creating and maintaining an environment that is safe for our team and patients. Employees are required to wear Personal Protective Equipment (PPE) including face masks, gloves, gowns, and more as needed and in accordance with CDC standards. Benefits Summary At ProSmile, we are committed to supporting the health and well-being of our employees and their families. We offer the following benefits for Full Time Benefits Eligible Positions (35+ hours per week) and Part Time Benefits Eligible Positions (30-35 hours per week): • Medical Insurance: Choice of five comprehensive Aetna medical plans, including options with low copays, deductible-sharing, and national provider networks., • Dental Insurance: MetLife plans offering preventative, basic, major, and orthodontic coverage options., • Vision Insurance: Davis and UHC vision plans with annual exams, eyewear allowances, and contact lens benefits., • Flexible Spending & Health Savings Accounts: Pre-tax savings accounts for medical, dependent care, and healthcare expenses., • Life & Disability Insurance: Employer-paid basic life and AD&D insurance, with voluntary life, short-term, and long-term disability plans., • Additional Perks:, • Employee Assistance Program (EAP), • Identity Theft & Fraud Protection, • Legal Support Services, • Discount Programs (including pet insurance, travel, theme parks, electronics, etc.), • Wellness Programs The Company reserves the right to modify the job description based upon its needs and may require the employee to perform functions beyond those mentioned above. Neither this job description nor any other communication creates an employment contract between the Company and the employee. Equal Employment Our culture encourages individual development, embraces an inclusive environment, rewards innovative excellence, and leads in provider and patient satisfaction. Prosmile values diversity, inclusion, and equity as matters of fairness and effectiveness. We are committed to hiring and retaining a staff that reflects the diversity of the communities we serve, fostering an inclusive working environment where staff of all backgrounds feel welcomed and engaged. ProSmile is an Equal Opportunity Employer and encourages applications from individuals underrepresented in the medical sector, including people of color, and persons with non-traditional work and educational experience. All who believe they meet the stated qualifications are invited to apply. Company Safety We believe that the best care for our patients starts with the best care for our employees. ProSmile is committed to proactively creating and maintaining an environment that is safe for our team and patients. Employees are required to wear Personal Protective Equipment (PPE) including face masks, gloves, gowns, and more as needed and in accordance with CDC standards. Powered by JazzHR 91kfwKsqVO

Job DescriptionCompany Description MAKE GREAT PIZZA — AND MORE — POSSIBLE Be a part of the world's #1 Pizza company and watch your career grow! Job Description The supervisor oversees a team of drivers [Class A and B] delivering to Domino’s Pizza stores. The supervisor is responsible for scheduling drivers, routing trucks, reviewing trip sheets for accuracy, and ensuring compliance with DOT regulations, state, local laws, and company policies and programs. Effectively and efficiently handle customer complaints and concerns. Train new drivers in job duties, safely, and complete Job Safety Observations (JSO). The supervisor must be comfortable working in a diverse, fast-paced environment. RESPONSIBILITIES AND DUTIES Shift- Sunday- Thursday 3:00pm- Finish Compensation- 90k-100K (based off experience) 10% bonus Leadership: · Recruit, interview, select, and mentor new and tenured drivers · Support driver engagement initiatives · Monitor drivers performance and hold accountable when performance is below expectations, using coaching and/or progressive discipline, as needed · Complete driver’s annual performance reviews · Review driver’s lytx and logs and coach according to company · Collaborate in drivers onboarding and training · Ensure safe work environment in compliance with FMCSA, OSHA, company standards, local, state, and federal requirements · Effectively communicate day-to-day with drivers, departments and vendors · Create positive environment, morale and respect among team members · Attend and participate in classroom or virtual Leadership & Development trainings · Coordinate safety/team/quarterly meetings Reporting/Budget: · Prepare and assist with Transportation generated reports · Monitor budget and fuel cards to ensure funds are maximized · Participate in the development of budgets Routing, Scheduling, Hours of Service, and Maintenance: · Weekly schedule driver routes and re-routing as necessary to ensure route coverage · Conduct route analysis and recommend saving opportunities to Manager · Monitor driver hours of service via onboard system · Conduct route observations to ensure Drivers are safely performing their duties as required by company and DOT standards (The numbers of observations per period are determined by the number of drivers at the SCC) · Maintain and monitor food safety standards in compliance with company and franchisee requirements · Perform payroll duties when necessary and review driver payroll for accuracy · Monitor mis-deliveries, and make recommendations to Manager on avoidance strategies · Maintain driver qualification file · Schedule truck maintenance and maintain fleet image · Conduct accident investigations · Coordinate deliveries and backhauls activities · Assist the Transportation Manager with truck leasing meetings to ensure PMs are met to Domino’s standard and repairs are completed in a timely manner · Perform other duties as assigned by leadership · As needed, if qualified, drive company vehicle or straight truck for deliveries or to leasing company for service/maintenance, and on occasion work the yard Customer Relations: · Answer Slice of Pie complaints and keep leadership informed of findings · Maintain positive customer relationships · Customer Surveys Qualifications · High School Diploma, some college hours, 2-year degree preferred · 2-3 years of documented supervisory experience · 2-3 years route scheduling experience · Knowledge of Department of Transportation, FMSCA rules and regulations · MS Office, SAP, Transportation Management Systems (TMS), computers, and scanner equipment/software · Willingness to support a 24-hour operation, including carrying an emergency cell phone as needed · Results-oriented with strong organizational, decision making and people skills · Successfully pass a background check every third year on your anniversary date · Commercial Driver’s License Class A, a plus PHYSICAL REQUIREMENTS · Ability to stand and/or walk for extended periods of time, climb stairs, and lift to 25 lbs. frequently and 50 lbs. on occasion · Ability to bend, twist, reach, push, and pull throughout the shift · Ability to work in extreme temperatures (non-airconditioned warehouse), both indoors and outdoors, including refrigerated conditions [33-38] · Ability to work in environment with exposure to loud machinery · Must be able to work around yeast and flour Additional Information What you can expect from Domino’s: • Competitive pay, • Competitive benefits – Medical, Dental, & Vision on the first day of employment, • Company paid short term disability coverage, • Company paid Life Insurance, • 401k with company match up to 5%, • Paid Holiday and Vacations, • Professional and supportive management

Job Description Empowering Lives, Embracing Abilities: Their Place is dedicated to championing the rights and enhancing the quality of life for individuals with Intellectual and Developmental Disabilities (IDD). We strive to create a compassionate and inclusive community where every person, regardless of their abilities, is valued, supported, and empowered to reach their full potential. Department: Administration FLSA Status: Exempt Reports to: Chief Executive Officer Position Summary: This position is responsible for ensuring organization-wide compliance with all required DDD, New Jersey State, Federal regulatory standards and Medicaid guidelines. Essential Job Functions: • Administer the corporate compliance program for the organization and oversees all New Jersey Department of Human Services, Division of Developmental Disabilities (DDD) regulatory standards., • Identifies all DDD related compliance requirements in each area of the organization and assigns responsibility for ensuring that such compliance is maintained., • Prepares the Agency for organizational compliance audits, including DDD site visits, Medicaid and other related audits., • Collaborates with the COO and CEO to recommend changes in policy and procedure in order to ensure that compliance is attained throughout the organization., • Conducts all required internal audits, investigations and quality assurance training., • Works with agency Leadership, Directors, Managers, and other personnel to ensure that compliance within each individual area of the organization is attained., • Completes all required agency and DDD trainings., • Bachelor’s degree in Business, Public Administration or related field, Master’s degree preferred., • Minimum of 5 years of experience as a Quality Manager/Director., • Minimum of five years of related experience in the non-profit sector., • Expert knowledge of NJ State Department of Human Services, DDD regulations and standards., • Advanced knowledge of best practices related to Quality Management., • Knowledge of Medicaid regulations and standards., • Excellent written and oral communication skills., • Proficient with MS Office applications, Sharepoint, Therap and other technology platforms., • Ability to work independently and as part of a team., • Detail-oriented, • Integrity, • Teamwork & Collaboration, • Quality Management, • Reliability Benefits: • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off, • Retirement plan, • 8 hour shift, • Day shift Job Type: Full-time Pay: $75,000.00 - $80,000.00 per year Benefits: • 401(k) matching, • Dental insurance, • Employee discount, • Health insurance, • Paid time off, • Referral program, • Retirement plan, • Vision insurance Work Location: In person

Job Description Senior Quality Engineer – Medical Device Do you want to make a difference in the world? Do you want to help save lives? Come start or continue your career with us! MICRO is a contract manufacturer providing services for companies engaged in life-saving products and solutions. MICRO offers an excellent benefits package, compensation higher than industry average and a full complement of training programs dedicated to give our employees the skills and knowledge required to achieve their career goals. So don’t settle for a job when you can have a career that makes a difference! Are you ready to? MISSION The Senior Quality Assurance Engineer is responsible for conducting complex ongoing analysis of the production process inputs and outputs to ensure that customer quality requirements are being achieved. ESSENTIAL DUTIES AND RESPONSIBILITIES Research & Analysis • Collects production data and applies standard scientific and statistical methods to analyze, document, and diagram production processes. Conducts FMEA, DOE, and SPC analysis, • Performs complex data analysis and uses six sigma tools to resolve complex quality issues., • Provides input to the production control systems and designs control activities, • Provides input for new product equipment selection, installation and maintenance, • Maintains expert level of understanding of GD&T, • Leads investigations to determine root cause, development of corrective action plans, verification and effectiveness activities., • Leads projects, teams and complex product transitions., • Develops quality standards and processes related to customer specifications and process improvement, • Communicates with customers, suppliers and other resources to achieve the objectives, • Evaluates process stability and capability, • Analyzes processes and procedures to ensure they fit the organization’s quality standards., • Ensures quality processes and procedures comply with internal SOPs, • Assists with regulatory audits, • Performs inspections and sets quality assurance testing models for analysis of raw materials, materials in process, and finished products., • Writes detailed work instruction-level documents for Quality and related areas. Trains personnel in these instructions and other technical process controls, • Quarantines, documents and evaluates products and materials, • Ensures control plans and associated documentation are implemented effectively and maintained., • Monitors and reports on quality-related key performance indicators, • Ensures compliance and assists with adherence to quality management system ASQ certification is preferred EDUCATION AND EXPERIENCE • Bachelor’s degree in Engineering or a related field is required., • 4 - 6 years of quality experience in a manufacturing environment or equivalent combination of education and experience is required., • Experience reading and interpreting blueprints and gage design knowledge is required., • Experience with GD&T is required., • Experience with automate inspection systems is required., • Proficient in common quality methodologies, including: APQP, MSA, PPAP, SPC., • Strong manual and spatial dexterity skills is required., • Experience with Lean and Six Sigma methodologies is preferred., • Implementation of effective corrective action is strongly preferred., • Ability to work multiple projects., • Strong verbal and written communication skills as well as excellent interpersonal skills are required, • Must have exceptional organizational skills, ability to meet deadlines, thrive in a fast-paced environment and be able to problem solve effectively.

Job Description The Safety Specialist supports specific project needs by ensuring best practices are implemented, safety compliance requirements are met, and enhance a culture of safety. • Oversee all aspects of a commercial construction projects ensuring OSHA compliance, • Conduct daily safety meetings, • Complete accident reports and conduct accident investigations, • Ensure all personnel wear their personal protective equipment (PPE), • Daily safety audits and inspections, • Minimum 5 years direct construction safety experience required, • OSHA 30-hour Construction, • OSHA 510 required, • Hazwoper 40 a plus, • Advance knowledge of construction safety standards, • Excellent written and verbal communication skills required, • Proficient Microsoft Office skills Embody HazTek's Core Values of Integrity, Compassion, Dependability, Leadership, Accountability Company DescriptionHazTek Inc. is one of the nation’s largest and most experienced occupational health and safety management firms. We are known for our professional consulting services and premium safety training and we are trusted for our effectiveness in keeping workers safe today – so employees and businesses will be here tomorrow. Our team is dedicated to safety and saving lives through our Core Values of integrity, compassion, dependability, support, and accountability. This is an opportunity to be surrounded by fellow individuals who are dedicated to safety. We offer competitive compensation and a great benefits package including, but not limited to, medical, dental, life insurance, long-term disability, paid time off, 401(k), professional development, and education assistance HazTek Inc. is committed to building an environment of inclusion and acceptance that values diversity across all areas of the organization — an environment in which all employees have an opportunity to participate and contribute to the success of the business and are valued for their skills, experience, and unique perspectives. Every employee’s role in creating an inclusive culture is to demonstrate respect for colleagues and customers and recognize the broad range of ideas and viewpoints that are being contributed to the company every day. We work to increase awareness of diversity issues through integrity and accountability, and swiftly correct behaviors that are toxic, offensive, retaliatory, or exclusive. We strive to ensure that any environment our team members work in provides an atmosphere of inclusion, achieved through open-door policies, whistleblower protection, organizational training, and transparency. Equal Opportunity Employer (EOE): We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. HazTek will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.HazTek Inc. is one of the nation’s largest and most experienced occupational health and safety management firms. We are known for our professional consulting services and premium safety training and we are trusted for our effectiveness in keeping workers safe today – so employees and businesses will be here tomorrow. \r\n\r\nOur team is dedicated to safety and saving lives through our Core Values of integrity, compassion, dependability, support, and accountability. This is an opportunity to be surrounded by fellow individuals who are dedicated to safety.\r\nWe offer competitive compensation and a great benefits package including, but not limited to, medical, dental, life insurance, long-term disability, paid time off, 401(k), professional development, and education assistance\r\n\r\nHazTek Inc. is committed to building an environment of inclusion and acceptance that values diversity across all areas of the organization — an environment in which all employees have an opportunity to participate and contribute to the success of the business and are valued for their skills, experience, and unique perspectives. \r\n\r\nEvery employee’s role in creating an inclusive culture is to demonstrate respect for colleagues and customers and recognize the broad range of ideas and viewpoints that are being contributed to the company every day.\r\n\r\nWe work to increase awareness of diversity issues through integrity and accountability, and swiftly correct behaviors that are toxic, offensive, retaliatory, or exclusive. We strive to ensure that any environment our team members work in provides an atmosphere of inclusion, achieved through open-door policies, whistleblower protection, organizational training, and transparency.\r\n\r\nEqual Opportunity Employer (EOE): We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. HazTek will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

Job Description We are a full-service community bank with branch locations in New York and New Jersey. Each day, Northfield Bank upholds our mission to be the financial institution of choice for individuals and businesses by delivering innovative products and exceptional customer service. Founded in 1887, the Bank has always been proud of being “locally grown,” and credits our strength to our dedication to our customers and the communities that we serve. Job Title: Bank Secrecy Analyst (BSA) Job Location: BSA Department - Woodbridge, New Jersey Job Status: Full Time Job Summary: The BSA Analyst is responsible for collecting, analyzing and reporting on customer and account information in relation to all aspects of the Bank Secrecy Act, Sanctions laws and regulations, including USA Patriot Act. The incumbent must maintain a working knowledge of all policies, procedures and regulations to conduct in-depth analysis and investigations of suspicious activity. Responsibilities Include: • Review daily reports of customer transactions to identify potential fraudulent accounts or activities to be investigated, • Prepare monthly reports to review assigned alerts from the Anti-Money Laundering (AML) system and then conduct timely and detailed investigations of suspected fraudulent accounts or activities using internal and external resources. Document investigations and draft Suspicious Activity Report (SAR), when necessary., • Exercise sound judgment when examining sensitive account activities and escalate issues and concerns to management, as appropriate, • May interface with other departments and branches regarding customer activity and investigations, • Conduct all background research, analysis, and due diligence that will be included in summary section of the SARs, and record all transaction detail through thorough documentation, • Assist in the implementation of new methods, processes and procedures to make daily operations more efficient, • Responsible for complying with all relevant bank policies and procedures including the Bank Secrecy Act, Anti-Money Laundering, and government compliance, • May require occasional travel for business meetings or training Job Requirements: • High school diploma or equivalent required. Bachelor’s degree preferred., • Minimum of 2 years experience in BSA monitoring or related function preferred, • Knowledge of BSA regulations preferred, • Experience with Fiserv FCRM Anti-Money Laundering systems preferred, • Ability to analyze and interpret data to determine the risk associated with moderate to high-risk transactions required, • Knowledge of internal controls, • Effective written and verbal communication skills, • Must work timely and accurately very deadline oriented and organized, • Proficiency in Microsoft Office, Word, Excel, and Outlook Salary Pay Range: $33.65-38.46/hour (This range is for informational purposes only. Offer of employment will be made based on level of experience and skill qualifications within this range) **Equal opportunity employer-vets/disabled.

Job Description * HUMAN RESOURCES MANAGER The HORIBA Group, which consists of 47 companies in 28 countries and regions, provides analytical and measurement solutions throughout the world. Our business is evolving with our innovative analysis and measurement technologies in the three megatrend fields of Energy & Environment, Bio & Healthcare, and Materials & Semiconductor, which are essential to our lives. Our technologies are employed in various areas, including the utilization of hydrogen and other new energy sources, carbon dioxide capture, research & development and quality control in the pharmaceutical field, as well as the advancement of semiconductor manufacturing processes. We believe it is our mission to contribute to creating a sustainable society by offering optimal solutions for customers’ needs. With our corporate motto of “Joy and Fun” we have incorporated the desire to spend our days with more Joy and Fun into our company principle, in the spirit handed down since the company was founded. Around the world, there are approximately 8,900 HORIBARIANs (our term for HORIBA employees) who embody their own unique spirit of “Joy and Fun”. HORIBA Instruments Incorporated is looking for the ideal individual to join our team as Human Resources Manager at our Piscataway, NJ office. Key Responsibilities include: • Culture and Engagement: Educate employees on HORIBA’s philosophy, culture, policies and practices, fostering a work environment that encourages and provides for open and productive communications; consistently deliver excellent customer service and demonstrates respect, initiative, and follow-through in each encounter with internal and external customers and other business contacts., • Strategic Partnership: Become a key resource to employees and leadership team and collaborate with business leaders to understand key objectives and organizational challenges in order to develop and align supportive HR strategies., • Employee Development: Partner with leadership to establish succession planning and conduct needs analysis to determine training needs and oversee, including sourcing, developing and delivering, training programs focused on career development., • Talent Acquisition: Work with leadership team to identify talent needs and build plans to recruit, develop and retain key talent; oversee full recruitment cycle of sourcing, screening, selection and effectively onboarding new team members., • Performance Management: Support managers to establish team performance goals and identify opportunities to coach employees and create development plans to enhance employee skills performance., • Employee Relations: Facilitate conflict resolution and coach managers on how to effectively address and resolve complex employee matters; conduct investigations of internal/external complaints., • HR Policies and Compliance: Ensure company policies and procedures are up-to-date and compliant with local, state and national regulations; provide guidance to employees and management on interpretation and application of human resources policies, ensuring consistency and balance between company and employee concerns., • Compensation and Benefits: Administer compensation processes that ensure competitiveness in attracting and retaining employees and provide equity based on job requirements and employee skill-level; educate employees about health insurance and other programs and assisting employees to ensure claims are processed correctly. Key Requirements Include: • Excellent customer service, communication, organizational, strategic thinking and problem-solving skills, with the ability to build effective relationships at all levels of the organization., • High level of integrity and confidentiality as well as initiative., • Proven leadership and demonstrated ability to develop and implement HR strategies that drive business results., • Possession of strong employee relations and talent management skills, as well as knowledge of local, state and federal regulations and human resources best practices., • 10+ plus years of progressively responsible generalist human resources experience including at least five years of on-site HR management., • Proficiency in Microsoft 365 and ADP Workforce Now HRIS., • Bachelor’s degree in human resources, business administration or a related field or equivalent experience; master’s degree and HR certification a plus., • Some domestic travel will be required. Compensation Package: HORIBA Instruments Incorporated offers a competitive compensation package that includes a 401(k) plan with match; employee group dental, vision, life, and disability (short and long-term) paid for by the company; medical insurance, family dental and vision insurance, and supplemental life insurance available with reasonable employee contributions; employee assistance program; paid holidays, vacation, and sick time; flexible spending accounts; and educational reimbursement and commuter benefit programs. Qualified candidates can expect to earn between $110k - $125 in this role, depending on experience. If you are an individual with a disability and need an accommodation during the application/hiring process, please email or call (949) 344-0152 for assistance. HORIBA will provide reasonable accommodations, upon request, to support individuals with disabilities to be able to participate in the hiring process. HORIBA is committed to making our workplace accessible for individuals with disabilities. Proud to be an Equal Opportunity Employer – EEO/Veteran Status/Disabilities

Job DescriptionSafety ManagerAbout Our Client Our client is a respected leader in the construction industry, committed to building excellence while maintaining the highest standards of safety and integrity. With over 20 years of experience specializing in commercial, manufacturing, and data centers, they have built a reputation for quality and reliability. They're seeking a dedicated Safety Manager to help ensure their work environments remain safe and compliant. Position Overview We are seeking a full-time, onsite Safety Manager to oversee health and safety programs across our construction projects. The successful candidate will develop, implement, and monitor safety protocols that protect our team members while maintaining productivity and quality standards. Key Responsibilities • Develop, implement, and enforce comprehensive safety programs and policies in compliance with OSHA regulations and industry best practices, • Conduct regular site inspections to identify potential hazards and ensure regulatory compliance, • Lead safety training sessions and toolbox talks for employees at all levels, • Investigate incidents, accidents, and near-misses to determine root causes and implement corrective actions, • Maintain accurate safety records and prepare required documentation and reports, • Collaborate with project managers and superintendents to integrate safety considerations into project planning, • Stay current with changes in safety regulations and recommend program updates accordingly, • Serve as the primary liaison with regulatory agencies during inspections or investigations, • Create and foster a culture of safety awareness throughout the organizationQualifications, • Bachelor's degree in Occupational Safety and Health, Construction Management, or related field preferred, • 3+ years of safety management experience in the construction industry, • Thorough knowledge of OSHA construction regulations and industry safety standards, • OSHA 30-hour certification required; additional safety certifications (CSP, CHST, etc.) strongly preferred, • Experience developing and delivering safety training programs, • Strong analytical and problem-solving skills, • Excellent written and verbal communication abilities, • Proficiency with safety management software and Microsoft Office applicationsPhysical Requirements, • Ability to access all areas of construction sites, including climbing ladders, navigating uneven terrain, and entering confined spaces when necessary, • Capable of wearing required personal protective equipment, • Valid driver's license and ability to travel between multiple project sites as neededWhat We Offer, • Competitive salary based on experience and qualifications, • Comprehensive benefits package including health insurance, retirement plan, and paid time off, • Opportunities for professional development and continuing education Our client is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law. Our client is an EEOC Employer and encourages all minority groups to apply. By applying to this job, as part of our typical recruiting process, from time to time, we may contact you regarding positions that we feel are a good fit for you or engage with you during the recruiting process via SMS text message. Message and data rates may apply, depending on your mobile phone service plan. At any time you can get more help by replying HELP to these texts, or you can opt-out completely by replying STOP. Our Terms of Service are available at . Powered by JazzHR GgLi8n2hXz

Job DescriptionSpeech Pathologist needed for a contract-to-hire opportunity with Yoh Scientific’s client located in New Brunswick, NJ. Open to candidates interested in direct-hire only. This position is for a major public research university and the ideal candidate is someone with a master's degree in Speech-Language Pathology and a New Jersey State Speech-Language Pathology license and Speech Language Specialist Standard Certificate. Requires ASHA Certificate of Clinical Competence (CCC) or Clinical Fellow (CF). Responsibilities Among the key duties of this position are the following: • Conducts comprehensive assessments of the language, communication, feeding, and social needs of the students enrolled at the DDDC., • Analyze and interpret diagnostic data, including standardized and non-standardized tests, observations, and parent/teacher input., • Develop and implement specific therapeutic interventions (programs)., • Provide direct and indirect therapy services, individual or small groups., • Monitor and document student progress, adjusting interventions as needed., • Participate in IEP meetings and parent conferences., • Master's degree in Speech-Language Pathology or an equivalent education., • Requires a New Jersey State Speech-Language Pathology license and Speech Language Specialist Standard Certificate., • Requires ASHA Certificate of Clinical Competence (CCC) or Clinical Fellow (CF)., • Preferred, 2 years of experience to include experience with students with autism, • Requires good communication and interpersonal skills, and computer literacy., • Selected candidates will be subject to a criminal history background check. In accordance with New Jersey State law, applicants must agree to undergo and authorize the University to conduct fingerprint, criminal history and/or child abuse record checks with various law enforcement agencies, including, but not limited to: the Federal Bureau of Investigation, Identification Division and/or the New Jersey Division of State Police, Bureau of Identification. Applicants must also assume any costs incurred by the University associated with the background investigations, whether required by statute or not., • In accordance with state mandated requirements, candidates must be able to provide documentation of a negative Mantoux test or will be administered to the successful applicant to verify the absence of tuberculosis. In addition, the successful applicant, at the cost of the University, will be required to be inoculated against Hepatitis B unless the successful applicant waives this vaccination in writing., • Employees must be physically active and be on foot most of the day. Duties may involve running and playing active games with individuals with autism (ages 3 1/2 – 21 years). Following training must be physically capable of safely providing crisis management techniques including restraining, lifting, blocking individuals with challenging behavior. Individuals in this position must be able to withstand blows to the chest, head, and other areas, and must be able to assist and lift physically restrain individuals with developmental disabilities., • Assists in providing behavioral programs for students with severe behavior challenges. Salary: $45 - $50 per hour depending on experience. Recruiter: Ery Baniqued What’s In It For You? We welcome you to be a part of one of the largest global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. • Medical, Dental & Vision Benefits, • 401K Retirement Saving Plan, • Life & Disability Insurance, • Direct Deposit & weekly ePayroll, • Employee Discount Programs, • Referral Bonus Programs Yoh makes finding and applying for jobs simple. Partner with Yoh to find the right opportunities across multiple industries in the US and UK. Find out more here! Estimated Min Rate: $45.00 Estimated Max Rate: $50.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week), • Health Savings Account (HSA) (for employees working 20+ hours per week), • Life & Disability Insurance (for employees working 20+ hours per week), • MetLife Voluntary Benefits, • Employee Assistance Program (EAP), • 401K Retirement Savings Plan, • Direct Deposit & weekly epayroll, • Referral Bonus Programs Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Company DescriptionFounded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day & Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations. Company Website: in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day & Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.\r\nCompany Website:

Job Description iCreditWorks, one of the fastest-growing FinTech platforms in the United States, offers innovative “Point-of-Sale” (POS) lending and digital payment technologies, including the first-in-market native mobile App that reinvents B2B/B2B2C lending. We seek an experienced, BSA-fluent Senior Compliance Specialist to support our Compliance function. Reporting to the Chief Compliance Officer (CCO), the role is ideal for a seasoned BSA professional who thrives in a dynamic environment and takes ownership of complex regulatory matters. The ideal candidate should be detail-oriented and organized, with a strong business acumen. Excellent written and verbal communication skills are essential. iCreditWorks is a fast-paced environment and managing multiple projects under concurrent deadlines is the norm. What You’ll Do • Monitor daily transactions and alerts for suspicious activity using AML software systems., • Investigate potential suspicious transactions and escalate cases as appropriate., • Prepare suspicious activity reports in a timely and accurate manner., • Conduct enhanced due diligence (EDD) reviews on high-risk customers., • Assist with the Customer Identification Program (CIP) and Customer Due Diligence (CDD) processes., • Review OFAC alerts and ensure compliance with sanctions screening., • Maintain accurate records and audit trails of investigations and decisions., • Participate in internal and external audits and regulatory examinations., • Assist in updating BSA/AML policies and procedures., • Stay current with regulatory changes and industry best practices. Desired Qualifications: • Bachelor's degree in Finance, Criminal Justice, Business, or a related field; equivalent work experience may be considered., • 2+ years of experience in BSA/AML compliance, preferably in a financial institution., • Strong understanding of the Bank Secrecy Act, USA PATRIOT Act, OFAC, and related regulations., • Strong analytical, investigative, and writing skills., • Ability to work independently and manage multiple priorities under tight deadlines. Compensation Competitive compensation based on experience and includes health, dental, and vision insurance plus 401k plan. Company DescriptioniCreditWorks, one of the fastest-growing FinTech platforms in the United States, offers innovative “Point-of-Sale” lending and digital payment technologies, including the first-in-market native mobile App that reinvents B2B/B2B2C lending.iCreditWorks, one of the fastest-growing FinTech platforms in the United States, offers innovative “Point-of-Sale” lending and digital payment technologies, including the first-in-market native mobile App that reinvents B2B/B2B2C lending.

Job DescriptionJob Title: Aseptic Technician Job Description The Aseptic Technician will be responsible for supporting the production of sterile injectable pharmaceutical products in accordance with cGMP, FDA, and quality standards. This role involves operating, cleaning, and maintaining aseptic manufacturing equipment while adhering to strict safety, quality, and documentation practices. The technician may be assigned to various activities within Granulation, Blending, Compression, Coating, Dispensing, Sterile Manufacturing, or Technical Service. Responsibilities • Follow all policies, SOPs, and regulatory requirements for pharmaceutical manufacturing., • Perform aseptic gowning and operate within classified cleanroom environments (ISO 5–7)., • Set up, clean, and operate production equipment including autoclaves, depyrogenation tunnels, sterile filling machines, and lyophilizers., • Manufacture products according to cGMP and GDP standards, ensuring accuracy and compliance in all documentation., • Conduct inventory checks and maintain adequate consumable stock levels., • Partner with Quality Assurance for line clearance and with Engineering for equipment/facility issues, ensuring timely work order follow-up., • Participate in training programs; serve as a trainer/mentor for new operators as assigned., • Support deviation investigations, CAPAs, and continuous improvement initiatives.Essential Skills, • 2-3 years of Aseptic Gowning experience in sterile processing., • Pharma GMP experience in Compounding, Mixing, Blending, and Compressing., • Strong documentation skills., • Be alert and present, with abilities in sterilization, visual inspection, production, cGMP, assembly, and filling.Additional Skills & Qualifications, • High school diploma or equivalent; further technical/scientific education preferred., • Experience in sterile pharmaceutical manufacturing strongly desired; sterile injectable experience preferred., • Knowledge of pharmaceutical manufacturing equipment and aseptic processing principles., • Ability to troubleshoot technical issues in assigned production areas., • Strong communication skills with the ability to work effectively across departments., • Flexibility to work shifts, weekends, and overtime as required.Work Environment Work is primarily performed in cleanroom/manufacturing environments (Grade A/B, ISO 5–7). The position requires aseptic gowning, standing for extended periods, lifting up to 50 lbs, and repetitive manual tasks. There is exposure to sterilization equipment and regulated production processes. The department is growing and offers a family-like environment with a lot of opportunities available, including shifts from Monday to Friday, 7:00 AM to 3:30 PM. Job Type & Location This is a Contract position based out of Cranbury, New Jersey. Pay and Benefits The pay range for this position is $28.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in New Brunswick,NJ. Application Deadline This position is anticipated to close on Sep 12, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Are you highly motivated, hard-working, and seeking to join a growth-focused consulting & engineering firm? Are you looking for a company that will invest in your development and grow your professional skills? If so, consider a career with Apex! Powered by record sales, extraordinary client retention, strategic acquisitions, and an entrepreneurial spirit, Apex Companies is one of the fastest growing engineering and environmental consulting firms in the US. We were recently recognized by the Zweig Group as one of the fastest growing firms in the AEC industry. We take pride in providing our clients with exceptional service and have earned numerous awards for project excellence. We continue to grow, and we want you to grow with us. Position: Industrial Hygiene Professional Industry: Science Technical Location: Iselin, NJ Apex Companies, LLC seeks candidates for a full-time, experienced Certified Industrial Hygienist (CIH) or certified-eligible, to provide personnel and area exposure assessment services to local, regional, and national clients. Qualified candidates must have the skill, technical experience and training to self-perform or manage industrial hygiene projects ranging from small to large. All candidates must be capable of researching and accurately referencing standards (e.g., OSHA, ACGIH, etc.) and have a working knowledge of health and safety regulations and best practices. Additional requirements include developing cost estimates, preparation of proposals and sampling plans, advising and mentoring junior level staff as well as managing/interfacing with clients (building of relationships). Strong interpersonal and writing skills are necessary. OSHA and previous consulting experience are required. Your Responsibilities as an Industrial Hygiene Professional: You will be responsible for evaluating workplace health exposure risks for a wide variety of clients in various industries. Qualified candidates should have experience performing the following tasks: • Conduct qualitative exposure assessments, including basic characterization, identification of similar exposure groups, and development of sampling plans., • Plan and conduct industrial hygiene sampling surveys for chemical, physical and biological hazards., • Interpret exposure monitoring results and develop appropriate recommendations to control exposures., • Author detailed technical reports supported with sampling, analysis, and/or evaluation data; citation of applicable references, and recommendations to remove or manage the exposure risk., • Recognize and investigate the potential for health effects associated with chemical agents without authoritative occupational exposure limits., • Defines fundamental concepts of inferential and deterministic statistics in order to select appropriate statistical tools (both parametric and non-parametric) to determine exposure outcomes., • Applies statistical techniques to analyze exposure trends over time., • Defines strategies for ongoing exposure monitoring to assure timely identification of deviations in exposure profiles and to ensure controls continue to be effective., • Assesses compliance with state and/or federal health-based standards., • Develops and presents industrial hygiene training programs at client sites., • BS in Industrial Hygiene, Environmental Science, or other related field., • Client facing skills with ability to grow opportunities., • MS or MSPH or MPH preferred but not needed., • 5-8 years of experience providing industrial hygiene consulting services or management of industrial hygiene programs including technical writing, technical oversight, and project management., • Certification or eligibility to earn certification in the comprehensive practice of industrial hygiene (CIH) from the American Board of Industrial Hygiene., • Ability to mentor and train staff., • Strong technical writing and communication skills., • Strong safety awareness and a good record and understanding of safe work practices., • Proficiency with Microsoft Office suite. Why you'll love working with us: • Company-subsidized medical and dental, • Company-paid life, short, and long-term disability, • 401k match, tuition assistance, and more, • Cross-training and the ability to work on a variety of projects, • Performance-based bonuses or other incentives, • Working with the best and brightest in the industry, • 1,700+ employee national firm with 50+ locations across the US Apex Job Title: Project Manager Annual Expected Pay Range$115,000—$120,000 USD We believe in equality for all and celebrate the diversity and differences of our employees, customers, and communities. We do not discriminate based on gender, race or color, ethnicity or national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status, or any other applicable characteristics protected by law. Apex aims to make apexcos.com accessible to all users. If you have a disability or special need that requires accommodation to navigate our website or complete the application process, please contact or (301) 417-0200. Likewise, feel free to reach out to us if you would like to view or discuss Apex policy related to equal employment opportunity or have any related concerns. EO/AA/VEV/Disabled Employer TO ALL RECRUITMENT AGENCIES: Apex Companies does not accept unsolicited agency resumes. Please do not forward resumes for any of our job postings to our career's sites, or to any employees of Apex Companies or affiliates. Apex Companies is not responsible for any fees related to unsolicited resumes.

Job Description Job Title: Compliance Officer Reporting Supervisor: Director of Compliance Position Summary: The Compliance Officer is tasked with instituting proactive systems and methods to include quality, risk & incident management as well as investigations and plans of correction. The overarching responsibility of this position is to eliminate any perils, exposure and liability that could negatively impact or harm APluscare, employees, or the individuals in their care. This professional must implement policies based on DDD and other regulations and ensure the health, safety and welfare of all stakeholders. Job Duties: ● Ensures quality of life of the client served and protected by minimizing risk to the entire Agency and surrounding community. ● Conducts spontaneous and scheduled visits and inspections. ● Creates and revises systems and procedures by analyzing compliance policies and practices. ● Identifies potential weaknesses and risks in operations, documenting needs for improvement, creating corrective plans, and ensuring correction. ● Review Practices on an ongoing basis to ensure prevention of incidents or violations. ● Audits and corrects employee documentation at the residential or individual/ client level. ● Reviews and updates internal policies; recommends and formulates policies, procedures and guidelines. ● Responds to internal and external inquiries related to licensing and compliance issues. ● Creates and maintains compliance and audit documents. ● Resolves compliance and risk problems by analyzing regulations and identifying solutions. ● Facilitates Agency governance filings, licensing, registrations and corporate records for oversight entities. ● Assists in the development and implementation of corporate governance policies, guidelines and templates. ● Maintains professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies, as applicable. ● Responsible for compliance activities to include reporting, risk assessments, training and follow up reviews of compliance investigations and notifications. ● Responsible for ensuring that all employees receive all required trainings upon hire and annually thereafter. ● Responsible for ensuring that additional employee development opportunities are available on an ongoing basis to all staff. ● Attends Agency and departmental meetings, trainings, and activities. ● Operates Agency vehicles in accordance with agency standards and policies. ● Is available for after hours on-call duties for urgent facility matters. ● All other duties as requested or assigned by APluscare. Skills/Qualifications: ● Bachelor's Degree is required. ● 3 to 5 years progressive and comprehensive experience or training in internal auditing and regulatory compliance in healthcare. ● Certified in Healthcare Compliance (CHC) by the Health Care Compliance Association preferred. ● Must possess thorough knowledge of laws, rules and regulations pertaining to DDD and provider operations (including Stark, antikickback and other fraud and abuse laws), and principles, practices and techniques of compliance management, including program planning and implementation, fiscal/financial analysis and basic accounting. ● 1-3 years of experience working in the field with individuals with developmental disabilities. ● 2+ years of experience in health care administration. ● Valid Driver's License ● Excellent verbal and written communications. ● Employee must cooperate with the licensee and DHS department staff in any inspection or investigation. ● Employee must successfully complete and demonstrate proficiency in all areas of required training. ● All other duties as required or assigned by APluscare. Physical Demands/Working Conditions: ● Handles detailed work and highly complex problems, balancing multiple tasks simultaneously. ● The ability to effectively communicate (orally and written) and interact with others, including diverse, inter-disciplinary, cross-functional teams ● The ability to read, concentrate and learn ● Physical requirements include: sitting, standing, lifting up to 50lbs, and computer work for long periods of time ● The ability to verbally express ideas in a way that is easily understood by others who are unfamiliar with the topic, including delivering a presentation, giving accurate information or acting as a spokesperson. ● The ability to write concisely and convey meaning in a manner appropriate to different readers, presenting a persuasive argument. ● The ability to handle numbers, gathering statistical data and being able to analyze, interpret and present it in a clear and accurate way. ● Flexible team player who thrives in environments requiring ability to effectively prioritize and juggle multiple concurrent projects. ● The ability to apply clinical knowledge to program implementation and educational development of staff. ● The ability to design, plan, organize, and implement projects and tasks within an allotted timeframe. ● Support and maintain all corporate policies, procedures, and quality and confidentiality standards ● Duties and responsibilities may be added, deleted or changed to meet the needs of the organization

Job Description Hey! We are looking for great candidates who have a great eye for detail! We are looking for a Quality Assurance Specialist in Somerset, NJ. This is a Monday-Friday, 8 am 5 pm position. Must have 2+ years of experience in quality assurance or quality control. Main duties: This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. Responsibility: -Conduct inspections and statistical audits of incoming textile shipments -Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments. -Document inspection results and maintain accurate quality records and reports -Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance. -Assist in the development and refinement of QA/QC procedures and standards -Analyze quality data and trends to support continuous improvement initiatives. Experience required: • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash, • Proficiency in Microsoft Excel and data entry/reporting tools. Position offers benefits such as health, dental, and vision! Ambassador Personnel, Inc. is an Equal Opportunity Employer. We do not discriminate based on race, color, national origin, religion, sex, disability status, protected veteran status, gender identity, or any other attribute protected by law.

Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description We are seeking an experienced and highly motivated Raw Material Chemist to join our team. As a Raw Material Chemist, you will play a critical role in the testing, evaluation, and quality control of raw material samples. Your expertise will drive product innovation, quality assurance, and cost-effectiveness while ensuring compliance with industry regulations. Key Responsibilities: • Conduct detailed chemical and physical analyses of raw materials using techniques such as the following, including but not limited to:, • Spectroscopy (FTIR, UV-Vis), • Chromatography (HPLC, GC, TLC), • Dissolution, • Potentiometric Titrations / Assay, • Viscosity, • pH, • Conductivity, • Karl Fisher, • Specific Gravity, • Loss on Drying, • Residue on Ignition, • Oversee the quality control of incoming raw materials and ensure their compliance with company standards. Troubleshoot any material-related issues., • Proven ability to analyze raw material issues, identify root causes, and implement effective solutions., • Strong experience with HPLC and GC testing/techniques and Empower software, • Ability to troubleshoot instrument / equipment issues, • Perform method verifications / validations on new methods, • Perform calibration of instrument / equipment, • Maintain meticulous, accurate and precise records of specifications, test methods, testing data, results, and any deviations from standard procedures., • Evaluate test results for accuracy, • Review / Release raw data, documentation and results for Certificate of Analysis, • Prepare detailed reports for management and regulatory purposes., • Author / revise technical documents including but not limited to specifications, test methods, method verification / validation / transfer protocol or reports, SOPs, investigations, etc., • Ensure that all raw materials comply with industry regulations and safety standards, • Knowledge of current GMP, FDA regulations, ICH guidelines, ISO 17025 and other regulatory requirements as applicable., • Working knowledge of computer skills., • Strong attention to detail, ensuring accurate and precise testing and documentation., • Excellent written and verbal communication skills to effectively report findings and collaborate with cross-functional teams., • Ability to maintain a safe, clean, and orderly laboratory environment., • Ability to work independently and as part of a team, with minimal supervisionQualifications, • Education: Bachelor’s / Master’s degree in Chemistry or other science related field, • Experience: Bachelor’s: Minimum of 6 years or Master’s: Minimum of 4 years of experience in a raw material, chemistry, or quality control role, preferably in pharmaceuticals, manufacturing, cosmetics. Additional Information Positions are full-time, working Monday-Friday 8am-5pm, overtime as needed. Candidates currently living within commutable distance to North Brunswick, NJ are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options • Annual compensation between $90,000 and $100,000, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Job Description Date 02/2024 Location 1300 Airport Road, North Brunswick NJ Title Lead, Quality Control Chemist Department Quality Control Reports to Manager, Quality Control Laboratory FLSA (Exempt or Non-Exempt Exempt Role Overview The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains & organizes testing’s and compliance while working in a fast-paced environment with changing priorities. Areas of Responsibility • Performs assigned sampling, physical, chemical tests and assay on raw materials, active dietary ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer., • Troubleshoots HPLC, GC, QC instruments for specific tests in order to assist in determining the root cause of aberrant results and help in performing Lab investigations / OOS., • Evaluates daily raw data sheets for product samples and release, if needed., • Coordinates annual review of STPS / SOPS as per USPL procedures., • Prepare new methods and test procedures for new or existing raw materials and finished products., • Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements., • Perform floor supervision of QC Chemists for routine testing, if required., • Prepares and reviews QC related documents during and finishing of testing of sample. Submit all testing related documents like data sheets, chromatograms, spectras, instruments print outs in timely manner to Qc Documentation department to release the batch of raw material / finished product., • Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned., • Performs maintenance and calibrations of laboratory instruments /equipment, if required to help in-house calibrations., • Assures GMP compliance according to FDA CFR Part 111 and USPL SOPs / guidelines., • Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, GLP, documentation) when performing the assigned activity., • Trains new QC Chemists to perform instrumental testing., • Must be able to work extended hours as needed and occasional weekends., • Works in a safe and responsible manner to create an injury-free and incident-free workplace., • Complies with all job-related safety and other training requirements. Education & Qualification: • BS/MS in Chemistry or related scientific disciplines., • Five (5) years of basic chemistry techniques (can be academic) is a plus., • Ability to maintain integrity and honesty at all times and to communicate with transparency., • Ability to work independently or as part of a team., • Solid understanding of cGMP’s and GLP and is familiar with 21 CFR Part 11., • Strong working knowledge of Microsoft Word, Excel., • Good documentation practices and able to write simple, clear reports., • Meets commitments on time and practices time-management skills., • Seeks to identify continuous improvement needs., • Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters, • Ability to navigate office, lab, and/or plant floor working environments., • Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment., • Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators., • Work is regularly performed inside a laboratory environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents., • May execute up to 20% of their work at the bench level either standing or sitting on a stool., • Work performed in a standard office environment is without unpleasant or hazardous conditions. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Office Hours: 8:30 AM - 5:00 PM 9:00 AM - 5:30 PM

Job DescriptionObjective Reporting to the Senior Director, CMC Operations, the Scientist, GMP Data Reviewer & Technical Writer is responsible for supporting Perspective Therapeutics’ pipeline of radiopharmaceutical products, including radioisotope-labeled peptides and related biologics. This individual will lead and support phase-appropriate analytical method development, validation, and qualification activities. In addition, the role requires thorough review and interpretation of analytical data for raw materials, in-process controls, and finished product testing in compliance with GMP expectations. Working in a fast-paced, integrated, and multidisciplinary environment, the successful candidate will bring a deep understanding of analytical instrumentation, regulatory standards, equipment qualification, method lifecycle management, and GMP documentation. The individual is expected to collaborate cross-functionally while also delivering strong independent contributions that support product advancement from clinical development to commercialization.Essential Functions • Lead or contribute to analytical method development, validation, and transfer efforts for clinical and commercial programs., • Review, interpret, and approve raw data, laboratory reports, and validation documentation for accuracy and compliance with applicable GMP and ICH guidelines., • Troubleshoot analytical issues and propose scientifically sound solutions in collaboration with internal teams and external partners., • Contribute to cross-functional investigations (e.g., deviations, OOS, OOT) and author supporting documentation., • Draft and revise technical protocols, method validation plans, SOPs, and final reports., • Serve as subject matter expert for analytical instrumentation and associated software (e.g., HPLC, GC, UV-Vis, LSC)., • Collaborate with QA, QC, Manufacturing, and Regulatory teams to ensure project milestones and submission timelines are met., • Support audits, inspections, and regulatory filings by providing documentation and responding to analytical inquiries.QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.Education/Experience, • M.S in Analytical chemistry with 3+ years of relevant industry experience, or B.S. in Analytical Chemistry or related field with at least 5+ years of relevant industry experience in an FDA regulated laboratory environment., • Minimum of 5 years of experience working in an FDA-regulated laboratory environment, with a strong understanding of cGMP standards., • Deep expertise in regulatory frameworks (FDA, EMA), and commercial manufacturing compliance, with strong emphasis on quality, safety, and environmental impact., • Demonstrated hands-on experience with method development and validation per ICH Q2 guidelines., • Strong working knowledge of US and EU regulatory expectations for analytical controls and data integrity., • Familiarity with quality systems, electronic lab systems, and document management systems., • Experience in radiopharmaceuticals or isotope-based therapeutics is strongly preferred., • Experience with MS Office Suite required.Knowledge / Skill / Ability, • Strong working knowledge of method validation principles, equipment qualification (IQ/OQ/PQ), and GMP laboratory operations., • Experience reviewing data in alignment with GLP/GMP requirements, with a focus on accuracy, traceability, and compliance., • Ability to prepare detailed study protocols and interpret complex datasets across multiple techniques., • Excellent communication skills, including the ability to explain technical concepts to cross-functional teams., • Prior radiochemistry experience and knowledge of radioactive material handling are a plus., • Strong organizational skills, with the ability to manage multiple priorities and meet tight deadlines., • Availability for occasional off-hours or weekend work as needed to support critical timelines.Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions., • Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels., • May be required to sit or stand for long periods of 8+ hours a day while performing duties., • Willingness to complete safety training within allotted time limits, and work in a team-based environment. Yqz0Dt86qX

Job Description Role Description: The QA Specialist is responsible for managing processes such as (Document Control and Corrective Action and Preventive Action) and conducting quality assurance auditsof the quality management system to ensure compliance with ISO 13485:2016 standard and applicable regulatory requirements. Essential Duties and Responsibilities: · Participates in preparation for and hosting of external audits and FDA inspections in collaboration with the Sr. VP Regulatory Affairs. · Conduct Quality Assurance Audits as scheduled and ensure the effective and timely facilitation of suppliers and internal quality audits and follows-up on CAPAs/Observations. · Assists in the preparation of periodic Management Review meetings which are held to meet regulatory requirements. · Stay current with new or potential business opportunities and prepare for all QA activities. · Manage the POD (Point of Distribution) labeling process for OUS labeling requirements. · Ensures that the Document Control System is maintained including SOPs, methods, production records, change controls, deviations, validation documents, operation manuals, training documents and any other relevant controlled documents in compliance with cGMPs, and international policies and procedures. · Maintains and helps improve current quality systems, processes, tools, policies, SOPs and validations to ensure compliance with regulatory requirements. · Assists with recording and provides regulatory reportability decisions on complaints. · Assists with generating and submitting medical device event reports to appropriate authorities and government agencies as requested and as required by applicable laws and regulations. · Manages the Corrective Action and Preventive Action process and the Non-Conforming Material process. · Performs root cause investigations and is involved in CAPA (Corrective and Preventive Action) activities. · Collects CAPA data and process metrics to capture and generate trend reports. · Review and approve batch production records for accuracy, completeness, and compliance with established procedures. · Analyze sterilization reports and validation data to ensure sterility assurance levels meet regulatory requirements Skills and Competencies: · Interpersonal Effectiveness: Actively seeks to understand perspectives and interpersonal needs and expectations of others at all levels, builds self-awareness, flexes personal style appropriately, and works through conflicts constructively and appropriately · Communication: Effectively uses all mediums of communication as appropriate, presents well to groups, actively listens, and continuously identifies opportunities to build communication skills · Collaboration & Teamwork: Actively works together with formal and informal team members to build relationships and achieve team goals · Prioritization: Effectively prioritizes work to ensure timely completion of work within scope · Technical Expertise: Continuously builds functional and technical expertise, and pro-actively applies that technical expertise in progressively broader scope · Continuous Improvement: Learns and uses best practices tools and methodologies to assess, identify, and executes on opportunities to improve; Focus on learningand building new capabilities into self · Problem Solving & Problem Prevention: Learns and uses strong problem-solving methodologies and tools, focuses on root cause analysis, and shows orientation towards problem prevention · Accountability: Focuses on results, takes initiative without direction, takes ownership for all work within scope, builds relationships and works across departments, functions, or areas of responsibility Role Qualifications (Education & Experience): · Bachelor's degree in technical, scientific, or business-related discipline preferred. · 3 years related work experience as a complaint handler in the medical device industry, performing all duties described above. · Knowledge of medical terms and Medical Device Reporting regulations · Exceptional organizational skills and attention to detail. · Able to perform job function with minimal supervision and work independently, taking initiative to make independent decisions, where appropriate. Physical Demands (if any) as well as how much travel the job requires: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job: · Work safely and follow all OSHA regulations and company safety policies and procedures. · For all on-the-job injuries or accidents, must notify manager/supervisor immediately. · Ability to regularly sit or stand for extended periods of time.

Job DescriptionSalary: $25 - $28 per hour DOE Founded in 1986 and located in Middlesex NJ, BAMCO inc. is an award-winning industry leader in the design, manufacture and erection of building envelope systems servicing the architectural, developer and general contracting communities. We specialize in engineering, custom fabrication, bending, routing, welding and finishing in all types of metals from aluminum, galvanized and stainless to the exotics with a focus on safety, green initiatives and Lean Kaizen principles throughout. Our primary markets are pharmaceutical, health care, industrial, institutional and high-rise office and residential in the northeast corridor for installation and we service all 48 states with design and fabrication offerings as well. BAMCO is a 100% employee-owned company (ESOP) that prides itself with an unparalleled commitment to excellence for our customers, our company and all our stakeholders. We are currently seeking a detail-oriented and hands-onInventory/Materials Coordinatorto maintain inventory operations across multiple local facilities. This role combines inventory management, materials movement, and coordination with purchasing, production and logistics teams. Key Responsibilities • Maintain accurate stock levels, manage reorder points, and lead cycle counts and quarter-end audits., • Track all incoming/outgoing items, document supply movements, and retrieve materials efficiently., • Verify incoming materials, stage for storage and shop use, andpull and prep orders for outbound truck shipments., • Oversee inventory distribution, manage line supply, and coordinate specialty job-related purchases., • Use Excel to monitor trends and support forecasting efforts., • Communicate inventory status with office and field teams; proactively notify when supplies are low., • Maintain organized storage systems and logical inventory layouts., • Manage tagging system, SOPs, and photo documentation., • Ensure accuracy of returned packing slips and interpret vendor codes., • Cooperate in safety programs, initiatives and investigations. Comply with all safety procedures., • Participate in clean-up responsibilities and maintains daily good housekeeping practices according to 5S procedures., • Perform other duties and tasks as required. Required Qualifications: • High School Diploma or GED Equivalent., • 1-3 years experience in inventory management or processes, • Valid drivers license (required for local transport between facilities), • Forklift experience, • Strong organizational and communication skills, • Proficient in Microsoft Excel and warehouse operations Desired Qualifications: • Excellent time management and organizational skills., • Experience working in a collaborative environment promoting a teamwork mentality., • Strong sense of personal accountability. Benefits: • 401(k), • 401(k) matching, • ESOP - Employee Stock Ownership Plan, • Health insurance, • Dental insurance, • Vision insurance, • Life insurance, • Paid time off (Holidays/Vacation), • Professional Development BAMCO inc. is not accepting unsolicited assistance from search firms. All resumes submitted by search firms to any employee of BAMCO inc. in any fashion without a valid written search agreement in place will be deemed the sole property of BAMCO inc. No fee will be paid if a candidate is hired by BAMCO inc. based upon an unsolicited referral. BAMCO inc. is an Equal Opportunity Employer.

Job DescriptionOverview Advance Your Career in Insurance Claims with Allied Universal® Compliance and Investigation Services. Allied Universal® Compliance and Investigation Services is the premier destination for a career in insurance claim investigation. As a global leader, we provide dynamic opportunities for claim investigators, SIU investigators, and surveillance investigators. Our team is committed to innovation and excellence, making a significant impact in the insurance industry. If you're ready to grow with the best, explore a career with us and make a difference. Enjoy comprehensive benefits for most full-time positions, including medical, dental, and vision coverage, life insurance, retirement plans, employee assistance programs, and exclusive perks. Job Description Allied Universal® is hiring a Special Investigations Unit (SIU) Investigator. Special Investigations Unit (SIU) Specialists investigate claims with red flags that suggest fraudulent behavior In relation to an Insurance claim. The SIU Specialist must use their extensive knowledge of Insurance policies and the components of fraud to determine If claims warrant reporting to the appropriate state agency for prosecution. • Must possess a valid driver's license with at least one year of driving experience, • Candidate must reside in state listed in job posting, • Pay Rate: $27 - $32 / hr RESPONSIBILITIES: • Independently investigate suspected fraudulent insurance claims for a variety of coverage to include workers' compensation, general liability, property and casualty and disability, • Acquire and gather information through use of own discretion, and guidance from clients and case managers, by means of data collection, interviews, research and collaboration with other SIU entities, law enforcement and state Departments of Insurance, • Create and maintain detailed documentation for investigations, file reviews, audits, training tasks, consulting projects, and other assignments as directed, • Produce professional and expert reports, memos, and letters that are clear, concise, and grammatically correct, • Run appropriate database indices if necessary and verify the accuracy of results found, • Must possess one or more of the following:, • Bachelor's degree in Criminal Justice, • High School diploma or higher with a minimum of five (5) years of demonstrated professional law enforcement experience with specific attention to investigations related to fraud, • Ability to be properly licensed as a Private Investigator as required by the state where work Is completed, • Post offer, must be able to successfully complete the Allied Universal Investigations training/orientation course, • Minimum of five (5) years of demonstrated experience conducting complex insurance investigations or adjusting complex insurance claims, • Proficient understanding and application of anti-fraud laws, insurance regulations, and compliance standards within their home state and designated regional area., • Proficient in utilizing laptop computers and cell phones., • Special Investigative Unit (SIU) Compliance knowledge, • Ability to type 40+ words per minute with minimum error, • Flexibility to work varied and irregular hours and days including weekends and holidays, • Military experience, • Law enforcement, • Insurance administration experience, • Familiarity with California SIU regulations, • One or more of the following professional industry certifications:, • Certified Fraud Investigator (CFE), • Certified Insurance Fraud Investigator (CIFI), • Fraud Claim Law Associate (FCLA), • Fraud Claim Law Specialist (FCLS), • Certified Protection Professional (CPP), • Associate in Claims (AIC), • Medical, dental, vision, basic life, AD&D, and disability insurance, • Enrollment in our company's 401(k)plan, subject to eligibility requirements, • Seven paid holidays annually, sick days available where required by law If you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: . Requisition ID 2025-1414359

Job Description Come work for a great company at APluscare! The Quality assurance Coordinator is responsible for preserving the standard of the services of the agency. Quality assurance personnel are accountable for assisting to create and execute quality control and management methods and systems. Personnel are accountable for monitoring that the services of the agency meet the standard and are error free. Job Duties: The principal responsibility of quality assurance personnel is to make sure quality of the services provided by APluscare is at the highest level. Quality assurance employees must review the business statistics and then determine areas requiring enhancement. A quality assurance employee should also inspect the samples and formulate policies concerning improvement of the present quality standards. Personnel should ensure that the services take place in accordance with the standards established. Additional responsibilities include all other duties as assigned by APluscare. The Quality Assurance Coordinator is required to: • Oversee and ensure agency's compliance with DDD regulations at all levels of operations., • Demonstrate broad knowledge of New Jersey Division of Developmental Disabilities (DDD) and Department of Human Services (DHS) licensing standards, regulations, and circulars., • Maintain agency's residential/other programs compliance with DDD, DHS, Medicaid, and other applicable state and federal regulations., • Cooperate and coordinate with state and other relevant officials during investigations of incidents that involve APluscare and/or its personnel., • Ensure agency's compliance with applicable federal and state laws, regulations, and licensing requirements., • Ensure agency's compliance with applicable accrediting bodies., • Suggest and participate in policy and procedure development, modification, renewal, as well as adherence while maintaining compliance with applicable requirements., • Provide weekly training and In-service to all staff involved in providing services and supports to clients of APluscare., • Conduct weekly visits and audits of all DDD licensed programs in order to maintain continuous compliance with DDD licensing standards., • Identify program deficiencies for all residential programs on a weekly basis and supervise program staff as needed to correct deficiencies., • Maintain DDD licensure renewal for all agency programs that are licensed by the division., • Maintains all company vehicles including registration, insurance, preventative maintenance, repairs, and equipment inventory according to APluscare policies and licensing standards., • Maintains all licenses/certificates for each APluscare program and prepares homes on a regular basis and for licensing inspections., • Prepare new programs for initial DDD licensing inspection and secure licensure., • Maintain continuous program integrity for all agency programs through quality assurance surveys and reviews., • Track and report on quality-related indicators, including areas of risk management and compliance., • Conduct weekly quality assurance surveys for all DDD licensed programs, • Maintain agency compliance with all local, state, and federal regulations for all agency programs, • Conduct monthly visits and audits of all residential and other programs, • Prepare and submit program integrity and quality assurance weekly report to the Executive Director Identify program deficiencies for all residential and other programs on a monthly basis and supervise program staff as needed to correct deficiencies The Quality Assurance Coordinator is expected to posse s excellent interpersonal skills, including the ability to communicate effectively with in individuals with intellectual and developmental disabilities and their families, colleagues, and other parties as necessary for employment with APluscare. Outstanding negotiation skills, customer-oriented approach, excellent analytical skills, effective leadership capability to lead projects, fundamental knowledge of operational software and understanding concerning concepts, equipment and various other quality management techniques. Employee must cooperate with the officer of licensing and/or any department of Human Service staff in any inspection or investigation • Employee must successfully complete and demonstrate proficiency in all areas of required training., • Valid Driver's License Handles detailed, basic to complex, and specialized concepts and problems, balancing multiple tasks simultaneously. • The ability to effectively communicate (orally and written) and interact with others, including diverse, interdisciplinary, cross-functional teams, • The ability to read, concentrate and learn, • Physical requirements include sitting, standing, walking, and computer work for long periods of time, • Pushing, pulling, and lifting up to 50lbs, • Driving and travel locally and between agency sites and other required locations, • Support and maintain all corporate policies, procedures, and quality and confidentiality standards, • Duties and responsibilities may be added, deleted or changed to meet the needs of the organization

Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

Job Description The Quality Assurance Engineer I is responsible for conducting ongoing analysis of the production process inputs and outputs to ensure that customer quality requirements are being achieved. The Quality Engineer I is expected to: • Maintain SPC limit at or above the corporate target., • Keep customer complaints less than or equal to previous year, • Manage CAR containment and root cause investigation, corrective action plan and completions on time · Collects production data and applies standard scientific and statistical methods to analyze, document, and diagram production processes. Conducts FMEA, DOE, and SPC analysis • Applies GD&T and measurement techniques to review and interpret part print design, quality and intention., • Provides input to the production control systems and designs control activities, • Provides input for new product equipment selection, installation and maintenance, • Identifies opportunities for cost reduction and quality improvements., • Audits work processes and evaluates any non-value-added activities or variations in the processes., • Use appropriate statistical techniques to analyze data and make/recommend decisions, • Participates in root cause investigations and development of corrective action plans. Leads verification and effectiveness activities., • Performs inspections and sets quality assurance testing models for analysis of raw materials, materials in process, and finished products., • Writes detailed work instruction-level documents for Quality and related areas. Trains personnel in these instructions and other technical process controls, • Troubleshoots quality assurance equipment and processes., • Quarantines, documents and evaluates products and materials and generates Material Review Board (MRB) Case(s) as appropriate., • Provides communication to Calibration Technicians of any additions, deletions, or changes to the process gages and equipment, • Ensures control plans and associated documentation are implemented effectively and maintained., • Monitors and reports on quality-related key performance indicators EDUCATION AND EXPERIENCE · Bachelor’s degree in Engineering or a related field is required. · 2-4 years of quality experience in a manufacturing environment or equivalent combination of education and experience is required. LICENSE AND CERTIFICATION · ASQ certification is preferred TECHNICAL SKILLS · Blueprint reading and interpretation · Gage design knowledge · APQP · MSA · PPAP · SPC · GD & T · Automated inspection software · MS Office Suite OTHER SKILLS · Manual dexterity · Spatial dexterity · Problem solving o Root cause analysis o Corrective Action · Multitasking · Written communication · Verbal communication · Organizational skills · Time Management While performing the duties of this Job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk and hear. The employee is occasionally required to stoop, kneel, crouch, or crawl. The employee must frequently lift, push, pull, carry and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing this Job, the employee is regularly required to demonstrate manual and spatial dexterity sufficient to operate machinery for precision work While performing the duties of this Job, the employee is regularly exposed to moving mechanical parts and vibration. The employee is frequently exposed to risk of electrical shock. The employee is occasionally exposed to wet and/or humid conditions and odors, dusts, mists, fumes and/or airborne particles. The noise level in the work environment is usually moderate.

Job Description Job Description: Primary responsibilities of this role include the following: • With Supervision, review documents/records and provide batch release authorization to 3PL service provider for products manufactured outside of the US., • Support Drug Product Complaint management; forwarding to respective drug product manufacturing site and coordinate with corporate QA for investigations., • Support Drug Product Recall/Field alert management., • Assist with review of Quality Agreements., • For applicable products, coordinate with Contract Testing Laboratories for Analytical Method Transfer activities, Drug Product testing, any OOS results, and test method issues., • With supervision, review deviations/investigations related to Strides Pharma Inc. (Strides) frontend products., • Assist with SOP management for Strides’ US corporate office., • Support with quality matters for disposition of product returns., • Excellent verbal and written communication skills are necessary., • With supervision and direction, effectively prioritizes competing tasks in a fast-paced and dynamic environment., • BS degree in Pharmacy, Chemistry, Biology or Microbiology is preferred. 1-2 years of Quality Assurance or related pharmaceutical industry experience is preferred. Recent graduates will be considered for this role.

Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

Job Description The Textile Quality Specialist is responsible for executing quality assurance (QA) and quality control (QC) activities on textile products received from the manufacturer. This role ensures that all products meet established quality standards before distribution to hospitality clients. The position also supports investigations into manufacturing failures and non-compliance issues. The ideal candidate will bring a strong understanding of textile performance, laundry processes, and quality systems, and will be capable of working independently with minimal supervision. Responsibility: • Conduct inspections and statistical audits of incoming textile shipments to verify compliance with product specifications and quality standards., • Perform physical testing of textiles, including test washing, dimensional checks, colorfastness, and durability assessments., • Document inspection results and maintain accurate quality records and reports., • Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues., • Collaborate with suppliers, internal teams, and laundry operations to resolve quality concerns and improve product performance., • Assist in the development and refinement of QA/QC procedures and standards., • Analyze quality data and trends to support continuous improvement initiatives. High school diploma or equivalent; associate degree or technical certification in textiles, quality control, or a related field preferred. Experience: • 2+ years of experience in quality assurance or quality control, preferably in textiles or manufacturing., • Familiarity with textile testing methods and standards (e.g., AATCC, ASTM)., • Experience with laundry processes and evaluating textile performance post-wash., • Proficiency in Microsoft Excel and data entry/reporting tools., • Strong attention to detail and analytical skills., • Ability to work independently and manage time effectively., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment., • This position requires travel between multiple local facilities., • Primarily warehouse or test laundry-based environment with occasional exposure to production or shipping areas., • May require lifting of textile samples and use of testing equipment.

The position also supports investigations into manufacturing failures and non-compliance issues. Support root cause analysis and corrective action processes for manufacturing failures and non-compliance issues.

Job Description FULL TIME EXPERIENCED WAREHOUSE COMPOUNDER Edison, New Jersey A full-time position is available in our Edison, New Jersey chemical blending plant for an organized, detail oriented, friendly, and adaptable individual. Work for a profitable and private 120 year old, international water treatment chemical company that promotes from within. Garratt-Callahan treats industrial boilers and cooling towers to keep them energy efficient and environmentally friendly. We are registered to ISO 9001:2015 and sell an industry leading line of “green" solutions, G-C GreenTech. The Edison plant prepares and blends chemicals for our customers in the Northeast Region of the United States. The hours for the Compounder position are Monday through Friday, 7:30 AM to 4:30 PM. Salary is $25.00 to $30.00 per hour depending on experience. Benefits are available. Medical, dental, 401k. Duties and Requirements for the Warehouse Compounder position include the following: • The compounder is responsible for the production of liquid and dry materials into finished goods ready for distribution to our industrial customers., • Loads blending tanks with raw materials and blends material into finished product according to work orders., • General warehouse work, including moving totes, drums, and pallets., • General Maintenance work., • Samples and tests finished blended product and records findings. Create work orders, MSDS and labels according to ISO procedures., • Recognizes, applies and responds appropriately to chemical hazard information. Maintains current knowledge of the use and handling of all chemical used in the facility., • Loads finished and tested product into properly labeled containers from blending tanks according to weight, making sure containers are properly sealed so they are leak free and leak proof and ready for shipment., • Places raw material into stocks, and maintains the raw material inventory., • Prepares and labels containers with up to date documents., • Must be able to safely operate and maintain forklift, and maintain forklift records and logbook., • Must be able to operate and calibrate equipment used in testing and weighing manufactured products and record findings into logbook., • Assists with projects and activities for shipping and receiving and with administrative tasks for the Plant., • Must be forklift trained and certified. We offer stability, a friendly work environment, great benefits, stability, and day time working hours. Thank you for considering Garratt-Callahan Company. Garratt-Callahan is an EEO/AAE employer. Minorities and Women are encouraged to apply. If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at 650.697.5811. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan. Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants. Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.

Job DescriptionSalary: $20 - $24 per hour DOE Founded in 1986 and located in Middlesex NJ, BAMCO inc. is an award-winning industry leader in the design, manufacture and erection of building envelope systems servicing the architectural, developer and general contracting communities. We specialize in engineering, custom fabrication, bending, routing, welding and finishing in all types of metals from aluminum, galvanized and stainless to the exotics with a focus on safety, green initiatives and Lean Kaizen principles throughout. Our primary markets are pharmaceutical, health care, industrial, institutional and high-rise office and residential in the northeast corridor for installation and we service all 48 states with design and fabrication offerings as well. BAMCO is a 100% employee-owned company (ESOP) that prides itself with an unparalleled commitment to excellence for our customers, our company and all our stakeholders. We are currently seeking a dependable and safety-consciousMaterial Handlerto join our growing team. This position plays a key role in supporting daily operations by ensuring materials are efficiently moved, stored, and prepared for use. The Material Handler must be capable of organizing and prioritizing materials in coordination with department managers, maintaining a clean and safe workspace, as well as loading and unloading as needed. This role also includes routine equipment inspections and general warehouse support. Key Responsibilities: • Operate forklifts, pallet jacks, and other material handling equipment safely, • Load, unload, and transport materials as needed to support production and ensure smooth workflow, • Bundle and tag completed trim and angle materials; store them neatly in designated areas, • Ensure work areas are clean, organized, and free of hazards both inside and outside the facility with materials easily accessible, • Ensure materials that cannot be stored in wet conditions are properly protected or relocated, • Organize and stage materials for production or shipment, • Follow and implement instructions from supervisors, • Perform daily forklift inspections and submit weekly inspection reports, • Cooperate in safety programs, initiatives and investigations. Comply with all safety procedures., • Participate in clean-up responsibilities and maintains daily good housekeeping practices according to 5S procedures., • Perform other duties and tasks as required. Requirements/Qualifications: • High School Diploma or GED Equivalent., • Previous experience in material handling, warehouse operations, or a similar role, • Ability to lift and move heavy materials safely, • Strong organizational skills and attention to detail, • Ability to follow instructions and work independently or as part of a team, • Commitment to maintaining a clean and safe work environment, • Previous experience operating a variety of powered industrial vehicles, (forklifts, etc.), • Proven ability to accept and apply feedback and directives from supervisors and other team members., • Workers are required to be on time for every shift. Desired Qualifications: • Excellent time management and organizational skills., • Experience working in a collaborative environment promoting a teamwork mentality., • Strong sense of personal accountability. Benefits: • 401(k), • 401(k) matching, • ESOP - Employee Stock Ownership Plan, • Health insurance, • Dental insurance, • Vision insurance, • Life insurance, • Paid time off (Holidays/Vacation), • Professional Development BAMCO inc. is not accepting unsolicited assistance from search firms. All resumes submitted by search firms to any employee of BAMCO inc. in any fashion without a valid written search agreement in place will be deemed the sole property of BAMCO inc. No fee will be paid if a candidate is hired by BAMCO inc. based upon an unsolicited referral. BAMCO inc. is an Equal Opportunity Employer. BAMCO inc. participates in E-Verify.

Job DescriptionSalary: $18 - $23 per hour DOE Founded in 1986 and located in Middlesex NJ, BAMCO inc. is an award-winning industry leader in the design, manufacture and erection of building envelope systems servicing the architectural, developer and general contracting communities. We specialize in engineering, custom fabrication, bending, routing, welding and finishing in all types of metals from aluminum, galvanized and stainless to the exotics with a focus on safety, green initiatives and Lean Kaizen principles throughout. Our primary markets are pharmaceutical, health care, industrial, institutional and high-rise office and residential in the northeast corridor for installation and we service all 48 states with design and fabrication offerings as well. BAMCO is a 100% employee-owned company (ESOP) that prides itself with an unparalleled commitment to excellence for our customers, our company and all our stakeholders. We are currently seeking a Fabrication Operator II to join our growing team. This position reports to the Fabrication Lead. The Fabrication Operator II must be capable of fabricating our complicated aluminum panels independently, have the ability to read drawings and use hand tools. The ideal candidatewill be familiar with the aluminum panel fabrication processes, guide and mentors others, work with line supervisors, and keep up with the workflow in their designated area. Responsibilities: • Follows drawings and/or cutsheets to fabricate multi-bend panels and then Epoxy welds those panels together comprised of two or more pieces., • Trains, mentors and assists new and lower-level crew members, promoting a positive and productive work environment., • Follows and implements instructions from supervisors., • Maintains a steady workflow., • Inspects work performed for adherence to quality standards and project specifications., • Cooperates in safety programs, initiatives and investigations. Complies with all safety procedures., • Participates in clean-up responsibilities and maintains daily good housekeeping practices at workstations and throughout the shop according to 5S procedures., • Inspires others to improve., • Performs other duties and tasks as required. Required Qualifications: • High School Diploma or GED Equivalent., • 2+ years experience in fabrication and/or construction., • Proven ability to accept and apply feedback and directives from supervisors and other team members., • Experience using both hand and power tools., • Experience reading cut sheet/drawings., • Experience handling sheet metal. Desired Qualifications: • Leadership mentality and strong attention to detail., • Experience working in a collaborative environment promoting a teamwork mentality., • Strong sense of personal accountability. Benefits: • 401(k), • 401(k) matching, • ESOP - Employee Stock Ownership Plan, • Health insurance, • Dental insurance, • Vision insurance, • Life insurance, • Paid time off (Holidays/Vacation), • Professional Development BAMCO inc. is not accepting unsolicited assistance from search firms. All resumes submitted by search firms to any employee of BAMCO inc. in any fashion without a valid written search agreement in place will be deemed the sole property of BAMCO inc. No fee will be paid if a candidate is hired by BAMCO inc. based upon an unsolicited referral. BAMCO inc. is an Equal Opportunity Employer. BAMCO inc. participates with E-Verify.

The position advertised has been exempted from the federal civilian hiring freeze. Plan and conduct investigations of potential violations of federal laws, cybersecurity, and public safety. Create and maintain effective liaison relationships with federal, state, local, tribal, territorial, and inter

Description: Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community. Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change. Under the general direction of the Physician Billing (PB) Director of Coding and Manager of Education and Audit, this position supervises the Coding Education and Audit team and conducts audits for medical provider documentation while adhering to Centers for Medicare and Medicaid Services (CMS) and Office of Inspector General (OIG) guidelines for Hackensack Meridian Health (HMH). Works professionally, exercising good judgment and ethical standards. Interacts effectively and builds respectful working relationships across the organization. Demonstrates integrity by adhering to high standards of personal and professional conduct. Reliable and maintains a high level of confidentiality within all aspects of job functions and performance. Responsibilties: A day in the life of a Supervisor, Education/Audit, Physician Billing at Hackensack Meridian Health includes: • Monitor all Coding Educators and Auditors in the department to ensure internal workflows are being followed., • Ensure that the productivity and actions of the Coding Educators and Auditors meet and support the overall operational goals of the department and institution., • Counsel Coding Education and Audit teams on actions required to meet minimum performance requirements., • Create and facilitate educational programs/presentations for Providers & Staff as they relate to new coding concepts., • Prepare educational communications of annual coding updates for all Providers and Staff., • Provide coaching and advice to team members for performance and effectiveness including helping team members prioritize daily tasks and resolve complex coding issues., • Participate in hiring employees and address individual and team performance needs., • Conduct investigations/audits and communicate, educate, and work with the leadership team to troubleshoot issues and/or revise workflows to ensure documentation compliance., • Research assigned issues through the use of research skills, automated analysis tools, online research tools, etc., • Provide manager coverage as needed., • Other duties and/or projects as assigned., • Bachelor's degree or higher; or High School diploma, general equivalency diploma (GED), and/or GED equivalent programs plus 5 years of supervisory coding experience., • Minimum of 3 years of physician coding experience in a multi-specialty practice., • Minimum 3 years of quality improvement audit experience., • Exhibit strong project management and presentation skills., • High-level understanding of coding and auditing concepts, American Medical Association (AMA)/Centers for Medicare and Medicaid Services (CMS)/Office of Inspector General (OIG)/Federal/State regulations & guidelines., • Must have advanced coding education and training with a strong foundation in E/M Coding., • Certified Professional Medical Auditor within 1 years of entering position.

Weston is seeking an Environmental Air Scientist for scheduled and time-critical responses to site-related environmental issues, including disaster/emergency response, environmental investigations and remedial alternative analysis. Assist in environmental site assessments consistent with US EPA stan