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Job DescriptionCompany Description MAKE GREAT PIZZA — AND MORE — POSSIBLE Be a part of the world's #1 Pizza company! Job Description Shift: Multiple shifts available Compensation: $30-$40 hourly based off experience; bi-weekly pay The Maintenance Technician for the Domino’s Pizza Supply Chain Center will repair and install Bakery equipment in a distribution manufacturing facility. They will use their technical skills to design, evaluate, and troubleshoot the PLC interface for diagnostics, perform preventative maintenance, and troubleshoot on JLS delta-style robotics. The Maintenance Technician will use their skills in Electrical, Mechanical, Plumbing, Hydraulics, Pneumatics, Hydraulics, and Computer Controls to perform this role. In addition, the Maintenance Technician will work safely on mechanical and electrical equipment. RESPONSIBILITIES AND DUTIES (60%) Inspect, test, troubleshoot, repair, and install machinery and equipment • Monitor equipment to detect malfunctions, • Discuss machine operation variations with a supervisor or other team members to diagnose problems and repair machines, • Install, repair, or replace electrical devices such as transformers, relays, circuit breakers, starters, and safety and limit switches, • Layout, assemble, install, and maintain pipe systems and related hydraulic and pneumatic equipment, • Install, program, and troubleshoot automated machinery., • Install, troubleshoot, and repair refrigeration and Heating Ventilation Air Conditioning (HVAC) equipment, • Service and repair material handling equipment, • Monitor the main electrical panel and troubleshoot as necessary, • Repair and maintain boilers, water heaters, water conditioning equipment, and all water distribution systems, • Follow established preventative maintenance guidelines, • Perform all necessary maintenance and update logs as necessary, • Repair and maintain the physical structure of the establishment, • Identify safety issues with machines; document issues; develop an action plan to resolve concerns; follow up to ensure problems are resolved, • Assist in the control and scheduling of projects, • Monitor inventory and order parts as necessary, • Monitor energy usage and provide recommendations for better usage Qualifications, • HS Diploma and Technical School Training of two years, and 5 plus years related experience in distribution or manufacturing environment, and licensed journeyman of a skilled trade, • Advanced knowledge of hydraulics, PLC logic, plumbing, general contracting, welding, HVAC/refrigeration, etc., preferred, • Advanced Windows-based computer systems and spreadsheets, • Read and interpret blueprints, mechanical and electrical schematic diagrams, • Solid communication skills, verbal and written, • Identify problems and draw conclusions, • Working knowledge of 5s and Six Sigma, • Ability to safely operate a forklift and manual/electrical pallet jack, • EPA REFRIGERATION CERTIFICATION (Type II or Universal) Federal requirement – Team Leader or Maintenance Tech Servicing or Handling Refrigeration equipment While performing the duties of this job, the team member is frequently exposed to moving mechanical parts. The team member is occasionally exposed to wet and humid conditions, outside weather conditions, extreme cold, extreme heat, and risk of electrical shock, explosion, and vibration. The noise level in the work environment is usually moderate but can be high. The team member must have a strong safety awareness to ensure a safe and healthy workplace. Additional Information Domino's offers: • Competitive wages, • Paid Holidays and Vacation, • Positive work environment, • Benefits on the first day of employment!, • 401k matching contributions, • 15% off the purchase price of stock, • Company bonus, • Referral bonuses

Job Description CNC Machinist Reports to: Manufacturing Supervisor Accountability This position is responsible for ensuring safe and efficient operation of manufacturing machines for production of quality parts. Organizational Relationship The Machinist position reports to the Manufacturing Supervisor, receiving advice, counsel and direction. Duties and Responsibilities 1. Reviews job package in its entirety, including routing, blueprints, specifications and other documentation as appropriate to fully understand the process plan, part configuration (dimensions & tolerances), material, tooling and equipment to be used to produce the end product., 2. Builds setup per documented plan, utilizing knowledge of proper setup procedures, machining practices, material properties and tooling. Setups are built on equipment he/she has been previously qualified to operate, such as lathes, milling machines, and/or grinders, both CNC and conventional., 3. Operates production equipment utilizing knowledge of machining practices and safe operation techniques to produce components and/or services that meet customer needs. Initiates change to the setup and/or operation to optimize production efficiency. 4. Verifies conformance of work piece to specifications using appropriate measuring instruments., 5. Evaluates deviations identified in the machining process to determine the cause and initiates corrective action if appropriate. Reports all deviations identified via Process Discrepancy Report (PDR). 6. Trains less experienced machinists in advanced machining techniques to aid in developing a higher level of technical competence in the machine labor force., 7. Maintains a professional & personable relationship with superiors, peers and subordinates, being responsive to their needs as well as those of the company., 8. Performs other duties or functions as requested by his/her supervisor or other authorized Midstate Machine personnel. Shift open as Indicated: Shift A: Mon – Thu 6:00 AM to 4:00 PM Shift B: Mon – Thu 6:00 PM to 4:00 AM Shift C: Fri – Sun 6:00 AM to 6:00 PM (Work 36 hours, but paid for 40 hours) CMM Quality Inspector Reports to: Quality Manager or Supervisor Accountability The CMM Quality Inspector’s function is to verify that in-process and completed materials are in compliance with all requirements as defined by Midstate Machine and/or customer specification. This function serves the same purpose as the Quality Inspector’s function but requires a working knowledge of CMM Programming. Organizational Relationship The position of CMM Quality Inspector reports directly to the Quality Manager and/or Quality Supervisor, receiving advice, council and direction on issues related to the Inspection function. The incumbent serves on the Quality department staff, obtaining and providing information, advice and service regarding the Inspection function, primarily but not limited to other members of the Midstate Machine organization. Principal Accountabilities To ensure that product is manufactured and supplied to Midstate and customer required specifications. Principal Challenges and Decision Authority 1. Responsible to assure all documentation and materials are in accordance with customer requirements prior to the release for subsequent processing by vendors and/or shipment to the customer., 2. Responsible for inspecting characteristics involved in specific operations using different gages whenever possible and practical. Inspections will be extended to the point where it can be determined that present operation has/will not affect prior or subsequent operations., 3. Aids in maintaining traceability and established filing., 4. Responsible to initial and date operations and/or dimensions inspected., 5. Responsible for notifying production supervisors or lead men of deviations found in their operations., 6. Maintains clear and concise instructions/programs of proper CMM inspection methods for specific part operations to ensure all CMM capable personnel follow the same guidelines., 7. Responsible for using a secondary method for verifying deviations with the CMM when applicable., 8. Responsible for tagging and segregating non-conforming material., 9. Responsible for providing inspection forms when required and to perform inspections in a timely manner., 10. Responsible for inspecting and documenting results on appropriate paperwork., 11. Reports and tags any gages found needing repair., 12. Maintains a clean and safe working environment within Midstate Machine., 13. Maintains a professional and personable relationship with customers, vendors and Midstate Machine staff, being responsive to their needs as well as those of the company, 14. Displays and generates a “readiness to work” attitude with all employees., 15. Working knowledge of CMM Programming required., 16. Performs other duties or functions as requested by the Quality Manager. Following 2 shifts open need two Candidates Shift B: Mon – Thu 6:00 PM to 4:00 AM Shift C: Fri – Sun 6:00 AM to 6:00 PM (Work 36 hours, but paid for 40 hours)

Job Description Fluid Path Products manufactures components for Biotech, Pharmaceutical, and Food Processing industries. We are dedicated to delivering high-quality products to our customers. We pride ourselves on our commitment to efficiency, innovation, and customer satisfaction. We are looking for a motivated and detail-oriented Shipping Clerk to join our team. Job Overview: The Shipping Clerk is responsible for assembling products, packaging them for shipment, ensuring timely and accurate delivery to our customers, and receiving products. This role requires attention to detail, strong organizational skills, and the ability to work in a fast-paced environment. Key Responsibilities: • Assemble products according to specifications and guidelines., • Perform quality checks to ensure products meet company standards., • Report any defects or discrepancies to the supervisor., • Package products securely and efficiently to prevent damage during transit., • Label packages accurately with the correct shipping information., • Maintain a clean and organized workspace., • Assist with inventory management, including stock counts and restocking shelves., • Strong attention to detail and accuracy., • Ability to lift and move heavy packages, • Basic computer skills, • Excellent organizational and time management skills., • Ability to work independently and as part of a team., • Positive demeanor and strong work ethicCompany DescriptionWe offer an exciting and rewarding opportunity for an enterprising manufacturing professional to be part of multiple and related start-up success stories in the biotech and biopharma industries.We offer an exciting and rewarding opportunity for an enterprising manufacturing professional to be part of multiple and related start-up success stories in the biotech and biopharma industries.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Summary: We are seeking a detail-oriented and proactive Analytical Associate Scientist or Scientist to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards. Key Responsibilities: • Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required., • Prepare reagents, standards, and samples according to established protocols., • Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation., • Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations., • Assist in method development, validation, and troubleshooting of analytical procedures., • Collaborate with cross-functional teams to support project timelines and deliverables., • Participate in the review and update of SOPs, batch records, and other quality documentation., • BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization., • Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred., • Strong attention to detail, organizational skills, and commitment to data integrity., • Ability to work independently and collaboratively in a fast-paced team environment., • Good communication skills and the ability to clearly document and present data., • Experience working in a CRO or CDMO setting is an advantage. #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job Description 2nd and 3rd Shift Supervisor/Foreman for Injection Molding - $25 to $30 / HR. Qualified candidates must have previous supervisory experience in a manufacturing environment. Experience with plastic injection molding is strongly preferred. The Molding Supervisor is responsible for providing leadership and guidance to the molding department to ensure production schedules are met. Specific responsibilities include: • Performs process and equipment adjustments when necessary., • Monitors work of associates to ensure production requirements are met in Small and Large Molding., • Verifies that associates are adhering to Safety rules within department., • Ensures quality standards are met by auditing the operators work., • Monitors cleanliness of the worksite., • Performs product problem solving and corrective action., • Completes required forms, paperwork, and data entry in a timely manner. (Regrind utilization, and Part auditing), • Notifies responsible departments on potential safety, quality, and equipment issues to address the problems, • Monitors and tracks area performance to target., • Promotes positive working relationships with associates., • Needs to have the ability to react to changing conditions and environment. Be able to make decisions with little or no direction., • Effectively communicate to other shifts and/or departments to resolve Mfg. issues., • Repairs minor machine problems., • Supervising a team of 13 employees., • Performs other duties as necessary. Requirements • Must have 3+ years of plastic injection molding experience, • Excellent leadership skills, ability to communicate well, both orally and written • Thorough understanding of injection molding equipment and processes, excellent troubleshooting skills is preferred. • Knowledge of the overall operations of a manufacturing facility • Bi-Lingual is a plus Company DescriptionWe are custom Injection Molding Manufacturer.We are custom Injection Molding Manufacturer.

Job DescriptionWe are looking for an Electronic Technician – Full–Time - $35 - $42/hr.***Job Summary: The Electronic Technician will modify, repair, and improve existing electronic products, equipment, and controls and will assist in developing new or updated electronic systems, components, or products. Primary Responsibilities: • Interfaces with maintenance department to identify replacement parts or components as needed., • Has knowledge of commonly used concepts, practices, and procedures within a particular field., • Applies principles and techniques of engineering to accomplish goals., • Relies on experience and judgment to plan and accomplish goals. Instructions and pre-established guidelines to perform the functions of the job., • Performs a variety of complicated tasks., • Primary job functions typically require exercising independent judgment., • Reports potentially dangerous electrical equipment to supervisor and takes steps to resolve the issue., • Performs safety checks to ensure design plans are feasible in various conditions., • May lead and direct the work of others., • Develops and maintains a high degree of positive employee attitude as applied to their jobs and fellow employees., • Typically reports to a supervisor or manager. A wide degree of creativity and latitude is expected., • Will be responsible for back up duties of Maintenance Manager as needed., • Responsible for other duties as assigned by Maintenance Manager. Qualification Requirements: To 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. • Ability to perform high level math aptitude functions., • Ability to read, comprehend and practice necessary safety procedures, signs, etc., • Thorough understanding of electronics principles and design., • Proficient in Microsoft Office Suite or related software., • Detail-oriented and organized., • Excellent problem-solving ability., • PLC, HMI and Temperature Controllers’ knowledge., • Electronics trouble shooting, repairs and installations., • Knowledge of 24v, 110v, 220v and 480v., • Troubleshooting, installing and programing of VFD’s., • Troubleshooting/repair/installation of relay logic circuits., • Basic electrical circuitry., • Multimeter proficient., • Ability to follow highly complex directions., • Excellent verbal and written communication skills throughout the organization at all levels., • Bi-lingual a plus., • Experience in a manufacturing environment is a strong plus. Education and/or Experience: • Requires a bachelor's degree in electrical/electronic engineering and/or a minimum of 5 years of experience in the field or in a related area. Work Environment: • This position normally works in a manufacturing environment., • Hearing, eye and foot protection are mandatory when engaged in activities in the plant., • Ability to work in 110-degree environment Physical Requirements: • Moderate physical activity involved., • A great deal of walking., • Lifting required., • Ability to distinguish various colors of wires and distinguish electronic system sections and wiringWorking Hours: Monday to Friday, 8:00 AM to 5:00 PM***Pay Range is based on experienceReasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Job DescriptionBenefits: • Dental insurance, • Health insurance Position Overview A fast-paced, refrigerated food manufacturing and distribution facility is seeking an experienced Maintenance Supervisor to lead its maintenance team. This role is responsible for overseeing daily mechanical and electrical maintenance activities, ensuring minimal production downtime, and driving a culture of safety, preventive maintenance, and continuous improvement. Key Responsibilities • Supervise a team of maintenance technicians across multiple shifts, providing direction, training, and performance feedback, • Lead mechanical troubleshooting, repair, and preventive maintenance activities on conveyor systems, motors, gearboxes, pneumatics, VFDs, photoeyes, sensors, and other production equipment, • Coordinate and prioritize work orders to minimize production downtime and meet operational goals, • Oversee electrical diagnostics, including wiring, control panels, PLCs, and 3-phase systems (role split: ~70% mechanical, ~30% electrical), • Manage the preventive maintenance (PM) program, ensuring schedules are followed and maintenance records are accurately kept, • Collaborate closely with production, sanitation, and quality teams to ensure equipment operates safely and efficiently in compliance with GMP, OSHA, and food safety standards, • Assist in vendor coordination, spare parts inventory, and capital project support, • 5+ years of maintenance experience in a manufacturing or food production environment, with at least 2 years in a supervisory or lead role, • Strong mechanical troubleshooting and repair skills; solid electrical knowledge preferred, • Experience working with conveyors, motors, gearboxes, pneumatic systems, and production equipment, • Familiarity with PLC troubleshooting, VFDs, control systems, and basic electrical diagnostics, • Strong organizational and communication skills, with the ability to manage competing priorities in a high-pressure setting, • Experience using preventive maintenance systems (CMMS) and applying maintenance best practices, • Knowledge of GMP, OSHA, and food safety compliance standards, • Previous experience in refrigerated or food manufacturing environments, • Bilingual (English/Spanish) a plus, • Technical certifications in mechanical, electrical, or automation systems

Job DescriptionDescription: Job Summary: Oversees the activities of plant and facility maintenance for a 55,000 square foot building and is responsible for managing the installation and maintenance of equipment, machinery and buildings of the company. Also responsible for planning, budgeting and scheduling facility modifications - including estimates on equipment, labor materials and other related costs. Essential Functions: • Ensures production equipment operates safely, efficiently, and predictably by supervising and performing scheduled equipment maintenance., • Supervises the daily, weekly and monthly preventative/predictive maintenance activities., • Schedules and leads the daily activity of a maintenance team of 5-15 associates and develops effective and relevant metrics for direct reports., • Selects and develops talent to match the maintenance needs of plant operations., • Leads safety initiatives for the maintenance department including:, • Conducts safety compliance inspections of the production and shop equipment to eliminate hazards, • Actively participates in the site safety committee, • Plans and enforces safe work practices through effective PPE, lockout/tagout, and other behaviors, • Ensures compliance with all OSHA, HLAC and environmental regulations and other local, state and federal government regulations., • Develops and executes a maintenance operating plan that meets budgeted expenses., • Manages spare parts and supplies procurement and inventory and maintains effective vendor relationships., • Ensures that Company facilities, including buildings and grounds, are maintained to Company standards., • Provides technical assistance to Production Managers and associates including training on equipment operation, equipment start-up, and operator preventative maintenance., • Develops effective troubleshooting and repair/adjustment to production and maintenance equipment., • Communicates effectively with all levels of the organization and provides periodic reporting on results and metrics., • Selects and provides direction to all outside contractors., • Seeks new technologies and automation opportunities in lowering the overall cost of manufacturing., • Must have well developed communication and basic math skills, organizational, analytical, and decision-making skills, efficient multi tasking abilities, ability to supervise multiple workers in an often fast-paced environment, organizational skills, and able to foster a positive team working environment., • The ability to stand, sit and/or walk repeatedly throughout most of the workday., • When in the plant, subject to the outside environment with possible exposure to extreme temperatures (heat, cold, humidity, etc.)., • Position is occasionally exposed to fumes, odors, dust, mists, airborne particles, chemicals, heights, cramped quarters, oil, grease and dirt., • Normal lifting of up to 50 pounds is possible., • Mobility is necessary in order to perform assigned functions., • Noise level is moderate to heavy as the work area is a production environment., • Position requires the ability to occasionally work different shifts to monitor plant performance., • Bachelor’s Degree or equivalent work experience along with 5+ years of industrial maintenance/management experience required., • This position requires the knowledge of hydraulics, pneumatics, electrical, electronics (PLC), hydraulics, heating ventilation, air conditioning, carpentry, welding, machining and fabricating. The position also requires proficiency in troubleshooting the before listed categories., • Technical knowledge of maintenance equipment and capital project activities and experience leading associates of various skill levels required., • Must have well developed communication and basic math skills, organizational, analytical, and decision-making skills, efficient multi-tasking abilities, ability to supervise multiple workers in an often fast-paced environment, organizational skills, and able to foster a positive team working environment. Disclaimer: This description does not state or imply that the duties listed above are the only duties to be performed by the Associate. Associates are required to follow job-related instructions and perform other job-related activities requested by their supervisor. All requirements are subject to possible modifications in order to provide a reasonable accommodation to individuals with physical or mental disabilities as defined in the Americans with Disabilities Act. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other Associates. Nixon Medical is an equal opportunity employer. #IND1

Job DescriptionDescription: The Plant Engineer position will be responsible for leading engineering and maintenance activities at a site. Working under limited supervision, the Plant Engineer maintains production and quality by ensuring operation of machinery and the condition of the site. This position oversees skilled Technicians to maintain the facility, including grounds, buildings, equipment, and assets. The Plant Engineer will need to ensure compliance with safety, regulatory, and plant reliability to align equipment availability with operating requirements. Requirements: Essential Functions: • Create a high level of equipment availability through Planned Maintenance to minimize unscheduled repairs or equipment failures as measured by the departments KPI’s., • Through daily huddles and technician coaching sessions, maintain consistent communications with plant operations for scheduling, planning, and training purposes. Meet or exceed agreed KPI’s and individual goals., • Ensures Maintenance and Project expenses and objectives under span of control are met and on budget., • Use Lean concepts to identify and implement continuous improvement and systematic problem solving to remedy root causes for improved plant performance., • Coordinates activities with management to review planned maintenance, projects, objectives, timelines, and communications within the plant., • Responsibilities may include performing research, designing smaller or large projects within financial and operational scope, and implementing these projects, or sub-sets of complex projects., • Mentor and support the development of facility operations and maintenance personnel., • Delivery and support of cost saving initiatives to accomplish productivity targets., • Active support and participation in driving reliability and safety initiatives through root cause analysis, idea generation and task execution., • Oversees Maintenance Technicians and provides ongoing training to maximize the efficiency of the work force and meet operational requirements., • Process safety stewardship in all aspects; change management, hazard analysis and abnormal situation management., • Provides mechanical maintenance information by answering questions and requests and ensures operation of machinery by completing preventive maintenance requirements by following diagrams, sketches, manuals, manufacturer's instructions, and engineering specifications and troubleshooting malfunctions., • Maintains a safe and clean working environment by complying with site level Environmental and OSHA procedures, rules, and regulations. Upholds site level Environmental and OSHA records and reports as appropriate., • Strong leadership and interpersonal skills, project management, organization, decision making ability, relationship building and interfaces well with others. Specific skill-based competencies required to satisfactorily perform the functions of the job include adhering to safety practices; and operating equipment used in technical maintenance trades., • Ability to present information to others. Specific knowledge-based competencies required to satisfactorily perform the functions of the job include safety practices and procedures, and advanced fundamentals of MEP and general building preservation., • The ability to stand, sit and/or walk repeatedly throughout most of the workday., • When in the plant, subject to the outside environment with possible exposure to extreme temperatures (heat, cold, humidity, etc.)., • Position is occasionally exposed to fumes, odors, dust, mists, airborne particles, chemicals, heights, cramped quarters, oil, grease and dirt., • Normal lifting of up to 50 pounds is possible., • Mobility is necessary in order to perform assigned functions., • Noise level is moderate to heavy as the work area is a production environment., • Position requires the ability to occasionally work different shifts to monitor plant performance., • BS in Engineering preferred with a minimum of Five years’ experience in manufacturing systems or Ten plus years of experience leading a Technical team in a manufacturing environment., • This position requires the knowledge of hydraulics, pneumatics, electrical, electronics (PLC), hydraulics, heating ventilation, air conditioning, carpentry, welding, machining and fabricating. The position also requires proficiency in troubleshooting the before listed categories., • Technical knowledge of maintenance equipment and capital project activities and experience leading associates of various skill levels required. This description does not state or imply that the duties listed above are the only duties to be performed by the Associate. Associates are required to follow job-related instructions and perform other job-related activities requested by their supervisor. All requirements are subject to possible modifications in order to provide a reasonable accommodation to individuals with physical or mental disabilities as defined in the Americans with Disabilities Act. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other Associates. Nixon Medical is an equal opportunity employer. #IND1

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Title: Procurement Supervisor, Direct Materials Location: Piscataway, NJ (Fully onsite) Employment Status: Full Time Reports to: Senior Procurement Manager Overview: The role is responsible for leading the direct procurement team, managing end-to-end sourcing and procurement of direct materials and consumables to support production. Key duties include ensuring daily operations meet SLA and KPI targets, overseeing material planning for critical items, and driving strategic sourcing initiatives. The candidate will manage vendor relationships, negotiate contracts, and identify cost-saving opportunities through category management and market analysis. Close collaboration with cross-functional teams is essential to ensure supply continuity, compliance with quality and regulatory standards, and readiness for audit requirements. Location: Piscataway, NJ The estimated salary range is $80,000 - $100,000, based on experience. Job Responsibilities: • Supervise the direct procurement team to ensure smooth daily operations and compliance with SLA and KPI targets, and effectively manage team performance., • Oversee material planning for Green Channel item replenishment to meet inventory KPIs while ensuring continuity of supply., • Lead strategic sourcing and manage the procurement process for direct materials and consumables used in production, ensuring alignment with cost objectives, quality standards, and regulatory requirements., • Develop alternative vendors for critical materials and components to ensure supply continuity and mitigate supply chain risks., • Conduct category management to identify cost-saving opportunities through vendor consolidation and the use of alternative materials or components., • Leverage negotiation, analytical, and market research skills to drive value through cost reduction initiatives. Track and report KPIs related to cost savings, cost avoidance, on-time delivery (OTD), and efficiency improvements., • Execute vendor management by building supplier profiles, conducting regular business reviews, and securing both short- and long-term pricing contracts and Master Supply Agreements (MSAs)., • Serve as the primary point of contact for negotiating and executing contracts and agreements in coordination with the legal team., • Collaborate closely with production team to provide effective procurement support by understanding production processes, tracking changes in material consumption, and proactively addressing critical issues with urgency., • Maintain active communication with suppliers of critical materials to stay updated on market conditions, ensure timely deliveries, and identify potential risks and opportunities., • Work cross-functionally with quality, finance, and other departments to ensure procurement processes remain compliant with company policies and regulatory standards., • Bachelor's degree or higher in Business, Supply Chain Management, Biology and Chemistry, or other related fields., • 5+ years of experience in procurement, strategic sourcing or planning of direct materials, preferably in the biotech or pharmaceutical industries, • Demonstrated leadership through previous experience in people management or project management, • Strong negotiation, analytical, and communication skill., • Good knowledge of materials used in biotech/pharma production, including raw materials, consumables and packing materials., • Ability to effectively communicate complex situations and demonstrate agility in identifying opportunities for cost reduction and problem-solving., • Proficiency in ERP systems of SAP and S2P is a plus #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

We are seeking an experienced Upstream Manufacturing Scientist to join our team in Piscataway, NJ. This is a crucial role responsible for executing mammalian cell culture processes, with a focus on producing recombinant proteins for biosimilars in a cGMP environment. You will work with a collaborative team on engineering and clinical-scale batches from 50 L to 1000 L volumes. Responsibilities: • Execute mammalian cell culture and bioreactor operations at multiple scales, specifically working with CHO (Chinese Hamster Ovary) cells., • Perform on-line adjustments to products, instruments, or equipment by collecting and evaluating operating data., • Review executed manufacturing and packaging batch records, protocols, and other technical documents., • Initiate and coordinate investigations for issues and deviations found during batch execution., • Take the lead in following GMP and EHS policies and provide strong technical expertise in cell biology and bioreactor operations., • Work both independently with minimal supervision and as a collaborative team member. Qualifications: • A minimum of 1+ years of relevant experience in the biopharmaceutical industry., • Expertise in independently designing, executing, analyzing, and documenting process development., • Previous experience in a cGMP and aseptic manufacturing environment is required., • Experience with single-use manufacturing consumables (e.g., bags, tube sets, process manifolds)., • Knowledgeable in GMP batch manufacturing, documentation, and cleaning verification/validation., • Experience with bioreactors (Sartorius, Thermo, Abec, Excelleris) is a plus. Salary & Schedule: • Pay: $75,000 - $110,000+ (depending on experience level), • Shift: 2nd shift (2:00 PM - 10:00 PM, Monday - Friday) with occasional weekend rotation and off hour work. This is a Direct Hire position with a clear path for career growth to Lead and Supervisor roles. Apply today if you're interested in your next Upstream Manufacturing opportunity!

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Overview: The Laboratory Supervisor is responsible for overseeing and guiding the daily operations of the laboratory, ensuring that the work is conducted efficiently and accurately. This position requires a background in laboratory studies or work and extensive team management experience. The candidate should be able to set and break down team goals, establish employee performance assessment criteria (PBC/KPI), and drive the team towards achieving its objectives. Key Responsibilities: Team Management: • Lead and manage the laboratory team, assign tasks, and monitor progress., • Set annual and quarterly team goals and break them down into actionable tasks., • Maintain open communication channels, regularly communicate with team members, and provide feedback and guidance., • Resolve internal team conflicts and issues, fostering a positive work environment., • Identify training and development needs of employees, develop and implement training plans., • Mentor and cultivate employees, helping them improve skills and advance their careers., • Apply lean principles to optimize laboratory processes, enhancing efficiency and quality., • Implement site management practices to ensure effective use of laboratory equipment and resources., • Develop and maintain laboratory SOPs, ensuring all operations comply with industry best practices and regulatory requirements., • Regularly review and update SOPs to adapt to new technologies and methods., • Apply comprehensive thinking to analyze problems from perspectives such as personnel, equipment, materials, methods, and environment., • Identify potential issues and develop preventive measures to reduce impacts on laboratory operations., • Represent the team in developing and executing strategies to achieve laboratory goals., • Monitor project progress, make necessary adjustments to ensure goals are met., • Possess a degree in a relevant field and laboratory work experience., • Extensive team management experience with the ability to set and achieve goals., • Familiarity with lean management principles and site management practices., • Excellent communication and coordination skills, able to effectively resolve issues., • Ability to mentor and develop employees, supporting the team's continuous growth. #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job Description The QC Laboratory Supervisor is responsible for overseeing daily operations in the laboratory, ensuring the accuracy, timeliness, and reliability of testing results. This role involves supervising laboratory personnel, maintaining quality control standards, ensuring compliance with safety and regulatory guidelines, and assisting with administrative tasks including scheduling and inventory management. ESSENTIAL FUNCTIONS: • Supervise laboratory staff including assigning tasks, monitoring performance, and providing guidance and training., • Ensure that laboratory tests are performed accurately and efficiently in accordance with standard operating procedures (SOPs) and regulatory guidelines, • Maintain laboratory quality control and quality assurance programs., • Collaborate with management to implement laboratory policies and procedures., • Monitor inventory levels and order laboratory supplies and equipment as needed., • Ensure compliance with safety regulations and maintain a safe work environment., • Troubleshoot technical problems with laboratory equipment and procedures., • Maintain accurate records of laboratory activities, results, and incidents., • Participate in audits and inspections; ensure readiness for regulatory reviews., • Stay updated with new laboratory technologies and procedures., • Evaluate OOS results and assist in determining acceptable deviations, • BS/BA in Chemistry, Food Science, Biology or related Science Field, • Minimum of 3–5 years of laboratory experience with at least 1–2 years in a supervisory or lead role., • Strong Leadership and communication abilities, • Solid understanding of laboratory practices and safety regulations, • Excellent problem solving and decision-making skills, • Knowledge of statistical toolsCompany DescriptionReliance Vitamin is a high growth consumer products company in the very “on trend” natural and organic space, and is comprised of three divisions: · Private Labeling of premium branded and private label products for various companies/retailers using 450 stock products and differentiating with over 50 Patented and Trademarked raw materials. · Contract Manufacturing of premium powders, tablets and capsules differentiating with over 50 patented and trademarked raw materials, specializing in probiotics and plant proteins. Customer base is branded, domestic and international companies. With over 30+ years in business, Reliance provides expertise and resources to deliver nutritional innovation that truly makes a difference in consumer’s lives. The Company is in the process of transforming to maximize its entrepreneurial culture and heritage while building enterprise practices to achieve sustainable performance.Reliance Vitamin is a high growth consumer products company in the very “on trend” natural and organic space, and is comprised of three divisions:\r\n\r\n· Private Labeling of premium branded and private label products for various companies/retailers using 450 stock products and differentiating with over 50 \r\n Patented and Trademarked raw materials.\r\n\r\n· Contract Manufacturing of premium powders, tablets and capsules differentiating with over 50 patented and trademarked raw materials, specializing in probiotics \r\n and plant proteins. Customer base is branded, domestic and international companies. \r\n\r\nWith over 30+ years in business, Reliance provides expertise and resources to deliver nutritional innovation that truly makes a difference in consumer’s lives. The Company is in the process of transforming to maximize its entrepreneurial culture and heritage while building enterprise practices to achieve sustainable performance.

Job Description Senior Supervisor Tax Accounting - Public Accounting Firm $80-90,000 Westfield, NJ Established and growth-oriented CPA Firm is currently looking to add to their team! This CPA Firm offers a diverse mix of work and clientele. In your role you will be responsible for tax preparation and review of individual, corporate and partnership returns. You will also assist with some accounting compilation and review work, but the primary focus will be on taxes. Clients range in size from $500,000 to 50 million and are in a variety of industries from professional service to manufacturing to construction. If you are looking for a career in public accounting and looking to join a professional and pleasant team - this opportunity is for you. Qualified candidates will have: BS in Accounting 3-10 years of recent public accounting experience including solid TAX background in preparation and review of business and personal returns Must have good tax return review experience Solid understanding of GAAP accounting - Financial Statements Experience dealing with tax authorities and working directly with clients Good computer skills - Microsoft office suite +, CCH Axcess and CCH Engagement a plus or similar product CPA or pursuing certification

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: Product Managers (PM) lead a cross-functional role for existing and new products. PMs are involved with all product management aspects associated with product definition, product development, forecasting, pricing, market introduction, sales tools, sales training and promotion plans. Serving as the primary marketing resource for supporting catalog product overall strategy and revenue goals in US. This ideal candidate will have a blend of skills including technical knowledge, stakeholder management, excellent project management, and strong communication. Please note that this position is based onsite in Piscataway, NJ. The estimated salary range is $80,000 - $100,000, based on experience. Responsibilities: • Promote product portfolio in North America and international regions, while working across product lines and workflows., • Coordinate promotional activities with product line managers and the sales teams., • General promotional assets, including landing pages, flyers, brochures, etc., • Execute promotional activities including sampling programs, advertisement, conference/tradeshow booking and/or attendance, product demonstrations, and customer presentations., • Demonstrate product expertise when attending conferences or tradeshows, • Categorize customer types and analyze effectiveness of territory performances based on client category, promotional activities and help execute improvement plan., • Analyze each portfolio in different territories, market needs and gather market information through surveys and client discussions to identify potential areas of growth or improvement., • Provide trainings, guidance and recommendations to Sales, Product Line Managers, R&D, and Production groups based on recognizing customers' current and future needs during continued business relationship., • Organize and provide training for customers, sales, and external distributors by delivering presentations or/and demos., • Collaborate with internal teams/departments to achieve sustainable growth, • Minimum bachelor degree in relevant life science disciplines, such as biology, protein chemistry, biochemistry, cell biology, immunology, molecular biology, biotechnology, etc., • Marketing experience highly preferred., • Exceptional verbal and written communication and presentation skills, • Must be customer-centered and proactive/action-oriented, • Excellent analytical skills & problem-solving skills, able to grasp new concepts quickly, • Strong organization skills with great attention to detail, • Enjoy working in a fast-paced and team-oriented environment, • Quick learner and well organized with good time managements and multitasking skills., • Solid business sense is a plus, • Must have basic computer skills in Microsoft Office #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job DescriptionDescription: About the Company: At Lincoln Electric Products Co. Inc., we specialize in the design, manufacture, and distribution of custom equipment tailored to meet the specific applications and requirements of our customers. Our product range includes: • Panelboards: Up to 2000A, • Service and Distribution Switchboards: Up to 8000A, • Generator Connection Boxes, • Generator Output Switchboards, • Single and Double-Ended Substations Lincoln Electric Products Co. Inc. we are seeking a proven Switchgear Project Manager to join its dynamic team and the growing organization. This role is available immediately and provides a great growth opportunity for the right candidate. It is a full-time, exempt position, and the candidate will report directly to the Project Manager-Supervisor. The successful candidate will be responsible for the initial design and project Management Of Electrical Distribution Equipment, including Panelboards, Switchboards, and Circuit breakers. At Lincoln Electric Products Co. Inc., Project Management begins at Stage 1, which is Engineering. This means the Project Manager is involved right from the start of the project lifecycle, leading the coordination of engineering activities, ensuring design specifications are met, and setting the foundation for successful execution. It's a hands-on role that combines technical understanding with cross-functional leadership. Job Responsibilities • Focus is switchgear projects for commercial construction, commercial facilities, and OEMs., • Collaborate with sales, engineering, and manufacturing teams., • Designing and drawing Switchboards/ Panelboards., • Reviewing outgoing engineering submittal drawings for technical and contractual accuracy., • Evaluating and interpreting customer specifications and drawings to create an accurate bill of materials., • Providing phone support and direct interaction with customers and employees to obtain sales, • Reviewing returned drawings and submittals of same, analyzing and processing mark-up/comments, and communicating changes to the internal and external stakeholders, • Review contract documents, interpret technical specifications to ensure product compliance, and prepare change order pricing and quotations if needed., • Coordinate and facilitate the completion of Short Circuit and Coordination Studies., • Releasing equipment for production and delivery to an in-house shop., • Coordinating deliveries with customers., • Enter orders into the company ERP software system., • Configure and order long lead time major materials/components for the project., • Perform visits to survey site layout and logistical challenges as needed., • Provide post-sales support for equipment. Requirements: Job Requirements • Bachelor’s degree in Electrical Engineering., • 3+ years within the industry., • Thorough knowledge of electrical power systems, • Good knowledge of Industry UL standards and NEC standards, • Proficiency with MS Excel., • Ability to collaborate with team members.

Job Description Tenth Revolution has partnered with a Food Manufacture to find a Food Production Supervisor. The bilingual Food Production Supervisor (Spanish/English) will lead daily operations on the production floor. This role is responsible for overseeing production staff, ensuring food safety and quality standards, and meeting production targets in a fast-paced, high-volume environment. The ideal candidate will be a hands-on leader with strong communication skills and experience in food manufacturing. Key Responsibilities • Supervise and coordinate daily production activities to meet output, quality, and safety goals, • Lead, train, and motivate a diverse team of production workers, ensuring clear communication in both Spanish and English, • Monitor production lines for efficiency, accuracy, and compliance with food safety regulations (GMP, HACCP, SQF), • Ensure proper handling, roasting, seasoning, and packaging of nut products, • Collaborate with Quality Assurance, Maintenance, and Warehouse teams to resolve issues and maintain workflow, • Maintain accurate production records, shift reports, and inventory logs, • Identify process improvements and implement best practices to reduce waste and downtime, • Enforce company policies and safety procedures to maintain a clean and safe work environment, • Participate in audits, inspections, and continuous improvement initiatives Qualifications • High school diploma or equivalent required; associate or bachelor’s degree in Food Science, Operations, or related field preferred, • 3+ years of supervisory experience in food manufacturing or production environment, • Fluency in both Spanish and English is required, • Strong leadership, organizational, and problem-solving skills, • Working knowledge of food safety standards and manufacturing best practices, • Ability to work flexible shifts, including weekends or evenings as needed, • Proficient in Microsoft Office and production tracking systems

Job Description Tablet Press Operator will set up, maintain, and run capsule machine. Operator will also be responsible for recording logs every 30 minutes, submitting samples to QC for approval, and for capsule quality. Capsule operator must not leave machine unattended while machine is running. Product quality to be checked at start up and after breaks. ESSENTIAL FUNCTIONS: · Set up press with floor supervisor. · Verify correct punches are used and in good order. · Feed material to hopper to run press. · Verify correct blend is being used. · Bring samples to QC for approval. · During run, controls for weights, thickness, and hardness are taken and recorded into a log every 30 minutes. · Responsible for keeping a log for every break, change in operator, and machine being stopped. · Monitor tablets coming off punch and dropped into container. · Responsible for tablet quality. · Must remain at machine while machine is running. · Responsible for machine’s routine maintenance and cleaning by following SOP instructions. · Responsible for taking samples from beginning, middle, and end of run and recording on log. · Label containers with correct information as described on batch ticket. · Work area must be kept in accordance with Good Manufacturing Practices. · Remove all trash at the end of the shift and clean room thoroughly. · Keep current equipment use and cleaning log. QUALIFICATIONS: Education: · Preferred experience in nutraceutical or solid dosage manufacturing. KNOWLEDGE, SKILLS AND ABILITIES: · Must be able to lift 50 lbs. · Must be able to bend, stretch, and stand for extended time intervals during work shift · Must have good oral communication skills to be able to complete work tasks as instructed · Ability to understand written and verbal instructions in English Company DescriptionReliance Vitamin is a high growth consumer products company in the very “on trend” natural and organic space, and is comprised of three divisions: · Private Labeling of premium branded and private label products for various companies/retailers using 450 stock products and differentiating with over 50 Patented and Trademarked raw materials. · Contract Manufacturing of premium powders, tablets and capsules differentiating with over 50 patented and trademarked raw materials, specializing in probiotics and plant proteins. Customer base is branded, domestic and international companies. With over 30+ years in business, Reliance provides expertise and resources to deliver nutritional innovation that truly makes a difference in consumer’s lives. The Company is in the process of transforming to maximize its entrepreneurial culture and heritage while building enterprise practices to achieve sustainable performance.Reliance Vitamin is a high growth consumer products company in the very “on trend” natural and organic space, and is comprised of three divisions:\r\n\r\n· Private Labeling of premium branded and private label products for various companies/retailers using 450 stock products and differentiating with over 50 \r\n Patented and Trademarked raw materials.\r\n\r\n· Contract Manufacturing of premium powders, tablets and capsules differentiating with over 50 patented and trademarked raw materials, specializing in probiotics \r\n and plant proteins. Customer base is branded, domestic and international companies. \r\n\r\nWith over 30+ years in business, Reliance provides expertise and resources to deliver nutritional innovation that truly makes a difference in consumer’s lives. The Company is in the process of transforming to maximize its entrepreneurial culture and heritage while building enterprise practices to achieve sustainable performance.

A+ Personnel celebrates its 38th Anniversary in the staffing industry in 2025! We have successfully been placing qualified candidates with top corporations, from entry to C-Level, in New Jersey and New York.Interested in learning more about this job Scroll down and find out what skills, experience a

Job Description • We are hiring immediately for full time JANITOR positions., • Location: L'Oreal - 175 Terminal Avenue, Clark, New Jersey 07066. Note: online applications accepted only., • Schedule: Full time; Monday through Friday, 1:30 pm to 10:00 pm. More details upon interview., • Requirement: Prior cleaning experience is preferred. Willing to train!, • Fixed Pay Rate: $16.50 per hour. ESFM is the corporate Integrated Facilities Management (IFM) division of Compass Group USA and a Keystone member of the International WELL Building Institute (IWBI). We Make Applying Easy! Want to apply to this job via text messaging? Text JOB to 75000 and search requisition ID number 1473934. The advertised program is a conversational recruiting assistant that helps you apply to jobs with Compass Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or HELP for help. Terms and conditions: Rooted in hospitality, ESFM elevates the workplace experience as the single source of innovative FM solutions that ensure a safe, healthy, and sustainable environment. ESFM’s clients include many household names from Life Science, Technology, Oil & Gas and Manufacturing markets. ESFM self-performs 80% of all IFM solutions provided to clients. Their portfolio of service categories includes Environment, Health & Safety, Facilities Maintenance & Engineering, Sustainability, Janitorial & Industrial Cleaning, Laboratory Support and Workplace solutions. This self-performance model creates a consistent hospitality experience for clients, resulting in higher engagement and productivity from their employees. In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management Achievement from the International Facilities Management Association (IFMA). Job Summary Summary: Keeps buildings clean and orderly. Performs heavy cleaning duties, including cleaning floors, shampooing rugs, washing walls and glass, and removing rubbish. Essential Duties and Responsibilities: • Collects and disposes of trash following approved procedures and infection control plans., • Dusts and damp mops floors following approved procedures., • Moves equipment and furniture for proper cleaning and place furniture back in correct placement., • Cleans assigned areas with the use of assigned materials and equipment. Sanitize all surfaces. Follows the eight-step cleaning procedure., • Washes walls, windows, furniture, baseboards and other items to maintain a clean, safe environment for patients, visitors and staff., • Seeks out areas requiring cleaning; takes initiative to complete the task., • Completes all tasks assigned by supervisor., • Performs tasks in accordance with all federal, state and county guidelines., • Strips, scrubs, buffs and refinishes floors; shampoos carpet., • Contributes to the team; exhibits professionalism with customers, fellow employees and others. Full-time and part-time positions offer the following benefits to associates: Retirement Plan, Associate Shopping Program, Health and Wellness Programs, Discount Marketplace, Identity Theft Protection, Pet Insurance, Voluntary Benefits, including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program Full-time positions also offer the following benefits to associates: Medical, Dental, Vision, Life Insurance/AD, Disability Insurance, Commuter Benefits, Employee Assistance Program, Flexible Spending Accounts (FSAs) Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws. For positions in Washington State, Maryland, or to be performed Remotely, click here for paid time off benefits information. About Compass Group: Achieving leadership in the foodservice and facility management industry Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law. Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. Applications are accepted on an ongoing basis. ESFM maintains a drug-free workplace. ESFM

Job Description Maximum Quality Foods, Inc. Job Description Job Title: Forklift Operator FLSA/Grade: Non-Exempt/Hourly Reports to: Warehouse Supervisor Department: Operations Position Summary: The Forklift Operator is responsible for maintaining all stock inventory and pulling orders for manufacturing per designated work orders by performing the following duties. The position of Forklift Operator is not exempt from the overtime provisions of the Federal Fair Labor Standards Act and shall be entitled to overtime compensation for hours worked more than 40 in any one work week. The Forklift Operator shall be accountable and supervised by the Warehouse Manager. Essential Duties & Responsibilities: Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. • Oversees and maintains all stock inventories for warehouse daily., • Follows daily manufacturing work orders giving special attention to various materials., • Maneuvers heavy materials with the use of forklift, pallet and hand truck as required., • Unloads shipping trucks as required., • Maintains and ensures all machines are functioning per established work standards., • Assists shipping area with package procedures as requested., • Reports any concerns or discrepancies to management., • Maintains tools and equipment in a clean, orderly and safe manner., • Complies with company policies and procedures giving special attention to safety regulations., • Oral Communication Skills, • Written Communication Skills, • Reading Skills, • Dexterity Skills, • Math Skills, • Professionalism, • RF/WMS experience preferred.

We are seeking an innovative and highly motivated Manufacturing Supervisor for Cell Therapy Operations to join our team who will be responsible for ramp-up and oversight of the cGMP operations within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufa

Join Silgans Production Management Development Program and gain the skills and hands-on experience you need to excel in operations management at one of the largest metal food container manufacturing companies in the food packaging industry. This pro Management, Production, Operations Supervisor, Tra

Shift Supervisor – Springfield, NJ - $70k - $75k d/o/e This growing client needs your expertise to oversee all daily operations of the plant from production and manufacturing to ensuring policies and procedures are followed. Prior experience working in a food, pharmaceutical, cosmetic, or related

Citizen with the ability to communicate clearly in English.Only local NJ/NYC area people will be considered.Must reside within commuting distance of the Whippany New Jersey area.To qualify for this position you need to have experience with Panel Wiring, PLCs.HMI, Motor Drives, Control Systems, Varia

Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Creates employee schedules around manufacturing production hours and needs. Executes

Job Summary: The Senior Manufacturing Engineer will play a pivotal role in shaping and optimizing Roche's diagnostic manufacturing processes, ensuring high efficiency, quality, and compliance with regulatory standards. Competitive advantage: Opportunity to influence large-scale manufacturing improve

Develop and maintain manufacturing documentation (SOPs, records, specs).

Manufacturing Engineering Manager Location: Fairfield, NJ Direct Hire | Salary: $130,000 – $140,000 (DOE) We are seeking an experienced Manufacturing Engineering Manager for a direct hire opportunity with our client in Fairfield, NJ. This position combines leadership in engineering, manufacturing,

We are seeking a Senior Manufacturing Systems Engineer to lead the design, delivery, and maintenance of Manufacturing Execution Systems (MES). Job Title: Senior Manufacturing Systems Engineer. Lead the delivery, support, and optimization of global MES solutions in alignment with IT and manufacturing

The Production Supervisor will work closely with the Sr Manager of Fulfillment and Operations Manager to oversee all operational aspects of the distribution center, ensuring efficient product flow, accurate order fulfillment, and timely delivery by managing staff, optimizing processes, maintaining i

Provide leadership and direction for the day-to-day manufacturing operations to meet demand based on customer needs. Lead teams in solving manufacturing problems when gaps are detected. Recommend process and operational changes to overcome process issues, avoid deviations, and improve productivity b

A Depot Supervisor will be responsible for overseeing the operations and management of a depot dedicated to autonomous vehicles.

The Supervisor, QC Micro is an exempt level position with responsibilities for supervising the operation and workflow of the quality control microbiology laboratories in support of cell therapy manufacturing. Legend Biotech is seeking Supervisor, QC Micro as part of the Quality team based in Raritan

PrideStaff - 560337 [Warehouse Associate / Forklift Operator] As a Clamp Truck Operator at PrideStaff, you'll: Operate clamp trucks to load and unload materials safely and efficiently; Maintain accurate inventory records and ensure proper storage of goods; Conduct routine inspections and maintenance

Senior Quality Engineer Needed For Leading Manufacturing Company. Manufacturing & Process Quality.

As the Production Supervisor, you play a vital role in ensuring employee safety, maintaining product quality, and optimizing asset performance, all while adhering to the production schedule. As a role model, the Production Supervisor must lead by example, cultivating a workplace culture that inspire

What you need to succeed as a Freight Operations Supervisor at XPO Minimum qualifications: 2 years of related work experience in a warehouse, distribution, supply chain, transportation or similar environment Knowledge of the Less-than-Truckload (LTL) industry, hazardous materials regulations and DOT

Manufacturing Operator (2nd Shift) for a cGMP-regulated solid oral dosage facility. Ideal for mechanically inclined, detail-driven operators who want consistent hours, hands-on work, and clear growth in regulated manufacturing.

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Under the supervision of the Executive Director of the Movement Control and Communications Unit (MCCU), the Supervisor of MCCU is responsible for the oversight, supervision, and daily functioning of a team of direct reports in the centralized and around-the-clock communication and transfer hub for t

Job Title: Senior Materials Engineer Location: Mahwah, NJ Hours/Schedule: 8:00am to 5:00pm Compensation: $53.Type: Contract Responsibilities Develops and modifies process formulations, methods and controls to meet quality standards.In order to make an application, simply read through the following j

Knowledge of Fishbowl or Manufacturing/Inventory software a plus.

Serve as Acting Picking Supervisor in the absence of the Picking Manager.

Jewelry Manufacturing & E-Commerce. The ideal candidate is detail-oriented, organized, and thrives in a fast-paced manufacturing environment.

We are seeking a Senior Manufacturing Systems Engineer to lead the design, delivery, and maintenance of Manufacturing Execution Systems (MES). Job Title: Senior Manufacturing Systems Engineer. Lead the delivery, support, and optimization of global MES solutions in alignment with IT and manufacturing

The Second Shift Site Manager will lead and coordinate all second shift operations across Manufacturing, Warehouse, Maintenance, Quality, and Safety departments in a food manufacturing facility. Industry Leading Manufacturing Company Urgently Hiring A Second Shift Site Manager!. Supervise department

We’re seeking a Senior Engineer, Process Development to execute innovation and development projects with a focus on manufacturing processes, technology, and procedures for new products. Provide training for manufacturing team members. Solid knowledge of manufacturing processes, materials, product,