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Job Description POSITION OVERVIEW Data One Construction is seeking an experienced Site Superintendent to serve as the on-site leader and primary liaison between Data One project management, subcontractors, and stakeholders on mission-critical data center construction projects. In this role, you will be the bridge connecting all parties—ensuring seamless coordination, clear communication, and flawless execution. As Site Superintendent, you are responsible for day-to-day field operations, subcontractor management and coordination, stakeholder communication, safety oversight, quality assurance, and schedule adherence. You will manage multiple trades simultaneously, resolve on-site issues collaboratively, maintain transparent communication with all parties, and ensure all work meets Data One's rigorous standards. This is a leadership position requiring exceptional communication skills, collaborative problem-solving ability, and the capacity to lead through influence rather than authority. If you excel at coordinating complex operations while keeping all stakeholders aligned and satisfied, this is your opportunity. KEY RESPONSIBILITIES Subcontractor Coordination & Management • Serve as primary on-site interface with all subcontractors and specialty contractors, • Conduct pre-work meetings with each trade to clarify scope, sequencing, expectations, and project requirements, • Verify subcontractor qualifications, insurance, safety certifications, and compliance documentation, • Monitor subcontractor performance including schedule adherence, quality of work, and safety compliance, • Address performance issues directly and collaboratively; implement corrective actions as needed, • Coordinate work sequencing to prevent conflicts and maintain efficient project flow, • Manage subcontractor change orders, time tracking, and documentation, • Build positive working relationships with subcontractors while maintaining professional accountability, • Facilitate communication between subcontractors when coordination between trades is required, • Resolve day-to-day subcontractor issues and escalate complex matters to Project Manager PM & Project Management Liaison • Serve as primary on-site representative and direct liaison to Data One Project Manager, • Provide regular project updates to PM including daily progress, issues, risks, and schedule status, • Communicate design clarifications, change orders, and scope modifications from engineering to field teams, • Execute PM directives and ensure field implementation aligns with project requirements, • Escalate critical issues, safety concerns, or schedule risks immediately to PM, • Maintain accurate field documentation and daily reporting for PM review, • Coordinate PE/engineer site visits and support engineering assessments, • Support project management with cost tracking, budget updates, and schedule forecasting Stakeholder Communication & Liaison • Serve as primary on-site communication point for project stakeholders (client, owner representatives, consultants, architects, engineers), • Conduct weekly coordination meetings with stakeholders addressing schedule, quality, and operational issues, • Provide transparent, professional updates on project status, progress toward milestones, and any concerns, • Manage stakeholder expectations regarding schedule, quality, and cost through proactive communication, • Address stakeholder questions and concerns professionally and promptly, • Represent Data One professionally in all stakeholder interactions, • Facilitate site visits and project tours for stakeholders as needed, • Maintain positive relationships while advocating for Data One's interests and project requirements Field Operations & Project Leadership • Manage daily construction operations and coordinate field team activities, • Oversee job site layout, equipment staging, material delivery coordination, and logistics, • Enforce strict adherence to project schedule while maintaining quality standards and safety protocols, • Identify and resolve on-site conflicts, bottlenecks, and operational challenges in real-time, • Support project manager with field reporting, daily logs, and project documentation, • Ensure efficient workflow across multiple trades and activities Safety & Compliance Oversight • Maintain overall responsibility for site-wide safety culture and OSHA compliance, • Conduct daily jobsite safety inspections and toolbox talks, • Verify that all subcontractors maintain required safety certifications and training, • Investigate safety incidents, near misses, and hazardous conditions; implement corrective actions, • Monitor PPE compliance, equipment safety, and adherence to jobsite safety protocols, • Enforce zero-tolerance safety standards and coordinate with company safety leadership, • Support emergency response procedures and maintain incident documentation Quality Assurance & Inspection • Verify that all construction work meets specifications, blueprints, and quality standards, • Conduct daily quality inspections and document deficiencies, • Coordinate with inspectors, testing companies, and third-party verification entities, • Ensure proper documentation of inspections, testing results, and compliance records, • Identify quality issues early and implement corrective actions before escalation, • Support punch-list compilation and final inspections prior to project closeout Schedule Management & Documentation • Monitor daily progress against project schedule and identify variances, • Track subcontractor productivity and identify schedule risks, • Coordinate activities to maintain critical path and meet project milestones, • Maintain daily jobsite logs including weather, productivity, staffing, and incidents, • Document delays, changes, and impacts to schedule, • Prepare weekly progress reports for project management, • Support schedule updates and forecasting with accurate field data REQUIRED QUALIFICATIONS • 8+ years of construction superintendent or project management experience on commercial, industrial, or data center projects, • Proven experience coordinating and managing multiple subcontractors and diverse trades, • Exceptional communication skills with ability to interface effectively with subcontractors, clients, engineers, and stakeholders, • OSHA 30 Certification or willingness to obtain within first 90 days, • Deep knowledge of construction processes, sequencing, and scheduling, • Ability to read and interpret construction blueprints and specifications, • Understanding of construction contracts, change orders, and project documentation, • Proficiency with construction management software (scheduling, budgeting, documentation), • Valid driver's license and reliable transportation, • Ability to work full-time on-site in Franklinville, New Jersey, • Physical capability to work in construction environments (climbing, bending, standing, walking jobsites), • High school diploma or equivalent; Bachelor's degree in construction management preferredCompany DescriptionAt Data One Construction, you’ll be part of building the infrastructure that powers today’s digital world. Specializing in data center construction, our projects are fast-paced, high-impact, and essential to keeping businesses and communities connected. We offer a strong pipeline of work, a collaborative team environment, and the opportunity to contribute to complex, cutting-edge builds where quality, safety, and precision matter every day.At Data One Construction, you’ll be part of building the infrastructure that powers today’s digital world. Specializing in data center construction, our projects are fast-paced, high-impact, and essential to keeping businesses and communities connected. We offer a strong pipeline of work, a collaborative team environment, and the opportunity to contribute to complex, cutting-edge builds where quality, safety, and precision matter every day.

WCS Healthcare Partners is seeking a local contract nurse RN Labor and Delivery for a local contract nursing job in Vineland, New Jersey. Job Description & Requirements • Specialty: Labor and Delivery, • Discipline: RN, • Duration: 13 weeks, • 36 hours per week, • Shift: 12 hours, • Employment Type: Local Contract WCS Healthcare is currently seeking a Labor and Delivery Nurse for a contract assignment at a Prestigious Hospital in Vineland, NJ. Job Function: \n • Shift: Nights, 6:45pm to 7:15am\n, • Categorizes patients in the appropriate level of classification. \n, • Applies external fetal monitor and interprets fetal heart tracing and uterine activity. \n, • Implements intervention appropriately based on fetal heart rate pattern and maternal status during labor. \n, • Identifies emergency situations, observes age and notifies provider accordingly. \n, • Administers medication according to the 5 rights of safety and infection control guidelines and or per Provider's orders. \n, • Screens patients for pain during the initial assessment and reassess according to guidelines. \n, • Assists the physicians/midwife during a delivery \n\n Job Requirements:\n • 3 years of experience\n, • Must have postpartum couplet care experience\n, • EPIC experience required \n, • BLS, NRP & ACLS\n\n Disclosure: The hourly rates and/or salaries listed may or may not reflect total compensation packages including bonus and fringe benefits, etc., nor are the advertisement(s) posted a guarantee of a certain compensation package for a position or bona fide offer of employment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. \n \n ITAC1 \n #LI-DNP \n 45978 White Cap Search Partners Job ID #45978. Posted job title: RN - L&D About WCS Healthcare Partners With WCS Healthcare Partners, every Job Seeker grows stronger, moving one step forward with each job placement. We take the time to get to know the needs and qualifications of each Healthcare professional to match you with the right clinical setting, patient population, merging your compensation and career goals with your desired work environment. Our recruiters are experts at navigating the dynamic nature of healthcare employers to get your resume in front of the right decision makers. NURSING ● Registered Nurses (RN) ● Licensed Practical Nurses (LPN) ● Travel Nursing ● Quality Assurance/Review, Performance Improvement, HEDIS ● Nursing Leadership ● Case Management ALLIED HEALTH ● Technologists: Medical, Laboratory, Cardiac, RadTech, X-Ray ● Therapy: Physical, Occupational and Speech Therapy ● Social Work: LCSW/LMSW, Case Management, Care Coordination ● Med Support: Medical Assistants, Phlebotomy, Surgical/Sterile Techs ● Pharmacists and Pharmacy Techs ● Dental Hygienist, Dental Assistants OPERATIONS & FINANCE ● Practice Management ● Clinical Operations ● Administrative Support ● Reception, Clerical, Call Center ● Claims Appeals/Denials/Reimbursement ● Insurance Pre-Authorizations ● Medical Billing/Coding Benefits • 401k retirement plan, • Weekly pay

Job Description POSITION: Machine Operator (Multiple Positions due to expansion) We are growing!!! Shift: Thursday, Friday, Saturday — 4:45 p.m. to 5:00 a.m. (Open to being flexible to work other shifts) About the Role We are looking for a Machine Operator to join our Vineland production team on the V5 schedule. This role is responsible for safely operating production equipment, monitoring performance, performing basic troubleshooting, and keeping accurate computer-based records. A strong comfort level with both machine operation and computer systems is essential. Key Responsibilities Operate production machinery safely and efficiently Perform equipment start-up, adjustments, and basic troubleshooting during operation Monitor machine performance and communicate any issues to leadership or maintenance Use computer systems to enter production data, track runs, document downtime, and complete digital forms Ensure product quality meets company standards Follow all safety, GMP, and food safety procedures Support continuous improvement by identifying opportunities to optimize performance Requirements Strong computer skills — ability to navigate production software, input data accurately, and complete digital documentation Operator experience in a manufacturing or food production environment Ability to troubleshoot routine mechanical or operational issues SAP ERP experience is highly recommended Must be able to work independently and reliably on the V5 schedule (Thursday–Saturday, 4:45 p.m.–5:00 a.m.) Ability to work in a fast-paced environment and stand for extended periods What You’ll Do You’ll play a key role in bringing high-quality bakery products to life by supporting the full production process: • Ensure strict compliance with food safety and quality standards at every stage of production, • Accurately measure, weigh, and prepare ingredients for production runs, • Mix and blend ingredients according to established formulas and specifications, • Set up, calibrate, and operate production equipment for efficient runs, • Monitor processes to ensure consistency, quality, and performance targets are met, • Maintain a clean, safe, and organized work environment alongside your team, • Use ERP/MRP systems to support inventory tracking, production scheduling, and workflow accuracy, • Participate in continuous improvement efforts to help make our processes even betterWhat We’re Looking For We’re seeking individuals who are ready to grow, take ownership, and build a long-term career: • Experience in food and beverage manufacturing or production environments, • Strong understanding of food safety and quality assurance practices, • Hands-on experience with measuring, weighing, and ingredient preparation, • Familiarity with mixing, blending, or batching processes, • Exposure to ERP/MRP systems (or ability to learn quickly), • Ability to set up and operate production machinery, • Strong attention to detail and commitment to doing things the right way, • A team-focused mindset with good communication skillsWhat We Offer Bridor USA believes in rewarding great work and supporting long-term career growth. We offer a comprehensive benefits package, including: • Medical, Dental, and Vision Insurance, • Paid Time Off (Vacation, Sick Time, and Paid Holidays), • 401(k) Retirement Plan with Company Match, • Life Insurance and Disability Coverage, • Training and Development Opportunities, • Career Growth in a Fast-Growing Manufacturing EnvironmentWhy Bridor USA, • A growing company with real opportunities for advancement, • A strong focus on training, development, and internal growth, • A team-oriented environment where your work makes a daily impact, • Stability, structure, and the chance to build a long-term career—not just a jo #LI-DNI (Thursday–Saturday, 4:45 p.m.–5:00 a.m.)

Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Labcorp is seeking a Support Services Supervisor to join our team in Vineland, NJ. Work Schedule: Monday – Friday 6:00am-2:30pm, additional days and hours may be required Job Responsibilities: Supervise the day to day operations of the non-technical staff for the Accessioning and Phlebotomist departments Assist with preparation of laboratory specimens for analysis and testing Directly supervise, train, and mentor non-technical personnel of the department Monitor daily workflow in the lab and schedule adequate coverage Responsible for ensuring all shifts in the department are properly staffed Research and resolve any production errors while escalating when necessary Engage in continuous process and service level improvements Perform quality assurance checks to ensure efficiency and accuracy Prepare and maintain Quality Assurance records and documents Meet regularly with direct reports to provide coaching and feedback for their development Responsible for administering and managing policies and procedures Minimum Qualification: High school diploma or GED or equivalent 3 years or more experience in clinical laboratory environment Preferred Qualifications: Associates degree 1 year or more supervisory or leadership experience Current or prior Labcorp experience Additional Job Standards: Strong computer skills and working knowledge of Microsoft Office Excellent communication skills; both written and verbal High level of attention to detail with strong organizational and prioritization skills Strong critical thinking skills with the ability to make decisions in a fast paced environment Ability to handle the physical requirements of the position Familiarity with laboratory operations as well as policies and procedures Able to pass a standardized color blindness test Are you detail oriented, process focused, and enjoy leading others? Are you looking for an industry leading company that offers growth and stability? **Salary Range: $80,000 - $105,000 per year All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here. If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today! Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

ABOUT US Together, we are the Epic Special Education Staffing family and family is how we view each member of this incredible community. From our family to the nation’s schools, we remain focused on providing a world of opportunities for you to leverage your abilities and make an impact on special education. Apply today! POSITION DESCRIPTION Epic Special Education Staffing is partnering with an exceptional school district who is looking for a contract Deaf and Hard of Hearing Teacher for the 2026 - 2027 school year. · Duration: 10/19/2026 - 03/19/2027 · Location: Egg Harbor Township, NJ · Location Type: On-Site · Schedule: Full Time · Hours: 32.50 · Grade/Age Levels: Elementary School;Kindergarten;Pre-K · Weekly Pay Range: $38.25 – $43.99 per hour on a local contract BENEFITS We offer a variety of benefits for you and your loved ones. As a valued and respected part of the Epic family, you will enjoy: · Competitive compensation packages for both local and travel contracts · Medical, Dental, and Vision benefits · Infertility & Domestic Partner Coverage · Summer Insurance Coverage · Paid Non-Student Days & Holiday Pay · 401K matching · Wellness and Employee Assistance Program (EAP) · CEU & license reimbursements · Referral bonuses of $1000 QUALIFICATIONS The minimum qualifications for Deaf and Hard of Hearing Teacher: · 1 year of verifiable, professional experience as Deaf and Hard of Hearing Teacher within the last 3 years (may include residency or clinical practicum) · Valid Deaf and Hard of Hearing Teacher credential/license or in process in state of practice · Employees must be legally authorized to work in the United States and will be asked for proof upon hire. We are unable to sponsor or take over sponsorship of an employment Visa at this time. At Epic Special Education Staffing, you will have the opportunity to apply your unique experience and expertise with school-based special education as your singular focus. We offer stimulating and rewarding careers that provide an opportunity to make a difference in a child's life! By applying for this position, you agree that any calls from Epic Staffing Group and its subsidiaries may be monitored or recorded for training and quality assurance purposes. Epic Staffing Group 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, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us. Know someone great? Refer them and earn a $1,000 bonus for each referral who reaches their contract milestone, plus we’ll make a $250 donation to a special education–focused organization on your behalf.

Job Description Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further – Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company – we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. • Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement., • Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positively impact patients' lives., • Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry., • Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing., • Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today! This position will report directly to the Director of Corporate Quality and Compliance (PharmD). The Pharmacy Manager / Pharmacist-in-Charge (PIC) is responsible for applying clinical knowledge to appropriateness of formulation, processes, and procedures related to sterile pharmaceutical manufacturing and related activities in a 503B Outsourcing Facility. The Pharmacy Manager / PIC will work collaboratively with other pharmacists, technicians, and various staff members to manufacture sterile drug products to fill customer orders in compliance with all regulatory requirements and company policies and procedures. Quality Assurance Pharmacists and Regulatory Support Technicians will report to the Pharmacy Manager / PIC . Essential Functions: • Review and verify formulation (compounding) activities and documentation performed by technicians and other support staff for completeness, accuracy, and adherence to cGMPs. Such verifications may require ISO 8 cleanroom gowning attire and functions., • Perform the final review and release of batches., • Ensuring compliance with all federal, state, and local regulations related to facility activities, USP 797, cGMP, and controlled substances, • Author, review, and/or approve various cGMP documents such as customer complaint investigations, adverse drug event investigations, deviations, CAPAs, SOPs, Change Controls, Master Product Batch Records, and Annual Product Review reports., • Create, update, and approve product labels and determine appropriate label content per applicable regulations., • Train manufacturing technicians to perform pharmaceutical calculations., • Perform DEA recordkeeping activities., • Perform required federal and state regulatory reporting as applicable., • Efficiently utilize tools and metrics (KPI’s) to monitor staff productivity, deliverables, timelines, and quality of work product to adjust staffing levels and operational processes as needed to ensure operational effectiveness., • Participate in internal audits, regulatory inspections, and customer audits as necessary., • Answer clinical questions from physicians, nurses, and other healthcare providers., • Work collaboratively with members from various teams to achieve company goals., • Maintaining active pharmacist licenses in all states that require PIC licensing., • Other duties as assigned. Supervisory Responsibilities: • Directly supervise Quality Assurance Pharmacists and Regulatory Support Technicians., • Foster a positive and productive work environment, providing guidance, coaching, and mentoring., • Conduct regular 1:1’s to address performance, feedback and relationship building., • Identify training and development needs within the team and facilitate as able. Experience and Necessary Skills: • Pharmacy Degree (PharmD preferred), • Licensed Pharmacist in the state of site location (New Jersey) and all states that require PIC licensing. Candidates without all required licenses will be required to obtain all necessary licenses after hire., • 3 years’ experience in a 503(b) outsourcing facility OR R&D or pharmacovigilance role in the pharmaceutical industry OR other relevant management experience required, 5 years preferred., • Familiarity & Understanding of Sterile Manufacturing/Processing (USP testing, sterilization techniques, etc.) preferred, • Familiarity & Comprehension of regulations including DQSA, 21 CFR 211 and USP guidelines, as applicable., • Good computer skills, including but not limited to Word, Excel, PowerPoint, • Excellent interpersonal and communication skills, both verbal and written, • Ability to assume responsibility and act on own initiative, • Ability to lead and influence a team to achieve desired goals, • Good self-management, organizational and planning skills, • Ability to adhere to strict deadlines and procedures, • Excellent reasoning and critical thinking skills, • Hands- on approach with a “can-do” attitude and results orientation, • Good listener, but proactive in group discussions Benefits: • Smart healthcare coverage options that rewards wellness (and puts money back in your pocket!), • Flexible Spending & Health Savings Accounts (FSA & HSA) available, • Dental & Vision insurance, • Employer Paid Life Insurance & Employee Assistance Program, • Short Term & Long-Term Disability Insurance, • Up to 4% 401K Matching (100% vested on day one!), • Generous Paid Time Off Options – vacation, sick, paid leave and holidays!, • $5,250 Annual Tuition Reimbursement after 6 months, • $1,000 Referral Bonus Program with no limit, • Eligible for annual bonus program Location: New Jersey Timeline: We will be accepting applications on an ongoing basis until position is filled. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. *Please note that we do not work with third-party recruiters or agencies for this position. If you are a qualified candidate and wish to apply for this job, please do so directly through our official application process. We appreciate your understanding and cooperation in this matter.

Job DescriptionCardiovascular Cath Lab Tech Location: Bricktown, New Jersey Job Type: Contract (13 Weeks) Local Pay Rate: $2,800 - $2,900 Weekly Traveler Pay Rate: $3,250 - $3,350 Weekly Weekly Hours: 40 Hours Shift: Days Schedule: 7:00 AM – 5:30 PM Position Overview We are seeking an experienced Cardiovascular Cath Lab Tech to support physicians and clinical teams during diagnostic and interventional cardiovascular procedures. The ideal candidate will have strong Cath Lab experience, expertise with cardiovascular imaging equipment, and the ability to thrive in a fast-paced acute care environment. Required Qualifications • High School Diploma or equivalent required., • Minimum two (2) years of Cardiac Catheterization Lab experience in an acute care hospital., • ARRT Certification required., • Current BLS Certification required., • Radiologic State License required where applicable., • Experience operating C-arm and fluoroscopy imaging equipment., • Knowledge of hemodynamic monitoring systems and sterile procedural techniques., • Ability to participate in on-call coverage and emergency procedures., • Bachelor's Degree preferred. Responsibilities • Prepare sterile trays and organize procedure-specific equipment., • Prepare patients for cardiac catheterization and cardiovascular procedures., • Attach EKG leads and perform patient preparation according to established protocols., • Assist physicians during diagnostic and interventional cardiac procedures., • Operate C-arm and X-ray imaging equipment during procedures., • Load and operate power injectors., • Calibrate and monitor hemodynamic equipment., • Assist with vascular closure devices and sheath removal procedures., • Maintain digital imaging systems and procedural documentation., • Support emergency interventions and patient stabilization efforts., • Assist with inventory management and supply control., • Participate in equipment maintenance, calibration, and quality assurance activities., • Maintain compliance with infection prevention, safety, and hospital policies. Contact Information For more details contact at hdavda@navitashealth.com or Call / Text at 516-862-1169. About Navitas Healthcare, LLC It is a Joint Commission Certified / WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. We offer the most competitive pay for every position we cater. We understand this is a partnership. You will not be blindsided and your salary will be discussed upfront.

Job Description Summer Tutor in Vineland & Paulsboro Start date: July 6- July 30, 2026 Reports To: Site Coordinator Subordinate Staff: none Site Information • Locations:, • BGC Vineland (304 W. Plum Street Vineland NJ 08360), • BGC Paulsboro (916 Penn Line Rd. Paulsboro 08066), • Summer schedule from 9am-12pm, • 3-4 days per week; Monday - Thursday, • Hours do not exceed 12 hours per week BASIC FUNCTION The NJ| PA Tutoring Corps Inc. provides high-impact tutoring for K through Grade 8 students in math and literacy to close learning gaps. The New Jersey Tutoring Corps seeks to hire tutors to work with scholars in partnership with the Boys and Girls Club in Vineland or Paulsboro. Tutors will work with small groups of scholars, typically in groups of 1-4, in grades K-8, in building skills in math and literacy. ESSENTIAL FUNCTIONS • Engage and communicate instructions with scholars in grades K- 8th to build on existing mathematics and/or literacy skills;, • Complete daily records, including attendance (digitally) on scholar progress and site needs using the tools provided;, • Tutors must be able to sit with scholars for 4-6 hours a day;, • Prepare lessons digitally, use the data to drive instruction, and maintain respect for the confidentiality of all program data;, • Have proficient technology skills;, • Communicate regularly with your site coordinator to provide optimum learning experiences for scholars;, • Participate in coaching from an instructional coach and demonstrate the ability to receive and act upon feedback;, • Possess the desire to continuously grow and learn;, • Use an asset-based approach in working with scholars “glass half full”;, • Be responsive and work collaboratively with a team-oriented mindset; this includes, but is not limited to, collaborating with classroom teacher and building administration;, • Complete all training;, • Arrive to work on time,, • Complete other duties as assigned. EMPLOYER REQUIREMENTS • Individuals must have teaching/mentoring experience (or recently retired), or subbing (60 credit) experience, or tutoring experience, • Knowledge of NJ Student Learning Standards for Math & ELA;, • Maintain integrity, resilience, trustworthiness, and patience with scholars and teammates;, • Espouse the belief that all scholars deserve the highest-quality education;, • Professionalism—We do critical work to help grow scholars skills and confidence, and we do it with the highest degree of professionalism;, • Professional skills include attention to detail, timely and proactive communication, and job preparedness;, • MUST have a Gmail email address or be willing to create a Gmail account; and experience with Google Suite applications: Google Docs, Sheets, and Forms;, • Employees are encouraged to use their private computer device(s) to perform work-related assignments. If necessary, employees can ask for a company loaner;, • Genuine desire to work with young children in a small group tutoring/academic intervention capacity, building on foundational skills and closing learning gaps using formative and summative data and strong teaching pedagogy;, • New Jersey or Pennsylvania Fingerprint Certificate and Background Clearance- The final offer of employment is contingent upon the successful completion of a background check and employment authorization verification;, • Must adhere to local health department and school district requirements for the site at which you are working, including any mask rules that must be followed, if applicable., • Reliable transportation to travel to sites;, • Bilingual (optional, but a plus). APPLICATION • Please submit your resume via the online platform you are using to apply., • Before being hired, you will be asked to email your teaching certification (if applicable) and one professional letter., • Upon accepting an offer with NJ|PATC, you are required to have an active Criminal Background Fingerprint Certificate AND a Child Abuse History Clearance., • If you do not have a certificate, you will be required to obtain the required certificate upon working on-site., • Applications will be considered until all positions are filled., • The final offer of employment is contingent upon the successful uploading of required documents and completion of background and reference checks. JOB DISCLAIMER Please note that our school-year tutoring schedule is based on the school calendar for the partners we serve. These calendars include predictable break periods during which onsite staff may not be required to work. The predictable vacation periods include (but are not limited to) the following: • Winter break (mid-December to mid-January), • Spring break (mid-March to mid-April), • Summer break (mid-May to mid-September), • Detailed dates to follow Employees have reasonable assurance of returning to work after a predictable vacation period unless otherwise informed. COMPANY: New Jersey Tutoring Corps Inc. DEPARTMENT: Tutors COMPENSATION: $30- 40/hrs. Vary; Semi-monthly; Paid Training All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, veteran status, or any other characteristic protected by federal, state, or local law. New Jersey Tutoring Corps, Inc. makes reasonable accommodations wherever necessary for all employees or applicants, provided that the individual is otherwise qualified to safely perform the essential duties and assignments connected with the job and provided that the accommodations do not require significant difficulty or expense.

Job Description Join the dynamic team at Cumberland County Guidance Center as the Full-Time Director of Clinical Care Systems Operations in Millville, NJ! This is an exceptional opportunity for Licensed Clinical Social Workers with supervisory experience to lead transformative initiatives in healthcare. You’ll play a vital role, shaping clinical strategies that deliver empathetic and customer-centric care. Enjoy the excitement of working onsite, fostering a vibrant, energetic culture while collaborating with passionate professionals who share your commitment to problem-solving. With a competitive salary of $90,000, you’ll be rewarded for your expertise as you drive meaningful change in the community. This is more than just a job; it’s a chance to innovate and inspire in a role where your impact is felt every day. You will be provided great benefits such as Medical, Dental, Vision, 401(k), Life Insurance, Competitive Salary, Paid Time Off, and Employee Discounts. Are you ready to embark on this thrilling journey in healthcare leadership? Apply now! Who are we? An Introduction For over 60 years, The Guidance Center has been a primary mental health support agency, providing compassionate, professional care to individuals and families in Cumberland County, NJ. As a non-profit organization, our dedicated team of professionals, including doctors, nurses, therapists, and support staff, works to diagnose and treat all types of mental illness. Make a difference as a DIRECTOR- CLINICAL CARE SYSTEMS OPERATIONS As the Clinical Care Systems Director of Operations at Cumberland County Guidance Center, you will provide essential administrative and clinical leadership for our Outpatient and Community Support Services (CSS) programs. In this exciting role, you’ll oversee daily operations while offering clinical supervision to staff delivering vital behavioral health and substance use services. Your expertise will ensure compliance with state and federal guidelines and support ongoing staff development through evidence-based approaches like Motivational Interviewing (MI) and Cognitive Behavioral Therapy (CBT). You'll monitor employee productivity, facilitate interdisciplinary care, and uphold high standards for client engagement and treatment planning. Additionally, you'll prepare and manage contracts and budgets, collaborate with various departments, represent the agency at county and state meetings, and ensure HIPAA compliance. This is your chance to make a profound impact in a vibrant environment focused on quality assurance and continuous improvement! Requirements for this DIRECTOR- CLINICAL CARE SYSTEMS OPERATIONS job To thrive as the Clinical Care Systems Director of Operations at Cumberland County Guidance Center, a robust set of skills and qualifications is essential. Applicants must possess a Master's Degree in Behavioral Health Sciences or a related discipline, along with LCSW credentials. The role requires the CCS certification. A minimum of two years in the administration of behavioral health services, complemented by five years of clinical experience working with psychiatric and co-occurring disorders, will set candidates up for success. Additionally, strong leadership, problem-solving, and communication skills are paramount, as you will be overseeing program directors and fostering collaborative interdisciplinary care. A valid New Jersey driver's license with a clean five-year driving record that meets organizational standards is also necessary for this impactful position. Knowledge and skills required for the position are: • Master's Degree in the Behavioral Health Sciences or related discipline, • LCSW and CCS required at hire or obtained shortly thereafter with specialized training, • Two years of experience in administration of behavioral health services, • Five years of clinical experience working with psychiatric and co-occurring disorders, • Possession of a valid New Jersey driver's license with a clean five-year driving record that meets organizational standards and qualifies for insurance coverage.Our team needs you! We believe in taking care of our team, both on and off the job. That's why we offer a mobile-friendly application process - because we know your time is valuable. If you're ready to take your management skills to the next level and join a team that values hard work and good times, complete our application today! A Background Check is required Clear Five year driving record/abstract with ability to be insured by organizations carrier. Job Posted by ApplicantPro

We guarantee 15-25 hours per week with an hourly pay of between $25/hr. Be able to work 15-25 hours per week and commit to a certain routine. The hours are completely flexible and no previous experience is necessary.

Job DescriptionPathLink of New Jersey is seeking a full-time Anatomic & Clinical Pathologist to join our team in Vineland, NJ. The selected candidate will provide high-quality diagnostic services within a collaborative outpatient medical environment, supporting physicians and clinical teams in delivering accurate and timely patient care. Monday – Friday, 9:00 AM – 5:00 PM Key Responsibilities • Perform histopathologic and cytologic evaluations, • Interpret clinical pathology results and provide consultative support, • Correlate laboratory findings with patient clinical information, • Collaborate with physicians and multidisciplinary teams, • Ensure adherence to quality assurance and regulatory standardsQualifications, • MD or DO degree required, • Board Certified or Board Eligible in Anatomic & Clinical Pathology, • Active New Jersey medical license (required), • Strong diagnostic and interpersonal skillsWork Environment, • Outpatient medical center setting, • Case volume: approximately 30–60 cases per weekAbout PathLink of New Jersey PathLink of New Jersey is committed to delivering high-quality pathology services through a team-oriented and patient-focused approach. We pride ourselves on maintaining a collaborative work environment that supports professional growth and clinical excellence.

Tris Pharma in South Brunswick, NJ, seeks a Quality Assurance Research and Development Chemist I to support Quality Control and Analytical R&D activities.

Quality Analyst The Quality Analyst is responsible for the oversight and execution of Quality Management Systems and compliance at the Distribution Center. The Quality Analyst serves as a single point of contact to the Sr. Manager, Janssen Commercial Quality and Supply Chain partners on compliance related matters and is the liaison with multiple Quality and Compliance organizations to drive timely resolution of quality and compliance related issues. The Quality Analyst identifies business issues, identifies opportunities to continuously improve quality and compliance and leads improvement opportunities and problem solutions. The Quality Analyst implements and executes quality and compliance programs to ensure effective and consistent processes with established standards. Roles & Responsibilities: Quality and compliance product receiving process, including, but not limited to receiving inspection activities such as review of temperature monitoring devices and systematic transactions in Warehouse Management System and/or SAP Monitoring and following Quarantine/Hold/Stop-Ship/Recall processes and notices Product refusals process activities, including, but not limited to inspection and disposition Serve as single point of contact to internal and external partners on Distribution Quality related matters and liaise with multiple Quality organizations to drive timely resolution of Quality related issues Responsible for adherence to the Deviation, Corrective and Preventative Action (CAPA), and Change Controls processes and Interface collaboratively with other business partners and stakeholders Provide training to new hires (FTEs) and/or Contractors Operate in a team-based environment with minimum supervision Supports 24/7 operations of the Distribution Center Monitor and review temperature data for the Distribution Center and ancillary areas Compliance oversight for the end-to-end Re-Pack-Re-Label processes, including, but not limited to Batch Record/Protocol activities Compliance oversight for the end-to-end clinical supply chain processes, including, but not limited to re-stickering and other labelling activities Responsible for making quality decisions based upon assessments of compliance risks balanced with the overall business needs Evaluate the overall compliance risk and recommending corrective actions and tracking progress Ensures compliance and remaining current with local, state, federal, and international regulations and standards Support of New Product Launch activities at the Distribution Center, including, but not limited to Master Data (sIDMa) set-up Perform gap assessments in local procedures to Pharmaceutical Global Standards, Business processes, and External Standards Identify business issues, communicates to management, prioritizes for action, and leads improvement opportunities and problem solutions in collaboration with other Supply Chain partners. Identifies opportunities to continuously improve quality, cost and time factors, consistent with both Janssen Commercial Quality and DELIVER Supply Chain business objectives Drives innovation within functional areas while ensuring functional initiatives are delivered in a compliant and safe manner Develop and review of Standard Operating Procedures (SOPs), Work Instructions (WI) and other documents, as needed Provide data/information/metrics to management for Quality System Management Reviews Notify/escalate critical quality issues to management in a timely manner Provide quality and compliance oversight for execution of Protocols Plans, support, and coordinates quality and compliance programs designed to ensure effective and consistent processes with established standards by performing the duties personally Supporting internal and external audits Responsible for adhering to the Training process Responsible for adherence to the Records Management and Retention processes Education & Experience: A minimum of bachelor's degree in an Engineering, Life Science, and Technical scientific or related discipline is preferred. In absence of a bachelor's degree, special consideration would be considered for individuals who have related and background experience. A minimum of 2 years of experience in a highly regulated industry is required. Quality and Compliance experience in the Medical Device, Pharmaceutical or Consumer products industry and experience in distribution is preferred. Strong communication, teamwork, problem solving, decision-making, and root cause analysis skills are required. Experience with Warehouse Management Systems and SAP is preferred. Experience with Quality Management Systems such as COMET is preferred. Proficiency in organizational and project management skills is preferred. Experience with Temperature Control is preferred. This position may require up to a 10% of domestic travel. #J-18808-Ljbffr

Join our team as a QC/Production Associate I, where you'll play a key role in producing life-changing drug products and ensuring their quality through hands-on work with advanced radiosynthesizers and analytical equipment. Title | QC/Production Associate I Department | Network Operations Reports To | Facility Manager Compensation: $25-$27/hr Overview The QC/Production Associate I will operate the radiosynthesizers for the production of drug product, as well as operate analytical equipment for the quality control of drug product. Essential Duties and Responsibilities • Perform FDG and NaF synthesis according to Standard Operating Procedures (SOPs):, • Ensure all materials/reagents are accepted according to SOPs and within expiry, • Ensure all equipment is appropriately qualified prior to use, • Operate the synthesis unit according to SOPs, • Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit, • Perform FDG and NaF quality control (QC) processes according to SOPs:, • Assist with basic maintenance of QC equipment, • Ensure all equipment is appropriately calibrated and qualified prior to use, • Operate the QC equipment according to SOPs, • Ensure completion of applicable cGMP documentation., • Assist with inventory management:, • Maintain production/QC/cleaning supply levels as appropriate, • Assist with inventory reporting, • Perform material acceptance according to SOPs, • Communicate with local and Network support resources to troubleshoot equipment, production, or QC issues., • Perform basic computer-controlled cyclotron operations for FDG and NaF production under the advisement of site Cyclotron and Facility Engineer., • Maintain a clean and safe working environment., • Perform radiation safety duties according to SOFIE's Corporate Radiation Compliance Program and site licensing requirements., • Maintain all qualification and validation requirements for entering ISO classified area., • Clean classified and non-classified areas according to SOPs., • Perform environmental monitoring of classified areas according to SOPs., • Report manufacturing metrics into data repository as required., • Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:, • Investigations, • Corrective and Preventative Actions, • Deviations, • Out of Specifications, • No or Atypical Yields, • Manufacturing and QC Records, • Logbooks, • Attend internal meetings as required., • Other assigned duties as required. Qualifications • High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred., • Technical experience with computer-controlled automation preferred., • Efficient in the use of MS Office Suite required., • Ability to work various shifts and weekends required., • Ability to be detail-oriented, accountable, patient, organized, and work in a team environment required., • Ability to communicate professionally with colleagues and customers, have excellent attention to detail, and be dependable and responsible in a fast-paced, highly technical environment required., • Ability to lift ~50 lbs. required., • Up to 5% travel required.

Overview Aviation Electronics, Electrical and Computer Systems Technicians keep Navy aircraft mission ready by maintaining, troubleshooting, and repairing the electrical power, avionics, and computer based systems that enable radar, communications, navigation, flight controls, and weapons at sea and ashore. Qualified Sailors may also volunteer as Naval Aircrewmen and perform in flight systems operations and mission support. Key Responsibilities Troubleshoot and repair complex aircraft systems including digital computers, fiber optics, radar, laser electronics, infrared detection, and communications and navigation suites. Maintain aircraft electrical power generation and distribution systems. Test and calibrate aircraft instruments and automatic flight controls. Perform micro miniature circuit card repair for qualified technicians. Install modifications and upgrades to aircraft avionics and electrical systems. Use diagnostic equipment and interpret schematics and wiring diagrams to restore systems to full mission capability. What to Expect A mix of hands‑on flight line maintenance and bench diagnostics in hangars, avionics shops, and aboard aircraft carriers; frequent troubleshooting under time pressure to return aircraft to service; work around high‑tempo flight operations with rotating shifts, nights, and weekends while deployed; strict adherence to safety, tool control, foreign object damage prevention, tag‑out procedures, and quality assurance standards; opportunities to qualify as a work center leader or collateral duty inspector as you gain experience. Work Environment Assignments with squadrons at naval air stations and aboard aircraft carriers worldwide; work in hangars, avionics labs, and outdoors on flight lines in all weather conditions and high noise environments; close teamwork with other aviation ratings and aircrew in a structured maintenance organization; potential temporary duty with detachments and deployments supporting carrier or expeditionary operations. Pathways, Training & Advancement Recruit Training followed by ClassA School in Pensacola, Florida, covering aviation theory, electrical systems, electronics fundamentals, and technical skills; assignment after A School into either the Aviation Electrician's Mate or Aviation Electronics Technician rating based on performance and Navy needs; advanced platform specific schools for particular aircraft and mission systems; opportunities to qualify for micro miniature repair and, for volunteers who qualify, to attend Naval Aircrew training. Enlist for the Aviation Electronics and Electrical pipeline, with final placement into AE or AT after A School based on performance and service needs; qualified Sailors may later volunteer for Naval Aircrew duty after initial rating qualification and screening. Qualifications All Navy jobs require meeting general enlistment or commissioning standards, which typically include: Eligibility to serve in the United States Navy, which may involve United States citizenship or other legal residency and work status, depending on the program and current law and policy. A high school diploma or equivalent for enlisted positions, and a bachelor's or qualifying professional degree for officer positions. Meeting age limits that vary by program and are set in law and Navy policy. Meeting medical, vision, and dental standards, including body composition and physical fitness requirements, with some jobs requiring more demanding standards. Meeting character and conduct standards, including background screening. Achieving required test scores for your program, such as the Armed Services Vocational Aptitude Battery for enlisted roles or officer qualification tests for officer programs. Eligibility for a security clearance when required for your rating or designator. Additional qualifications for this job may include: United States citizenship and eligibility for a security clearance. Normal color perception; interest in aviation and working around aircraft. Strong aptitude in electronics, computers, and precision technical work. Manual dexterity, good memory, and physical fitness sufficient to work safely on flight lines, in hangars, and on shipboard aircraft. Education Education benefits are available through standard Navy programs such as Tuition Assistance, the Post‑9/11 GI Bill, ACE‑recommended college credit for Navy training, Navy COOL‑funded certifications, USMAP apprenticeships, and other Navy College Program opportunities. Specific options depend on the Sailor's status, training, and current Navy policy. Pay, Benefits & Service Pay, benefits, and service commitments follow standard Navy Active and / or Reserve policies for this type of role, including basic pay, allowances when eligible, health coverage, and retirement options. Exact entitlements, special pays, and service obligations depend on program, component, years of service, and current law and Navy guidance. Incentives Incentives such as bonuses, special pays, and loan repayment may be available at times for specific ratings or communities, but they change frequently and cannot be guaranteed. Applicants must confirm current incentives and eligibility with an official Navy recruiter or authoritative Navy source. Notes and Disclaimers This description is a general overview of typical duties, training, and opportunities in this community. It does not replace official Navy instructions, policies, or contracts and does not guarantee specific assignments, training, incentives, or outcomes. Actual opportunities depend on Navy needs, individual performance, screening results, and current law and policy. #J-18808-Ljbffr

About Atrium: What you do matters. Guided by our Applicant-Centric approach, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated. Join us and become part of an inclusive team committed to your growth and success. Client Overview: Our client is a specialty clinic dealing with Spine and Pain Management. They are currently expanding their team and looking to add a Medical Scribe to their team. Salary/Hourly Rate: $22/hr - $28/hr DOE Position Overview: The Medical Scribe plays a critical role in supporting physicians and clinical teams by ensuring accurate, timely, and complete documentation of patient encounters. This position focuses on reviewing, editing, and finalizing medical records within the EMR, while collaborating with providers to maintain high documentation standards and support quality patient care. Responsibilities of the Medical Scribe: • Review of physician documentation for accuracy, completeness, and compliance., • Edit and finalize patient encounter notes within the EMR system., • Review operative reports and clinical documentation for clarity and consistency., • Communicate with physicians and providers regarding missing, unclear, or incomplete information., • Support chart completion and quality assurance workflows., • Ensure documentation aligns with regulatory and organizational standards. Required Experience/Skills for the Medical Scribe:, • Strong attention to detail and accuracy in documentation., • Excellent written and verbal communication skills., • Familiarity with electronic medical records (EMR) systems., • Ability to multitask and manage time effectively in a fast-paced clinical environment., • Basic understanding of medical terminology and clinical workflows. Preferred Experience/Skills for the Medical Scribe:, • Prior experience as a Medical Scribe or in a clinical documentation role., • Background in healthcare, life sciences, or pre-medical studies (MD or similar track is preferred)., • Experience reviewing operative reports or specialty-specific documentation., • Knowledge of healthcare compliance and documentation standards. Education Requirements:, • High school diploma or equivalent is required., • Associate's or Bachelor's degree in a healthcare-related field is preferred. Benefits:, • Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off)., • Apply now By applying to this job, you agree to receive calls, AI-generated calls, text messages, and/or emails from Atrium and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to opt out on any message you receive. For more details, please review our Terms of Use and Privacy Policy . As a woman-owned firm, we value diversity. We are an equal opportunity and affirmative action employer and will consider all applications without regard to race, sex (including gender, pregnancy, sexual orientation and gender identity), age, color, religion or creed, national origin or ancestry, veteran status, disability (physical or mental), genetic information, citizenship or any other characteristic protected by law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Candidates who apply for roles through the Atrium website will be added to our candidate pool and may be considered for additional roles of a similar title. Please contact us to request an accommodation. EOE/M/F/D/V/SO

Located in Monmouth Junction, New Jersey, Tris has an immediate opening for a QA R&D Analytical Chemist, I SUMMARY The Quality Assurance (QA) Research and Development (R&D) Chemist I supports Quality Control (QC) and Analytical R&D (AR&D) activities by initiating appropriate change controls and upd

Job Description Pathlink is seeking a Board Certified Cytopathologist for a full-time position in Vineland, NJ and Mullica Hill, NJ Full Time 40 hours per week. Ideal candidate will have experience with All specimen types – Hematopathology & Cytopathology with some general Surgical Pathology Surgical Specimen experience About the Role: The Cytopathologist plays a critical role in the diagnosis and management of diseases at the cellular level by examining samples obtained through various minimally invasive procedures. This position involves the detailed microscopic evaluation of cells from body fluids, fine needle aspirations, and exfoliative cytology to detect malignancies, infections, and other pathological conditions. The Cytopathologist collaborates closely with clinical teams to provide accurate and timely diagnostic information that directly influences patient treatment plans. Additionally, the role includes overseeing laboratory operations related to cytopathology, ensuring quality control, and maintaining compliance with regulatory standards. Ultimately, the Cytopathologist contributes to advancing patient care through expert interpretation of cytological specimens and participation in multidisciplinary case discussions. Minimum Qualifications: • Medical degree (MD or DO) from an accredited institution., • Completion of residency training in pathology with subspecialty fellowship training in cytopathology., • Board certification or eligibility in Anatomic Pathology and Cytopathology by the American Board of Pathology., • Valid New Jersey medical license to practice pathology in the United States., • Demonstrated experience in diagnostic cytopathology. Preferred Qualifications: • Experience with molecular diagnostic techniques and integration of molecular data in cytopathology., • Familiarity with digital pathology and telecytology platforms., • Prior involvement in academic research or publication in peer-reviewed journals., • Strong background in quality management systems and laboratory accreditation processes., • Excellent communication skills for effective interdisciplinary collaboration and teaching. Responsibilities: • Perform microscopic examination and interpretation of cytological specimens including fine needle aspirations, body fluids, and exfoliative samples., • Provide accurate and timely diagnostic reports to guide clinical decision-making and patient management., • Collaborate with pathologists, oncologists, and other healthcare professionals to correlate cytological findings with clinical and radiological data., • Oversee quality assurance and quality control processes within the cytopathology laboratory to maintain high standards of diagnostic accuracy., • Participate in continuing education, research activities, and multidisciplinary tumor boards to stay current with advances in cytopathology and related fields. Skills: The Cytopathologist utilizes advanced microscopic and analytical skills daily to interpret complex cellular specimens accurately. Strong diagnostic acumen is essential to differentiate benign from malignant processes and to identify subtle pathological changes. Effective communication skills are employed to convey findings clearly to clinical teams and to participate in multidisciplinary discussions. Organizational and leadership skills are important for managing laboratory workflows, ensuring compliance with regulatory standards, and mentoring junior staff or trainees. Additionally, proficiency with emerging technologies such as digital pathology enhances diagnostic efficiency and supports remote consultations. Monday - Friday 8am-4pm 40 hrs per week