Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning…
Skills: Leadership, Pharmaceutical manufacturing, Manual visual inspection, cGMP, FDA compliance
Greenville, North Carolina, United States · On-site
About Us We are a full-service mechanical contractor providing customers in the commercial, residential, and industrial sectors with innovative, energy-efficient heating and air conditioning services, automation and cont…
Skills: Electrical conduit installation, Control wiring, HVAC unit accessories installation, Blueprint reading, Wiring schematics
Greenville, North Carolina, United States · On-site
$90k–$130k/yr
The Area MRF Manager oversees Material Recovery Facilities (MRFs) across North Carolina, Virginia, and Georgia, with accountability for safe operations, regulatory compliance, staff leadership, cost control, and performa…
Skills: Material recovery facility operations, Recycling processes, Sorting systems, Operational management, Staff leadership
Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description Job Summary: The Staff Medic…
Skills: Autoinjector Expertise, Pharmaceutical Engineering, GMP Compliance, FAT/SAT, Vendor Management
Greenville, North Carolina, United States · Hybrid
Job Title Environmental Health & Safety (EHS) Specialist I-II Job Category Environmental Health and Safety Job Description What starts with YOU, moves the world! Put a LIFT in your career with Hyster-Yale Materials Handl…
Skills: Workers' Compensation Case Management, Accident Investigation, EHS Training Development, OSHA Compliance, ISO 14001
Greenville, North Carolina, United States · On-site
Work Schedule Standard Office Hours (40/wk) Environmental Conditions Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Job ove…
Skills: Technology Transfer, Manufacturing Process Development, Formulation, Freeze Drying, Steriles Processing
Greenville, North Carolina, United States · On-site
Job Seekers can review the Job Applicant Privacy Policy by clicking here. Job Description: Summary The Operations Management Trainee will support the shop management process and assist in cost savings, customer retention…
Skills: Customer relationship management, Fleet maintenance, Operations management, Issue resolution, Time management
Greenville, North Carolina, United States · On-site
Job Purpose & Summary: As Warehouse Manager, you'll protect the flow of product and service that keeps customers supplied-by running warehouse operations with discipline, accuracy, and compliance. This role exists to imp…
Skills: Warehouse operations, Team management, Scheduling, Inventory management, Logistics
Greenville, North Carolina, United States · On-site
Pharmaceutical Technician I About Site Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development thr…
Skills: GMP manufacturing, Oral solid dose manufacturing, Dispensing, Compounding, Compressing
Greenville, North Carolina, United States · On-site
Work Schedule Standard Office Hours (40/wk) Environmental Conditions Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Job ove…
Skills: Technology Transfer, Manufacturing Process Development, Injectables, Experimental Design, Formulation
Greenville, North Carolina, United States · On-site
Laboratory Team Leader Position Summary Work Schedule: Monday-Friday, Days. This position is 100% on-site at the Greenville site. Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral…
Skills: People Leadership, Project Management, Pharmaceutical Analytical Chemistry, Method Development, Method Validation
Greenville, North Carolina, United States · On-site
About Us We are a full-service mechanical contractor providing customers in the commercial, residential, and industrial sectors with innovative, energy-efficient heating and air conditioning services, automation and cont…
Skills: HVAC maintenance, Refrigerant charging, Gas furnace repair, Duct system installation, Wiring confirmation
Greenville, North Carolina, United States · Hybrid
Job Title Electrical & Systems Test Engineer Job Category Engineering Job Description What starts with YOU, moves the world! Hyster-Yale Materials Handling, Inc, a world-class manufacturer of industrial lift trucks, has …
Skills: Test planning, Validation methods, Technical documentation, Data acquisition, Instrumentation
Greenville, North Carolina, United States · On-site
The Film Technician is responsible for the set-up, operation, prevention and troubleshooting of issues and housekeeping of equipment as assigned. The operation of Life Protection equipment is expected to be done in accor…
Skills: Equipment troubleshooting, Manufacturing operations, Quality monitoring, Inventory management, Mechanical competency
Greenville, North Carolina, United States · On-site
The UD Inspector will set up, operate, adjust and clean the inspection equipment required to inspect and pack finish product into boxes in accordance to work instructions and standard operating procedures. Maintain recor…
Skills: Equipment operation, Inspection, Quality control, Troubleshooting, Mechanical skills
Greenville, North Carolina, United States · On-site
About Us We are a full-service mechanical contractor providing customers in the commercial, residential, and industrial sectors with innovative, energy-efficient heating and air conditioning services, automation and cont…
Skills: Autodesk Revit, Autodesk Navisworks, BIM Modeling, Mechanical HVAC systems, Ductwork routing
Greenville, North Carolina, United States · Hybrid
Job Title Supply Chain Rotational I Program Job Category Supply Chain Management Job Description What starts with YOU, moves the world! Hyster-Yale Materials Handling, Inc, a world-class manufacturer of industrial lift t…
Skills: Supply chain management, Project management, Analytical skills, Problem solving, Presentation skills
Greenville, North Carolina, United States · On-site
Laboratory Analyst About Site Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through comm…
Skills: Analytical testing, Data integrity, Documentation practices, Laboratory instrumentation, Calibration
Greenville, North Carolina, United States · On-site
About Us Arc3 Gases is a family-owned, independent distributor of industrial gases, welding supplies, safety products, and hardgoods used in metal fabrication industries. We prioritize family values and a focus on people…
Skills: Sales, Customer Service, Welding Product Knowledge, Technical Expertise, Inventory Management
Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaning…
Skills: Quality assurance, Change control, GMP compliance, GxP regulations, ISO standards
Greenville, North Carolina, United States • On-site
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The Packaging/Labeling Supervisor will lead a team of 35-40 employees in sterile pharmaceutical operations, ensuring production readiness and compliance with cGMP standards. This role involves driving daily production priorities, coaching staff, and partnering with cross-functional teams to maintain quality and operational efficiency.
Candidates must possess a combination of education and relevant experience, ranging from an advanced degree with 3+ years of experience to a high school diploma with 9+ years of experience. Strong knowledge of FDA-regulated manufacturing environments, leadership capabilities, and proficiency in documentation practices are required.
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
As a Packaging/Labeling Supervisor at our Greenville, NC site, you will provide hands-on leadership for approximately 35–40 colleagues supporting three manual visual inspection (MVI) rooms within our sterile pharmaceutical operations. Your team supports multiple customers and inspects sterile injectable products, including liquid vials, lyophilized vials, and liquid syringes.
This is a highly visible, floor-based leadership role for someone who enjoys driving daily production, developing people, strengthening compliance, and improving how work gets done. You will ensure each area is ready to run safely and compliantly, reinforce strong documentation practices, and build greater ownership and accountability within the team.
You will also gain broad cross-functional exposure through regular partnership with Quality, Validation, Customer Service and other operational teams, creating opportunities to expand your leadership capabilities and grow within the organization.
Lead day-to-day operations across assigned manual visual inspection areas, maintaining a strong and consistent presence on the production floor.
Direct and develop approximately 35–40 employees, setting clear expectations for safety, quality, productivity, attendance, performance and accountability.
Assess daily production readiness, including staffing, batch status, documentation, systems, materials and other requirements needed to execute the production schedule.
Drive daily production priorities and coordinate resources across inspection rooms to meet customer commitments while maintaining quality and compliance.
Ensure manual visual inspection activities are performed in accordance with current Good Manufacturing Practices (cGMP), approved procedures and applicable regulatory requirements.
Strengthen Good Documentation Practices (GDP) by reviewing production and batch documentation for completeness and accuracy and addressing recurring documentation errors.
Conduct routine self-audits of assigned areas to identify compliance, documentation and technique gaps before they become audit observations or downstream issues.
Promote right-first-time execution by coaching employees on inspection technique, documentation accuracy and adherence to established procedures.
Identify production, quality and compliance issues, escalate when appropriate, and partner with cross-functional teams to determine and implement effective solutions.
Coach, develop and motivate employees while providing clear, timely and constructive performance feedback.
Reinforce consistent application of procedures, policies and performance expectations while creating an environment of ownership and continuous improvement.
Support new projects, process changes and onboarding of new work, helping the team adapt successfully as business and customer needs evolve.
Identify opportunities to improve workflow, productivity, quality and operational performance and help implement sustainable improvements.
Partner closely with Quality, Validation, Customer Service and other functions to resolve issues and support successful execution for multiple customers.
One of the following combinations of education and relevant experience:
Advanced degree with 3+ years of relevant experience in pharmaceutical manufacturing, packaging, visual inspection or another FDA-regulated manufacturing environment; or
Bachelor’s degree with 5+ years of relevant experience; or
High school diploma or equivalent with 9+ years of relevant experience.
Relevant degrees may include Business, Management, Engineering, a scientific discipline or a related field.
Experience working in a cGMP/FDA-regulated manufacturing environment, with a strong understanding of quality, compliance and documentation expectations.
Demonstrated leadership experience in a manufacturing or operations environment, such as direct people leadership, team lead responsibilities or significant responsibility for leading teams and daily production activities.
Ability to lead a large frontline workforce, establish clear expectations, address performance concerns and hold employees accountable while maintaining respectful and effective working relationships.
Strong knowledge of Good Documentation Practices and the ability to review production and batch records for accuracy and completeness.
Ability to manage daily production priorities, staffing needs and competing operational demands in a deadline-driven environment.
Strong problem-solving skills with the ability to identify issues, evaluate root causes and drive timely resolution.
Effective written and verbal communication skills with the ability to collaborate across operations, Quality, Validation, Customer Service and other functions.
Ability to work independently, make sound decisions and appropriately escalate issues that may affect safety, quality, compliance or delivery.
Demonstrated initiative, adaptability and willingness to challenge established ways of working when opportunities exist to improve performance.
Proficiency with Microsoft Office and experience working with electronic manufacturing and/or quality systems.
Experience with manual visual inspection (MVI) of pharmaceutical products, particularly sterile injectable products.
Previous experience leading teams in pharmaceutical manufacturing, sterile operations, packaging, inspection or a similarly regulated production environment.
Experience with TrackWise and SAP.
Experience supporting new product, process or project onboarding in a changing manufacturing environment.
Experience with Lean Manufacturing or continuous improvement tools and methodologies.
Lean, Six Sigma or Project Management certification.
This position is fully onsite in Greenville, North Carolina.
Regular schedule is approximately 6:00 a.m.–4:30 p.m. Monday through Thursday and 6:00 a.m.–2:30 p.m. Friday.
Saturday overtime may be required based on production backlog and business needs. Supervisors rotate Saturday coverage, which is typically approximately 6:00 a.m.–12:00 p.m. when required.
The position requires regular presence in manufacturing and manual visual inspection areas and the ability to stand and walk for extended periods.
Must be able to meet applicable visual acuity and color vision requirements associated with the manufacturing environment.
Must be able to lift up to 50 pounds and work in applicable production environmental conditions.
At Thermo Fisher Scientific, each one of our extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
There are currently 118 open manufacturing positions in Greenville, NC listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Thermo Fisher Scientific, Catalent, Avient Corporation, Hyster-Yale Materials Handling, Attindas Hygiene Partners, among others. Browse the listings above to see every active employer.
Yes — 12 of the 118 open manufacturing positions offer remote or hybrid work (2 remote, 10 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
