Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, pro…
Skills: Process Validation, Project Management, Sterilization Validation, cGMP Compliance, FDA Regulatory Affairs
Greenville, North Carolina, United States · Hybrid
Job Title Pricing Analyst I (Tactical) Job Category Finance Job Description What starts with YOU, moves the world! Hyster-Yale Materials Handling, Inc, a world-class manufacturer of industrial lift trucks, has an outstan…
Skills: Pricing Analysis, Market Research, Financial Analysis, Tactical Pricing, Database Research
Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facia…
Skills: Contamination Control Strategy, Environmental Monitoring, Aseptic Processing, Media Fill Program, Sterilization Processes
Greenville, North Carolina, United States · On-site
$167k–$310k/yr
At Fluor, we are proud to design and build projects and careers. We are committed to fostering a welcoming and collaborative work environment that encourages big-picture thinking, brings out the best in our employees, an…
Skills: Construction management, Semiconductor facility standards, Project management, Subcontractor management, Safety culture training
Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
Skills: Site Master Planning, Capital Project Management, cGMP, Operational Excellence, Stakeholder Management
Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
Skills: GMP Regulations, ISO 9001, ISO 13485, FDA Compliance, EMA Compliance
Greenville, North Carolina, United States · On-site
Work Schedule Rotational shift nights Environmental Conditions Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed Job Description As part of the Thermo Fishe…
Skills: Aseptic Manufacturing, cGMP, Sterile Filtration, Filter Integrity Testing, Equipment Troubleshooting
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 Discover Impactful Work: As part of the Thermo Fisher Scientific team…
Skills: Technical Writing, Data Analysis, Validation Protocols, GMP Compliance, IQ/OQ/PQ
Greenville, North Carolina, United States · On-site
ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health cha…
Skills: Process Validation, Validation Protocol Development & Execution, Smoke Studies, Pharmaceutical Manufacturing Experience, cGMP Knowledge
Consolidated Pipe & Supply Co., IncGreenville, North Carolina, United States · On-site
Consolidated Pipe & Supply is a full-line supplier, fabricator, and manufacturer of pipe, valve, and fitting products and services for natural gas, waterworks, energy, and industrial sectors. Summary: The ideal candidate…
Skills: Material Takeoffs, Contract Specification Analysis, Cost Analysis, Project Tracking Software, Microsoft Excel
Greenville, North Carolina, United States · On-site
Work Schedule 12 hr shift/nights Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail …
Skills: cGMP Regulations, Aseptic Techniques, Sterile Drug Manufacturing, SOP Compliance, Troubleshooting
Greenville, North Carolina, United States · On-site
$40/hr–$50/hr
Position: Part-Time Industrial Injury Prevention Specialist (Part-Time, 1099 Contractor) Location: Greenville, NC Compensation: $40 - $50 per hour, depending on experience and credentials Start Date: Immediate Hours: Fle…
Skills: Ergonomic Assessment, Body Mechanics Coaching, Deep Tissue Therapy, Injury Prevention, Risk Assessment
Greenville, North Carolina, United States · On-site
$20/hr–$30/hr
Service Center Greenville NCEvery day, over 20,000 car accidents disrupt lives. When our customers face one, we step in to make things right — quickly, confidently, and with care. At Caliber, fixing fenders has its benef…
Skills: Collision Repair, Frame Straightening, Structural Repair, Blueprint Execution, Welding
Greenville, North Carolina, United States · On-site
Tomorrow RDS, LLC is a well-established company whose core business is recycling, processing, and marketing of materials. RDS operates four different facilities across three different states, servicing the recycling need…
Skills: Material Sorting, Waste Segregation, Equipment Operation, Teamwork, Communication
Greenville, North Carolina, United States · On-site
Press Operator Trainee Learn a Skilled Trade. Build a Career We are looking for a dependable, hard-working individual to join our printing team. No previous press experience required. We are willing to train the right pe…
Skills: Press Operation, Equipment Maintenance, Mechanical Aptitude, Problem Solving, Teamwork
Greenville, North Carolina, United States · On-site
$40k–$90k/yr
Benefits: Bonus based on performance Competitive salary Health insurance Opportunity for advancement PIRTEK, the nation’s leading provider for on-site hydraulic and industrial hose replacement is hiring for the position …
Skills: Prospecting, B2B Sales, Account Acquisition, Relationship Building, Time Management
Greenville, North Carolina, United States · On-site
Attindas Hygiene Partners designs, manufactures, and markets absorbent hygiene products. The company sells adult incontinence and infant diapers, among other products, into the healthcare, retail, and direct-to-consumer …
Skills: Product Design, Product Development, Project Management, Statistical Techniques, Data Analysis
Greenville, North Carolina, United States · On-site
Full-Cycle Recruiting – Hourly Manufacturing Manage full-cycle recruitment for hourly manufacturing roles from requisition intake through start date, maintaining competitive time-to-fill benchmarks aligned with productio…
Skills: Full-Cycle Recruiting, Candidate Screening, Sourcing, Interviewing, Talent Pipeline Management
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Manage professional staff and contractors responsible for the design, implementation, and documentation of validation for manufacturing equipment, facilities, and processes. Represent the department during FDA audits and meetings while ensuring compliance with regulatory requirements.
Requires a Bachelor's degree in a scientific or engineering discipline and over 10 years of validation experience. Must have at least five years of pharmaceutical/biotechnical industry experience and two years of sterilization validation expertise.
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
Location/Division Specific Information
Greenville, NC | Drug Product - North America
Manage a professional support staff and contractors responsible for process validation of all products marketed by the company and produced by the company, independent contractors, and international company subsidiaries to include the design, implementation, and documentation of validation for manufacturing equipment, utility systems, facilities, and manufacturing processes. Negotiate specific process validation criteria and required external resources. Coordinate interdepartmental process validation programs. Represent the department regarding process validation issues during FDA meetings and audits. Identify and resolve validation issues on a timely basis to avoid regulatory action and make recommendations to senior management. Perform a wide range of managerial duties pertaining to employees including hiring, on-the-job training, career development, appraising performance, promoting, disciplining and firing. Identify opportunities and provide the means for employees to pursue career growth.
Manages the activities of several functional groups of the Validation Department consisting of supervisory, professional, and technical employees. Manages design, implementation, and documentation of validation for manufacturing equipment, utility systems, facilities, and manufacturing processes and computer/information/automation validation.
Develops, approves, executes, and presents all validation master plans and associated documentation in the NDA drug approval process under the FDA Pre-Approval Inspection programs. Represents the department during audits, meetings, and teleconferences regarding process validation issues with the FDA. Provides responses to FDA deficiency letters and audit observations.
Manages multi-disciplinary validation teams, approve testing protocol and establish acceptance criteria for validation projects that impact on the production and control of externally produced products, both in clinical supply and trade product manufacturing. Negotiates the scheduling and commitment of specific resources outside the department required for validation projects.
Audits, evaluates, and qualifies all vendors or contractors. Negotiates validation requirements with these vendors. Plans and establishes technical communications, document flow, testing requirements, and financial resources necessary to produce the validation of the system. Reviews and approves all vendor-supplied documents. Coordinates the audits of inter-departmental validation programs.
Selects bidders, awards and administers contracts involved for consulting, laboratory, and process validation engineering services. Prepares and defends five-year plans and annual budgets for the department by assessing manpower and capital needs
Participates in project team activities and process design to insure Current Good Manufacturing Practices (cGMP) compliance as the validation representative on engineering project teams. Develops and maintains a plant wide change control system to review, authorize and document changes to validated systems.
Provides process validation guidance to domestic contractors and other subsidiaries of the Company supplying US markets regarding current FDA requirements for facility and product approval. Determines FDA’s current regulatory and enforcement policies regarding process validation of drug manufacturing for domestic and foreign sites and implement procedures accordingly.
Represents the Company as an active participant on internal (GQD) and external (ISPE/PDA/PMA) professional committees establishing policy guidelines relating to validation issues.
Complies with all job-related safety and other training requirements.
Performs other duties as assigned.
Bachelor's degree in a scientific, production, or engineering related discipline is highly preferred.
10+ years of validation experience is required, with five to eight years of progressive leadership experience preferred.
Pharmaceutical or Biotechnical Industry experience should exceed five years.
Minimum of two years of demonstrated experience in sterilization validation.
Must have strong project management experience
Equivalent combinations of education, training, and relevant work experience may be considered. 12 to 15+ years of applicable experience may be considered for equivalency to education.
Demonstrated ability to manage and lead professional staff in order to achieve goals, evaluate and resolve complex technical problems.
Ability to motivate, energize, and retain key staff by direct interactions with supervisors and staff.
Outstanding attention to detail and organizational skills.
Self-starter, mature, independent and dependable.
Ability to work in a fast paced environment under pressure, able to multi-task and is results-oriented.
Demonstrated ability to maintain a high degree of confidentiality.
Effective time management and prioritization skills. Requires discretion and independent judgment.
Very high degree of interpersonal skills to establish and maintain effective working relationships with employees and the public, including tact to handle sensitive matters.
Highly effective verbal and written communication skills.
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand and walk; ability to lift and/or carry light objects of up to 25 lbs. for brief periods.
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.
