Greenville, North Carolina, United States · On-site
Work Schedule First Shift (Days) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/cold, Laboratory Setting, Lou…
Skills: Good Manufacturing Practices, Technical Writing, SOP Development, Batch Records, CAPA
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 (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
$76k–$111k/yr
Position Summary The Infection Preventionist (IP) is responsible for the Infection Prevention and Control Program, developed to control the spread of infections and/or outbreaks. Track and monitor transmissible diseases …
Skills: Infection surveillance, Regulatory compliance, NHSN reporting, Hand hygiene monitoring, Risk assessment
Greenville, North Carolina, United States · On-site
At HonorBridge, our mission is to build connections that save and heal lives through organ and tissue donation. Every donation opportunity depends on strong partnerships, clinical expertise, and compassionate professiona…
Skills: Clinical assessment, Family support, Healthcare collaboration, Donation advocacy, Relationship building
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
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
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
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
$17/hr–$21/hr
Summary A Medical Lab Assistant/Phlebotomist serves patients by identifying the best method for collecting specimens; accurately ordering and preparing specimens for laboratory testing; performing other laboratory testin…
Skills: Phlebotomy, Venipuncture, Specimen collection, Laboratory testing, Data entry
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
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
Pharmaceutical Technician II The Pharmaceutical Technician II is responsible for the dispensing, compounding, compressing, encapsulating, tablet coating and printing of good manufacturing practice (GMP) commercial batche…
Skills: Pharmaceutical manufacturing, GMP compliance, Equipment maintenance, Troubleshooting, Batch record documentation
Greenville, North Carolina, United States · On-site
Position Summary The Medical Laboratory Scientist (MLS) performs clinical laboratory tests by standard operating policies and procedures. Understands method principles, performs quality control & calibrations, performs p…
Skills: Clinical laboratory testing, Quality control, Calibration, Preventive maintenance, Specimen preparation
Greenville, North Carolina, United States · On-site
Work Schedule Standard Office Hours (40/wk) 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. Jo…
Skills: Strategic Sourcing, Category Management, Supplier Relationship Management, Project Management, Supply Chain Management
Greenville, North Carolina, United States · On-site
Work Schedule First Shift (Days) Environmental Conditions Office Job Description Job Description Location/Division Specific Information As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a…
Skills: Quality Assurance, Quality Control, Document Review, Regulatory Compliance, Risk Assessment
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: Validation, GMP, Oral Solid Dose, Packaging Validation, Automated Visual Inspection
Greenville, North Carolina, United States · On-site
Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description The R&D Scientist II-Reviewer independently performs complex data reviews in support of validations, development testing, proto…
Skills: Cgmp, Analytical Data Review, Hplc, Empower, Uv
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: Technology Transfer, Manufacturing Process Development, Good Manufacturing Practices, Formulation, Steriles Processing
Greenville, North Carolina, United States · On-site
Work Schedule First Shift (Days) 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: Product complaint investigations, Root cause analysis, Cgmp regulations, Quality systems, Technical writing
Greenville, North Carolina, United States • On-site
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The Manufacturing Scientist II supports day-to-day Manufacturing Sciences and Technology activities, including process design, validation, and problem-solving. They are responsible for authoring SOPs, managing CAPA investigations, and ensuring compliance with GMP and safety standards.
The role requires a Bachelor of Science or STEM degree and 2-4 years of scientific experience, preferably within the pharmaceutical industry. Candidates must possess strong technical writing skills and a thorough knowledge of Good Manufacturing Practices.
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.
How will you make an impact?
Technically supports day-to-day Manufacturing Sciences and Technology in the Manufacturing, Filling, Freeze Drying, and/or Packaging areas of the Steriles business unit.
Investigates, creates, and validates scientific methodologies used to control raw materials, production intermediates, and final products on a complex scope of processes, products, and projects.
May be involved in pre-clinical, clinical, and/or post-marketing stages of drug development.
Works on technical/scientific process/product/project activities to execute strategies and technical solutions that meet client needs and expectations.
Evaluates and contributes to the design of manufacturing processes and supports problem solving as necessary with independent judgment.
Makes decisions that require developing new options to solve complex problems.
What will you do?
Author and improve procedures including SOPs, Batch Records, Protocols, training documents, etc. Author Change Controls, etc. in electronic Quality Management System and Document Management System.
Leads cross functional investigation teams in CAPA closure.
Present recommendations internally.
Leads assignments, including managing project timelines and deliverables.
Liaises with internal Quality, Operations, Engineering, Validation, and other functional areas to meet team objectives.
Guides and advises documentation and training strategies during implementation of new methodologies and processes.
Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices and Safety guidelines.
Maintains the necessary compliance status required by company and facility standards.
How will you get here?
Qualifications
Bachelor of Science in any Science or STEM degree preferred. Other Education and time in industry can be considered.
2-4 years of scientific experience (preferred), preferably in the pharmaceutical industry. Education, time in the industry, and other applicable experience can be considered.
Experience with technical writing is a plus
Equivalent combinations of education, training, and relevant work experience may be considered.
Knowledge, Skills, Abilities
Thorough knowledge of Good Manufacturing Practices.
Strong proficiency in Microsoft Office Suite (including Word, Excel, and PowerPoint).
Excellent critical and logical thinking skills.
Effective written, interpersonal, and presentation skills, including managing technical discussions with internal and external clients.
Ability to work on multiple projects simultaneously.
Ability to develop knowledge and skills in pharmaceutical processes, equipment, instrumentation, and procedures.
Ability to keep current with scientific literature and industry trends relating to process technologies.
Ability to develop technical solutions.
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 117 open science & research positions in Greenville, NC listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Thermo Fisher Scientific, ECU Health, Grace Federal Solutions,LLC, Catalent, Physicians East, among others. Browse the listings above to see every active employer.
Yes — 7 of the 117 open science & research positions offer remote or hybrid work (1 remote, 6 hybrid).
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