Quality Specialist III, Batch Record Review

Thermo Fisher Scientific

Greenville, North Carolina

JOB DETAILS
SKILLS
Administrative Skills, Asepsis, Biology, Biotech and Pharmaceutical, Change Control, Chemistry, Communication Skills, Continuous Improvement, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Detail Oriented, Documentation, Drug Development, Drug Manufacturing, External Audit, GMP (Good Manufacturing Practices), Internal Audit, Lift/Move 40 Pounds, Maintain Compliance, Manufacturing, Manufacturing Operations, Manufacturing/Industrial Processes, Microsoft Office, Patient Safety, Presentation/Verbal Skills, Product Reviews, Product Safety, Product Support, Quality Assurance, Quality Control, Quality Metrics, Regulatory Compliance, Regulatory Requirements, Root Cause Analysis, Team Player, Time Management, Writing Skills
LOCATION
Greenville, North Carolina
POSTED
30+ days ago

Work Schedule

First Shift (Days)

Environmental Conditions

Able to lift 40 lbs. without assistance, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

About Thermo Fisher Scientific
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the world healthier, cleaner and safer. We support our colleagues with the resources needed to achieve individual career goals while advancing solutions to some of the world’s toughest challenges.

 

About the Business
Our Pharma Services Group (PSG) is a global leader in integrated drug development and manufacturing solutions for pharmaceutical and biotech companies. The Greenville, NC site specializes in sterile and oral solid dose (OSD) manufacturing, supported by advanced technologies and a collaborative, quality-focused environment.

 

Discover Impactful Work
The Quality Assurance Specialist III – Batch Release plays a critical role in ensuring that manufactured products meet all quality and regulatory requirements prior to release. This position supports site-wide batch disposition activities, with a strong focus on sterile/aseptic manufacturing processes. You will partner cross-functionally to ensure compliance with GMP standards while driving timely and accurate batch review and release.

 

A Day in the Life

•Perform comprehensive batch record review to support product release in compliance with GMP and regulatory requirements

•Ensure all documentation, deviations, and investigations are complete, accurate, and aligned with quality standards

•Collaborate with Manufacturing, Quality Control, and other cross-functional teams to resolve batch-related issues

•Evaluate deviations, change controls, and CAPAs for impact on product quality and release decisions

•Support inspection readiness and participate in internal and external audits

•Communicate effectively across all organizational levels to ensure alignment on quality expectations

          •Contribute to continuous improvement initiatives within the Quality organization

 

Keys to Success

 

Education & Experience

•Bachelor’s degree in Life Sciences, Chemistry, Engineering, or related field required

•Minimum 5 years of Quality Assurance experience in a regulated pharmaceutical environment

•Required: Experience with sterile/aseptic manufacturing and batch release activities

 

Knowledge, Skills & Abilities

•Strong knowledge of GMP/GxPregulations and quality systems

•Proven experience in batch record review and product disposition

•Familiarity with deviation management, CAPA, and change control processes

•Strong investigation and root cause analysis capabilities

•Excellent attention to detail and documentation skills

•Effective written and verbal communication skills across all levels

•Ability to work both independently and collaboratively in a team environment

•Proficiency with quality systems (e.g., TrackWise) and Microsoft Office

 

Working Conditions

Standard Monday–Friday business hours

Work performed in both office and manufacturing environments requiring appropriate PPE

 

Why Join Us?
You will be part of a high-performing Quality team supporting critical pharmaceutical manufacturing operations. This role offers the opportunity to directly impact patient safety and product quality while working in a collaborative and growth-oriented environment.

About the Company

T

Thermo Fisher Scientific

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of nearly $11 billion, we have approximately 37,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through two premier brands, Thermo Scientific and Fisher Scientific, which offer a unique combination of continuous technology development and the most convenient purchasing options. Our products and services help accelerate the pace of scientific discovery, and solve analytical challenges ranging from complex research to routine testing to field applications.

All of our employees share a common set of values - Integrity, Intensity, Innovation and Involvement. Our ability to grow year after year is driven by our ability to attract, develop and retain world-class people who will thrive in our environment and share in our desire to improve mankind by enabling our customers to make the world healthier, cleaner and safer.

If you share in our values and if you're looking for an employer who is strongly committed to developing talent and rewarding achievement, come grow with us at Thermo Fisher Scientific.

Thermo Fisher Scientific is an Equal Employment Opportunity and Affirmative Action employer.

COMPANY SIZE
10,000 employees or more
INDUSTRY
All
WEBSITE
https://corporate.thermofisher.com/en/home.html