hirly

Thermo Fisher

QA Supervisor (1 Day Shift & 2 Night Shift Positions)

Greenville, North Carolina, USA

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Thermo Fisher first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Mid level
Country
US
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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 polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse

Job Description

Title: QA Supervisor (Day Shift & Night Shift Openings)

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.

Division/Site Specific Information

As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization.

This position has 3 openings. One is day shift/12-hour Say Shift (6am-6pm), and two are night shift/12-hour Night shift from 6pm-6am on a 3-2-2 rotation. Flexibility to work overtime as needed.

Discover Impactful Work:

Join our Quality Assurance team at Thermo Fisher Scientific, where you'll contribute to ensuring product quality and regulatory compliance. As a QA Supervisor, you'll lead and develop a team of quality professionals while overseeing quality operations including batch record review, quality monitoring, and continuous improvement initiatives.

A Day in the Life:

You'll collaborate with cross-functional teams to enhance quality excellence and maintain our high standards for product safety and compliance.

This position offers the opportunity to contribute by helping ensure the quality of products that enable our customers to make the world healthier, cleaner and safer.

Keys to Success:

Education

BS degree required.

Preferred Fields of Study: Biology, Chemistry, Engineering

Advanced degree preferred.

Professional certifications (e.g., CQE, ASQ) desirable.

Experience

Advanced Degree plus 2 years of experience, or bachelor's degree plus 3-5 years of experience in quality assurance in a regulated manufacturing environment required (pharmaceutical, medical device, or related industry preferred).

2 -5 years of supervisory/leadership experience required.

Experience with batch record review, deviation management, and CAPA systems

Experience developing and delivering quality-related training.

Experience hosting regulatory inspections and customer audits.

Knowledge, Skills, Abilities

Comprehensive knowledge of cGMP regulations, ISO standards, and quality systems

Strong understanding of quality risk management principles and tools

Demonstrated success in implementing quality improvements and leading change initiatives

Expertise in quality documentation systems and electronic quality management tools

Excellent project management and organizational skills

Strong analytical and problem-solving abilities

Excellent written and verbal communication skills

Ability to build relationships and collaborate across all organizational levels

Proficiency with quality management software systems (e.g., TrackWise, SAP)

Comprehensive understanding of validation principles and requirements

Demonstrated ability to support quality culture and continuous improvement

Strong decision-making skills with focus on risk-based approaches

Ability to effectively manage multiple responsibilities in a deadline-oriented environment

Benefits

We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.

Original posting on Thermo Fisher's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job