QA Associate – GMP Documentation Reviewer
ManpowerGroup, Winchester, KY, United States
Our client, a leading Pharmaceutical & Biotech Manufacturing company, is seeking a QA Associate (GMP Documentation Reviewer) to join their team. As a QA Associate, you will be part of the Quality Assurance department supporting Analytical, QC, and Manufacturing operations. The ideal candidate will have strong GMP documentation skills, excellent critical thinking, and the ability to work independently in a fast‑paced quality environment.
Job Title:
QA Associate – GMP Documentation Reviewer
Location:
Onsite (Catalent location provided by client)
Shift:
Friday, Saturday, Sunday — 6PM to 6AM (Night Shift, 3×12 schedule)
Pay Range:
$27.64/hr Temp-to-Hire – 6‑month assignment
What’s the Job?
Review analytical
release and stability data
with minimal supervision. Evaluate compliance of
test methods, protocols, and specifications
under GMP guidelines. Review and approve
controlled documents
within QA systems. Partner with Analytical, QC, and Manufacturing teams to resolve documentation gaps. Ensure all documentation meets
GMP, regulatory, and internal quality standards .
What’s Needed?
Minimum
3 years of GMP experience
(QA, QC, Analytical Lab, or Manufacturing). Bachelor’s degree in a scientific field— Chemistry or Biochemistry preferred . Strong command of
GMP documentation practices
and data integrity principles. Ability to make
independent decisions
based on regulatory and quality requirements. Excellent attention to detail, organization, and written/verbal communication.
What’s in it for me?
Temp‑to‑Hire opportunity
with long‑term career potential in pharma/GMP. 36‑hour workweek
(full-time hours in 3 days). Gain experience with a major
pharmaceutical manufacturing site . Be part of a
stable and growing industry
with advancement potential. Work in a
collaborative QA environment
committed to high standards.
If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are consistently recognized for our diversity and ethics, including being named one of the World’s Most Ethical Companies for the 13th year in 2022.
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Job Title:
QA Associate – GMP Documentation Reviewer
Location:
Onsite (Catalent location provided by client)
Shift:
Friday, Saturday, Sunday — 6PM to 6AM (Night Shift, 3×12 schedule)
Pay Range:
$27.64/hr Temp-to-Hire – 6‑month assignment
What’s the Job?
Review analytical
release and stability data
with minimal supervision. Evaluate compliance of
test methods, protocols, and specifications
under GMP guidelines. Review and approve
controlled documents
within QA systems. Partner with Analytical, QC, and Manufacturing teams to resolve documentation gaps. Ensure all documentation meets
GMP, regulatory, and internal quality standards .
What’s Needed?
Minimum
3 years of GMP experience
(QA, QC, Analytical Lab, or Manufacturing). Bachelor’s degree in a scientific field— Chemistry or Biochemistry preferred . Strong command of
GMP documentation practices
and data integrity principles. Ability to make
independent decisions
based on regulatory and quality requirements. Excellent attention to detail, organization, and written/verbal communication.
What’s in it for me?
Temp‑to‑Hire opportunity
with long‑term career potential in pharma/GMP. 36‑hour workweek
(full-time hours in 3 days). Gain experience with a major
pharmaceutical manufacturing site . Be part of a
stable and growing industry
with advancement potential. Work in a
collaborative QA environment
committed to high standards.
If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are consistently recognized for our diversity and ethics, including being named one of the World’s Most Ethical Companies for the 13th year in 2022.
#J-18808-Ljbffr