QA Associate - GMP Documentation Reviewer
Manpower Group Inc., Winchester, KY, United States
Our client, a leading Pharmaceutical & Biotech Manufacturing organization, 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 QC, Analytical, and Manufacturing operations. The ideal candidate will have strong GMP documentation experience, critical thinking skills, and the ability to independently evaluate analytical data and controlled documents in a fast-paced, quality-focused environment.
Job Title:
QA Associate - GMP Documentation Reviewer
Location:
Onsite (Catalent location provided upon submission)
Shift:
Monday - Friday, 2:00 PM to 10:30 PM (2nd Shift)
Pay Range:
$26.44/hr
Temp-to-Hire - 6-month duration
What's the Job?
Review analytical
release and stability data
with minimal supervision.
Evaluate compliance of
test methods, protocols, and specifications
within GMP frameworks.
Review and approve
controlled documents
in QA systems.
Partner with QA, QC, and Manufacturing teams to resolve documentation discrepancies.
Maintain high documentation standards aligned with
regulatory, GMP, and internal quality requirements
.
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 working knowledge of
GMP documentation systems
and data integrity.
Ability to make
independent decisions
based on regulatory and internal guidelines.
Excellent communication, organization, and attention to detail.
What's in it for me?
Temp-to-Hire opportunity
with strong long-term growth potential in pharmaceutical QA.
Consistent
Monday-Friday 2nd shift
, no weekends required.
Work directly with
high-impact GMP documentation
supporting product quality.
Be part of a reputable, fast-growing pharmaceutical manufacturing site.
Join a collaborative, quality-driven environment with opportunities to advance.
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 recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality, and Disability - and in 2022, ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.
Job Title:
QA Associate - GMP Documentation Reviewer
Location:
Onsite (Catalent location provided upon submission)
Shift:
Monday - Friday, 2:00 PM to 10:30 PM (2nd Shift)
Pay Range:
$26.44/hr
Temp-to-Hire - 6-month duration
What's the Job?
Review analytical
release and stability data
with minimal supervision.
Evaluate compliance of
test methods, protocols, and specifications
within GMP frameworks.
Review and approve
controlled documents
in QA systems.
Partner with QA, QC, and Manufacturing teams to resolve documentation discrepancies.
Maintain high documentation standards aligned with
regulatory, GMP, and internal quality requirements
.
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 working knowledge of
GMP documentation systems
and data integrity.
Ability to make
independent decisions
based on regulatory and internal guidelines.
Excellent communication, organization, and attention to detail.
What's in it for me?
Temp-to-Hire opportunity
with strong long-term growth potential in pharmaceutical QA.
Consistent
Monday-Friday 2nd shift
, no weekends required.
Work directly with
high-impact GMP documentation
supporting product quality.
Be part of a reputable, fast-growing pharmaceutical manufacturing site.
Join a collaborative, quality-driven environment with opportunities to advance.
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 recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality, and Disability - and in 2022, ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.