GMP QA Specialist
The Voluntary Protection Programs Participants' Association, Inc, Smyrna, GA, United States
Job Summary
We are seeking a
QA Specialist with GMP experience
to provide
basic quality support
for a pharmaceutical manufacturing environment. This role will support day-to-day
quality assurance activities , with a strong focus on
deviation management and GMP documentation . The ideal candidate will have experience working in a regulated pharmaceutical setting and be comfortable supporting investigations and quality systems.
This position is
on-site in Smyrna, GA
and is a
one-year contract role
supporting quality operations.
Key Responsibilities
Provide
Quality Assurance support
for manufacturing and quality systems in a
GMP-regulated pharmaceutical environment .
Review and assist with
deviation investigations , ensuring timely documentation and closure.
Support
GMP documentation review , including batch records, SOPs, and quality records.
Assist in
root cause analysis and corrective/preventive actions (CAPA)
related to deviations.
Ensure compliance with
GMP regulations and internal quality standards .
Collaborate with
manufacturing, quality control, and regulatory teams
to resolve quality issues.
Maintain accurate documentation and support
inspection readiness .
Participate in quality meetings and provide
basic QA support across quality systems .
Qualifications Required
Bachelor’s degree in
Life Sciences, Chemistry, Biology, or related field .
1–3+ years of experience
in the pharmaceutical or biotech industry.
Experience working in a
GMP-regulated environment .
Hands‑on experience with
deviation investigations
and quality documentation.
#J-18808-Ljbffr
QA Specialist with GMP experience
to provide
basic quality support
for a pharmaceutical manufacturing environment. This role will support day-to-day
quality assurance activities , with a strong focus on
deviation management and GMP documentation . The ideal candidate will have experience working in a regulated pharmaceutical setting and be comfortable supporting investigations and quality systems.
This position is
on-site in Smyrna, GA
and is a
one-year contract role
supporting quality operations.
Key Responsibilities
Provide
Quality Assurance support
for manufacturing and quality systems in a
GMP-regulated pharmaceutical environment .
Review and assist with
deviation investigations , ensuring timely documentation and closure.
Support
GMP documentation review , including batch records, SOPs, and quality records.
Assist in
root cause analysis and corrective/preventive actions (CAPA)
related to deviations.
Ensure compliance with
GMP regulations and internal quality standards .
Collaborate with
manufacturing, quality control, and regulatory teams
to resolve quality issues.
Maintain accurate documentation and support
inspection readiness .
Participate in quality meetings and provide
basic QA support across quality systems .
Qualifications Required
Bachelor’s degree in
Life Sciences, Chemistry, Biology, or related field .
1–3+ years of experience
in the pharmaceutical or biotech industry.
Experience working in a
GMP-regulated environment .
Hands‑on experience with
deviation investigations
and quality documentation.
#J-18808-Ljbffr