GMP QA Specialist

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

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

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