Documentation Analyst
Kelly Professional & Industrial, Athens, GA, United States
Documentation Analyst – Johnson & Johnson (via Kelly Services) | Athens, GA
Kelly Services is excited to partner with a Johnson & Johnson company to recruit a Documentation Analyst to support their Quality Control team in Athens, GA.
Schedule: Monday through Friday, 8:00 AM – 5:00 PM
Contract: 2 years
Pay: $18.43/hr
Key Responsibilities
Manage, organize, and maintain Quality Control documents, including SOPs, work instructions, test methods, and specifications.
Prepare, review, and track change control records.
Ensure all documents meet regulatory compliance and are audit‑ready.
Support QC operations by coordinating training and collaborating with cross‑functional teams.
Required Qualifications
High school diploma with 2–3 years of relevant experience, preferably in a GMP environment.
Experience with document control systems and change control processes.
Strong attention to detail and knowledge of regulatory requirements.
Preferred Qualifications
Bachelor’s degree in a scientific field.
Experience supporting QC laboratories and familiarity with EDMS/eLIMS.
Understanding of FDA, cGMP, and data integrity requirements.
Why Join Us? This role offers the opportunity to gain valuable experience with a globally recognized pharmaceutical leader. Enjoy a stable work schedule, competitive pay, and the chance to contribute to a meaningful mission.
Interested candidates are encouraged to apply and become part of a dynamic, dedicated team.
#DocumentationAnalyst #QualityControl #AthensGA #PharmaceuticalJobs #KellyServices #Hiring
#J-18808-Ljbffr
Schedule: Monday through Friday, 8:00 AM – 5:00 PM
Contract: 2 years
Pay: $18.43/hr
Key Responsibilities
Manage, organize, and maintain Quality Control documents, including SOPs, work instructions, test methods, and specifications.
Prepare, review, and track change control records.
Ensure all documents meet regulatory compliance and are audit‑ready.
Support QC operations by coordinating training and collaborating with cross‑functional teams.
Required Qualifications
High school diploma with 2–3 years of relevant experience, preferably in a GMP environment.
Experience with document control systems and change control processes.
Strong attention to detail and knowledge of regulatory requirements.
Preferred Qualifications
Bachelor’s degree in a scientific field.
Experience supporting QC laboratories and familiarity with EDMS/eLIMS.
Understanding of FDA, cGMP, and data integrity requirements.
Why Join Us? This role offers the opportunity to gain valuable experience with a globally recognized pharmaceutical leader. Enjoy a stable work schedule, competitive pay, and the chance to contribute to a meaningful mission.
Interested candidates are encouraged to apply and become part of a dynamic, dedicated team.
#DocumentationAnalyst #QualityControl #AthensGA #PharmaceuticalJobs #KellyServices #Hiring
#J-18808-Ljbffr