QA Batch Records Specialist - Pharma
$20 - $24.5 per hourjob summary:
Advance your career with a top-tier global pharmaceutical leader in Melrose Park, IL! We are seeking a detail-oriented QA Records Specialist for a 3-month contract role (with potential extension or FTE conversion) to manage and maintain critical master documentation for manufacturing, packaging, and testing operations. location: Melrose Park, Illinois
job type: Contract
salary: $20.00 - 24.50 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
qualifications:
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on us.fitly.work.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Advance your career with a top-tier global pharmaceutical leader in Melrose Park, IL! We are seeking a detail-oriented QA Records Specialist for a 3-month contract role (with potential extension or FTE conversion) to manage and maintain critical master documentation for manufacturing, packaging, and testing operations. location: Melrose Park, Illinois
job type: Contract
salary: $20.00 - 24.50 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Analyze and coordinate scheduled production batches to ensure complete and accurate manufacturing document availability.
- Prioritize and issue Master Batch Records, testing specifications, and laboratory documentation while calculating product expiration dates.
- Identify and resolve documentation discrepancies using platforms like TrackWise and Documentum.
- Develop customized batch records to fulfill validation protocols, special studies, and component qualification needs.
- Collaborate cross-functionally and monitor daily production schedules to align documentation delivery with dynamic shift requirements.
qualifications:
- Bachelor's degree (preferably in Business, Chemistry, or a related field).
- 3+ years of quality assurance documentation experience within the pharmaceutical or medical device industry.
- Advanced expertise in MS Word along with proficiency in EDMS platforms (TrackWise, Documentum).
- Exceptional organizational, proofreading, and cross-functional communication skills.
- Ability to work independently with minimal supervision in a fast-paced environment.
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on us.fitly.work.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Vacancy posted 1 day ago
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