Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Randstad USA

QA Batch Records Specialist - Pharma

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
55
out of 100
Average of individual scores

Were these scores useful?

Job Description

qa batch records specialist - pharma.melrose park, illinoisposted today job detailssummary$20 - $24.50 per hourcontractbachelor degreecategorylife, physical, and social science occupations reference 54577 job details job 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: 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. #LI-ST1 skills: Good Manufacturing Practices (GMP), Quality Assurance (QA),
Batch Record 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 HRsupport@randstadusa.com. 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.

Benefits

  • 401(k) Plans
  • Dental Insurance
  • Disability Insurance
  • Life Insurance