QA Compliance & Documentation Specialist (Life Sciences)
$35 - $38 per hourjob summary:
Join a top-tier global life sciences leader in Round Rock, TX as a Quality Assurance Specialist. This on-site, 12-month contract position offers temp-to-perm potential for high performers looking to advance their QA career in a highly regulated ISO environment. location: Round Rock, Texas
job type: Contract
salary: $35 - 38 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
qualifications:
Required:
skills: Biology, Chemistry, Quality Assurance (QA), Quality Control (QC)
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.
Join a top-tier global life sciences leader in Round Rock, TX as a Quality Assurance Specialist. This on-site, 12-month contract position offers temp-to-perm potential for high performers looking to advance their QA career in a highly regulated ISO environment. location: Round Rock, Texas
job type: Contract
salary: $35 - 38 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Perform final review and approval of completed batch records, equipment qualifications, calibration records, raw material data, and stability protocols.
- Generate and approve Certificates of Analysis (CoA) for custom and catalog project deliverables.
- Review Standard Operating Procedures (SOPs) to ensure strict adherence to regulatory and internal quality standards.
- Support external and internal compliance audits, including customer, ISO, and DEA inspections.
- Track, compile, and present quarterly quality metrics covering production and documentation activities.
- Escalate quality concerns, delays, or discrepancies proactively to QA management.
qualifications:
Required:
- Bachelor's Degree in Chemistry, Biology, or a related Life Science discipline.
- 5+ years of quality assurance experience operating within an ISO-regulated environment.
- Strong document review capabilities with acute attention to detail and procedure discrepancies.
- Working knowledge of pharmaceutical or clinical quality system requirements (ISO 9001, 17025, 17034, 14001).
- Hands-on experience with Root Cause Analysis and electronic Quality Management Systems (eQMS) such as Veeva.
skills: Biology, Chemistry, Quality Assurance (QA), Quality Control (QC)
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 23 days ago
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