Quality Control Analyst II

Join a dynamic Quality Control team at a leading biopharmaceutical manufacturing site in Swiftwater, PA, where groundbreaking work in vaccine and biologics production is supported by rigorous quality systems. This is a full-time, onsite QC Analyst II role ideal for candidates with hands-on chemistry lab experience, especially in raw material and wet chemistry testing. You'll contribute directly to the safety and integrity of life-saving products by executing analytical methods, troubleshooting discrepancies, and maintaining strict compliance with cGMP standards.

This opportunity is well-suited for early-career professionals with a Bachelor's in Chemistry and 2-4 years of experience in pharma or GMP-regulated labs. The role offers consistent daytime hours (Monday through Friday, 8 AM-5 PM) and requires excellent attention to detail, strong documentation skills, and comfort with chemical handling and lab instrumentation. The Swiftwater facility plays a vital role in producing critical health products, making this position a valuable stepping stone in your pharmaceutical career.

location: Swiftwater, Pennsylvania
job type: Contract
salary: $37.00 - 39.49 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

• Perform QC testing in accordance with cGMP, SOPs, Pharmacopeia, and regulatory guidelines
• Conduct raw material and wet chemistry assays, pH and buffer testing, TOC and conductivity testing for water
• Prepare, operate, and maintain analytical lab equipment and instrumentation
• Troubleshoot discrepancies and perform peer review of assay documentation
• Complete sample preparation and coordinate contract lab testing as needed
• Clean laboratory spaces and handle chemical materials using proper PPE
• Attend and contribute to team, departmental, and safety meetings
• Ensure all documentation and test records are accurate, complete, and audit-ready

qualifications:
Required:

• Bachelor's degree in Chemistry or closely related scientific field
• 2-4 years of hands-on experience in a pharmaceutical or cGMP-regulated laboratory (academia or industry)
• Familiarity with analytical techniques and wet chemistry methods (e.g., titration, photometry)
• Excellent attention to detail and accurate documentation practices
• Strong communication skills and ability to work in a team setting
• Willingness to work onsite full-time and handle chemicals with appropriate PPE

Preferred:

• Experience with raw material testing, water system testing (TOC/conductivity), and analytical equipment operation
• Knowledge of relevant pharmacopeia and regulatory standards
• Prior work in a high-throughput QC environment supporting manufacturing operations
• Flexibility to support weekend or holiday work if needed
• Local candidates preferred; relocation at candidate's own expense considered

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skills: Quality control, Chemistry, GMP (Good Manufacturing Practice)

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 ....

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.