QC Sample and Contract Laboratory Management Associate (Secondment 12 Months)

Why Patients Need You

Every day everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture which is both science and risk-based is flexible innovative and customer-oriented. Whether you are engaged in development maintenance compliance or analysis through research programs your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the needs of those we serve. By being part of our team you play a crucial role in maintaining this high standard and making a difference in the lives of patients.

What You Will Achieve

In this role you will:

• Conduct and support laboratory operations including sample plan review data collection and analysis.

• Apply technical skills to assignments ensuring high-quality results and solving moderately complex problems with sound judgment.

• Follow procedures with general instructions maintaining compliance with regulatory standards and working under moderate supervision.

• Identify activities to support team goals contributing to overall project success and ensuring adherence to project timelines.

• Independently write Standard Operating Procedures technical reports memos project plans and/or other documents.

• Create purchase orders for external testing and trend annual spend.

• Review documentation in support of Quality Control operations and testing.

Qualifications

Must-Have

• BA/BS with at least 3 years of experience.

• Demonstrated experience in manufacturing quality or engineering within the biotech or pharmaceutical industry.

• Solid understanding of Quality Control sample requirements.

• Ability to establish strong relationships within business lines.

• Excellent written and verbal communication and interpersonal skills.

• Proficiency in laboratory information management systems and data analysis software.

• Strong problem-solving skills and attention to detail.

• Solid understanding of Vaccine or mAb manufacturing processes and sampling requirements.

Nice-to-Have

• MBA/MS with any years of experience.

• Experience in Quality Operations.

• Laboratory experience including Cell Culture Bioassay Aseptic Technique and Compendial monographs.

• Familiarity with regulatory requirements and compliance standards.

• Ability to work independently and as part of a team.

• Strong organizational and time management skills.

• Ability to adapt to changing priorities and work in a fast-paced environment.

• Education or experience forecasting anticipated external spend and generation of purchase orders.

Work Location Assignment:On Premise

Other Job Details

• Last Date to Apply for Job:September 26 2025

• Additional Location Information:NO

• Eligible for Relocation Package NO

• Secondment 12 months

• If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

• There will be no change to your current work location.

• Note: This secondment offers a valuable opportunity for professional growth. It will need to be funded by the secondees home market.

Relocation assistance may be available based on business needs and/or eligibility.