Production Scientists I & II

SLS Services Limited; Oxford; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading biopharmaceutical company in the UK is seeking a GMP Production Scientist I or II to contribute to cutting-edge therapies. The ideal candidate has a BSc and at least 2 years' experience in a GMP lab, strong cell culture skills, and exceptional attention to detail. This role offers the opportunity to work in a state-of-the-art environment and make a tangible impact on global healthcare.

Benefits

Dynamic team environment

Opportunities for growth

Contribution to cutting-edge therapies

Qualifications

• At least 2 years of hands-on experience in a biomedical or GMP lab.
• Expertise in GMP for ATMPs and quality management systems.

Responsibilities

• Master cutting-edge processes like cryopreservation, cell culture, and raw material preparation.
• Employ advanced techniques to ensure products meet quality standards.
• Maintain meticulous records to ensure GMP compliance.

Skills

Cell culture techniques

Attention to detail

Communication skills

Education

BSc in a relevant scientific discipline

Job description

Position: GMP Production Scientist I & II
Department: Production
Reports To: Senior Scientist

Are you ready to be at the forefront of cutting-edge science and revolutionize patient care? Join a passionate GMP manufacturing team as a GMP Production Scientist I or II, where you’ll play a critical role in producing Advanced Therapeutic Medicinal Products (ATMPs) for groundbreaking clinical applications.

Why Join Us?

• Be part of a mission-driven team dedicated to delivering life-changing cellular therapies.

• Thrive in a state-of-the-art environment, working on projects that push the boundaries of science and innovation.

• Collaborate with experts across production, quality assurance, and research to make a tangible impact on global healthcare.

What You’ll Do

• Cellular Therapy Production: Master cutting-edge processes like cryopreservation, cell culture, and raw material preparation in a sterile GMP environment.

• Quality Control Expertise: Employ advanced techniques such as flow cytometry, ELISA, and ELISPOT assays to ensure products meet rigorous standards.

• Documentation & Compliance: Maintain meticulous records, from Batch Manufacturing Records to SOPs, ensuring GMP compliance at every step.

• Process & Equipment Validation: Spearhead the validation of innovative cellular therapy processes and new equipment to support clinical excellence.

• Daily GMP Operations: Take ownership of housekeeping, stock control, and environmental monitoring, ensuring seamless day-to-day operations.

What You Bring

Required:

• A BSc in a relevant scientific discipline and at least 2 years of hands-on experience in a biomedical or GMP lab.

• Expertise in cell culture techniques and a solid understanding of GMP for ATMPs.

• Exceptional attention to detail, communication skills, and a proactive, adaptable mindset.

Preferred:

• Experience with aseptic manufacturing, viral vector production, or gene therapy techniques.

• Familiarity with quality management systems and process troubleshooting.

What We Offer

• A dynamic, supportive team environment where your work truly matters.

• Opportunities for growth, learning, and contributing to cutting-edge therapies that transform lives.

• A chance to shape the future of cellular therapy production in a thriving sector.

Ready to Make a Difference?

If you’re a detail-oriented scientist with a passion for innovation and collaboration, we’d love to hear from you! Join us in delivering tomorrow’s therapies, today.

Apply now and let’s pioneer the future of medicine together.