Biotech jobs in United Kingdom
Manufacturing Contractor I
BioPharma Consulting JAD Group
Senior Counsel
Danaher - Global
Senior Scientific Officer - Dr Patricia Centeno & Prof Owen Sansom
CRUK Scotland Institute
Biotechnologist (GRIT) Programme
SANOFI-AVENTIS SINGAPORE PTE. LTD.
Lead Chemoinformatics Scientist for Drug Discovery (Hybrid)
OMass Therapeutics
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Biocatalysts Ltd
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Moderna
Global GCP Quality Auditor — Remote/Hybrid
Amgen, Inc.
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Regeneron Pharmaceuticals
Cleanroom Manufacturing Technician – Microfluidics
STEMCELL Technologies
Manufacturing Technician
STEMCELL Technologies
Senior Director, QC — On-Site Operations
Replimune, Inc.
Senior Director of Quality Control — Drive GMP Excellence
Replimune, Inc.
GMP Manufacturing Technician (12-Month Contract)
BioLegend, Inc.
Information Security Analyst
Medpace, Inc.
Biologics GMP Technician - Cleanroom & Autoclave Ops
Charles River Labs
Biologics Manufacturing Assistant
Charles River Labs
Pharmaceutical Physician – London-based
Medpace
Manufacturing Contractor I
Job summary
A leading biopharma consulting firm in the UK is seeking a Production Technician for hands-on work with production equipment in manufacturing operations. The successful candidate will operate equipment, support compliance initiatives, and collaborate with various internal support teams. Required qualifications include a Bachelor's degree in Biotechnology and strong cGMP understanding. This role involves a 4x10 shift schedule from Wednesday to Saturday for a 1-year contract.
Qualifications
- Strong understanding of cGMP manufacturing processes and compliance principles.
- Ability to follow complex procedures and retain technical information effectively.
- Proven troubleshooting skills to identify and resolve issues quickly.
- Excellent communication and teamwork skills in a fast-paced environment.
Responsibilities
- Operate production equipment to produce clinical products safely and compliantly.
- Execute manufacturing tasks including weighing, dispensing, and equipment cleaning.
- Support materials handling and inventory management within manufacturing suites.
- Maintain accurate and detailed documentation in compliance with cGMP.
- Identify and communicate potential issues, assisting in troubleshooting.
Skills
Education
Tools
This role involves hands‑on work with production equipment and materials to support manufacturing operations, including weigh/dispense, solution preparation, equipment cleaning (CIP/COP), small parts cleaning, and materials handling. The position requires close collaboration with internal support técnicos such as Facilities, QC, QA, Materials Management, and EHS to maintain compliance and operational excellence.
<开展h3>Key Responsibilities- Operate production equipment in accordance with SOPs to produce clinical products safely and compliantly.
- Execute manufacturing tasks including weighing, dispensing, solution preparation, and equipment cleaning (CIP/COP).
- Support materials handling and inventory management within manufacturing suites.
- Maintain accurate and detailed batch records and documentation in compliance with cGMP.
- Collaborate with cross‑functional support groups (Facilities, QC, QA, EHS) to ensure smooth operations.
- Identify and communicate potential issues, assisting in troubleshooting and process improvements.
- Participate in equipment setup, calibration, and shutdown activities as needed.
- Ensure adherence to safety procedures and quality standards at all times.
- Bachelor’s degree in Biotechnology or a related scientific field (required).
- Strong understanding of cGMP manufacturing processes and compliance principles.
- Ability to follow complex procedures and retain technical information effectively.
- Proven troubleshooting skills with the ability to identify and resolve issues quickly.
- Excellent communication and teamwork skills; comfortable collaborating in a fast‑paced environment.
- Hands‑on experience with Tangential Flow Filtration (TFF) or Ultrafiltration/Diafiltration (UFF) operations.
- Familiarity with HPLC systems.
- Exposure to automation systems such as DeltaV or similar.
- Basic understanding of automated manufacturing systems and process controls.
- Shift: 4x10 Weds-Sat 6am-4pm
- 1 year contract
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.