Manufacturing Contractor I

BioPharma Consulting JAD Group; Norton-on-Derwent; On-site; GBP 30,000 - 50,000; Full time

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

cGMP manufacturing processes

Troubleshooting skills

Communication

Teamwork

Education

Bachelor’s degree in Biotechnology or a related scientific field

Tools

HPLC systems

DeltaV automation systems

Job description

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.

Qualifications

• 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.

Preferred Experience

• 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