Production Technician

Experis; Stevenage; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading global technology provider is seeking a Production Technician in Stevenage. This role involves undertaking routine manufacturing activities, adhering to cGMP standards, and participating in compliance inspections. Ideal candidates should have 2 years' manufacturing experience or a relevant scientific degree. Opportunities for extensions and permanent placement are available, along with working in state-of-the-art facilities.

Benefits

Work in brand new state of the art facilities

Opportunities for extensions and permanent placement

Work on exciting projects

Qualifications

• 2 years' experience in a Manufacturing environment or a relevant scientific degree with lab work.
• Ability to comply with and understand production work instructions.
• Experience in writing Standard Operating Procedures and Manufacturing Batch Records.

Responsibilities

• Undertake routine manufacturing activities to produce membrane products.
• Perform daily lab activities including calibrations and checks.
• Support NPI introduction and compliance inspections.

Skills

Self-starter

Knowledge of cGMP standards

Team player

Ability to work overtime

Education

Relevant scientific degree

Tools

Standard Operating Procedures

Job description

Overview

Role: Production Technician

Rate: £16 per hour PAYE 37 hours per week

Term: 6 - 12 Months - Potential for Permanent Placement & Extension

Location: Stevenage (SG1)

The Client

Our client are a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics.

Their portfolio ranges from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Their job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.

Responsibilities

• Undertake the routine manufacturing activities to produce membrane products.
• Perform daily lab activities including calibrations and checks using appropriate records and logs.
• Provide support for NPI introduction including method transfer and validation activities.
• Assist in compliance inspections and EHS program implementation to maintain high level of EHS compliance.
• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
• Undertake training in all Q/C processes required for all membrane manufacturing.
• Complete all training within the defined deadlines.
• Identify and report any quality or compliance concerns and take immediate corrective action as required.
• Knowledge and understanding of production work instructions, SOP's and manufacturing batch records and operates within them.
• Ensures the creation of accurate, complete, and timely records.
• Maintain cGMP at all times

Expected areas of competence

• Self-starter, willing to work alone or in team as required by the business.
• Willing to work overtime from time to time at reasonable notice to support the business needs.
• Knowledgeable in terms of cGMP and lab standards
• Demonstratable experience with writing Standard Operating Procedures, Work instructions and Manufacturing Batch Records.
• 2 years' experience in a Manufacturing environment OR Degree in relevant scientific field with proven lab work.

Other Bonuses

• Work in brand new state of the art, £4million facilities on a day-to-day basis
• Extensions and Permanent placement opportunities available
• Work on an exciting project looking to launch new products in 2026
• Join an already established and well-oiled team
• Joining an Industry Leading company in the Life Sciences and Pharmaceutical Industry