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Production Technician

Reference: BBBH28915
Date posted: 23/03/2026
Job details
Specialism
Technical Operations
Expertise
Quality Control
Location
Milton Keynes, Buckinghamshire, England
Job type
Contract
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Description

Join the frontline of sterile manufacturing, ensuring safe, high‑quality products that keep biotech operations running flawlessly.

R&D Partners is seeking a Production Technician to join a leading biotechnology company in Milton Keynes. This role focuses on supporting sterile product manufacturing within a cleanroom environment, ensuring compliance with Good Manufacturing Practices (GMP), and contributing to the overall operational efficiency of the facility.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Aseptic Manufacturing: Prepare and produce sterile products using aseptic techniques in a cleanroom environment.
  • Environmental Monitoring: Conduct daily and routine environmental monitoring activities to ensure compliance with regulatory and internal standards.
  • Documentation Compliance: Follow Standard Operating Procedures (SOPs) and complete batch documentation accurately, ensuring all records meet GMP requirements.
  • Quality System Activities: Raise deviations within the Quality Management System (QMS) and manage associated non-investigative records. Initiate and close Corrective and Preventive Actions (CAPAs) as required.
  • Safety & COSHH: Participate in Control of Substances Hazardous to Health (COSHH) safety assessments and apply safe working practices at all times.
  • Operational Flexibility: Support business needs by training in and performing tasks across additional operational areas when required.
  • Area Maintenance & Cleaning: Assist with routine cleaning activities to maintain the cleanliness and readiness of the production area.
  • Workload & Availability: Be available for occasional overtime, including extended workdays or weekend work, to support operations.
  • Safety Audits: Ensure monthly safety audits are completed accurately and within required timelines.
  • Issue Escalation: Report any building-related issues promptly to the Team Leader or SES Manager.

Key Skills and Requirements:

Experience:

  • Experience in a pharmaceutical environment is advantageous but not essential.
  • Background in a manufacturing setting is beneficial but not mandatory.
  • Prior experience working in graded cleanroom environments is desirable.
  • Familiarity with SAP or similar ERP systems is an advantage.
  • Proven ability to maintain high levels of accuracy and attention to detail.
  • Demonstrated capability to follow GMP and adhere to SOPs.

Personal Attributes:

  • Strong communication skills with the ability to interact effectively at all levels and across multiple functions.
  • Effective time management skills, especially within fast-paced, high-volume production environments.
  • Adaptable and able to respond positively to shifting priorities and business needs.
  • Consistently demonstrates strong attention to detail in all tasks.

For more information, please contact Grant Van Schalkwyk.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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