Technologist

Technologist

Contract Type:

Contractor

Location:

Slough

Industry:

Pharmaceuticals

Contact Name:

Flora Pollack

Contact Phone:

Date Published:

06-Jun-2025

Technologist

Slough, UK

Schedule: Standard Office Hours

Duration: 12-Month Contract

Pay:$20-24/ph



Job Responsibilities:

In this role, you will perform analytical testing to assess the quality and stability of therapeutic proteins. Key responsibilities include:

  • Ensuring all work is carried out in compliance with cGMP regulations and local EHS policies.
  • Performing analytical testing independently and accurately on various sample types, including in-process, drug substance, and drug product release/stability samples.
  • Planning and completing assigned tasks within timelines, escalating issues to Group Leader or scientific lead when necessary.
  • Collaborating with reviewers and study directors to support assay review and closeout.
  • Interpreting analytical results against established specifications and identifying trends.
  • Supporting investigations, deviations, CAPAs, and change control activities.
  • Assisting in general lab maintenance including equipment monitoring and inventory control.
  • Collaborating with cross-functional teams to meet regulatory and customer expectations.
  • Performing other related duties as assigned.



    Essential Duties and Job Functions:
  • Execute HPLC, electrophoresis, ELISA, and spectrophotometry methods for therapeutic protein analysis.
  • Work independently in a GMP-regulated laboratory environment.
  • Document all activities in accordance with SOPs and regulatory requirements.
  • Maintain personal training profile and ensure compliance with safety and operational procedures.
  • Assist in the interpretation and reporting of analytical data.
  • Monitor laboratory equipment and coordinate calibration/maintenance as needed.
  • Engage in continuous improvement initiatives related to lab operations and data quality.
  • Participate in audits and provide support during regulatory inspections.
  • Ensure proper lab housekeeping and reagent supply management.



    Knowledge & Skills:
  • Strong foundation in analytical chemistry and protein biochemistry.
  • Hands-on experience with HPLC, ELISA, CE-SDS, and icIEF.
  • Familiarity with GMP principles and regulatory requirements.
  • Excellent documentation and data interpretation skills.
  • Effective communication and collaboration in a team-oriented environment.
  • Meticulous attention to detail and commitment to data integrity.
  • Strong problem-solving and organizational capabilities.
  • Ability to adapt to changing priorities and multi-task in a fast-paced setting.
  • Competency in using laboratory software systems and analytical instrumentation.



    Education & Experience:
  • HND or BSc in Chemistry, Biochemistry, or related life sciences field.
  • 0–2 years of relevant experience in a GMP-compliant pharmaceutical or biotech QC environment.
  • Experience working with therapeutic proteins, particularly monoclonal antibodies.
  • Prior QC laboratory or analytical experience preferred.
  • Understanding of quality systems, documentation standards, and compliance frameworks.

...

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