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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