QC Technologist

JR United Kingdom; Reading; On-site; Full time

Job summary

A leading biopharmaceutical company is seeking a QC Technologist to join their team in Slough. The role involves conducting analytical testing to assess the quality of therapeutic proteins while adhering to GMP standards. Suitable candidates will have a degree in Biochemistry or Chemistry and 1-2 years of relevant industry experience, including familiarity with HPLC or ELISA.

Qualifications

• 1-2 years of industry experience is essential.
• GMP experience is essential.
• Experience with Monoclonal Antibodies is desirable.

Responsibilities

• Perform analytical testing on various sample types in compliance with SOPs.
• Ensure safety and compliance with EHS policies and cGMP guidelines.
• Interpret data and support timely completion of investigations.

Skills

Analytical Testing

Protein Biochemistry

GMP Compliance

Education

Bachelors/Masters in Biochemistry or Chemistry

Tools

HPLC

ELISA

Job description

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Job Title: QC Technologist – Global Biopharmaceutical

Contract: 12 months

Location: Slough

Salary: £16.41 per hour

Hours: 37.5 hours per week

This is a great opportunity for a graduate in a biochemistry related degree looking for their first role in the industry. 1-2 years industry experience is required for this role.

To perform analytical testing e.g. HPLC (size exclusion, ion exchange etc.), electrophoresis (e.g. CE SDS, icIEF), spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) for the purpose of assessing the quality and stability of therapeutic proteins. All work is expected to be carried out in a safe and compliant manner in accordance with local EHS policies and cGMP guidelines.

Key Responsibilities will include:

• Performs experimental work independently in accordance with SOPs on a variety of sample types e.g drug substance and drug product release and stability samples, in-process samples
• Performs work in a safe, compliant manner, ensuring training profile is maintained and up to date at all times.
• Plans and completes assigned tasks within the required timeframe and escalates any issues/delays to the Group Leader and/or scientific lead as appropriate
• Liaise with reviewers and study directors to close out technical review of assays.
• Interpret data against specifications and identify trends within data
• Support, as needed, with the timely completion of investigations, deviations, CAPAs and change controls.
• Actively contributes to QC department general lab housekeeping, ensuring the laboratory is adequately stocked with reagents and consumables as needed and may support with the monitoring and maintenance of equipment e.g. IMS
• Work collaboratively in a team to ensure business, regulatory and customer needs are met

Candidate Requirements:

• Bachelors/Masters in Biochemistry or Chemistry
• 1-2 years experience in the industry is essential.
• GMP experience is essential.
• Experience in Protein Biochemistry and Monoclonal Antibodies would be desirable.
• Experience with HPLC or ELISA would be desirable.