QC Technologist

SRG; Slough; On-site; GBP 34,000 - 46,000; Full time

Job summary

SRG is seeking a QC Technologist for a 12-month contract in Slough. This entry-level role requires a Biochemistry or Chemistry graduate with 1-2 years of industry experience. The successful candidate will perform analytical testing, collaborate with a team, and support quality control processes in accordance with GMP standards.

Qualifications

• 1-2 years experience in the industry is essential.
• GMP experience is crucial.
• Experience in Protein Biochemistry and Monoclonal Antibodies would be desirable.

Responsibilities

• Perform analytical testing in accordance with SOPs.
• Plan and complete assigned tasks, ensuring timely delivery.
• Support timely completion of investigations and laboratory housekeeping.

Skills

Analytical Testing

HPLC

Electrophoresis

General Characteristic Analysis

Data Interpretation

Team Collaboration

Education

Bachelors/Masters in Biochemistry or Chemistry

Job description

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.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Pharmaceutical Manufacturing

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