QC Analyst

CK Group- Science, Clinical and Technical; Dundee; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading pharmaceutical organization is seeking a QC Analyst to work on-site in Dundee for a contract of 6 months. The role involves performing analytical testing of raw materials and finished products to support quality control processes. Applicants should have a degree in Chemistry or Biology and experience in HPLC or GC techniques. Strong knowledge of GMP and excellent troubleshooting skills are required. This position offers an opportunity to enhance your analytical skills within a dynamic team.

Qualifications

• Educated to degree level or equivalent in a relevant scientific discipline.
• Experienced analytical chemist with experience in chromatographic techniques.
• Strong knowledge of GMP and data integrity requirements in QC.
• Proven troubleshooting skills.

Responsibilities

• Perform analytical testing of raw materials and final product.
• Document test results to ensure accuracy per cGMP.
• Contribute towards the development and revision of SOPs.
• Support departmental improvement projects.

Skills

Analytical skills

Chromatographic techniques (HPLC, GC)

Troubleshooting skills

Knowledge of GMP

Education

Degree in Chemistry or Biology

Tools

Chromeleon Software

HPLC instruments

Job description

CK Group are recruiting for a QC Analyst, to work within a Quality Control Laboratory, for a leading pharmaceutical organisation that develop and manufacture veterinary products.

The QC Analyst will be working on site in Dundee, on a contract basis for 6 months.

Key Responsibilities

• Perform analytical testing of raw materials, product packaging and final product to support the release, stability and in process testing of materials for production or products for commercial use.
• Accurately follow relevant SOPs, performing all activities in accordance with cGMP requirements, reporting anomalies. Initiate and complete laboratory discrepancy events on time.
• Document test results to ensure completeness and accuracy per cGMP, keeping accurate documentation.
• Demonstrate hands‑on knowledge of operating, maintenance and troubleshooting skills for HPLC instruments as well as quality / regulatory requirements pertinent to quality control environments / laboratories.
• Performing moderate to complex equipment / instrumentation troubleshooting.
• Contribute towards the development and revision of SOPs, investigations, the preparation laboratory investigation reports and implement corrective & preventative actions (CAPAs).
• Support departmental improvement projects related to release goals, the identification of root cause for investigations and the improvement of laboratory methods.

Your Background

• Educated to degree level or equivalent in a relevant scientific discipline such as Chemistry or Biology.
• Experienced analytical chemist with experience in chromatographic (HPLC and or GC) techniques.
• Strong knowledge of GMP and Data integrity requirements in QC environments.
• Strong troubleshooting skills.
• Industry background in a Pharmaceutical, Laboratory or related environment.
• Ability to conduct Laboratory investigations.
• Experienced with chromatography systems & software such as Chromeleon Software.

Apply

It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.