QC Analyst

Idibu; Dundee; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading pharmaceutical organisation is seeking a QC Analyst to work on-site in Dundee for a 6-month contract. The role involves performing analytical testing of materials, adhering to cGMP, and contributing to laboratory investigations. Applicants should hold a degree in a relevant scientific discipline and possess strong analytical and troubleshooting skills in a pharmaceutical laboratory environment. This full-time position requires entitlement to work in the UK.

Qualifications

• 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.

Responsibilities

• Perform analytical testing of raw materials and final products.
• Accurately follow relevant SOPs and report anomalies.
• Document test results to ensure completeness and accuracy.
• Demonstrate hands-on knowledge of HPLC instruments.

Skills

Analytical testing

Chromatographic techniques (HPLC/GC)

Troubleshooting skills

Knowledge of GMP

Data integrity requirements

Education

Degree in a relevant science (Chemistry/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 and initiating and completing 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.
• Perform 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 171 455 in all correspondence.

Employment Type : Full Time

Experience: years

Vacancy: 1