Quality Control Analyst - Dartford
Posted 2 days ago by Planet Pharma
Negotiable
Undetermined
Undetermined
Dartford, England, United Kingdom
Summary: The Quality Control Analyst role involves supporting production in a GMP-regulated laboratory by performing timely and accurate QC testing on in-process and finished samples. The position requires collaboration within a QC team to ensure compliance with GMP and EHS standards while contributing to data generation and release activities. Candidates will utilize various analytical techniques and maintain documentation to uphold product quality. This role offers hands-on experience in a fast-paced environment focused on continuous improvement.
Key Responsibilities:
- Perform analytical testing using techniques such as HPLC, FTIR, Raman, DSC, particle size analysis, and Karl Fischer
- Support cleaning verification, swabbing, and method validation activities
- Review and report data for QC release in line with procedures
- Maintain accurate GMP documentation and support investigations (OOS, deviations, CAPA)
- Ensure lab equipment is calibrated and used correctly
- Contribute to audit readiness and continuous improvement initiatives
- Carry out microbiological/environmental sampling activities
Key Skills:
- Degree in a scientific discipline (or equivalent industry experience)
- Experience working in a GMP or regulated laboratory environment
- Understanding of core analytical techniques and lab systems
- Strong attention to detail and documentation skills
- Proactive, team-oriented, and able to manage priorities effectively
Salary (Rate): undetermined
City: Dartford
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
We are currently supporting an exciting opportunity for a QC Analyst to join a fast-paced, GMP-regulated laboratory environment.
The Role
You’ll support production by carrying out timely, accurate QC testing on in-process and finished samples, ensuring all work meets GMP and EHS standards. Working under supervision, you’ll contribute to data generation, review, and release activities critical to product quality.
Key Responsibilities
- Perform analytical testing using techniques such as HPLC, FTIR, Raman, DSC, particle size analysis, and Karl Fischer
- Support cleaning verification, swabbing, and method validation activities
- Review and report data for QC release in line with procedures
- Maintain accurate GMP documentation and support investigations (OOS, deviations, CAPA)
- Ensure lab equipment is calibrated and used correctly
- Contribute to audit readiness and continuous improvement initiatives
- Carry out microbiological/environmental sampling activities
About You
Degree in a scientific discipline (or equivalent industry experience)
Experience working in a GMP or regulated laboratory environment
Understanding of core analytical techniques and lab systems
Strong attention to detail and documentation skills
Proactive, team-oriented, and able to manage priorities effectively
This is a fantastic opportunity to join a collaborative QC team where you’ll gain hands-on experience across a wide range of analytical techniques and play a key role in maintaining product quality and compliance.