Quality Control Analyst
Posted Today by Planet Pharma
Negotiable
Undetermined
Undetermined
Dartford, England, United Kingdom
Summary: The Quality Control Analyst role involves conducting high-quality analytical testing in a laboratory setting to support production while ensuring compliance with GMP and EHS standards. The position requires proficiency in various analytical techniques and instruments, alongside responsibilities in method development, data review, and reporting. The ideal candidate will possess a science degree and relevant laboratory experience, demonstrating strong attention to detail and effective communication skills. This role offers a structured shift pattern and the opportunity to work in a professional lab environment focused on quality and safety.
Key Responsibilities:
- Perform routine and specialized analytical testing on in-process and composite samples.
- Prepare and review analytical reports, certificates of analysis, and validation documentation.
- Maintain lab cleanliness and adhere to all GMP and EHS procedures.
- Identify and escalate deviations, CAPAs, or changes under supervision.
- Use laboratory IT systems, including Oracle, Trackwise, ComplianceWire, and Minitab.
- Communicate effectively with colleagues, management, and clients.
- Stay up-to-date with industry developments related to particle size analysis and cleaning validation.
Key Skills:
- Science graduate or higher with laboratory experience in a cGxP environment, or extensive industry experience.
- Knowledge of GMP and EHS principles.
- Strong attention to detail, accurate documentation, and time management skills.
- Self-motivated with a professional and positive attitude.
- Ability to work independently or as part of a team.
Salary (Rate): undetermined
City: Dartford
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
About the Role
We are seeking a motivated and detail-oriented QC Analyst to join our laboratory team. You will conduct high-quality analytical testing to support production, ensuring compliance with GMP and EHS standards . You will work with a range of analytical techniques and instruments, including particle size analysis, HPLC, FTIR, Raman, DSC, microscopy, and more. The role involves testing, method development, data review, and reporting, as well as maintaining laboratory compliance and safety standards.
Key Responsibilities
- Perform routine and specialized analytical testing on in-process and composite samples.
- Prepare and review analytical reports, certificates of analysis, and validation documentation.
- Maintain lab cleanliness and adhere to all GMP and EHS procedures.
- Identify and escalate deviations, CAPAs, or changes under supervision.
- Use laboratory IT systems, including Oracle, Trackwise, ComplianceWire, and Minitab.
- Communicate effectively with colleagues, management, and clients.
- Stay up-to-date with industry developments related to particle size analysis and cleaning validation.
Who We’re Looking For
Science graduate or higher with laboratory experience in a cGxP environment , or extensive industry experience. Knowledge of GMP and EHS principles. Strong attention to detail, accurate documentation, and time management skills. Self-motivated with a professional and positive attitude. Ability to work independently or as part of a team.
Shift Pattern: 3-week rotation Early Shift: 6:00am – 2:00pm (Mon-Fri) Late Shift: 1:30pm – 10:00pm (Mon-Thu), 1:30pm – 7:00pm (Fri) Night Shift: 9:00pm – 7:00am
Why Join Us
Work in a supportive, professional lab environment. Opportunity to gain hands-on experience with a wide range of analytical techniques. Be part of a team committed to quality, safety, and continuous improvement.