QC Analyst

SRG; Glasgow; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading pharmaceutical company based in Glasgow is seeking a talented QC Analyst III to ensure that products meet the highest quality standards. You'll conduct various tests and work closely with production teams in a strong, supportive environment focused on learning and development. Ideal candidates will have a degree in chemistry and experience in quality control.

Benefits

Supportive work environment

Opportunities for learning and development

Qualifications

• Previous experience in a quality control laboratory environment.
• Experience with complex HPLC analysis/validation essential.
• Knowledge of GLP and GMP regulatory requirements.

Responsibilities

• Conduct testing on in-process and finished products.
• Review data and documentation as required.
• Liaise with production supervisors for scheduling tests.

Skills

Troubleshooting skills

Method development

Attention to detail

Collaboration

Education

Degree in chemistry or a related field

Tools

HPLC

UV

IR

GC

Job description

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Exciting QC Analyst III Opportunity in Glasgow

Are you a talented Quality Control Analyst looking to join a dynamic and growing company? This could be the perfect opportunity for you!

We are working on a role for a very experienced QC Analyst from the pharmaceutical industry to play a key role in the QC team.

If you are currently an experience Analyst or Senior, then this could be the job for you.

The Role

The QC Analyst is a crucial member of the team, responsible for ensuring that the company's products meet the highest quality standards. As a QC Analyst, you will be involved in a variety of tasks, including:

• Conducting testing on in-process, finished product, and raw materials using a range of analytical techniques including but not limited to HPLC analysis, UV, IR, GC, and particle size analysis, in accordance with the relevant procedures and cGMP
• Reviewing data and documentation as required in line with regulatory requirements
• Liaising with production supervisors to schedule and report on in-process testing
• Documenting test results and interpreting data to identify any out-of-specification or out-of-trend results
• Assisting with laboratory investigations and implementing corrective and preventive actions
• Maintaining a clean and organized working environment within the Quality Control Laboratory

What We're Looking For

To be successful in this role, you will need:

• A degree in chemistry or a related field
• Previous experience working in a similar quality control laboratory environment
• Strong troubleshooting and method development skills, particularly with HPLC
• Experience in with complex HPLC (UV-VIS, CAD, IC) analysis/validation essential
• Knowledge of regulatory requirements such as GLP and GMP
• Excellent attention to detail and the ability to work to tight deadlines
• A customer-focused attitude and the ability to collaborate effectively with colleagues
• Ability to work in a fast-paced and changing environment

Why Join This Company?

This company offers a positive and supportive work environment, with plenty of opportunities for learning and development. You'll be part of a talented team that is committed to excellence and making a real difference in the pharmaceutical and biotechnology industries.

If you're excited about the prospect of joining the QC Analyst team, we'd love to hear from you. Apply now and take the first step towards an rewarding and fulfilling career!