Quality Control Analsyt

PE Global (UK); Sligo; On-site; EUR 45,000 - 60,000; Full time

Job summary

PE Global (UK) is currently seeking an Analytical Scientist for a leading multi‑national Pharma client located in Sligo. This contract position involves testing and managing analytical data, ensuring quality control, and providing laboratory support.

The ideal candidate will possess a relevant degree and at least 5 years of experience in the pharmaceutical sector, along with proficiency in analytical techniques and strong technical writing skills. Interested candidates should submit their CV to the provided email.

Qualifications

• At least 5 years of relevant experience in a pharmaceutical/healthcare environment.
• Proficient in Microsoft Office applications.
• Self-starter capable of working on own initiative.

Responsibilities

• Testing of in process, stability, and finished product samples.
• Review and authorisation of Lab Data.
• Support Analytical Technical Transfer activity testing reports.

Skills

Analytical techniques such as HPLC, CE, SDS-PAGE, IEF

Microsoft Word and Excel proficiency

Technical writing skills

Troubleshooting and problem solving abilities

Teamwork skills

Detail-oriented and self-motivated

Education

Degree/Diploma in Biochemistry, Chemistry, Biology, Biotechnology or similar

Job description

PE Global is currently recruiting for an Analytical Scientist for a leading multi‑national Pharma client based in Sligo.

This is a contract position.

Role:

• Testing of in process, stability and finished product samples e.g. HPLC, CE, SDS‑PAGE, IEF analytical testing, characterization and sample and data management.
• Review and authorisation of Lab Data.
• Support Analytical Technical Transfer activity testing reports and documentation.
• Document review/updates when required.
• Equipment Calibration, Maintenance and Trouble Shooting.
• Method Validation/Verification.
• Training of QC Chemistry Laboratory colleagues.
• Laboratory Investigation support.
• Laboratory Housekeeping and maintaining GMP standards.
• Assisting in regulatory audits.

Responsibilities:

• Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.
• Have at least 5 years relevant experience in a pharmaceutical/healthcare environment (this is more 3 to 5 year’s experience).
• Be very proficient in the use of Microsoft Word, Excel etc.
• Have strong technical writing skills.
• Be detail oriented, self‑motivated with good troubleshooting and problem solving abilities.
• Be a self‑starter and capable of working on own initiative.
• Strong team work skills.
• Proven track record of meeting deadlines.
• Experience with analytical techniques such as HPLC, CE, SDS‑PAGE, IEF testing would also be advantageous.

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up to date CV to [e-mail]

Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.