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Analytical Chemist, Pharmaceutical (HPLC)

Capio Spine Center Stockholm

Derby

On-site

GBP 25,000 - 33,000

Full time

7 days ago
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Job summary

An established industry player is seeking an experienced HPLC/GC Analyst to join their reputable pharmaceutical manufacturing team. This role offers a defined career progression path within a growing organization known for its commitment to quality and innovation. You will be responsible for conducting analytical testing, ensuring compliance with cGMP/GLP standards, and supporting quality control processes. If you are passionate about analytical chemistry and looking for a role that offers both challenge and opportunity, this position is perfect for you.

Qualifications

  • Solid experience in HPLC-UV and GC testing in a GLP/GMP setting.
  • Experience in method development and validation is ideal.

Responsibilities

  • Conduct analytical testing according to cGMP/GLP and SOPs.
  • Perform QC testing on raw materials and finished products.
  • Calibrate and maintain laboratory equipment.

Skills

HPLC
GC
Analytical Chemistry
Wet Chemistry Techniques
Troubleshooting

Education

Degree in a relevant scientific discipline

Tools

LIMS system
GC/MS

Job description

Type: Permanent
Location: Derby
Salary: £25000 - £32900 depending on experience (company bonus included too)
Hours: Days (Mon - Friday)

Our client, a leading Pharmaceutical manufacturer (CMO), is looking to recruit for an experienced HPLC/GC Analyst. The successful candidate will gain further career progression working for a growing pharmaceutical manufacturing company that offers a pre-defined development path. The company has a great reputation in the industry, and their brands can be recognized in any major retailer.

The Role
  1. Analytical testing according to cGMP/GLP, SOPs and Work Instructions
  2. Raw Material and Finished product QC testing
  3. Assisting with batch release
  4. Routine Quality Control testing using Analytical and Wet Chemistry techniques (HPLC, GC/MS, pH, titrations, etc.)
  5. Updating results onto the LIMS system accurately and promptly
  6. Working to departmental efficiency targets, ensuring timely completion of results
  7. Adhering to the QMS and GMP/GLP standards at all times
  8. Reporting and investigating any QC issues that may arise from test work
  9. Calibrating and maintaining equipment
  10. Ability to troubleshoot analytical and equipment problems, be proactive
  11. Escalate non-resolvable technical/quality issues to management
  12. Assist with training of laboratory staff
  13. Ensure the laboratory is kept to a standard that meets cGMP and would pass all audits
  14. Support other areas of the laboratory as required including calibration and cleaning responsibilities
  15. Provide support in the execution of project tasks and paperwork
The Person
  1. Will hold a Degree in a relevant scientific discipline (Analytical based - Pharmaceutical, Chemistry, etc.)
  2. Solid experience in HPLC-UV, GC testing with experience in troubleshooting in a GLP/GMP setting or similar
  3. The ideal candidate will have experience in method development and/or method validation

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