QC Chemistry Analyst

CV-Library

Posted on Sep 18, 2024 by CV-Library
Pentre Maelor, Clwyd, United Kingdom
Pharmaceutical
Immediate Start
£28k - £35k Annual
Full-Time
QC Chemistry Analyst – Pharmaceutical Manufacturer

Position: QC Chemistry Analyst
Location: Clwyd
Salary: £28,000 - £35,000 per annum
Role Type: Permanent, Full-Time

Job Summary

As the QC Chemistry Analyst, you will be responsible for the design and carry out of HPLC/UPLC/UV/GC analytical method validation and verification. You will support the department to monitor the quality of components, raw materials, products and production processes by sampling, inspection and analysis.

Qualifications and Skills

* A relevant science degree or equivalent qualification

* A sound understanding of current GMP, Health and Safety and COSHH regulations

* Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision

* The ability to take on a limited supervisory role would be an advantage

* Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation

* 3+ pharmaceutical experience

Benefits

* 33 days holiday inclusive of Bank Holidays

* Pension Contributions 7% employer / 7% employee

How to Apply

If this is a role that you feel you are suitable for, please send an updated copy of your CV using showcasing the relevant experience.

Please note, for this role you must have the full right to work in the UK

Reference: 222346859

https://jobs.careeraddict.com/post/95419716
CV-Library

QC Chemistry Analyst

CV-Library

Posted on Sep 18, 2024 by CV-Library

Pentre Maelor, Clwyd, United Kingdom
Pharmaceutical
Immediate Start
£28k - £35k Annual
Full-Time
QC Chemistry Analyst – Pharmaceutical Manufacturer

Position: QC Chemistry Analyst
Location: Clwyd
Salary: £28,000 - £35,000 per annum
Role Type: Permanent, Full-Time

Job Summary

As the QC Chemistry Analyst, you will be responsible for the design and carry out of HPLC/UPLC/UV/GC analytical method validation and verification. You will support the department to monitor the quality of components, raw materials, products and production processes by sampling, inspection and analysis.

Qualifications and Skills

* A relevant science degree or equivalent qualification

* A sound understanding of current GMP, Health and Safety and COSHH regulations

* Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision

* The ability to take on a limited supervisory role would be an advantage

* Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation

* 3+ pharmaceutical experience

Benefits

* 33 days holiday inclusive of Bank Holidays

* Pension Contributions 7% employer / 7% employee

How to Apply

If this is a role that you feel you are suitable for, please send an updated copy of your CV using showcasing the relevant experience.

Please note, for this role you must have the full right to work in the UK

Reference: 222346859

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