Stability Analyst, HPLC, Pharmaceutical
- Recruiter
- Confidential
- Location
- Derby
- Salary
- 22000.00 - 24000.00 GBP Annual
- Posted
- 12 May 2022
- Closes
- 25 May 2022
- Sectors
- Accountancy
- Contract Type
- Permanent
- Hours
- Full Time
Stability Analyst, HPLC, Pharmaceutical
Location: Derbyshire
Type: Permanent
Hours: Monday - Friday (days)
Salary: GBP23,000 CIRCA DOE
Russell-Taylor is delighted to be working alongside one of the UK's leading Pharmaceutical manufacturing companies; the successful candidate will be joining a team and company who continue to grow from strength to strength and offer career development as well as the chance to work with a vast product range.
The successful person will be working on some really - key projects/ programmes and will help support the QC lab. You will be involved in project management (drafting stability protocols and reports) and ensuring the smooth flow of the assigned stability programme.
The Person:
Will hold a Degree in a relevant/ Chemistry related discipline.
Extensive HPLC experience (method validation/ development not essential but preferable) - the ideal candidate will be able to troubleshoot (column change etc) and will have worked to GMP standards.
Will have a good understanding of stability within a GMP setting
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please get in touch on h u s s e l l - t a y l o r . c o . u k
Location: Derbyshire
Type: Permanent
Hours: Monday - Friday (days)
Salary: GBP23,000 CIRCA DOE
Russell-Taylor is delighted to be working alongside one of the UK's leading Pharmaceutical manufacturing companies; the successful candidate will be joining a team and company who continue to grow from strength to strength and offer career development as well as the chance to work with a vast product range.
The successful person will be working on some really - key projects/ programmes and will help support the QC lab. You will be involved in project management (drafting stability protocols and reports) and ensuring the smooth flow of the assigned stability programme.
The Person:
Will hold a Degree in a relevant/ Chemistry related discipline.
Extensive HPLC experience (method validation/ development not essential but preferable) - the ideal candidate will be able to troubleshoot (column change etc) and will have worked to GMP standards.
Will have a good understanding of stability within a GMP setting
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please get in touch on h u s s e l l - t a y l o r . c o . u k