Quaity Control Analyst
- Recruiter
- Confidential
- Location
- Huntingdon
- Salary
- 15.00 - 21.00 GBP Hourly
- Posted
- 16 Jul 2021
- Closes
- 13 Aug 2021
- Sectors
- Accountancy
- Contract Type
- Temporary
- Hours
- Full Time
At S3 Science, we are recruiting for our client's Drug Development department. We are looking to recruit a Quality Control Analyst on a fixed term contract until February 2022.
The CMC (Chemistry Manufacturing Controls) division provides end-to-end analytical solutions and testing services to ensure quality control of our clients manufactured drug products.
The company works with leading pharmaceutical and biotech clients to ensure that their manufactured drug product or API (Active pharmaceutical Ingredient) passes all quality testing. Once this testing is complete, it brings our clients one-step closer to successfully launching that drug product on the market; helping bring medicine to patients.
The Quality Control Analyst is responsible for performing analytical work on studies. They provide specialist technical advice and training to department staff and study sponsors.
Job responsibilities include:
* Keeping up to date with regulatory requirements and industry guidelines concerning the tests/procedures within area of responsibility, GMP/GLP requirements and company/department SOPs relevant to the work area
* Conducting all phases of experimental work and reporting of projects and studies
* Performing allocated analytical work on projects and studies, ensuring that work is performed to satisfactory scientific standards, in accordance with the project plan or protocol, GMP, GLP and the relevant SOPs
* Developing, improving and validating analytical procedures, ensuring that these meet the objectives of the study and the scientific standards required by clients and regulatory authorities
* Interpreting and analysing the results obtained from relevant studies and provide advice to department staff in data interpretation
Your background and experience:
* Experience or knowledge of analysis and analytical techniques such as Flow Cytometry, Potency assays and other Bioassays along with cell culture preferably in the pharmaceutical industry
* The post holder should have a relevant scientific degree
* An understanding of health and safety policies, Company policies and procedures, and an understanding of GxP
The CMC (Chemistry Manufacturing Controls) division provides end-to-end analytical solutions and testing services to ensure quality control of our clients manufactured drug products.
The company works with leading pharmaceutical and biotech clients to ensure that their manufactured drug product or API (Active pharmaceutical Ingredient) passes all quality testing. Once this testing is complete, it brings our clients one-step closer to successfully launching that drug product on the market; helping bring medicine to patients.
The Quality Control Analyst is responsible for performing analytical work on studies. They provide specialist technical advice and training to department staff and study sponsors.
Job responsibilities include:
* Keeping up to date with regulatory requirements and industry guidelines concerning the tests/procedures within area of responsibility, GMP/GLP requirements and company/department SOPs relevant to the work area
* Conducting all phases of experimental work and reporting of projects and studies
* Performing allocated analytical work on projects and studies, ensuring that work is performed to satisfactory scientific standards, in accordance with the project plan or protocol, GMP, GLP and the relevant SOPs
* Developing, improving and validating analytical procedures, ensuring that these meet the objectives of the study and the scientific standards required by clients and regulatory authorities
* Interpreting and analysing the results obtained from relevant studies and provide advice to department staff in data interpretation
Your background and experience:
* Experience or knowledge of analysis and analytical techniques such as Flow Cytometry, Potency assays and other Bioassays along with cell culture preferably in the pharmaceutical industry
* The post holder should have a relevant scientific degree
* An understanding of health and safety policies, Company policies and procedures, and an understanding of GxP