Quality Manager
- Recruiter
- Anonymous
- Location
- Hereford
- Salary
- 30000.00 - 40000.00 GBP Annual
- Posted
- 20 Jul 2018
- Closes
- 17 Aug 2018
- Sectors
- Manufacturing & Industrial
- Contract Type
- Permanent
- Hours
- Full Time
Quality Manager
This is a chance to join a rapidly growing ingredients and pharmaceuticals business based in the UK. The company has grown rapidly and is looking to bring people in the business to sustain and grow over the up and coming years. This company operates within the food supplement, flavourings and pharmaceutical markets.
There is currently an opportunity for an experienced Quality Manager to join their team.
Responsibilities:
* Lead the Quality department in carrying out analysis on incoming materials, components and finished products as well as data in support of the onsite manufacturing and QC functions.
* You will be required to manage the day to day workload of a team of 14 Analysts.
* Be the driving force behind the labs' compliance and integrity of work, ensuring agreed timelines are met.
* Ensure that the QC department operate in a fully current GMP manner and ensure all members of the lab have regular training in GMP practices where necessary.
* Ensure compliance with the approved and filed regulatory dossiers for product testing.
* Partake in the writing, reviewing and approving of SOPs
* You will need to ensure all SOP's, methods, protocols, method and equipment validation, method development / transfer and reports are implemented as required.
* You will be expected to act as a subject matter expert for the Quality Control Laboratory and all its functions to all internal and external stakeholders at all levels of seniority.
* Requirements:
* Degree in Chemistry, Pharmaceutical Science, Analytical based subject or similar is necessary
* Experience managing a Quality team
* Strong hands-on experience of undertaking testing, analysis and development using instrumentational analysis such as: HPLC, GC, ICP, UV Dissolution and FTIR in a GMP environment
* Extensive knowledge of GMP, ICH guidelines, BP/EP/USP methods with a strong understanding of QA processes and methodologies.
* Extensive knowledge and direct dealings with the MHRA, FDA and other leading governing bodies.
For more info please get in touch with Naomi Clarke at Core Talent
This is a chance to join a rapidly growing ingredients and pharmaceuticals business based in the UK. The company has grown rapidly and is looking to bring people in the business to sustain and grow over the up and coming years. This company operates within the food supplement, flavourings and pharmaceutical markets.
There is currently an opportunity for an experienced Quality Manager to join their team.
Responsibilities:
* Lead the Quality department in carrying out analysis on incoming materials, components and finished products as well as data in support of the onsite manufacturing and QC functions.
* You will be required to manage the day to day workload of a team of 14 Analysts.
* Be the driving force behind the labs' compliance and integrity of work, ensuring agreed timelines are met.
* Ensure that the QC department operate in a fully current GMP manner and ensure all members of the lab have regular training in GMP practices where necessary.
* Ensure compliance with the approved and filed regulatory dossiers for product testing.
* Partake in the writing, reviewing and approving of SOPs
* You will need to ensure all SOP's, methods, protocols, method and equipment validation, method development / transfer and reports are implemented as required.
* You will be expected to act as a subject matter expert for the Quality Control Laboratory and all its functions to all internal and external stakeholders at all levels of seniority.
* Requirements:
* Degree in Chemistry, Pharmaceutical Science, Analytical based subject or similar is necessary
* Experience managing a Quality team
* Strong hands-on experience of undertaking testing, analysis and development using instrumentational analysis such as: HPLC, GC, ICP, UV Dissolution and FTIR in a GMP environment
* Extensive knowledge of GMP, ICH guidelines, BP/EP/USP methods with a strong understanding of QA processes and methodologies.
* Extensive knowledge and direct dealings with the MHRA, FDA and other leading governing bodies.
For more info please get in touch with Naomi Clarke at Core Talent