Hyper Recruitment Solutions are currently looking for a Quality Assurance Officer to join a leading Pharmaceutical Ingredients company based in the He... View Job
Hyper Recruitment Solutions are currently looking for a Quality Assurance Officer to join a leading Pharmaceutical CMO based in the Wiltshire area. As... View Job
International QA Auditor
Hyper Recruitment Solutions are currently looking for a International QA Auditor to join a leading Bio-Pharmaceutical company based in the Scotland ar... View Job
Hyper Recruitment Solutions are currently looking for a QA Specialist to join a leading Pharmaceutical Ingredients company based in the Oxfordshire area. As the QA Specialist you will be responsible for maintaining cGMP compliance across the business function.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Specialist will be varied however the key duties and responsibilities are as follows:
1. You will represent the QA department across multiple business areas, interacting with the QC and Validation teams. You will demonstrate a complete understanding of cGMP procedures, and practice putting them into practice.
2. As the QA Specialist you will monitor Quality KPI's, identify trends, lead investigations and resolve any issues with your line manager, this will involve generation and review of QA procedures and other documentation, as well as supporting root cause analysis and driving CAPA implementation.
3. It will be your responsibility to participate in and lead internal and external audits/inspections, seeking continuous quality improvement across the site.
4. You will provide GMP training to your colleagues, maintain an on-site QMS, produce batch manufacturing records, and conduct in PQR's to keep the business and products GMP compliant.
To be successful in your application to this exciting opportunity as the QA Specialist we are looking to identify the following on your profile and past history:
1. Proven industry experience in Quality Assurance, with previous time spent working with API/Biologic's products.
2. A working knowledge and practical experience with GMP requirements, additional experience with equipment validation would be highly advantageous.
Key Words: Quality Assurance | Pharmaceuticals | QA | GMP | Quality | Compliance | CAPA | Change Control | Deviations | Audits | Regulations | Quality Management System | Non-conformance | Trackwise | Root Cause | SOP's | Biologics | Product Quality Review | API | Inspections | Batch Records | Compliance | Drug Discovery
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors and is made up of a collaboration of scientists supporting science. We look forward to helping you with your next career moves.