Our client is committed to developing a growing portfolio of superior pharmaceutical-based health care solutions with breakthrough medicines for conditions such as depression, schizophrenia, attention-deficit hyperactivity disorder, diabetes, osteoporosis and many more. They are currently seeking QA representative for a 6 month contract for their Liverpool office.
The QA Representative will ensure that manufacturing is carried out in accordance with cGMP and Regulatory commitments and that production records provide full and accurate documentation of batch manufacture in accordance with SOP.
PRINCIPAL RESPONSIBILITIES include:
Monitor trends and identify problems in quality
Write/revise/approve and give advise on quality documentation
Review and approve SOPs as appropriate
Advise on the investigation of customer complaints, approve customer
complaint reports and promote corrective/preventive actions
Participate in self-inspections and other audits of the manufacturing
Provide training, support, advice and proactive assistance
Advise on and support appropriate validation of plant, processes and new
Prepare Quality Agreements as appropriate
Liaise with Contract Manufacturers, as appropriate
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Life Science degree
Quality assurance and manufacturing experience
Fforde is acting as a recruitment agency/business.
KEY WORDS: Quality Assurance, QA, cGMP, Regulatory, Manufacture, Life Science, Pharmaceutical, CRO, Contract, Liverpool, UK