Work as a QMS Officer in London
QA/QMS Officer, Pharmaceutical
Location: Bolton/ North Manchester area
Type: Permanent
Salary: £24,500 - £27,000 DOE
Hours: Days (Monday - Friday), parking onsite
Our Client a Pharmaceutical company (part of a large Pharmaceutical group); is looking to strengthen their QA team and recruit an experienced QA Specialist. This is a GDP focused position and this person will play a key part in the growth and development of the team.
The role:
Batch release of manufactured products and Release of Third Party products or Products (when covering due to staff shortages)
Generation or review of SOPs and other documents (where applicable)
Providing support the customers and answering queries and product investigations
Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/ resolution
Participate in the internal audit programme to ensure continued GMP compliance of all site activities
Utilise scientific resources in order to work on improving quality of products and services
To maintain personal training folder in an auditable state
To undertake any task required by your Line manager, and for which you have received full training and or an explanation has been provided and understood
Generate new BMRs and offer technical assistance in product manufacturing as and when required (when covering staff shortages)
Respond to external and internal medicines information requests
Maintaining quality documentation system
Participate in quality improvement initiatives
Supporting in the process or maintaining and archiving documentation
Supporting and executing external audits where applicable
Supporting management when hosting regulatory audits
Ensuring training matrix is maintained site-wide
Generating worksheets and reviewing QC and R&D documents
Maintaining records of MHRA drug alerts and assessments
Supporting in generation of Quality Metric reports and tracking KPIs
Working on executing and maintaining the QMS, including but not limited to:
oRisk Assessments
oChange Controls
oCAPAs
oDeviations
oComplaints
oRecalls
oOOS/OOT
The Person:
Will have a Degree in a relevant- Scientific discipline
Will have good knowledge of GMP
Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous
Strong IT skills (Microsoft applications)
Good interpersonal skills and strong written/ verbal report writing skills
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 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 GDPR please get in touch with us here.
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