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Job Details

QA Manager - GMP

Company: ProClinical Ltd
Location: United Kingdom
Reference: QA.CR.10463
Closing Date: 26 Jan 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Our client, a pharmaceutical solutions company, is seeking a QA Manager to join their team in the North West of the UK.Job Role: To co-ordinate the Compliance function ensuring that quality standards and business needs are met.Support the quality function, as necessary, in the undertaking of general duties, ensuring adherence to the quality philosophy and the delivery of customer service targets. ...

Requirements:

Our client, a pharmaceutical solutions company, is seeking a QA Manager to join their team in the North West of the UK.

Job Role:

  • To co-ordinate the Compliance function ensuring that quality standards and business needs are met.
  • Support the quality function, as necessary, in the undertaking of general duties, ensuring adherence to the quality philosophy and the delivery of customer service targets.
  • To manage quality in production (warehouse) operators to ensure incoming inspection of starting materials (including bulk, intermediate and finished goods), primary, secondary and printed packaging materials meet with, customer, company and regulatory expectations.
  • Qualification of packaging equipment, cleaning validation, process validation, validation of IT systems where there is GMP bias.

Job Responsibilities:

  • Develop systems related directly to quality within the Bolton production environment to maximise quality and efficiency and ensure compliance with current regulations for all medicinal products managed/packed by the facility.
  • Monitor the performance and potential of the QIP (Warehouse) team and provide the direction and motivation necessary to secure optimum commitment and competence.
  • Generate or assist in the generation, review or approval of Standard Operating Procedures, Corporate Policy Statements and other defined critical documentation concerning validation.
  • Assist in the conduct of customer and regulatory audits and the resolution of any audit deficiencies in a timely manner.
  • Organise and participate in internal training sessions and co-ordinate training requirements with respect to validation/qualification systems, documentation and related deliverables.
  • Contribute to the continuous development and improvement of relevant Quality systems, processes and procedures.
  • Collate data on relevant aspects of the Quality function for incorporation into periodic reports.
  • Ensure the management of systems for the recording, investigation and response to deviations, customer quality complaints and product recalls.
  • Provide Quality subject matter expert support on deviations, complaints and change controls within the incoming area ensuring proper root cause analysis, impact assessment and CAPA.

Qualifications and Experience:

  • Graduate or relevant experience within Pharmaceutical Quality/GMP environment.
  • Preferable knowledge areas of key quality systems include non-conformance reporting, complaints, auditing/inspection.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Courtney Russell on +44 203 8141 315 or upload your CV on our website www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Apply for this job: QA Manager - GMP

Contact Information:

Address:  ProClinical Ltd
Eldon House Eldon Street London
EC2M 7LS
England
Tel:  0800 988 4437
Fax:  +44 (0)207 834 9470
Website:  Visit Our Web Site

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