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Contract - Qualified Person (Solid Dose) - Midlands



Business Type: Generics Company
Job Type: Quality Assurance - Control
Job Level: Experienced (non manager)
Position: Contract
Location: Nottinghamshire
Reference: DAFE#12469
Closing Date: 20/06/18
Background:

Contract - Qualified Person (Solid Dose) - Midlands

QP required for a Generics wholesale site. Contract opportunity to be responsible for Qualified Person (QP) stated in directives issued by EC and certify batches for sale or supply in compliance with regulations. Candidates must be eligible to work in the UK.


JOB TITLE

Qualified Person / QP

LOCATION

United Kingdom / Midlands

LENGTH

6 Months Initially

RATE

£700

ROLE/DESCRIPTION

  • Perform the duties of a Qualified Persons in accordance with the provision of Directive 2001/EC/ EU Guidance on GMP, Annex 16 requirements.
  • Approves Annual Product Quality Review, SOPs, Complaint investigations, Deviations (EQMS general investigations)
  • Participates in writing or suggesting changes to controlled documents
  • Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Distribution Practices (GDPs)
  • Participate in the writing of annual product reviews and the development of training programs regarding all aspects of producing quality products.

REQUIREMENTS

  • Must be qualified QP under the Directive 2001/83/EC relating to medicinal products for human use QP on a manufacturing license
  • Proficient in Good Manufacturing Practices (GMPs) and/or Good Distribution Practices (GDPs)
  • Experience of involvement across all departments, working at a senior level
  • Working knowledge of risk management tools
  • Critical thinker with excellent communication skills


ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Senior Recruitment Consultant David Fearnley on +44 (0)20 3189 0497, or email dfearnley@i-pharmconsulting.com. If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


KEY WORDS

Qualified Person / QP / QA / Manufacturing / GMP / GDP / Good Distribution Practices / Good Manufacturing Practices / UK / Midlands / Generics / Solid Dose / England



i-Pharm Consulting Posted by:: i-Pharm Consulting (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 13/06/2018 | NPJ Ref: 216287
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