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Job Details

Quality Manager (EMA and ROW) ** Ghent / Antwerpen / Brussels West *** Growing and dynamic company, QA GMP NPI type role

Company: Advanced S&S (Medical / Clinical)
Location: Ghent, Antwerpen, Brussels West
Reference: MGADV / 10342
Closing Date: 30 May 18
Type: Full Time
Salary (£): On Application
Benefits: On Application

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Job Summary:

This role is on exclusive assignment to Advanced Search & Selection. Please contact Theo Moore or Matt Greig initially on +44 20 7801 3380 or +44 7918 679 405 (until 9.00 pm CET and Saturday mornings) or send a full CV and contact information to theo@advregulatory.com or matt.greig@advregulatory.com who will support your assessment and onboarding process.

Requirements:

This is a new position due to expansion of the quality team following portfolio growth for a company generating 5 billion USD per annum, with a 10-15% growth, driven by new product introductions, further expansion of new markets, so this company is not sitting still, it is growing dynamically!

You will be an experienced GMP product quality manager, with good knowledge of supporting form a QA perspective new products and new dosage forms development (across the full spectrum, of topicals, solid dose, and aseptic) and most importantly, will have worked through stability and validation for new product introduction:-

  • You will be involved in NPI development and running the stability and validation to ensure quality manufacture
  • Monitoring existing products before and after release, managing deviations and changes to process, assess the change control assessment, dealing with stability investigations
  • Being involved in technical product transfers for site transfers for process validation, analytical methods, stability
  • Have experienced in as many of the following: Ointments, creams, liquids, syrups and suspensions, solids, effervescent tablets, triple layer tablets, sachets, patches, lozenges, sterile as well (medical devices aseptic packaging)
  • GMP experience with either Human Rx, Gx or OTC products or animal health
  • Early / previous manufacturing environment experience and understands the regulations.

You will be certified by the company for auditing, not because this is an audit role, but because you will audit and troubleshoot for 10% of your time, the CMOs supporting your product portfolio.

This role is reporting to an experienced senior quality manager, who really wants you to help with their drive to develop new products, manage third party CMOs, and keep existing products through deviation management, compliant and there for the patients.

The role comes with a company car, bonus, petrol card plus the normal Belgium benefits, including extra legal pension. The company are seeking local applicants for this role who want in a smaller company than a top 10 pharma, where people can grow and develop locally, without having to leave the country or field calls from the US every day!

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If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
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About Advanced

Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at www.advregulatory.com.

We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.

Keywords / Key words: Medical, Medical Affairs, MA, Medical jobs, MA jobs, Medical Affairs jobs, PhV QA, Jobs in PhV QA, Jobs in Quality Assurance, QA Manager, Global QA Manager, Quality Manager, QA, GMP, NPI

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Head Office Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3388
Website:  Visit Our Web Site

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