My client, European industry-leading specialist service provider for the Life Sciences industry, focused on delivering high quality professional services in the areas of Regulatory, Safety, Quality, Process alignment and Medical services.
Title: QP / Qualified Person
Type: 12 month contract
ROLE PURPOSE AND RESPONSIBILITIES
The role will include:
To ensure that an effective pharmaceutical quality management system (QMS) is operated and that all regulatory obligations of the authorization holder are fulfilled To certify batches (QP) Perform GMP/GDP compliance gap analysis and interact with the regulatory department Handle quality complaints, rejects, reworks, returns, recalls, deviations and CAPA, change control QA liaison with contract manufacturing organizations or third party logistic providers To accomplish QP/RP duties according to the applicable regulations (RD 14 Dec 2006) and as described in GMP/GDP and in the "Code of Practice for Qualified Persons in the Pharmaceutical Industry"(EIPG)
FEEL LIKE THIS IS FOR YOU?
The ideal candidate should have:
Qualified Person certified at FAMHP (Belgian Royal Decree of 14 Dec 2006 art. 48 ; EU Directive 2001/83/EC) At least 3 years experience in Quality Assurance or as a Qualified Person or Responsible Person Customer and Quality focus Result driven , accurate Good organizational, planning and communication skills Team motivator and team player Open to operate with people of different background and cultures and adapt to different work situations and work circumstances Fluent in English and Dutch and/or French Computer skills: MS Office; knowledge of SAP® and Trackwise® is a plus.
If you think that this is an opportunity that you have experience and motivations to take on, then please forward your application to or call . However if you feel that you might know someone who is better suited to take on this position why don't you get in touch? We give out £250 in holiday vouchers if we place a candidate that you refer to us!
If you are a Regulatory Affairs, Clinical Trials, Pharmacovigilance, Quality Assurance, Compliance professional for which this opportunity isn't what you're looking for then feel free to call JCW on (0) and ask for our Life Science team.
If you are a business looking to make a placement in the Technical and Regulated space of the Life Science space, please get in touch on our main number on (0) and ask to speak one of our specialist consultants across our specialist areas listed here.
JCW's Life Science division is a preferred supplier to a number of FTSE 100 businesses across the Life Sciences and Biotechnology spectrum as well as assisting many smaller SME's achieve their headcount growth targets.
Due to the specialist nature of the Risk and Governance market, our focus is on proactively generating candidates through direct approaches which ensures that we're able to access the best talent in response to our client's hiring needs, regardless of whether they're actively looking for new opportunities.
Each JCW Consultant operates as a specialist within their particular market 'vertical' meaning that they develop a specific network of relevant industry professionals as well as keeping abreast of industry developments and being able to relate these to recruitment pressures in the sector.
Key words: Pharmaceutical / QA / Quality Assurance/ SOP / Biotech / Biopharmaceutical / Validation / GC/ Quality Control / GMP/ GDP/ Quality Assurance / QP / Qualified Person / batch release / RP / Responsible person