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Quality Assurance Project Manager



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Introductie

Fagron is looking for a Quality Assurance Project Manager to manage different projects in order to optimize our quality processes in line with the business needs.

De functie / The role

You will be focusing on the quality within the complete flow from raw material to product for our different production sites. Your aim is to strive, to achieve optimum quality and to make the processes more efficient. As Qualified Person you will also responsible for the final release of the batch of our pharmaceutical product. In this role you review all the batch files, which encompass information from every involved department.

In first instance you will focus on our production site in Uitgeest, The Netherlands. On the mid-term, you may also become responsible for quality projects at other European production sites, inside and outside The Netherlands. In your role you will report to the European Quality Manager.

Your responsibilities include but are not limited to:

Determine the policy lines in the framework of the entire quality process
Translating the Global and European quality strategy into quality in actual projects for our production sites
Act as Qualified Person and ensure certification of each batch of the finished products
Developing and rolling out training material in the field of GMP for employees within the various locations
Following the principles and guidelines of GMP according to ICH, EU Annexes, and industry best practices. Ensure all requirements under references have been met prior to release of a batch
Validation of the principal manufacturing and testing processes
Checking all necessary tests have been performed
Ensuring that the legal requirements regarding imported products have been fully met
Providing QP GMP declarations in support of importation activities and maintaining an up-to-date awareness of regulatory issues
Carry out auditing of third party GMP facilities involved in the manufacturing of medicinal products, active pharmaceutical ingredients, excipients, and other necessary materials used in production or ancillary activities.
Drawing up action plans for inspections / audits and monitoring their follow-up
Identifying and eliminating GMP risks within the various locations

Het profiel / Your profile


Maak het verschil

Has a M.Sc. degree in Pharmacy, Biotechnology, Biology or equivalent?
Is licensed as QP as defined in the DIRECTIVE 2001/83/EC
Has at least five years of experience working in a GMP regulated environment
Has experience in performing audits of third-party providers and support of the internal audit program to enable permanent inspection readiness
Has an excellent proficiency in English and in Dutch.



Het aanbod / The offer

We offer a unique working environment where talent and ambition can develop to its fullest. We have an open and informal organization culture, where you need to be able to work independently. Fagron is a young, professional and ambitious company with plenty of growth opportunities and we will offer you a competitive compensation


Solliciteer hier
Indien solliciteer hier u verwijst naar een ongeldig webadres, is de vacature (hoogstwaarschijnlijk) inmiddels vervuld. Attendeer FMF hierop

Uw referentie aan www.fmfvacatures.nl wordt gewaardeerd.
Your referral to www.fmfvacatures.nl is appreciated.


Gegevens

Werkgever:
Fagron
Vacaturesteller:
Fagron
Standplaats:
Amsterdam

Geplaatst op FMF: 22 juli 2019

Branche: Farma & Biotech
Functie: QA / regulatory
Opleidingsniveau: WO/academisch / MSc
Werkervaring: 5-10 jaar, > 10 jaar