Vacature Technology Transfer Officer (ref. 927)
Vacaturenummer 927
Regio Randstad
Uren per week 40

Technology Transfer Officer (ref. 927)

Introductie

Are you experienced in process transfer to production in an pharmaceutical environment (cGMP) and searching for a new challange? Send us your application!!!

Organisatie

More information is available upon request.

De functie

As Technology Transfer Officer you take full ownership of a project. You lead the process transfer either from an external client or from internal client. You ensure a smooth and successful preparation for a GMP production within agreed timelines (writing Batch records, BOM and batch related documentation). You are responsible for implementation and execution of new and/or adjusted formulation processes in the production department. You train and instruct production personnel on these new projects and support the execution of the processes in the cleanroom. You will be responsible for the planning of the OTT-team and assign each of the team members to requested project activities. You assure the team acts at an adequate level, are properly trained and meet timelines of our clients. Furthermore, you take initiative to continuously improve general (production) processes and/or documentation (f.e. Study files, instructions and SOP’s). You are expected to take ownership to follow up on deviations that occur during GMP production and take the appropriate corrective and preventive measures. You will be the project lead in the project team representing GMP production and you are the main contact person between the project team, production and client.

Wat vragen wij?

You are thoroughgoing, solution- and resultsoriented person who has quality as a priority. You are client and service oriented, proactive and enterprising with excellent analytical skills. You are able to put matters in a companywide perspective. You are pragmatic and have a "Yes we can do" mentality.

 
You have at least a BSc-level education or equivalent, preferably in the area of (bio)chemistry (or process engineering?). You have at least five years of experience with cGMP in a pharmaceutical or biotechnological company. You have experience with working in various projects at the same time. You have excellent communication skills verbal and writing in Dutch as well as in English.

Wat bieden wij?

Terms of employment are of marked standard. More information is available upon request.

Inlichtingen

Jay Baktawar

+31 10 415 7822 or jay.baktawar@birdrecruitment.nl

Sollicitatie

Jay Baktawar

+31 10 415 7822 or jay.baktawar@birdrecruitment.nl

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