Talent Acquisition Manager - Life Science & Pharmaceuticals for Consultys - Vulcain Engineering Group
Who we are:
For 19 years, the largest laboratories have extended their trust in us. Specialised in pharmaceuticals, biotechnologies and medical devices, we support our customers from the research to the marketing of their products. As a human-sized company, we are committed to supporting and personally advancing our 600 employees recognised for their technical and scientific expertise.
Through our regional subsidiaries, we guarantee everyone geographical stability, without mobility clause on the main business areas in France, Belgium, Switzerland and Canada.
Much more than concepts, our 3 values "Respect, Recognition and Transparency" guide us and are the foundation of our history, the heart of our group’s success.
Responsibilities:
* Oversee the timely, quality and cost-optimized production of the assigned products in compliance with the relevant laws, regulations and guidelines regarding safety, quality, regulation, hygiene and the environment.
* Take responsibility for the timely and independent execution of the operational batch record review (manufacturing records, cleaning records in MES / DeltaV) in accordance with the internal work instructions.
* Ensure the correct preparation and execution or review of the risk analysis in the projects assigned to you and the implementation of the resulting measures.
* Conduct production campaigns according to cGMP guidelines, ensure batch execution, evaluate test results, troubleshoot problems, troubleshoot manufacturing equipment and propose solutions.
* Handle documentation of processes and process know-how as well as prepare campaign reports and participate in annual product reviews.
* Support the ongoing search for improvement opportunities in processes, equipment and procedures in cooperation with various project teams.
* Be responsible for the implementation of the relevant GMP documents for the respective area.
* Support the training of employees for the assigned products (campaign training).
Qualification Requirements:
* Minimum Bachelor’s degree, Master's degree preferred in a scientific topic (Pharmacy, Chemistry, Biology, Biotechnology, etc.).
* At least 2 years of experience in Biotechnology.
* Excellent knowledge of regulatory requirements, including GMP guidelines.
* Experience (min 1 year) executing and supervising Biotech Processes in GMP environment.
* Experience with DeltaV and Syncade systems is preferable.
* Previous experience with systems like Trackwise is preferable.
* Fluency in English and/or German is mandatory.
Do you want to join the consulting world in a human-sized company that values the individual and performance?
To share your skills within a cohesive team where experiences are freely shared?
CONSULTYS is open to all talents and is committed to diversity and inclusion.
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