Technicien développement galénique H/F
Offer details
Wanted profile
PROFILE :
- You have a 2 or 3-year higher education qualification in formulation or process engineering and you must have 2 to 3 years' experience in the pharmaceutical or cosmetics sector.
- Your skills include formulation and process development for liquid and semi-solid non-sterile products.
- You are fluent in both written and spoken professional English.
- You have good writing skills and can communicate effectively.
- More generally, you are a good team player and a rigorous worker.
- Your understanding of expectations and your responsiveness to requirements and deadlines will make all the difference.
Context
Our client, which specialises in the outsourced production of medicinal products, is looking for a Galenic Development Technician (M/F).
Open-ended contract to be filled directly on a production site employing around 600 people.
Reporting to the Development Project Manager, you will contribute to :
- the development of new drugs and the evolution of existing drugs through pre-formulation and formulation studies and the development of manufacturing processes,
- the manufacture of clinical batches,
- the transfer of developed or reformulated medicines to the selected production sites.
Mission
The main tasks of the Galenic Development Technician are as follows:
Participate in the formulation and definition of manufacturing processes:
- Carry out the manufacture, packaging and in-process controls of bench, pilot and clinical batches independently in accordance with an established protocol and document them in accordance with the procedures in force
- Take part in analysing the results and providing an initial summary of the data collected
- Ensuring that studies are implemented and monitored in accordance with what has been agreed with the customer in terms of technical expectations and deadlines
- Assisting the recipient sites with the production of the first batches (validation and/or first commercial batches) for medicines from Development
Draft the associated documentation:
- Drafting, correcting and archiving the documents and manufacturing files required for the activities
- Draw up protocols and reports on formulation, development and process validation in accordance with pre-established specifications
- Drawing up production protocols and operating procedures for all stages (bench, pilot and clinical) and checking industrial operating procedures.
- Drafting investigation reports on GMP equipment
Guaranteeing the availability of equipment and components
- Setting up and adjusting equipment adapted to galenic development trials
- Prepare orders for laboratory components and consumables, researching the various possible suppliers
Work environment
A major international player in the production of medicinal products, our client is expanding rapidly and, thanks to its leading position, aims to supply all forms of medicine.
Are you planning a career in pharmaceuticals and thinking about new opportunities?
Submit your application and we'll discuss your project together!
