Headquartered in Milan, Italy, Bracco Imaging is one of the world’s leading companies in the diagnostic imaging business. Bracco Imaging offers products and solutions for all key diagnostic imaging modalities: X-Ray Imaging (including Computed Tomography-CT), Magnetic Resonance Imaging (MRI), Ultrasound and Nuclear Medicine. For our Manufacturing Site based in Geneva (Plan-les-Ouates) and producing a lyophilized contrast agent exported in several countries, we are looking for a seasoned professional as a
Reporting to the Sterile Production Manager, you oversee the production of sterile products produced on our aseptic filling line 2 using isolator technology. You manage a team of approximately 6 production technicians and ensure continuity and reliability according to product quality standards.
In this role, you will be responsible for the following activities:
- To organize and supervise production and operations related tasks in line 2 as per current Good Manufacturing Practices (cGMPs) and according to our HSE rules.
- To approve instructions related to production operations and ensure their strict implementation.
- To manage production planning line 2.
- To ensure that products are produced and stored according to the appropriate processes to obtain the required quality.
- To ensure that production records are fully evaluated and signed by an authorized person before batch production record review by the Quality Unit.
- To ensure that the required training of his team is carried out and adapted according to the needs.
- To verify maintenance, qualification and validation processes performance as per established program.
- To participate in the issuance of GMP documents related to the activities and in Regulatory inspections.
- To contribute to our continuous improvement program.
Qualifications & Skills:
- Graduated in Life Sciences, (pharmacist or engineer) you have a solid track record in managing a team in a production environment.
- An experience in aseptic production line to produce sterile product using isolator technology is required.
- You master production processes and are experienced in cGMP environments as well as in FDA-approved sterile manufacturing sites.
- Good knowledge of continuous improvement methods (e.g. lean six sigma methods) is a plus.
- On top of your professional competencies, you are a good communicator, and your interpersonal skills help you rapidly establishing your leadership within your team as well as with local and international management.
- Fluency in English and French are required for the position (Italian is a plus).
We offer:
- The opportunity to join a well-established and successful company certified ISO 14001-45001 with bright prospects and state-of-the-art manufacturing site and production facilities.
- A great development perspective and the opportunity to bring and utilize your know-how and expertise.
- A benefit from the support of local and corporate management in making our production site a reference for the group. You will enjoy large autonomy in the daily management of your department.
If you recognize yourself in this profile and want to take up a new challenge, send us your complete application, (letter & CV) only by mail, through the JOBUP website.