Description
My client is one of the leading pharmaceutical companies in the world, for their Headquarter in Bern area, Switzerland i am looking for a:GMP Team Leader m/f
Responsible for defining objectives and activities related to GMP production within the process development department. Supervises those activities, personnel and equipment of the department to meet project demands.
Objectives:
- Timely delivery of product or intermediate product of the correct quality and quantity to meet project demands.
- Give input to and follow up on departmental goals.
- Supervision of the team and responsible for the development of staff, performance of appraisals.
- Define team objectives, translate them into activities and take responsibity for the overall results of those activities
- Supports technology transfer within the Development organization and cross functional with other parties.
- Assures that data from CTM manufacturing is prepared, analyzed, interpreted and retained accurately
- Write, review and approve Study Plans & Study Reports.
- Assure that the members of the team keep up to date with developments in own field and are adequately trained; represent own expertise field within and outside of the organization.
- Participates, as the USP/DSP production Subject Matter Expert, in regulatory inspections and is experienced with the required GMP and regulatory guidelines.
- Pilot plant representative in global & cross-functional scientific project teams.
- Maintain and continuously improve cGMP compliance within USP/DSP area; support maintenance and improvement of cGMP compliance of pilot plant facility with relation to USP/DSP area
- Strong cross- functional interaction with the other Team Leaders, the Development & Investigations team and with other site Bern departments and with the Scientific Leads at the Sites in Bern.
Requirements:
- Master's degree with 5-10 years of relevant experience
- Knowledge and experience of cGMP manufacturing of CTM and/or commercial drug substance
- SME experience in USP/DSP area ("Anaerobic" Fermentation, Centrifugation and Ultrafiltration) including pilot scale and technology transfer. *
- Several years' experience with leading teams.
- Advanced knowledge of goal setting, leader ship, problem solving, communication, mentoring and coaching techniques.
- Knowledge and interpretation/implementation ability of cGMP and current Regulatory Compliance Guidelines
Duration of the contract:
Immediately available until 31.05.2017 - high possibility for an extension
About me:
I am a specialised recruiter, currently taking care of various projects within the Life Science area in Switzerland. If this role is of interest to you or to someone from your network, please send your CV in Word format including your hourly rate expectation for immediate consideration.
You can reach me on or at