Als neue Jobbenachrichtigung einrichten
Als neue Jobbenachrichtigung einrichten
Geben Sie nachstehend Ihre E-Mail-Adresse ein, um Benachrichtigungen in Ihrem Posteingang zu erhalten, wenn ähnliche Stellenangebote vorliegen.
Indem Sie nachstehend auf „Ja, senden Sie mir Stellenangebote zu“ klicken, stimmen Sie zu, gemäß unserer Datenschutzrichtlinie Stellenangebote auf Basis der von Ihnen gewählten Suchkriterien in Ihrem Posteingang zu erhalten.
Indem Sie nachstehend auf „Ja, senden Sie mir Stellenangebote zu“ klicken, stimmen Sie zu, gemäß unserer Datenschutzrichtlinie Stellenangebote auf Basis der von Ihnen gewählten Suchkriterien in Ihrem Posteingang zu erhalten.
Vielen Dank für Ihre Registrierung zur Jobbenachrichtigung
15945en
- Contract
- English
- Mid-Senior level
- Research & Development
- Zug
- Healthcare & Life Sciences
Dieses Stellenangebot ist abgelaufen
On behalf of our client, a leading global pharmaceutical company, we are now looking for a Senior Quality Release Lead.
Start Date: As soon as possible
Location: Zug
Workload: 100%
Duration: Until December 31st, 2024 (extension possible)
Your mission:
- Review and verification of batch release documentation according to local procedures and product specific checklist.
- Preparation and approval of the certificates of conformance and market-specific release documentation.
- Quality-relevant Status changes of the inventory in the Company’s systems.
- Influence the strategy of the manufacturing of our products at the CMOs and to sustain without disruption of the supply chain.
- Able to identify and drive improvements/updates of the GMP documentation related to Release activities and CMO oversight from release perspective.
- Identify and communicate timely to the management any supply risk or risk of batch rejection.
- Decisions with patient, global or regulatory impact must be taken in collaboration with upper management.
Your background:
- Minimum Bachelor's degree, Master degree preferred, in a scientific topic (Pharmacy, Chemistry, Biology, Biochemistry etc.).
- A minimum of 6 years of experience in similar position in pharmaceutical or biotechnology industries.
- Experience in the pharmaceutical industry (small molecules and/or biotechnology and/or aseptic filling). Sound knowledge of cGMP requirements, EU/FDA regulations and
compliance. Experience in clinical products manufacturing and/or regulatory is an asset. Knowledge of medical device regulations and manufacturing is a plus.
- Ability to develop effective working relationships with internal/external sites and cross-functional project teams.
- Negotiation skills.
- Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
What’s Offered:
- Opportunity to work in a dynamic and innovative environment.
- Career development and growth opportunities within a global organization.
If you are interested in this opportunity and meet the qualifications outlined above, please apply here or email veronika.nakev@swisslinx.com with your updated resume.
Start Date: As soon as possible
Location: Zug
Workload: 100%
Duration: Until December 31st, 2024 (extension possible)
Your mission:
- Review and verification of batch release documentation according to local procedures and product specific checklist.
- Preparation and approval of the certificates of conformance and market-specific release documentation.
- Quality-relevant Status changes of the inventory in the Company’s systems.
- Influence the strategy of the manufacturing of our products at the CMOs and to sustain without disruption of the supply chain.
- Able to identify and drive improvements/updates of the GMP documentation related to Release activities and CMO oversight from release perspective.
- Identify and communicate timely to the management any supply risk or risk of batch rejection.
- Decisions with patient, global or regulatory impact must be taken in collaboration with upper management.
Your background:
- Minimum Bachelor's degree, Master degree preferred, in a scientific topic (Pharmacy, Chemistry, Biology, Biochemistry etc.).
- A minimum of 6 years of experience in similar position in pharmaceutical or biotechnology industries.
- Experience in the pharmaceutical industry (small molecules and/or biotechnology and/or aseptic filling). Sound knowledge of cGMP requirements, EU/FDA regulations and
compliance. Experience in clinical products manufacturing and/or regulatory is an asset. Knowledge of medical device regulations and manufacturing is a plus.
- Ability to develop effective working relationships with internal/external sites and cross-functional project teams.
- Negotiation skills.
- Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
What’s Offered:
- Opportunity to work in a dynamic and innovative environment.
- Career development and growth opportunities within a global organization.
If you are interested in this opportunity and meet the qualifications outlined above, please apply here or email veronika.nakev@swisslinx.com with your updated resume.
I manage this role