Quality Manager
Auf einen Blick
- Veröffentlicht:27 November 2024
- Pensum:100%
- Vertrag:Temporär
- Sprache:Englisch (Fliessend)
- Arbeitsort:Zurich
On behalf of our client, a global leader in the pharmaceutical industry, Swisslinx is seeking a QA Manager to join their dynamic team. In this role, you will take a central position in managing quality oversight of external partners and driving continuous improvement.
Contract type: Contract
Start Date: ASAP
Locations: Zürich, Switzerland / twice per month: Singen, Germany
Workload: 100%
Duration: 1.5 years
Your mission:
* Perform GMP-compliant batch record review and approval for externally manufactured products within Vaccine External Supplier Quality (ESQA).
* Ensure timely batch evaluation and preparation of documents for batch release by regulatory authorities.
* Manage deviations, changes, CAPAs, and other QMS documents for external products.
* Maintain daily collaboration and communication with external partners, representing the company professionally.
* Coordinate complaint handling with external partners and global/local functions.
* Support regulatory inspections, internal inspections, and global audits at external partners.
* Facilitate documentation required by the regulatory department for registration purposes.
* Oversee and coordinate Quality Agreements (QAGs).
* Contribute to the development of global quality metrics/KPIs for external partners.
Your background:
* Degree in Pharmacy, Microbiology, Life Sciences, or a related scientific discipline.
* Several years of professional experience in Quality Assurance, Quality Oversight, or Regulatory Compliance, ideally in the pharmaceutical/biotech industry.
* Solid knowledge of GMP regulations.
* Demonstrated written and oral communication skills and ability to work in a cross-functional team environment.
* Strong interest and commitment to digital transformation and continuous improvement through data analytics and automation is a plus.
* Capable of thriving in a fast-paced environment with minimal supervision.
* Precise, reliable working style and a team-oriented mindset.
* Fluent English is required; additional languages are an advantage.
What's on offer:
* 1.5-year fixed-term contract with a leading global pharmaceutical company.
* Opportunity to grow and develop your career in a dynamic and international environment.
* Work across Zürich or Singen, collaborating with an expert team on impactful projects.
If this sounds like you, don't hesitate to apply here or contact Veronika von Mentzer, Recruiter: Write an email
Contract type: Contract
Start Date: ASAP
Locations: Zürich, Switzerland / twice per month: Singen, Germany
Workload: 100%
Duration: 1.5 years
Your mission:
* Perform GMP-compliant batch record review and approval for externally manufactured products within Vaccine External Supplier Quality (ESQA).
* Ensure timely batch evaluation and preparation of documents for batch release by regulatory authorities.
* Manage deviations, changes, CAPAs, and other QMS documents for external products.
* Maintain daily collaboration and communication with external partners, representing the company professionally.
* Coordinate complaint handling with external partners and global/local functions.
* Support regulatory inspections, internal inspections, and global audits at external partners.
* Facilitate documentation required by the regulatory department for registration purposes.
* Oversee and coordinate Quality Agreements (QAGs).
* Contribute to the development of global quality metrics/KPIs for external partners.
Your background:
* Degree in Pharmacy, Microbiology, Life Sciences, or a related scientific discipline.
* Several years of professional experience in Quality Assurance, Quality Oversight, or Regulatory Compliance, ideally in the pharmaceutical/biotech industry.
* Solid knowledge of GMP regulations.
* Demonstrated written and oral communication skills and ability to work in a cross-functional team environment.
* Strong interest and commitment to digital transformation and continuous improvement through data analytics and automation is a plus.
* Capable of thriving in a fast-paced environment with minimal supervision.
* Precise, reliable working style and a team-oriented mindset.
* Fluent English is required; additional languages are an advantage.
What's on offer:
* 1.5-year fixed-term contract with a leading global pharmaceutical company.
* Opportunity to grow and develop your career in a dynamic and international environment.
* Work across Zürich or Singen, collaborating with an expert team on impactful projects.
If this sounds like you, don't hesitate to apply here or contact Veronika von Mentzer, Recruiter: Write an email
By applying for this position, I consent to the Swisslinx Group of companies:
- storing my personal information (including name, contact details, Identification and CV information etc.) on their internal or external servers for the purpose of informing me of potential employment opportunities
- using my personal information or
- supplying it to third parties upon express consent for the purpose of informing me of potential job opportunities
- transferring where applicable my personal information to a country outside the EEA/EFTA
I also hereby agree to the Swisslinx privacy policy (http://www.swisslinx.com/en/legal/privacy-policy) and Terms of Use (http://www.swisslinx.com/en/legal/disclaimer)
