EXPIRED – Quality Manager / ta-024

Location
CH-Zurich
Start
07.01.2025
End
06.07.2026
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
2.880

Deadline:

Deadline
EXPIRED

 

EXPIRED – Quality Manager / ta-024

Location
CH-Zurich
Workload
100 %

Start

07.01.2025

End

06.07.2026

DEADLINE

Deadline
EXPIRED

  • CH-Zurich
  • CH-Zurich07.01.202506.07.2026100 % 2.880rate negotiableDeadline
    EXPIRED

For our customer located in Zurich/Switzerland we are currently looking for a: Quality Manager (m/f/d)

  • Location: CH-Zurich (hybrid – 2 days a week in the office
    travel once or twice a month to germany- Singen site)
  • Branch: Pharma
  • Duration: 07.01.2025 – 06.07.2026

Tasks & Responsibilities

  • GMP-compliant batch record review and approval of batch documentation as well as timely batch evaluation for externally manufactured products within the responsibility of Vaccine External Supplier Quality (ESQA).

  • Preparation and approval of documents for batch release by the responsible institutes/authorities.

  • Management of deviations and changes as well as management and tracking of CAPA measures and other QMS documents for external products within the responsibility of ESQA.

  • Daily collaboration and communication with external partners, ensuring Takeda is professionally represented

  • Support in coordinating complaint handling with external partners as well as with global and local functions.

  • Support in the preparation of inspections by regulatory authorities, as well as internal inspections and global audits at external partners.

  • Coordination of documents required by the regulatory department for registration purposes.

  • Coordination of Quality Agreements (QAGs).

  • Support in the creation of global quality metrics/KPIs for external partners.

Must Haves

  • You have a degree in Pharmacy, Microbiology, Life Sciences, or an equivalent scientific discipline.

  • Several years of professional experience in Quality Assurance; Quality Oversight or Regulatory Compliance, ideally in the pharmaceutical or biotech industry.

  • Solid knowledge of GMP regulations is a given for you.

  • 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.

  • Able to thrive in a fast paced environment with minimal direction

  • You are characterized by a precise, reliable way of working and enjoy teamwork.

  • Fluent English skills complete your profile.

Nice to Haves

  • German fluent preferred

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Preferred Interview Dates

  • yyyy-mm-dd
Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Zurich
  • CH-Zurich07.01.202506.07.2026100 % 2.880rate negotiableDeadline
    EXPIRED

For our customer located in Zurich/Switzerland we are currently looking for a: Quality Manager (m/f/d)

  • Location: CH-Zurich (hybrid – 2 days a week in the office
    travel once or twice a month to germany- Singen site)
  • Branch: Pharma
  • Duration: 07.01.2025 – 06.07.2026

Tasks & Responsibilities

  • GMP-compliant batch record review and approval of batch documentation as well as timely batch evaluation for externally manufactured products within the responsibility of Vaccine External Supplier Quality (ESQA).

  • Preparation and approval of documents for batch release by the responsible institutes/authorities.

  • Management of deviations and changes as well as management and tracking of CAPA measures and other QMS documents for external products within the responsibility of ESQA.

  • Daily collaboration and communication with external partners, ensuring Takeda is professionally represented

  • Support in coordinating complaint handling with external partners as well as with global and local functions.

  • Support in the preparation of inspections by regulatory authorities, as well as internal inspections and global audits at external partners.

  • Coordination of documents required by the regulatory department for registration purposes.

  • Coordination of Quality Agreements (QAGs).

  • Support in the creation of global quality metrics/KPIs for external partners.

Must Haves

  • You have a degree in Pharmacy, Microbiology, Life Sciences, or an equivalent scientific discipline.

  • Several years of professional experience in Quality Assurance; Quality Oversight or Regulatory Compliance, ideally in the pharmaceutical or biotech industry.

  • Solid knowledge of GMP regulations is a given for you.

  • 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.

  • Able to thrive in a fast paced environment with minimal direction

  • You are characterized by a precise, reliable way of working and enjoy teamwork.

  • Fluent English skills complete your profile.

Nice to Haves

  • German fluent preferred

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Preferred Interview Dates

  • yyyy-mm-dd
Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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