QA Associate / no-628

Location
CH-Rotkreuz
Start
01.09.2024
End
31.08.2025
Workload
100 %
All-in / Hour
see job description
Total Hours
1664

Deadline:

Deadline
09.07.2024

 

QA Associate / no-628

Location
CH-Rotkreuz
Workload
100 %

Start

01.09.2024

End

31.08.2025

DEADLINE

Deadline
09.07.2024

  • CH-Rotkreuz
  • CH-Rotkreuz01.09.202431.08.2025100 % 1664see job descriptionDeadline
    09.07.2024

For our customer located in Rotkreuz/Switzerland we are currently looking for a: QA Associate (m/f/d)

 

  • Pay rate range of 44,40 – 55,5 chf/h

Tasks & Responsibilities

As a QA Associate, you drive and support the maintenance and development of the quality systems of the local quality organization. You ensure compliance with both local legislation and corporate regulations and the readiness for inspections and audits. In addition, you drive and support processes related to marketed products (e.g. batch release, complaints handling). At the interface between manufacturing and the market, you are the business partner for various functions.

  • Follows GxP and corporate guidelines in day-to-day work.
  • Acts as Subject Matter Expert (SME) in the own area of responsibility.
  • Takes over process ownership as assigned. The process owner ensures the proper functioning, monitoring and continuous development of a process within corporate regulations and local legal requirements. He/she responsible for the adequate handling of investigations and ensures appropriate training of relevant roles.
  • Responsible for the adequate handling and investigation of deviations including their CAPAs.
  • Is responsible for maintaining and updating the quality management system within the own area of responsibility.
  • Takes over administrative and supportive tasks, where required.
  • Supports readiness for all GxP regulatory inspections & audits, as well as self-inspections according to plan.
  • Meets Key Quality Indicators (KQI) in the own area of responsibility. Assesses, reports and proactively monitors Key Quality Indicators in the own area of responsibility, maintains good oversight and ensures gaps are appropriately addressed.
  • Drives and executes continuous improvement in his/her area of responsibility.

Must Haves

  • Minimum apprenticeship in Natural Science (e.g. laboratory technician, aide in Pharmacy, bachelor degree in natural sciences) or comparable education/scientific background with experience
    in GxP area.
  • Fluency in German and English (oral and written is mandatory)
  • Several (3-5) years of professional experience in pharmaceutical industry, analytics, quality assurance, production, distribution or pharmacy.
  • Strong interpersonal, communication, negotiation and problem-solving skills.
  • Skills in project management, including simplification mindset, strategic thinking and ability to implement changes.

Nice to Haves

  • French as advantage

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

  • week 30
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-Rotkreuz
  • CH-Rotkreuz01.09.202431.08.2025100 % 1664see job descriptionDeadline
    09.07.2024

For our customer located in Rotkreuz/Switzerland we are currently looking for a: QA Associate (m/f/d)

 

  • Pay rate range of 44,40 – 55,5 chf/h

Tasks & Responsibilities

As a QA Associate, you drive and support the maintenance and development of the quality systems of the local quality organization. You ensure compliance with both local legislation and corporate regulations and the readiness for inspections and audits. In addition, you drive and support processes related to marketed products (e.g. batch release, complaints handling). At the interface between manufacturing and the market, you are the business partner for various functions.

  • Follows GxP and corporate guidelines in day-to-day work.
  • Acts as Subject Matter Expert (SME) in the own area of responsibility.
  • Takes over process ownership as assigned. The process owner ensures the proper functioning, monitoring and continuous development of a process within corporate regulations and local legal requirements. He/she responsible for the adequate handling of investigations and ensures appropriate training of relevant roles.
  • Responsible for the adequate handling and investigation of deviations including their CAPAs.
  • Is responsible for maintaining and updating the quality management system within the own area of responsibility.
  • Takes over administrative and supportive tasks, where required.
  • Supports readiness for all GxP regulatory inspections & audits, as well as self-inspections according to plan.
  • Meets Key Quality Indicators (KQI) in the own area of responsibility. Assesses, reports and proactively monitors Key Quality Indicators in the own area of responsibility, maintains good oversight and ensures gaps are appropriately addressed.
  • Drives and executes continuous improvement in his/her area of responsibility.

Must Haves

  • Minimum apprenticeship in Natural Science (e.g. laboratory technician, aide in Pharmacy, bachelor degree in natural sciences) or comparable education/scientific background with experience
    in GxP area.
  • Fluency in German and English (oral and written is mandatory)
  • Several (3-5) years of professional experience in pharmaceutical industry, analytics, quality assurance, production, distribution or pharmacy.
  • Strong interpersonal, communication, negotiation and problem-solving skills.
  • Skills in project management, including simplification mindset, strategic thinking and ability to implement changes.

Nice to Haves

  • French as advantage

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

  • week 30
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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