Quality Control Specialist (F/M)

Quality Control Specialist (F/M)
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Quality Control Specialist (F/M)

Switzerland - Neuchâtel
Industrial Engineering and Life-Science
Permanent
5/30/2024
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About the role

To join our Life Sciences team in Neuchâtel, we are looking for a Quality Control Specialist (F/M) in the pharmaceutical sector.

 

The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories with a focus on:

- Laboratory Investigations

- Critical Material Qualification

- Laboratory Method Transfers

 

 

In addition, the job holder also supports daily QC activities following cGMP, client's policies and EHS requirements.

 

Validation and Qualification Activities

- Author transfer protocols and reports for assays

- Author qualification plans and reports for critical reagents

- Oversee validation and qualification activities executed by analysts, provide training and support

- Execute and documents experiments

 

Investigation Leads

- Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change

- Conduct/participate in risk assessments, root cause analysis and investigations

- Own Laboratory Investigations and CAPA

 

Quality Control Support Activities

- Support the application of industry specific compliance standards/regulations to assays life cycle management activities

- Participate to daily activities upon request (provide technical and statistical support)

To join our Life Sciences team in Neuchâtel, we are looking for a Quality Control Specialist (F/M) in the pharmaceutical sector.

 

The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories with a focus on:

- Laboratory Investigations

- Critical Material Qualification

- Laboratory Method Transfers

 

 

In addition, the job holder also supports daily QC activities following cGMP, client's policies and EHS requirements.

 

Validation and Qualification Activities

- Author transfer protocols and reports for assays

- Author qualification plans and reports for critical reagents

- Oversee validation and qualification activities executed by analysts, provide training and support

- Execute and documents experiments

 

Investigation Leads

- Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change

- Conduct/participate in risk assessments, root cause analysis and investigations

- Own Laboratory Investigations and CAPA

 

Quality Control Support Activities

- Support the application of industry specific compliance standards/regulations to assays life cycle management activities

- Participate to daily activities upon request (provide technical and statistical support)

Your profile

This is some text inside of a div block.

- Bachelor/Master in Engineering field (chemical, biotechnology) or equivalent,

- 3 years of experience within a biotech/pharmaceutical GMP manufacturing environment,

- Good knowledge of method transfer,

- Good knowledge of critical reagent qualification,

- Experience in problem solving and deviation management,

- Good knowledge of statistical tools,

- Proficiency in all aspects of standard IT tools,

- Fluent in French and English.

About Antaes

Founded in 2007, Antaes is a Swiss management and technology consulting company ranked among the top 15 consulting firms in Switzerland. We employ over 300 experienced consultants who share our passion.

 

With offices in Switzerland, Singapore, Hong Kong and France, we support our Swiss and international customers at clients in the following areas:

  • Organization and transformation consulting
  • Industrial Engineering
  • Information Systems Management

 

By joining our teams you will discover :

  • A dynamic team in a start-up spirit
  • Human support and career development monitoring
  • Challenges to help develop your network
  • Events: team building, meet-up, workshop, Winter Event ...
  • An @HappyAtWork certified company with a committed CSR policy (Ecovadis2023 Gold Medal)

APPLY
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Quality Control Specialist (F/M)

Switzerland - Neuchâtel
Industrial Engineering and Life-Science
Permanent

About the role

This is some text inside of a div block.

To join our Life Sciences team in Neuchâtel, we are looking for a Quality Control Specialist (F/M) in the pharmaceutical sector.

 

The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories with a focus on:

- Laboratory Investigations

- Critical Material Qualification

- Laboratory Method Transfers

 

 

In addition, the job holder also supports daily QC activities following cGMP, client's policies and EHS requirements.

 

Validation and Qualification Activities

- Author transfer protocols and reports for assays

- Author qualification plans and reports for critical reagents

- Oversee validation and qualification activities executed by analysts, provide training and support

- Execute and documents experiments

 

Investigation Leads

- Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change

- Conduct/participate in risk assessments, root cause analysis and investigations

- Own Laboratory Investigations and CAPA

 

Quality Control Support Activities

- Support the application of industry specific compliance standards/regulations to assays life cycle management activities

- Participate to daily activities upon request (provide technical and statistical support)

Your profile

This is some text inside of a div block.

- Bachelor/Master in Engineering field (chemical, biotechnology) or equivalent,

- 3 years of experience within a biotech/pharmaceutical GMP manufacturing environment,

- Good knowledge of method transfer,

- Good knowledge of critical reagent qualification,

- Experience in problem solving and deviation management,

- Good knowledge of statistical tools,

- Proficiency in all aspects of standard IT tools,

- Fluent in French and English.

Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.

About Antaes

Founded in 2007, Antaes is a Swiss management and technology consulting company ranked among the top 15 consulting firms in Switzerland. We employ over 300 experienced consultants who share our passion.

 

With offices in Switzerland, Singapore, Hong Kong and France, we support our Swiss and international customers at clients in the following areas:

  • Organization and transformation consulting
  • Industrial Engineering
  • Information Systems Management

 

By joining our teams you will discover :

  • A dynamic team in a start-up spirit
  • Human support and career development monitoring
  • Challenges to help develop your network
  • Events: team building, meet-up, workshop, Winter Event ...
  • An @HappyAtWork certified company with a committed CSR policy (Ecovadis2023 Gold Medal)