Quality Control Specialist (F/M)

Quality Control Specialist (F/M)
See all offers

Quality Control Specialist (F/M)

Switzerland - Neuchâtel
Industrial Engineering and Life-Science
Permanent
5/30/2024
APPLY

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
Our other offers

SAP Data Manager (M/F)

France - Haute-savoie
Permanent
Industrial Engineering and Life-Science

We are recruiting an SAP Data Manager (M/F) on a permanent contract to join our expertise center as part of a large-scale, long-term project to expand our partner's industrial activities.

 

As an SAP Data Manager (M/F), your role will be:

 

  • Creation of spare parts, views, and item master records in SAP.
  • Collection and integration of supplier data (prices, customs codes, technical information, EAR status, etc.).
  • Comparative analysis between new parts to be created and existing data in SAP.
  • Drafting of technical documentation (parts description sheets).
  • Monitoring of the document creation workflow (purchasing, quality, customs, release for sale).

 

See the offer

Supply Chain Data Analyst

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

We are recruiting a Supply Chain Data Analyst (M/F) on a permanent contract to join our expertise center as part of a large-scale, long-term project to expand our partner's activities.

 

As a Supply Chain Data Analyst, your responsibilities will include:

 

  • Participate in logistics initiatives and projects by providing analytical expertise through sizing studies and the definition of key performance indicators.
  • Understand business challenges in interaction with operational teams and clients in order to identify, formalize, and analyze needs, constraints, and objectives.
  • Map logistics flows by modeling physical and digital flows, and identifying data collection points and associated performance indicators.
  • Extract data from source systems (SAP, MES, LES, industrial equipment).
  • Process, structure, and ensure the reliability of data in order to guarantee its quality, consistency, and relevance for analysis.
  • Conduct in-depth analyses to identify trends and optimization levers, or to meet project requirements (choice of concepts, logistical organization).
  • Design dashboards and indicators for management and monitoring using Tableau.
  • Present results, analyses, and recommendations in a clear, concise, and impactful manner to facilitate decision-making.
See the offer

HMI Developer - Industrial Sector M/F

Switzerland - Fribourg
Permanent
Industrial Engineering and Life-Science

We are recruiting a HMI Developer - Industrial Sector M/F on a permanent contract to join our Industrial Expertise division, as part of a large-scale, long-term project to expand our partner's industrial activities.

 

As a HMI Developer - Industrial Sector M/F, your tasks will be :

 

  • Design the network architecture of the equipment and its integration into the client 's infrastructure;
  • Develop, configure and commission HMI applications, reporting tools and data collection systems for assembly machines;
  • Involvement in the entire project cycle: design, development, commissioning, testing and documentation;
  • Organize, plan and monitor projects in coordination with the team and the project manager;
  • Provide technical support and carry out on-site interventions at clients sites;
  • Contribute to R&D innovation projects, particularly in data analysis and machine learning.
See the offer

Industrial Data Scientist

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

We are recruiting an Industrial Data Scientist (M/F) on a permanent contract to join our expertise center as part of a large-scale, long-term project to expand our partner's industrial activities.

 

As an Industrial Data Scientist (M/F), your role will be:

 

  • Development of data science solutions that meet business needs.
  • Identification and formalization of requirements in collaboration with business units, facilitation of scoping workshops.
  • Drafting specifications for machine learning (ML) models.
  • Promotion of best practices for industrializing data science solutions.
  • Development of prototypes and demonstration of the value of the proposed solutions.
  • Design and execution of tests required for the production of data science deliverables.
  • Contribution to the industrialization of prototypes in collaboration with IT.
  • Participation in the design of interfaces facilitating the expanded use of ML models.
  • Supporting business lines in their transformation towards a data-driven organization.
  • Simplification and streamlining of data, proposal of appropriate analysis methodologies.
  • Simultaneous management of multiple projects.
See the offer

PLM Classification Project Manager

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

We are recruiting a PLM Classification Project Manager (M/F) on a permanent contract to join our expertise center as part of a large-scale, long-term project to expand our partner's industrial activities.

 

As PLM Classification Project Manager (M/F), your role will be:

 

  • Definition, structuring, maintenance, and application of the classification framework (families, subfamilies, attributes, authorized values, coding and naming rules).
  • Classification and codification of data according to PLM standards, with completeness and consistency checks.
  • Drafting and updating classification standards and procedures, ensuring compliance with best practices.
  • Management of special cases: qualification, treatment proposal, and escalation if necessary.
  • Preparation and facilitation of professional workshops: classification of types, collection of discrepancies, trade-offs, convergence towards a standard, and formalization of decisions.
  • Analysis of business needs and data types.
  • Preparation and participation in classification pilot tests: sample creation, execution, analysis of results, and adjustment of rules.
  • Post-migration compliance validation: classification checks, anomaly tracking, and implementation of corrections.
  • Monitoring and updating quality KPIs (compliance, error rate, reuse, duplicates).
  • One-time contribution to migration activities (post-loading checks, classification rules related to mapping).
  • Active participation in reporting on operations carried out in accordance with the schedule.
  • Maintaining an up-to-date understanding of the PLM data model, classification strategies, and their evolution.
  • Contribution to continuous improvement.
See the offer
APPLICATION FORM
* required fields
By submitting this form, you acknowledge that you have read our website's privacy policy, which includes your rights regarding your personal data.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

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)