- FR
Quality Assurance Associate
Quality Assurance Associate
About the role
Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Review and verify executed component batch records for accuracy and compliance with GMP/GDP requirements.
- Perform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures.
- Support Electronic Batch Record (EBR) review activities for production operations.
- Participate in Quality on the Floor (QOTF), GEMBA walks, and provide real-time guidance to operations personnel on documentation practices and GMP compliance.
- Assist in identifying and escalating documentation or process deviations during record review or shopfloor interactions.
- Collaborate cross-functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation.
- Support QA team in continuous improvement initiatives and data gathering for metrics and trend analysis.
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Your profile
Job Requirements:
- Degree in Biomedical Engineering, Biotechnology, Life Sciences, or an equivalent field
- 1–2 years of experience in Quality Assurance or Manufacturing within a GMP-regulated biologics or pharmaceutical environment.
- Familiarity with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
- Experience with SAP and Veeva Vault is preferred
- Candidates must be highly motivated, able to work both independently and as part of a team, and possess strong organizational and verbal and written communication skills
- Excellent communication skills, both written and verbal, in English
About Antaes
Founded in 2007, Antaes is a Swiss management and technology consulting firm ranked among the top 15 consulting firms in Switzerland. We have more than 300 experienced engineers who share our passion.
With offices in Switzerland, Singapore, Hong Kong, and France, we support our clients and international clients by providing services in the following areas:
- Organizational and Transformation Consulting
- Industrial Engineering
- Information Systems Management
When you join our team, you’ll discover:
- A dynamic team with a startup mindset
- Personalized support and guidance as your career progresses
- Challenges to help you grow your network
- Events: team-building activities, meetups, workshops, Winter Event …
-
A company certified by @HappyAtWork with a strong commitment to CSR (Ecovadis Gold Medal 2023)
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- Develop technical proposals
- Manage and monitor technical purchases
- Negotiate with suppliers
- Examine markets and identify potential suppliers
- Contribute to development and improvement initiatives
- Manage and track incidents of non-compliance
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Quality Assurance Associate
About the role
Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Review and verify executed component batch records for accuracy and compliance with GMP/GDP requirements.
- Perform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures.
- Support Electronic Batch Record (EBR) review activities for production operations.
- Participate in Quality on the Floor (QOTF), GEMBA walks, and provide real-time guidance to operations personnel on documentation practices and GMP compliance.
- Assist in identifying and escalating documentation or process deviations during record review or shopfloor interactions.
- Collaborate cross-functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation.
- Support QA team in continuous improvement initiatives and data gathering for metrics and trend analysis.
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Your profile
Job Requirements:
- Degree in Biomedical Engineering, Biotechnology, Life Sciences, or an equivalent field
- 1–2 years of experience in Quality Assurance or Manufacturing within a GMP-regulated biologics or pharmaceutical environment.
- Familiarity with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
- Experience with SAP and Veeva Vault is preferred
- Candidates must be highly motivated, able to work both independently and as part of a team, and possess strong organizational and verbal and written communication skills
- Excellent communication skills, both written and verbal, in English
About Antaes
Founded in 2007, Antaes is a Swiss management and technology consulting firm ranked among the top 15 consulting firms in Switzerland. We have more than 300 experienced engineers who share our passion.
With offices in Switzerland, Singapore, Hong Kong, and France, we support our clients and international clients by providing services in the following areas:
- Organizational and Transformation Consulting
- Industrial Engineering
- Information Systems Management
When you join our team, you’ll discover:
- A dynamic team with a startup mindset
- Personalized support and guidance as your career progresses
- Challenges to help you grow your network
- Events: team-building activities, meetups, workshops, Winter Event …
-
A company certified by @HappyAtWork with a strong commitment to CSR (Ecovadis Gold Medal 2023)
