QA Systems Manager
at DSM
Aesch, BL, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 12 Sep, 2024 | Not Specified | 17 Jun, 2024 | 2 year(s) or above | Good communication skills | No | No |
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Description:
DSM Pentapharm, part of the nutrition cluster of the DSM group, is a swiss SME with a long-standing tradition as an innovative and reliable supplier of active ingredients for the personal care, pharmaceutical and haemostasis industries.
POSITION
We are seeking a highly motivated individual to join our team as a QA Systems Manager. In this role, you will maintain a compliant Quality Management System (QMS), further develop the electronic QMS and ensure timely investigations and resolution of issues through scientific principles and root cause analysis.
QUALIFICATION & COMPETENCES
- Minimum MSc in Biology, Chemistry, Pharmacy or related fields or a Master’s in Quality
- 2+ years of experience with a proven track record in a GMP or ISO production environment
- Proficiency in product classification, definition of applicable standards and conformity assessment procedures
- Proficient with computer systems and strong record-keeping and documentation abilities
- Self-driven and results-oriented with the ability to work independently
- Excellent communication and presentation skills as well as exceptional organizational and detail-oriented skills
- Strong communication skills in German and English
Responsibilities:
- Manage and enhance the electronis QMS, ensuring its effectiveness and compliance
- Oversee the Corrective and Preventive Action (CAPA) process to address quality issues promptly and effectively
- Lead the training system, including onboarding, offboarding and planning GMP training sessions
- Conduct thorough investigations into customer complaints related to product release, considering all manufacturing processes, quality testing and customer requirements
- Maintain Quality Agreements with customers and subcontractors
- Provide support for supplier qualification process management
- Plan and oversee the external audit program for suppliers and lab contractors
- Evaluate quality aspects of new change control proposals and support the QA department with special projects as needed
- Identify and implement changes in established processes to enhance quality standards
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
MSc
Biology, Chemistry
Proficient
1
Aesch, BL, Switzerland