QA Systems Manager

at  DSM

Aesch, BL, Switzerland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate12 Sep, 2024Not Specified17 Jun, 20242 year(s) or aboveGood communication skillsNoNo
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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