Technical QA Manager (m/f/d) (EW) - BS
Key information
- Publication date:03 January 2025
- Workload:100%
- Contract type:Temporary
- Language:German (Fluent), English (Fluent)
- Place of work:Basel
MANPOWER AG - Your Career, Our Focus!
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ManpowerGroup is the world's leading workforce solutions provider.
With our three brands - Manpower, Experis, and Talent Solutions - we support companies from various industries with their recruitment needs. For 75 years, we have been active in over 75 countries, successfully helping our clients across Switzerland achieve their goals and implement their projects.
We are looking for a Technical QA Manager (m/f/d) (EW) - Metropolitan Area Basel
Tasks & Responsibilities:
* QA supervision of qualification- and validation-activities for GMP-relevant equipment for Synthetic Molecule production and/ or Quality Control
* Responsible to ensure QA oversight and setting guardrails for the operation facilities regarding GMP and Quality standards
* Support of implementation of DI requirements
* Provide sound technical and quality assurance expertise for review and approval of quality related documents (e.g. Qualification plans and reports, change and deviation management, CAPAs, SOPs, Risk Analysis etc.)
* Performing deep root cause analyses as a facilitator or expert to address and investigate complex problems independently
* Responsible for driving and optimization activities and improvements within IMP Quality Operations Switzerland Partner with stakeholders and provide guidance to ensure successful delivery of the IMP goals
* Represent and support your area of responsibility at HA inspections and internal audits
* Support of end to end cGMP activities, in maintaining the Right to Operate at the Swiss Technical R&D sites and in ensuring quality and compliance of IMP products according to Health Authority requirements and Company Standards for IMP products
Must Haves:
* Academical degree in Engineering, Chemistry, Life Science, Pharmacy or equivalent
* profound experience in the pharmaceutical industry
* Experience in equipment Qualification/Validation of synthetic molecules manufacturing and/or Quality Control
* Sound understanding on current DI (Data Integrity) requirements
* Profound knowledge of global quality and GMP requirements
* Strong team-player with a high level of self-motivation and the ability to effectively influence others across all levels of the organization
* Successful performance in health authority inspections and internal GMP audits
* Fluent German and English (spoken/written) is a must for this position
Nice to haves:
* Great communicator to stakeholders and in the team
* "Can-Do" attitude and self-confident to take over new responsibilities and tasks
* Ability to speak up, listening to other opinions and able to rethink the own way to ensure a highest level of success
* Knowledge of Pharmaceutical Development and about the special needs and road blocks regarding GMP-compliant production
Dissatisfied, underchallenged, or ready to discover something new?
What are you waiting for? Apply now, unlock your potential, and strive for greater satisfaction in your career.
I will support you with my expertise and guide you through the entire application process. I look forward to meeting you and hearing your story!
MANPOWER AG - Together, we shape your future!
