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Talent Acquisition Consultant at Coopers Group AG - Life Science
Location: Visp
We are looking for a person who will be in charge of managing and supporting various GMP-relevant deliverables for the organization, including deviation investigations, CAPAs, and CRs. The role involves supporting departments to ensure audit readiness and GMP compliance at all times.
Operational responsibilities include strict adherence to production and batch release schedules, timely completion and closure of deviations, CAPAs, CRs, etc., while maintaining high-quality standards:
* Provide a safe, controlled work environment in all areas of responsibility
* Work with stakeholders to ensure cGMP compliance in all GMP deliverables
* Collaborate with stakeholders and SMEs (e.g., Ops BPEs, MSAT, Engineering, QC) to improve process robustness via CAPA initiatives
* Manage deviation investigations, ensuring timely completion and investigation quality, acting as lead when required
* Create, review, and approve deviation investigation reports and CAPAs to ensure consistency and high standards
* Serve as Change Request manager for Manufacturing Operations when needed
* Support GMP documentation management (review, DMS workflows) for Manufacturing Operations
* Act as SME during audits or customer meetings regarding deliverables within scope
Requirements:
* 5-10 years in a cGMP-regulated environment, preferably manufacturing
* Strong leadership skills in team management
* Excellent communication and interpersonal skills
* Analytical thinking and problem-solving abilities
* High adaptability in dynamic environments
* Effective time management skills
* Proficiency in Microsoft Office Suite (Excel, Word, Project, PowerPoint)
Seniority level
* Mid-Senior level
Employment type
* Contract
Job function
* Other
Industries
* Biotechnology, Research, and Pharmaceutical Manufacturing
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