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Philips Sr Compliance Specialist Costa Rica 829208730
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Responsibilities
• Manage CAPA Process for Costa Rica Manufacturing Site, including weekly CAPA Review Boards
• Provide guidance to people on completing CAPAs, NCRs and other QA deliverables based on the procedure’s requirements.
• Follow up on CAPA, Quality Plans, and other QA deliverables
• Provide support, including reviewing responses to audit findings, CAPA evaluation/investigation for
completeness and effectiveness.
• Participates of the external audit team and work on the logistics and preparation.
• Prepare metrics and compliance information
• Lead the CAPA certification program
• People management
You are a part of
Senior Compliance Specialist (CAPA Program Facilitator) will manage the CAPA Process for Costa Rica Manufacturing Site, including preparation of metrics for CRB, report out to Top Management and guidance and training to new CAPA Owners.
Requirements
- Bachelor degree in engineering studies in industrial, microbiology, chemical or related area
- Intermediate to Advance English
- Minimum 5 years of experience in medical devices or pharma industry. (Quality Regulations)
- Analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.
- Ability to work under pressure.
- Excellent verbal / written communication, interpersonal, and organizational skills; must be able to multi-task, assimilate, and analyze information quickly.
- Ability to organize and prioritize workflow and to meet established timeframes.
- impact and influence
- Onsite
- Schedule: Administrative Shift
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