We're a dedicated team that's connected by a purpose to improve patient lives. We offer opportunities for lifelong learning, growth, and development, supported by benefit programs that empower the physical, mental, emotional, and financial health of our team members and their families.
Requirements
- Bachelor's degree in Engineering/Science Preferred OR Equivalent Experience in GMP pharmaceutical industry required
- Minimum of 5 years of experience in regulated industry with preferred at least 3 -5 years related experience analyzing information, documentation skills, promoting process improvement and corrective/preventive actions
- Minimum 1 year of project leadership experience
- Minimum 1 year investigative experience (DMAIC, A3, 8D, or similar processes)
- Experience with quality systems such as ISO 9001, ISO 15378 and ISO 13485, 21 CFR 820 preferred
- Experience Leading Internal / External Audits, and SAP preferred and Experience with customer interface and meeting customer expectations preferred
Benefits
- Community Involvement: West encourages volunteerism through its West without Borders initiative and other charitable programs that make a difference in local communities.
- Continuous Learning & Development: Opportunities for professional growth through training programs, tuition assistance, leadership development, and skill-certification initiatives.
- Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusionâwhere all voices are heard and respected in a supportive environment.
- Recognition & Rewards: Performance-based bonuses, service recognition, and employee appreciation initiatives celebrate dedication and impact.
- Relocation Assistance: This position offers relocation assistance.