Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, cutting-edge, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients.
What You Will Achieve
In this role, you will:
• Investigate quality issues within manufacturing and quality laboratories
• Examine deviations, out-of-specification results, and atypical investigations
• Identify root causes and suggest effective corrective action plans
• Ensure all reports comply with regulatory requirements and company policies
• Contribute to moderately complex projects, managing your own time to meet targets
• Develop plans for short-term work activities within a team-oriented team environment
• Apply skills and discipline knowledge to contribute to work within the Work Team
• Make decisions to resolve moderately complex problems in standard situations
• Work under supervision, following established procedures and general instructions
• Periodically review work, and may review the work of other colleagues in a mentor role
Here Is What You Need (Minimum Requirements)
• MBA/MS or associate's degree with at least 6 years of experience or high school diploma (or equivalent) with at least 8 years of relevant experience
• Proven record of problem-solving and decision-making skills
• Experience in the pharmaceutical industry
• Solid background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems
• Ability to work both independently and collaboratively
• Effective communication skills, both written and verbal
• Computer literate with superior skills in managing Excel spreadsheets