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, innovative, 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 collaborative team workplace
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
Strong 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
Bonus Points If You Have (Preferred Requirements)
Master's degree
Experience with investigations, including conducting