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Supervisor, Media & Process Development
On-site · Lenexa, Kansas, United States
Job Summary
Join our manufacturing team as a Formulation Manufacturing Supervisor, where you'll manage teams in producing pharmaceutical products. You'll maintain operational excellence while ensuring compliance with cGMP standards and FDA regulations. This role combines technical expertise with people leadership to deliver high-quality products that improve healthcare outcomes. You'll coordinate production schedules, oversee manufacturing processes, and support continuous improvement initiatives. Your leadership will be essential in maintaining quality standards, developing team members, and fostering a culture of safety and innovation.
Required Qualifications
- Advanced Degree (Master's or higher) in science, engineering, chemistry, or related STEM field with 3+ years in pharmaceutical/biotechnology manufacturing
- Bachelor's Degree with 5+ years in pharmaceutical/biotechnology manufacturing
- 2+ years of supervisory/leadership experience in a GMP environment
- Strong knowledge of cGMP regulations and FDA requirements
- Experience with aseptic processing and cleanroom operations
- Demonstrated ability to lead and develop teams
- Experience with batch record review and documentation
- Strong problem-solving and decision-making capabilities
- Excellent written and verbal communication skills
- Proficiency with Microsoft Office and manufacturing systems
- Ability to work rotating shifts, including nights/weekends
- Physical ability to stand for extended periods and lift up to 50 pounds
- Strong project management and organizational skills
- Experience with continuous improvement methodologies (Lean, Six Sigma)
- Knowledge of aseptic techniques and environmental monitoring
- Excellent interpersonal skills and ability to work cross-functionally
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