Production Scientist Job at MilliporeSigma | BS Graduates Apply
Join MilliporeSigma as a GMP Production Scientist and become a key player in manufacturing Active Pharmaceutical Ingredients (APIs) under strict FDA regulations. This role offers a unique opportunity to apply your scientific expertise in a dynamic, high-stakes environment where quality and precision are paramount. Discover the responsibilities, required qualifications, and the chance to contribute to human progress.
- Job Position: GMP Production Scientist
- Job ID: 291939
- Location: Miamisburg, Ohio, United States
- Salary Range: $68,700 – $115,400/year
About the Company:
MilliporeSigma is a global leader in science and technology, driving innovation in Healthcare, Life Science, and Electronics. The company fosters curiosity, diversity, and collaboration, empowering employees to solve challenges, advance research, and make a positive impact on people, communities, and the planet.
Qualifications:
Minimum Qualifications:
Bachelorโs Degree in Biochemistry, Biomedical Engineering, or related Life Science discipline.
Experience:
3+ years of experience in synthesis and chemical purification.
Production Scientist Job Description:
The GMP Production Scientist will be responsible for manufacturing Active Pharmaceutical Ingredients (APIs) in accordance with FDA regulations, ensuring compliance with current Good Manufacturing Practice (cGMP) guidelines. The role involves hands-on production work, technical leadership, and maintaining accurate documentation for all processes.
Production Scientist Job Key Responsibilities:
- Follow manufacturing protocols consistent with current Good Manufacturing Practice (cGMP) guidelines and accurately document all processes.
- Perform production operations and communicate production status to Manufacturing Supervision.
- Provide technical leadership during manufacturing processes.
- Ensure equipment is prepared, cleaned, and appropriately documented.
- Stage production areas, chemicals, and equipment for operations.
- Make critical decisions based on in-process analytical results.
- Write and revise Master Production Records, validation protocols, and reports.
- Prepare and review Operating Procedures to ensure compliance with FDA and cGMP guidelines.
Physical Requirements:
Ability to lift upto 40 lbs unassisted.
Preferred Skills:
- 1+ year of GMP experience.
- Detail-oriented with excellent organizational, written, and verbal communication skills.
- Strong problem-solving skills.
