Manager, Formulations, IA & Biologicals (FULLY ONSITE)
at Thermo Fisher Scientific
Middletown, VA 22645, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Nov, 2024 | Not Specified | 16 Aug, 2024 | 10 year(s) or above | Life Sciences,Chemistry,Disabilities,Perspectives,Cell Culture,Communication Skills,Pharmaceuticals,Biology | No | No |
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Description:
JOB DESCRIPTION
Thermo Fisher Scientific Inc. is seeking a highly motivated and experienced Manager, Formulations, IA & Biologicals to join our world-class team in Middletown, MD, USA. As the Formulation Manufacturing Manager, you will play a critical role in leading cGMP manufacturing activities for Immunoassays and Biologicals. You will be responsible for ensuring that our IA and biological formulations meet operational goals in safety, quality, delivery, and productivity. This is an exceptional opportunity to contribute to the development and manufacturing of materials for clinical trials and commercial use.
REQUIRED EXPERIENCE AND QUALIFICATIONS:
- Bachelor’s or master’s degree in biology, chemistry, life sciences, or a relevant field, or equivalent experience in a related role.
- Minimum of 10 years of formulation manufacturing experience, preferably in IVD, life sciences, cell culture, or pharmaceuticals
- Minimum of 3 years of people management experience
- Demonstrated ability to motivate employees and resolve conflicts
- Thorough knowledge of cGMPs
- Strong interpersonal and communication skills
- Ability to work in a fast-paced, dynamic environment
Thermo Fisher Scientific Inc. is an equal opportunity employer and provides reasonable accommodations for job seekers with disabilities. We value diversity and inclusion in our workforce, where diverse experiences, backgrounds, and perspectives are highly valued. Join our mission of enabling customers to make the world healthier, cleaner, and safer. Apply today at http://jobs.thermofisher.com
Responsibilities:
- Lead cGMP manufacturing activities for IA and biological formulations
- Collaborate with cross-functional teams to achieve production goals and timelines
- Review and approve batch records, change controls, and project plans
- Develop, review, and approve SOP’s and Work Instructions
- Support investigations and drive root cause/corrective action culture
- Coordinate manufacturing activities and supervise personnel
- Promote a positive and proactive work environment to sustain strong employee engagement levels
- Develop employees and provide feedback and coaching for performance improvement
- Drive innovation and continuous improvement activities to enhance compliance with quality procedures
- Other relevant responsibilities
REQUIREMENT SUMMARY
Min:10.0Max:15.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
A related role
Proficient
1
Middletown, VA 22645, USA