Operations Lead
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Role Summary
As the Operations Lead, you will ensure a reliable manufacturing supply through sound leadership and strict adherence to the production schedule. You will manage floor operations to maintain a safe, compliant environment, and oversee the implementation and maintenance of manufacturing activities for products and technologies in a cGMP setting. You will collaborate with support groups to guarantee the transfer of process changes and improvements into daily operations, integrate best practices where appropriate, and ensure the efficient use of materials, equipment, and personnel. Additionally, you will be committed to ongoing departmental improvement through staff collaboration and development, and serve as a trusted driver of floor operations by ensuring agreement on business, regulatory, and quality objectives, while fostering a culture of safety, excellence, and continuous improvement. You will report into the Manufacturing Area Department Heads.
Responsibilities
- Ensure a reliable manufacturing supply through sound leadership and adherence to the production schedule
- Manage the floor operations to ensure safety and compliance
- Oversee the planning, implementation and maintenance of manufacturing operations for new and/or existing products and technologies in a cGMP environment
- Collaborate with support groups to ensure accurate and well managed transfer of process changes/improvements to floor operations
- Be a trusted driver of floor operations, responsible for ensuring the right people, materials, and processes are in place to meet business, regulatory, and quality objectives—while championing a culture of safety, excellence, and continuous improvement
Qualifications
- Bachelor of Science degree and 2+ years of industry experience, or an equivalent level of education and/or related experience
- 2+ years as Supervisor or equivalent in a GMP Manufacturing facility
- Leadership experience in a regulated, technical manufacturing environment (preferably biopharma or similar)
- Technical knowledge of cGMP operations, production scheduling, and process improvement methodologies