Operations Supervisor

Responsibilities:

• Provide technical leadership in the implementation and sustainability of the visual inspection program.
• Develop, train, and lead a team of inspectors to meet compliance and quality standards.
• Establish visual inspection specifications to maintain consistent product quality.
• Create and manage process procedures related to inspection and packaging activities.
• Serve as the subject matter expert (SME) for visual inspection and packaging technologies.
• Ensure adherence to cGMP standards and regulatory compliance.
• Oversee day-to-day activities of inspection and packaging operations on 3rd shift.

Qualifications:

• Bachelor’s degree in Engineering, Science, or equivalent experience.
• Minimum of 8 years of experience in pharmaceutical inspection, packaging, or related manufacturing support.
• Proven leadership experience, preferably in a supervisory role.
• Ability to pass vision and health screening assessments, including annual eye checks.
• Strong understanding of aseptic techniques, inspection protocols, and packaging best practices.
• Knowledge of regulatory expectations and current trends in visual inspection and packaging.
• Excellent interpersonal and communication skills, with the ability to collaborate cross-functionally.

A leading biopharmaceutical contract development and manufacturing organization (CDMO) is seeking an experienced Operations Supervisorto join its team on 3rd shift. This is an exciting opportunity for an individual with deep expertise in the inspection and/or packaging of sterile drug products to play a pivotal role in launching and leading a visual inspection program within a fast-growing, state-of-the-art facility.