Lead Operator, Manufacturing

Key Responsibilities:

· Perform manufacture Medical Device products in multiple work departments (Manufacture Area) in accordance with current good manufacturing practices.

· Apply advanced departmental knowledge to facilitate problem resolution and implement process improvement

· Coordinate teamwork load, deployment and workflow on a daily basis

· Serve as designate to make corrections and countersign on production documentation

· Actively coach and mentor others on production topics to ensure departmental goals are met

· Coach others on procedures, teamwork and lead by example.

Always exemplifies positive behavior.

· Utilize Quality System and process documentation, converting raw material to finished goods in a GMP environment.

Maintain records to comply with regulatory requirements, GMP’s and standard operating procedures.

· Facilitate communication between manufacturing team and on shift Supervisors/Management.

· Willingly changes job duties and tasks (whether on a daily, weekly or monthly basis) to support the strategic priorities of the Manufacturing Operation

Minimum Requirements/Qualifications:

· High School Degree

· Requires a minimum of 2 years’ experience in a cGMP manufacturing environment equivalent experience and knowledge

· 1-3 years of Experience leadership capabilities are preferred

Personal attributes:

· Think systems, soft skills, and working in teams or support of one another

· Proficient with Microsoft Office

Non-Negotiable Hiring Criteria:

· Experience in an FDA regulated and/or cGMP environment required