Provide direction, problem solving, and training to employees in Cartoning, Sterilization, and PV Wet Lens Audit work areas.
Specific responsibilities include ensuring team understanding of SOPs; assist in training of procedure changes; ensure assigned end of shift activities are performed.
Instruct teammates in machine setup, operation, and finished product inspection requirements.
Informing shift Team Leader of any non-compliant condition.
Understand and execute daily staffing plan to ensure department quality and quantity objectives are achieved.
Assign resources to collect, enter, and report production numbers.
Report unusual conditions and problems to shift Team Leader.
Maintain confidentiality of sensitive information.
Support, encourage and participate in team related activities; report ideas or suggestions to Team Leader.
Ensure validation requirements are known and understood by teammates.
Ensure proper hand-off of validation requirements between shifts, monitor validation progress during shift and ensure personnel are processing the validations per procedure.
Perform manufacturing operations in addition to team guidance to maintain production throughput.
Other Duties and responsibilities include: performing job responsibilities to the best of an individual’s abilities and at the required skill levels; knowing and observing
B+L work /safety rules, policies and SOPs; protecting B+L assets and treating fellow employees with dignity and respect.
High school diploma or general education degree (GED)
Be available to work 12 hour night shift including everyother weekend
Good organizational skills a must.
Effective communication skills needed to provide clear and concise information to team members.
A minimum of 1 or more years experience in Medical Device Manufacturing.
Previous leadership experienced preferred.
Demonstrated knowledge of computers to include use of CAMS and email.
Knowledge and understanding of cGMPs and ISO standards.