Sr. Manufacturing Manager

STAAR Surgical Company•Monrovia, CA

43d•$140,000 - $180,000

About The Position

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Manage and coordinate the activities associated with various manufacturing processes in a cGMP-compliant manufacturing operation, including, but not limited to, assembly, sterilization, packaging, Clean Room operations, machining and material processing. 2. Manage and coordinate shelf life, qualification, and validation production runs between 3. Responsible and accountable for production schedule adherence, productivity and product quality 4. Ensure that Manufacturing personnel have been trained in required SOPs, in accordance with the established Training SOP. 5. Accountable for departmental compliance with production procedures, manufacturing specifications and regulatory requirements. 6. Review production operations and make recommendations for cost reduction and quality/productivity improvements. 7. Ensure that production activities are documented and records are maintained in accordance with applicable SOPs. 8. Maximize department, equipment and manpower utilization. 9. Ensure adherence to Company safety policies and procedures. 10. Provide employee development opportunities through coaching, delegating and cross-training. 11. Provide the leadership necessary to maximize the productivity of each employee, including active listening, ongoing feedback, meaningful development and growth opportunities as well as an effective documented review process. 12. Other duties as assigned. REQUIREMENTS

Requirements

A Bachelor's degree, science or engineering preferred or equivalent combination of education/experience.
3 years manufacturing experience in medical device, pharmaceutical or other FDA-regulated industry
Leadership experience
Demonstrated understanding of, and ability to practically implement, cGMP/QSR/ISO requirements
Excellent team building and interpersonal skills
Excellent prioritization, multi-tasking and organization skills

Nice To Haves

Graduate business degree a plus
Clean room operations experience a strong plus

Responsibilities

Manage and coordinate the activities associated with various manufacturing processes in a cGMP-compliant manufacturing operation, including, but not limited to, assembly, sterilization, packaging, Clean Room operations, machining and material processing.
Manage and coordinate shelf life, qualification, and validation production runs between
Responsible and accountable for production schedule adherence, productivity and product quality
Ensure that Manufacturing personnel have been trained in required SOPs, in accordance with the established Training SOP.
Accountable for departmental compliance with production procedures, manufacturing specifications and regulatory requirements.
Review production operations and make recommendations for cost reduction and quality/productivity improvements.
Ensure that production activities are documented and records are maintained in accordance with applicable SOPs.
Maximize department, equipment and manpower utilization.
Ensure adherence to Company safety policies and procedures.
Provide employee development opportunities through coaching, delegating and cross-training.
Provide the leadership necessary to maximize the productivity of each employee, including active listening, ongoing feedback, meaningful development and growth opportunities as well as an effective documented review process.
Other duties as assigned.