What are the responsibilities and job description for the Quality Control Supervisor position at RJ-Staffing?
Job Title: Quality Control Supervisor
Location: Orangeburg, NY
Shift: Full-Time Days Monday – Friday 9AM-6PM , On-Site
Salary: $80,000
Benefits: Health, dental, vision, pto, 401(k) savings plan with company match.
Overview: A global supplier of bonding solutions and manufacturer of adhesive-based products for the Healthcare and Industrial markets seeks a QC Supervisor. The QC Supervisor is responsible for oversight of the Quality Control Inspectors and ensuring the performance of the quality control process. Responsibilities include ensuring personnel, inspection equipment, and quality procedures throughout the manufacturing process are in place and product produced meets quality standards. Role is responsible for enforcing company policies and guidelines are met and ensuring a safe working environment. Role reports directly to the Quality Assurance Manager.
Responsibilities:
- Oversee day-to-day management of Quality Control (QC) Inspectors in the Cleanroom and Cartoon room. Including:
- Prioritize and schedule daily Inspectors workload in conjunction with Production to complete work effectively and efficiently.
- Create, modify, and approve procedures, work instructions, and forms for routine production and quality control activities.
- Periodically review work performed by QC Inspectors during the shift
- Manage workload of Inspectors.
- Ensure Inspectors adhere to all established start and break times
- Approve time cards and manage PTO requests.
- Train on company policies and on work related documentation and work instructions.
- Enforce company policies, hire, terminate, and promote employees with coordination of HR.
- Communicate and manage employee issues or conflicts with HR, and necessary parties, as needed.
- Monitor Cleanroom and the Cartoon room Inspectors performance and efficiency in order to provide continuous feedback, coaching, and improvement.
- Prepare and conduct performance reviews.
- Communicate and ensure all shift personnel conform to all Safety and Inspection Procedures/Work Instructions.
- Ensure pertinent information is communicated between different working shifts.
Essential experience:
• Minimum 5 years related experience in a quality role, preferably in the medical device or drug manufacturing environment.
• Demonstrated ability to read, understand, and apply the information contained on technical documentation, procedures, drawings, and understand basic geometric tolerances.
• Able to properly use standard inspection equipment (calipers, thickness gage and other, gages etc.).
• Previous experience leading or supervising personnel.
• Must be able to speak, write and read English. Bilingual skills are a plus.
Salary : $80,000
