Quality Supervisor Position Available In Naugatuck Valley Planning Region, Connecticut

Quality Supervisor Contract Medical Manufacturing, LLC Oxford, CT Job Details Full-time $75,000 – $80,000 a year 1 day ago Benefits Health insurance Dental insurance 401(k) Tuition reimbursement Paid time off Vision insurance 401(k) matching Life insurance Qualifications CGMP Strategy Development (Quality assurance practices) Process improvement

ISO 9001

Mid-level Analysis skills Supervising experience Quality assurance Attention to detail QA/QC Quality inspection Analytical thinking Coordinate measuring machine Communication skills

ISO 13485

Compliance Full Job Description Job Overview We are seeking a dedicated and detail-oriented Quality Supervisor to join our team. The ideal candidate will play a crucial role in ensuring that our products meet the highest quality standards and comply with industry regulations. This position requires a strong supervisory background. The Quality Supervisor will lead quality assurance initiatives, oversee quality inspections. Responsibilities Ensure responsibilities are well explained and employees understands and embrace accountability. Oversees Activities performed by Quality Inspectors, ensure all needs from Manufacturing are taken care of to ensure CMM meet OTD. Lead and communicate with Quality Floor Lead on last minute changes and discuss plans to provide support. Create and Monitor Productivity metric to ensure the right resources are in place. Take this as an input to Performance Reviews. Continuous monitoring to activities performed in the floor to be able to understand and provide quality process status of production lots, understand resources, and monitor completion throughout the process to ensure goals are going to be accomplished Initiate activities and Collaborate with Engineering to get resolution of problems identified. Ensure QIP work instructions and NC Procedures are followed, and records documented Properly. Ensure good communication between Manufacturing, Quality and Engineering Direct ReportsTraining Monitor data entry on Attribute charts to minimize errors Provide resources needed and collaborate with Engineering to complete PSWs documentation and approval of parts Ensure execution of Non-Viable Particle test program, Review of Records for compliance, initiate any action when required. Assess Quality Inspector’s documentation for accuracy. Release Non-Sterile Product DHRs Skills Strong knowledge of CGMP regulations and quality inspection methodologies. Ability to lead cross-functional teams effectively. Expertise in quality management systems including

ISO 13485, ISO

9001, HACCP, and QA/QC processes. Excellent analytical skills with a keen eye for detail to identify potential issues before they escalate. Strong communication skills to convey complex information clearly to diverse audiences. Proven problem-solving skills with a proactive approach to addressing challenges in the production process. Join us in our commitment to delivering exceptional products while maintaining the highest standards of quality assurance!

Job Type:

Full-time Pay:

$75,000.00 – $80,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Tuition reimbursement Vision insurance

Schedule:

8 hour shift Ability to

Commute:

Oxford, CT 06478 (Required) Ability to

Relocate:

Oxford, CT 06478: Relocate before starting work (Required)

Work Location:

In person