Supervisor, Quality Salary at Barclay Water Management Inc BETA

Job Description Job Description Quality Specialist Job Summary: We are seeking an experienced and detail-oriented Quality Specialist to join our team. The ideal candidate will possess expertise in inspecting and machining components, with a strong background in manufacturing environments. This role is critical in ensuring all quality standards are met and processes are continuously improved for optimal performance. The position may require a daily half-time split between our facilities in Rockland and Weymouth. Key Responsibilities: Inspect and machine components with precision and efficiency. Document processes with a focus on continuous improvement. Utilize statistical process control and apply the loss function concept for quality assurance. Record and verify standards for: Incoming Inspection In-process Inspection Gage Calibration Lot Control Routing Traveler Preventative Maintenance Non-conformance Reporting Assist with mechanical and electrical production inspection assignments d

Job Description Job Description Responsibilities: Incoming Material Inspection: Conduct inspections of incoming materials and components to ensure they meet established specifications and quality standards. Document inspection results, maintain inspection records, and communicate any deviations or non-conformances. Collaborate with suppliers and internal teams to address quality issues and perform root cause analysis. Document Control: Assist in the management, organization, and distribution of quality documentation in accordance with regulatory requirements. Ensure that documents are accurately reviewed, approved, and updated as needed to maintain compliance. Support the creation and maintenance of standard operating procedures (SOPs) and work instructions. Quality System Oversight: Help maintain the quality management system (QMS) to ensure compliance with relevant regulations and standards, such as ISO 13485 and FDA 21 CFR Part 820. Investigate quality issues, conduct root cause ana

**Supervisor, Quality Assurance - Operations** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. The Boston-area facility is Catalents global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America. Catalent Pharma Solutions is hiring a Supervisor, QA Operations who is responsible for supervising GMP Manufacturing Facility operations. This individual supervises the work of QA Specialists and Senior QA

**Quality Specialist** **Position Summary:** Looking for a Quality Specialist to support quality functions for our in-space propulsion products. The Quality Specialist will ensure products meet established quality standards and industry requirements; monitor processes and inspect incoming materials, in-process assemblies and finished product; propose product and process quality improvements to assure zero defects. The position is full-time located at our Boston, MA headquarters and is available to be filled immediately. **Responsibilities:** + Incoming material and component inspection and test + In-process assembly inspection and test + Review and analysis of inspection and test data + Creation of quality problem records driving and facilitating review and disposition approval + Assist in problem solving: root cause analysis and corrective action + Audit verification of corrective actions + Creation of quality management system documentation, inspection plans and instructions, quality

Job Description Job Description Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality Assurance professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Director, Quality Assurance at Vericel, this is a great opportunity to join a high growth company with a strong balance sheet supported by a talented team of professionals who are committed to improving the lives of the patients we serve. POSITION SUMMARY The Quality Operations (QAOps) Manager oversees the quality compliance activities associated with the day-to-day Quality Operations which includes CMO relationships. The individual will work cross functionally to support site projects as well as clinical and commercial products. This role will be focused on Vericel’s Medical Device products. DUTIES AND

Job Description Job Description Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality Assurance professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Director, Quality Assurance at Vericel, this is a great opportunity to join a high growth company with a strong balance sheet supported by a talented team of professionals who are committed to improving the lives of the patients we serve. POSITION SUMMARY The Quality Operations (QAOps) Manager oversees the quality compliance activities associated with the day-to-day Quality Operations which includes CMO relationships. The individual will work cross functionally to support site projects as well as clinical and commercial products. This role will be focused on Vericel’s Medical Device products. DUTIES AND

We are in search of a GMP Operational Quality Specialist for our client in Providence, RI. Job Summary: We are seeking an experienced GMP Operational Quality Specialist to join our team on a contract basis, focusing on compliance, quality processes, documentation control and quality control activities for our medical device manufacturing operations. The ideal candidate will have a strong background in Quality Assurance (QA) within the medical device (or similarly regulated) industry. This candidate will assist in incoming material inspections, supporting document control, quality system compliance, and other quality activities as needed. This role is ideal for someone with a keen eye for detail, a commitment to quality, and a desire to grow within the medical device field. Key Responsibilities: Incoming Material Inspection: Conduct inspections of incoming materials and components to ensure they meet established specifications and quality standards. Document inspection results, maintain

Job Description Job Description Title: Quality Specialist (Machine Shop) Hiring Organization: Connexion Systems & Engineering Job Description: SUMMARY OF RESPONSIBILITIES: The Quality Specialist primary responsibilities include manufacturing process work instruction and manufacturing equipment calibration procedure preparation, training and performance oversite, and continuous improvement. Additional responsibilities involve daily floor support of product non-conformance root cause investigation and propose corrective solutions for QA Leadership and QA Engineering disposition. ESSENTIAL RESPONSIBILITIES: • Provide “hands-on” quality assistance to Manufacturing, Materials, Product Engineering, and Sales, by applying knowledge and skills to develop, implement, and sustain process, product, and equipment performance. • Perform Incoming Inspection and/or QC Final Test responsibilities during surge capacity as product demand requires. • Basic understanding of manufacturing drawing interpret