Director, QC Salary at Golden Platter BETA

Our client is actively looking for a Director of Quality Control. This is an on-site position in Cranbury NJ. You should apply if you have: 15+ years of QC experience in pharma/biopharma environment Experience with sterile products Experience overseeing/building out QC labs Previous Director experience

Are you ready to take the lead in ensuring top-notch safety and quality in a dynamic food manufacturing environment? We're looking for a Director of Quality Assurance who is passionate about innovation and excellence. What You'll Do: Lead and Inspire: Oversee daily ESH operations, splitting your time between the floor and the office. Collaborate: Work closely with EHS, Quality, Manufacturing, Planning, Logistics, and Customer Service teams to drive continuous improvement. Innovate: Promote efficiency programs and foster a culture of safety across the facility. Strategize: Partner with senior leadership to develop and execute long-term business plans. Enhance Capabilities: Build processes to ensure COAs are readily available for customers. Ensure Compliance: Guide colleagues in meeting key regulatory certification requirements and uphold FDA, USDA, Kosher, Gluten-Free, and Organic regulations. Manage Recalls: Develop and maintain recall and traceability programs, including mock recalls.

Calling all Quality Champions! Are you a nurse or physician assistant ready to take your expertise to the next level? Our client, a Bronx-based healthcare system, is seeking a Director of Quality to join their diverse, academically driven, evidence-based, and Just Culture environment. Here’s the deal: you’ll lead the charge in performance improvement and quality outcomes, steering initiatives that directly impact patient safety, satisfaction, and care. You’ll be a key player in regulatory compliance, data analysis, and performance reporting—all while supporting hospital-wide committees, educating staff, and promoting continuous quality improvement. What You Should Bring: ✔ 3-5 years of hospital experience with regulatory know-how (Joint Commission, NYSDOH, OMH). ✔ Familiarity with quality metrics like NHQM, QCentrix, and eCQMs. ✔ RN/PA with a New York State license and an MSN preferred (but not required). ✔ Stellar communication, data analysis, and leadership skills. Step up, lead, and

Job Description Job Description About Us: Callen-Lorde is the global leader in LGBTQ+ healthcare. Since the days of Stonewall, we have been transforming lives in LGBTQ+ communities through excellent comprehensive care, provided free of judgment and regardless of ability to pay. In addition, we are continuously pioneering research, advocacy and education to drive positive change around the world, because we believe healthcare is a human right. Our Mission: Callen-Lorde Community Health Center provides sensitive, quality health care and related services targeted to New York’s lesbian, gay, bisexual, and transgender communities — in all their diversity — regardless of ability to pay. To further this mission, Callen-Lorde promotes health education and wellness, and advocates for LGBTQ+ health issues. About the Role: As the Director of Quality Improvement, you will play a critical role in ensuring the highest standards of care and operational efficiency at Callen-Lorde. You will lead the de

Must have experience working with an In Vitro Diagnostics (IVD) Devices in a manufacturing environment! Position: Director of Quality Assurance with FDA and In Vitro Diagnostics (IVD) devices. (IVD) Full-Time Direct Hire Salary Client Location: Toronto, Ontario Canada area Our direct client is looking for a Director of Quality Assurance (IVD & FDA) that has a background with In Vitro Diagnostics (IVD) devices. The Client is open to candidates located in Canada or based in the United States. client will pay travel expenses. Travel Requirement: Must be able to travel to Toronto, Canada, 50% of the time (client covers travel expenses). 50% Remote from Home and 2 weeks month onsite in Toronto Canada area Our client, an innovative and well-funded IVD company, is seeking a Director of Quality Assurance with expertise in In Vitro Diagnostics (IVD) devices and FDA compliance. This leader will oversee and grow the company's QMS, ensuring alignment with global regulations (Health Canada, FDA, EU

Job Description Job Description JOB SUMMARY: Provides leadership and guidance in the quality assurance function at both the Byram, and Fairfield facilities, which includes planning, directing, and controlling. Establishes, implements, coordinates and supervises the company’s Quality Management system including policies, objectives, plans, organization, procedures and appraisals. Ensures that the quality of products and services meet the requirements, specifications and quality standards established by the customer, company, and applicable governmental agencies. Interaction is with all levels of the organization. PRIMARY RESPONSIBILITIES: Directs and coordinates the activities of quality engineering, administration, and inspection and test functions to ensure that proposed and existing products and processes are reviewed for the purpose of avoiding or eliminating unnecessary quality difficulties; develop recommendation for improvements that increase product uniformity and reliability an

Job Description Job Description Director of Quality Assurance $170,000 - $180,000 + Bonus Global Manufacturing and Distribution Company Excellent opportunity to join a well-established and growth oriented privately held Global Manufacturing and Distribution company. Company is seeking an experienced Quality Assurance professional with demonstrated leadership skills and sound technical knowledge. In this role you will be part of the leadership team and drive all the quality and compliance related activities. This role will supervise a team and oversee the development, implementation, and maintenance of the Quality Systems and Procedures. You will also be responsible for fostering strong relationships with customers and addressing any concerns they may have. KEY QUALIFICATIONS: Bachelor's degree in related field / master's degree a plus 10-15 years of progressive experience in Quality Assurance in a Manufacturing environment Proven experience leading, training, and managing a QA team and

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Job Summary The Associate Director, GCP Quality Assurance works within the Global Clinical Quality team to conduct GCP compliance activities at Eisai, at our CROs and Investigator Sites, and leading GCP audits and inspection readiness. This position is responsible for ensuring high quality execution of clinical trials from first in h