Director, Quality Salary at Jesco Inc 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

Director Quality Assurance, G-III Warehouses Profile :The Director Quality Assurance is responsible for quality assurance operations at G-III warehouse and 3PL facilities, sampling incoming product to ensure vendors and manufacturers are following quality standards for shipping, packing, labeling, and production. Based in New Jersey, this role focuses on implementing and maintaining quality assurance processes within warehouse environments, addressing quality issues with overseas Quality Control team, and fostering a proactive culture of accountability and improvement .The Director Quality Assurance, G-III – Warehouses will play a critical role in bridging communication between warehouse operations, overseas Quality Control, production teams and vendors to ensure seamless quality control procedures. This role requires strong knowledge of Apparel product QC or QA and process, strong communication skills, analytics skills, and the ability to influence and build trust across cross functio

Senior Director of Quality Assurance (GCP) - Drive Excellence in Cutting-Edge Oncology Innovation! Backed by $500 MILLION in Funding | Transforming Oncology Treatments | A Culture of Innovation & Impact Are you a Quality Assurance leader passionate about revolutionizing oncology therapies? This is your chance to join a high-growth, well-funded biotech that is redefining cancer treatment through groundbreaking multispecific antibody and cell therapy advancements. With $500+ million in funding, this powerhouse is scaling rapidly and pushing the boundaries of scientific innovation. You'll be at the forefront of clinical quality strategy, ensuring compliance with global GCP regulations while shaping the future of cutting-edge oncology trials. Why You'll Love It Here: A mission-driven company dedicated to transforming patient outcomes. Elite scientific minds collaborating to drive real-world impact. A fast-paced, high-growth environment where your work directly shapes the future of medicine

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

Our client is actively looking for a Senior 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 overseeing/building out QC labs Experience working with outside testing laboratories Experience with sterile products 5+ years of Director experience or previous Senior Director experience

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

Reports to: Director, GMP Quality Assurance Location: Princeton, NJ (hybrid) This role is responsible for providing GMP QA expertise, oversight, and auditing support of contract manufacturing organizations of small molecule, oral dosage formulations. Additionally, this role supports PMV’s GxP procedures program, document control, and training activities, utilizing an electronic document management system. Responsibilities Support GMP QA activities spanning across CMC (Chemistry, Manufacturing & Controls) for drug substance, drug product, and clinical trial material, for all outsourced GMP activities. Ensure all API, drug product and packaged and labelled investigational material meet GMP regulations, as applicable to phase of development, and are released in a timely manner. Collaborate with CMC, Clinical Supplies Management, Regulatory Affairs, and other departments to resolve quality issues and implement process improvements. Review and approve GMP-related documents, including master