Quality Assurance Intern Salary at Estee Capital Llc BETA

Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the group’s own R&D facilities and through strategic partnerships with manufactures from around the world. The Senior Quality Assurance Manager reports to the Associate Vice President, Quality Assurance and will manage cGMP compliance assessment of contract manufacturers, the company SOP and Training systems, QA/QC Testing /Audit program, and Quality/Compliance decisions related to the Company’s ANDA products, as well as its products subject to OTC Monographs and FDA or other industry-accepted standards for Dietary Supplements, Medical Foods or Foods for special dietary use. DUTIES AND RESPONSIBILITIES: Perform, support and evaluate third party audits of current and proposed vendors for cGMP compliance Manage the SOP system, including writing/ revising and maintaining SOPs, SOP Tracking and SOP Training Manage market distributio

About the Company Sims Metal is the world’s leading publicly listed metal recycler, with operations encompassing the buying, processing, and selling ferrous and non-ferrous recycled metals. The metals recycling operations are geographically diverse, with operations on five continents. They comprise a network of processing facilities, many with deep-water port access, supported by an extensive network of feeder yards from which to source recyclable ferrous and non-ferrous metals. Purpose of the role Design, lead and drive the company's financial governance framework and related processes, ensuring the business has aligned its obligations and the group has confidence in the reported results. Ensure operational and financial policies are developed, reviewed, and updated (as applicable) to fit-for-purpose, simple, and meet the company’s strategic objectives and regulatory requirements. Oversee and ensure the alignment of improved financial controls across the organization aligned with the

Quality Assurance Manager – Overnight Shift (4 days) About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, developing our own radiopharmaceutical products and providing contract development and manufacturing services for other radiopharmaceutical companies. We also operate our own cutting edge cancer research laboratories. The company expects rapid growth in the next few years. Evergreen is a growing team, fostering a culture of collaboration and strong cross-functional communication to support end-to-end activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company into a cornerstone of the radiopharmaceutical industry. Partial equity-based compensation packages possible. Job Responsibilities Oversee all day-to-day QA operations and related activities for the overnight shift. Manage a team of Quality Assurance professi

We are a rapidly growing organization in the Rahway, NJ area. We are seeking to hire a Quality Control Manager (Spanish) to join our team of professionals. The ideal candidate will be responsible for but not limited to the following responsibilities: Quality Control Manager with a strong background in food manufacturing to join our team. The ideal candidate will oversee quality assurance processes, ensure compliance with food safety regulations, and lead a team in maintaining the highest product standards. This role requires hands-on leadership, excellent communication skills, and a deep understanding of food manufacturing quality systems. Job Responsibilities: Leadership & Team Management Supervise and train Quality Control (QC) technicians and staff. Promote a culture of quality and continuous improvement within the facility. Act as the primary liaison between the Quality department and other departments. Quality Assurance & Compliance Ensure compliance with food safety regulations,

Job Description Job Description Ingenus Pharmaceuticals offers a generous Paid Time Off policy, as well as, 14 paid holidays per year. Medical, Dental and Vision benefits are offered to all associates and are effective on the 1st day of the following month after hire. Enrollment in 401k after 90 days. The Manufacturing Operator/Technician II is responsible for all functions relating to the processing of drug products; consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP). Responsible for the safe and efficient execution of their job duties, while ensuring product compliance to established standards. Major Areas of Responsibility  Execute Batch Record and logbook documentation with clear details and accuracy.  Execute the procedures used to clean pharmaceutical production equipment and facilities.  Operates pharmaceutical production machinery and executes procedures for manufactur

Job Description Job Description We are seeking a highly motivated individual to join us as a Quality Assurance Manager. This individual will have the responsibility for Quality aspects related to Quality Systems in the packaging facility. The Quality Assurance Manager will ensure compliance with current Good Manufacturing Practices (cGMP) as they pertain to the local regulation and exporting countries regulation as applicable (such as FDA, MHRA, EMA, Health Canada). Overall Responsibilities For Quality Operations And Initiatives, Including • Quality Assurance management: • Documentation control (master batch record, specification and method) • Batch record review and product disposition • Investigations, complaints, deviations, CAPAs, APRs • Production and Pharmaceutical Development support • APRs, GMP training and SOP review • Validation / qualification documentation review and approval • QA Operations - inspection, sampling, and review of incoming materials, perform AQL inspections,

Job Description Job Description Our client, an insurance provider, is searching for a Director of Claims Quality. This is a permanent role where employees are required onsite 2 days per week. The full job description is as follows: Location: NYC (2 days per week onsite) Job Type: permanent About the role: The Director of Claims Quality has responsibility for the creation, delivery and ongoing facilitation of a data and metrics-driven Claims Quality Assurance and Performance oversight program to ensure payment accuracy, which includes defining frameworks/benchmarks, calibration and reporting of a program towards set benchmark while promoting a continuous improvement culture. Furthermore, the Director of Claims Quality will be responsible for the management/oversight of provider reimbursement and analytics, claims quality analysts, claims compliance, training and remediation and user acceptance testing (UAT). This will include overseeing staffing and implementing and maintaining policies

Position Overview The Director of Quality Control and Quality Assurance is responsible for overseeing the Quality Management and Assurance activities of the Commercial Unit, with a focus on maintaining and improving the Quality System. Reporting directly to the CEO in New York, this role serves as the Quality Functional Leader, ensuring compliance with all relevant regulations and fostering a culture of excellence within the organization. Key Responsibilities Leadership and Strategy Provide leadership for the Quality team by setting clear goals, objectives, and expectations. Oversee staffing, performance reviews, salary management, and succession planning. Develop long-term strategies and objectives to enhance Quality Management processes. Regulatory Compliance and System Management Ensure compliance with all applicable regulations, including GMP and GLP, per FDA guidelines. Maintain and continually improve the Commercial Unit's Quality System. Ensure the organization is consistently a