Head of Quality Assurance Salary at Formedix Ltd BETA

Title: US Head of Quality Location: Concord, MA, Remote Reporting to: Chief Operating Officer About the Company ITF Therapeutics is the U.S.-based rare disease division of Italfarmaco S.p.A., a private multinational group headquartered in Milan, Italy. Established in 1938, its mission has been to improve patient lives and overall well-being through pioneering research & development, high-quality production, and global marketing of branded prescription and non-prescription products. Operating in the pharmaceutical and API development, Italfarmaco Group has a presence in over 90 countries, employs 3,800 individuals, including 300 professionals across its four Research & Development Hubs, and generates a turnover exceeding 1 billion Euros. The group is known for its products in key therapeutic areas such as Women's Health, Neurology and Psychiatry, Cardiovascular and Metabolic, and Rare Disease. In January 2024, Italfarmaco launched ITF Therapeutics as a new division in the United States

Location: This role is based in the Lexington, MA area with a hybrid schedule of four days on-site and one day remote. We are looking for an experienced Senior Director of Quality Assurance to join a dynamic team. Reporting directly to the VP and Head of Quality, this role will be instrumental in developing, overseeing, and maintaining compliance standards across key third-party partnerships and within the organization’s internal Quality systems. This position holds primary responsibility for ensuring adherence to GMP protocols supporting product manufacturing and distribution, while also overseeing batch disposition processes for both clinical and commercial products. Key Responsibilities: Oversee the GMP Quality Assurance team to maintain quality and compliance standards. Develop and implement Quality objectives, managing risk and ensuring cross-functional compliance. Ensure quality control for manufacturing and distribution across clinical and commercial products. Manage compliance

About the Position This unique position will support both the Customer Quality Management (CQM) Team with warranty claims as well as support the organization with ISO audits and programs. You will support the CQM team by reviewing and responding to warranty replacement requests and product safety and liability claims through resolution, fielding and discussing technical issues, answering questions from internal and external customers on status of warranty claims. This position will be responsible for approving warranty payments within the limits described in the process. This position will work closely with the Head of Government Affairs and our Product Engineering team with ensuring our newly launched products meet federal, regional and local regulations. This position will also function as lead auditor for our ISO 9001 and ISO 14001 programs at our HQ facility. Customer Quality Engineering Support You will provide secondary support to our customer quality engineering team with resolv

About Tobin Scientific Tobin Scientific is a leading provider of cold chain, ambient storage, and transport & logistics services for the biopharma industry, and is one of the fastest growing companies in Massachusetts. Serving a diverse array of clients in life sciences, university, government, and more, we're recognized for our expertise in ensuring the safety and security of temperature-sensitive products during transport and storage. Our cGMP storage solutions are custom-built for the pharmaceutical and biotech industries, managing mission-critical consumables, equipment, raw materials, and finished goods with precision. Nationally acclaimed for laboratory relocation, principal investigator support, and other logistics services, Tobin Scientific's holistic approach and commitment to excellence make us an integral player in life science services. We are seeking a Manager of Quality Systems to drive our quality assurance initiatives and maintain compliance with industry standards. Thi

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. Position Summary: The Senior Director of Quality Control (QC) will be responsible for leading the Quality Control Unit at Ocular Therapeutix (OTX) as the Organization continues growing and expanding its clinical and commerci

Metal Production Operator Boston Metal is developing a new technology to lower the environmental impact of primary metals production while delivering higher quality at reduced cost. This fast-paced startup company is expanding its operations team to run its Molten Oxide Electrolysis (MOE) cells for the production of molten metal. The Metal Production Operator as a member of the Operations Team conducts 24 hour operations (7days a week) with three shifts. Duties include monitoring MOE cells, withdrawing molten metal and slag samples from the cells at regular intervals as well as supporting tapping and feeding operations. Additional duties may include cell rebuilding and commissioning. Cell rebuilding activities require operating heavy tools (such as jack hammers) for demolition operations or manipulating bags of refractory (similar to bags of concrete, 50+lbs) while conducting mixing and casting operations. Desired Experience and Skills: Experience or training in industrial fabrication/

Executive Director, Quality Control and Analytical Development ~ Burlington, MA ~ Local Candidates Only Please The Executive Director is accountable for overseeing all aspects of Quality Control and Analytical Development within the organization including QC systems, Analytical Chemistry, Microbiology (including Environmental Monitoring), Method Validation and Product Stability ensuring that the company QC practices comply with relevant industry standards, governmental regulations, and certifications. The Executive Director directs the development, planning, implementation, and is accountable for the Quality control methods, processes, and operations for all company development and commercial products and/or technologies. The Executive Director provides strategic and tactical leadership to the Quality Control and Analytical organization is accountable for the execution of Quality control and analytical development responsibilities within the Quality System. This position directly manag

Position Summary: The CMC Project Manager will support Technical Operations for Upstream Bio’s verekitug program. Responsibilities include supporting the team to advance the program to meet major milestones, and coordination and operational support of manufacturing and analytical activities conducted at CDMOs. Additionally, this role will interact with Program Management, Clinical Operations, Regulatory, Quality, external CROs, and cross-functional teams to identify dependencies for CMC activities related to technical development and manufacturing. This individual will also be responsible for tracking timelines, technical milestones, CDMO deliverables, and data to support regulatory filings. This role requires a strong background in pharmaceutical project management and technical expertise in CMC processes to ensure alignment with regulatory requirements and organizational goals. The successful candidate will report to the VP, Head of Technical Operations, and will be responsible for t