QC Lead Salary at Biopure Corp BETA

Job Title: Process Engineer/Gas Sterilization Location: Cambridge, MA Duration: 12 Months Responsibilities include but are not limited to: a) support/ lead process development and commercialization of gas sterilization processes of combination products b) coordinate/ lead manufacturing site requirements to support sterilization requirements c) support the design control process and qualification of primary components d) support/ lead tech transfer projects for combination products e) support/ lead the development and operational improvements with key primary component suppliers g) support development of characterization methods for mechanical and physical properties of primary components h) support on-going deviation/ CAPA and change control i) support/ lead supplier/ raw materials sterility assurance assessments j) collaborate extensively with internal and external stakeholders i.e. manufacturing, suppliers, quality, regulatory, senior management, etc. k) drive and influence key opini

About the Company - The Director of Quality has a critical role within Zevra that will provide strategic and technical leadership for the optimization and administration of Zevra’s Quality Management System (QMS). The position is responsible for developing and improving Zevra’s QMS and supporting operational processes. This position is further responsible for assuring that compliance with the established QMS and GxP (GMP, GCP, GDP and GLP) requirements in accordance with US, European and other country-specific regulations, both internally and in collaboration with our vendors and partners, is maintained. Key attributes of the incumbent include creativity and enthusiasm for building lasting organizational structure and systems suitable capable of growing with the organization. The qualified candidate must have experience building and maintaining sustainable and trusting cross-functional relationships with key strategic internal and external stakeholders. The incumbent must rapidly earn

Mori is a fast-paced anti-food waste Series C startup on a mission to create “More Food, Less Waste”, by transforming the food, agriculture, and packaging industries. Leveraging the unique properties of a naturally derived silk protein, Mori creates an all-natural food ingredient and coating which slows down the spoiling process of perishable foods. With Mori Silk, we can fundamentally change the food system by reducing our reliance on plastic packaging, reducing food and packaging waste, and increasing efficiency across the supply chain. Our Values Operate with Care: We respect where food comes from and where it is meant to go. Practice Humility: We communicate simply and specifically. Do Good Work: We show the data and prioritize practicality. Anything, Anytime, Anywhere: We do whatever it takes to get the job done. About the Role You will advance Mori’s mission of “More Food, Less Waste” by providing technical support to our Pilot Plant, which scales and ensures stability of new man

Location: Cambridge, MA (Onsite) Science: Microbiome Job Overview: As a Quality Systems Training and Documentation Specialist, you'll manage daily operations, training content via LMS, and documentation through EDMS across all GxP areas. Primary Job Responsibilities: Manage ComplianceWire LMS, streamlining training modules and roles for compliance. Collaborate on training impact assessments and develop targeted training content. Handle controlled document processes from creation to distribution to maintain compliance. Drive improvements in LMS and EDMS, supporting updates and training as necessary. Primary Job Requirements: Bachelor's degree with 1+ years industry experience focusing on GxP training and document management. Skilled in LMS and EDMS, preferably ComplianceWire and Veeva QualityDocs, with experience in record management. Strong in organization, communication, and project management, capable of leading cross-functional initiatives. About Stratacuity: Whether you are seeking

Responsibilities:Transform our prototype into a manufacturable product through DFM (Design for Manufacturability) refinementDevelop and implement a complete manufacturing strategy from small-batch to full-scale productionSource components and establish reliable supply chain relationshipsDesign assembly processes and production workflows for our sleep wearable devicesSet up and manage quality control systems and testing protocolsCoordinate with contract manufacturers and vendors to ensure product quality and timeline adherenceOversee the initial production run of prototype units and subsequent scalingDevelop comprehensive manufacturing documentation and production specificationsOptimize production costs while maintaining product quality and reliabilityCollaborate with engineering, design, and product teams to ensure manufacturabilityRequirements:Bachelors degree in Manufacturing Engineering, Mechanical Engineering, or related field5+ years of experience in hardware manufacturing, prefer

Responsibilities: Developed and optimized efficient, cost-effective, and validated manufacturing processes for medical devices, focusing on capital and/or disposable devices, including assembly, lot release testing, sterilization, and packaging. Produce production-level assembly and part drawings for all components and sub-assemblies. Incorporate Design for Manufacturing (DFM), Six Sigma, and LEAN principles into product and process designs to ensure manufacturability, minimize costs, and achieve optimal production efficiency through activities like DFMA reviews and cycle time optimization. Proactively identify and evaluate potential contract manufacturing partners by analysing quality, cost, delivery timelines, and regulatory compliance capabilities to recommend optimal providers. Lead and collaborate with contract manufacturers in selecting and developing the most efficient and reliable manufacturing processes and sites while fostering strong partnerships. ct as the liaison between C

About the Company: Landmark Bio translates groundbreaking research into life-changing medicines. We provide development, manufacturing, and regulatory capabilities to help early-stage life science innovators rapidly progress advanced therapies from bench to clinic. Launched in 2021, and based in Watertown, Mass. Landmark Bio is an unprecedented venture bringing together the best of industry, academia and research hospitals to accelerate life sciences innovation. A public benefit company, our work advances emerging technologies, demonstrates therapeutic potential, and improves human health. About the Role: We are seeking a highly motivated and team-oriented professional with entrepreneurial spirit to join our company! This is an exciting opportunity for a well-qualified candidate to join a rapidly growing company focused on turning today’s cutting-edge research into tomorrow’s breakthrough therapies. Responsibilities: Lead a process development team to develop clinical and commercial ma

You are applying for work with a franchisee of Taco Bell, not Taco Bell Corp. or any of its affiliates. If hired, the franchisee will be your only employer. Franchisees are independent business owners who set their own wage and benefit programs that can vary among franchisees.' Role: Support the RGM by running great shifts in a self-sufficient manner. Take ownership and responsibility to solve problems; seek help from others when appropriate; and be willing to provide help and guidance to others. Responsibilities and Accountabilities: Ensuring Consistent Customer Satisfaction Execute the MIC (Manager-In-Charge) Success Routine and ensure responsibilities under People, Customers and Service are completed. Ensure that all Team Members complete their Shift Excellence tasks for their assigned position(s). Ensure that all employees present a neat clean appearance and wear company uniform. Personally demonstrate the Customer needs are the highest priority. Ensure food safety, quality and acc