Ensures that the packaging line runs productively following all Packaging Operations SOPs and cGMPs Completes appropriate paperwork Monitors product from the line for accuracy and ensures proper packing procedure is utilized for shipment Complies with company policies and procedures and maintains regular work attendance Follows safety rules, SOP's and cGMP guidelines Main

Senior Director, Global Corporate Compliance Req. # 19854 Company Name Waters Division Category Legal Location US MA Milford Type Regular Full Time Overview Reporting to the General Counsel and supporting other members of the Legal Department, as well as managing other members of the Corporate Compliance function, this role will be key in advising and overseeing enterpris

Quality Assurance Analyst IT Prod Mgmt 0 && !infoField.enableCommand"> Job Tracking ID 512272 878258 0 && !infoField.enableCommand"> Job Location 0 && !infoField.enableCommand"> Job Level Any 0 && !infoField.enableCommand"> Level of Education BA/BS 0 && !infoField.enableCommand"> Job Type Full Time/Regular 0 && !infoField.enableCommand"> Date Updated 05/01/2024 0 && !info

Lead the development and continuous improvement of high performance optical coatings; Develop coating processes for e beam / IAD to improve yield and performance; Design optical thin film coatings for VIS and NIR products; Provide recipe development, parameter optimization and process documentation; Use characterization equipment to understand film uniformity and performa

The Safety Manager's primary role is to work with the assigned project teams and to oversee, plan and ensure the safety compliance of the construction project. Safety Managers will develop service plans for each assigned project including orientation and inspection schedules. Safety Managers shall ensure project risk assessments are complete and work with the Safety Direc

The Site EHS Specialist II, having completed level II competencies, will manage field personnel to ensure compliance with EHS policies, programs, procedures and legislative standards. Will communicate and contribute to the development of site based programs, conduct onsite EHS audits and inspections, and provide recommendations for improving EHS performance and creating a

Responsible for verification of purchased and in house manufactured products to ensure conformance to process and product requirements. Such verification can include inspection, test and audit functions or some combination thereof. II. MINIMUM KNOWLEDGE, EDUCATION AND SKILL REQUIREMENTS High school graduate or equivalent. 3 5 years' experience in Quality Control or in a m

This role will report to the senior manager of Product Development and focus on the design and transfer of implantable cell encapsulation devices for delivering proprietary cells. The successful candidate will join the Process Engineering Team and work closely with Research and Development, Device Quality Control, Device Quality Assurance, Regulatory Affairs, and Manufact

We are seeking a qualified Quality Inspection Supervisor to lead and manage the daily activities of our unionized inspection team in a manufacturing environment. As the Quality Supervisor, you will play a crucial role in ensuring production efficiencies, maintaining product quality, and meeting the production schedule. Your responsibilities will include overseeing the ins

Looking for an opportunity to make an impact? At Leidos , we deliver innovative solutions through the efforts of our diverse and talented people who are dedicated to our customer's success. We empower our teams, contribute to our communities, and operate sustainably. Everything we do is built on a commitment to do the right thing for our customers, our people, and our com

Quality Specialist II LOCATION Ayer, MA, US, 01432 REQ ID 46345 If you are a current employee click here to apply. Specific Responsibilities Include Inspects materials and products, for conformance to specifications, using fixed or preset measuring instruments. Ensures materials and products are in accordance with established tolerance levels for quality and performance.

IPG Medical , a wholly owned subsidiary of IPG Photonics (NASDAQ IPGP) , is focused on developing next generation products based on IPG Medical's state of the art laser technology. Headquartered in Marlborough, MA, we aspire to work together with our employees and customers to apply light in ways that improve life. Our mission is to develop innovative medical device laser

As part of the MSAT team, the Senior Manager of Drug Product Manufacturing Science and Technology, will manage tech transfer and process validation at contract drug product manufacturing sites. The Senior Manager of Drug Product MSAT is responsible for drug product process tech transfer, scale up, PPQ, and monitoring and optimization of the manufacturing process for the v

Reporting to the VP Quality & Controls Assurance, the incumbent is responsible for independent quality reviews of medical claims, and evaluating Call Center activities for compliance with policies and Standard Operating Procedures (SOP). Additionally, this role will review issuance of ID Cards, and Welcome Kits for accuracy. This role will also conduct reviews to verify a

Health & Safety Regional Lead Must have large EPC projects or off shore safety requirements experience Northeast/Upstate NY/Syracuse, NY We invite you to bring your attention to detail and ability to assess and analyze situations quickly to our safety team. You will contribute to a dynamic team supporting our US employees. To succeed in this role, you must have demonstrat