The QC Data Manger will be responsible for overseeing review for accuracy and interpretation of data generated internally from testing laboratory charged with the execution of all GMP bioassay and Nucleic Acids Testing (release and stability) related to Sarepta's Gene Therapy pipeline. The Data Manager will be responsible for oversight and review of release and stability d

This position is the subject matter expert for Punches, Dies, Cutting tools. A broad knowledge of stamping processes and Cutting tools will be utilized to develop and implement machinery, tools, and equipment for new and existing components. Plan, Manage, & coordinate all tooling functions for the NH and AR facility, including inter unit, purchasing, inventory control, re

of Role This role is responsible for leading Lantheus' Quality Systems & Compliance team. This role will oversee the global compliance function and related processes, providing multi site oversight of laboratory, manufacturing, and distribution operations. Manages and provides direction to Quality Systems, Compliance and Product Quality Complaints staff, ensuring that proc

The Sr. Manager, GxP Training position is responsible to manage Sarepta's global GxP Training Program. The position will reside on site in the Andover, MA facility, reporting to the Director of Global Quality Systems. The position encompasses a variety of training management responsibilities, including maintaining a compliant GxP Training Program in accordance with US and

TTM Technologies, Inc. Publicly Traded US Company, NASDAQ (TTMI) Top 5 Global Printed Circuit Board Manufacturer About TTM TTM Technologies, Inc. is a leading global manufacturer of technology solutions including engineered systems, radio frequency ("RF") components and RF microwave/microelectronic assemblies, and quick turn and technologically advanced printed circuit bo

Lead, develop and coordinate the activities of multiple crews in safely producing a quality, cost efficient work product consistent with the project goals and the expected standards established by Cianbro and our customers. Job Responsibilities Accept responsibility for team safety, leading the team to zero injuries. Be proactive in identifying hazards and managing risks

The objective of this position is to lead a maintenance team and ensure effective and efficient coordination of all manufacturing maintenance and support activities. Specifically, this role will ensure manufacturing operations are supported, and any necessary corrective or preventive maintenance will include appropriate job plans, materials, manpower estimates, safety, ch

Daily organization of resources and task prioritization to ensure On Time to Customer Request (OTR) goals are met and all production procedures are followed. Monitor future sales orders to identify all high volume builds and calculate the required process time in order to ensure materials and orders are released with sufficient time to assemble, test and ship. Develop and

A Day In The Life Hold pre shift meetings with previous shift Group Leader and organize plan. Direct associates to work stations as needed. Responsible in part for training & development of Associates including procedures and equipment. Run daily reports as required. Hold Toolbox Safety Meetings and participate in Safety Campaigns Assist in appraising the performance and

The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and takes a role in the design and execution of new projects , effectively ensuring alignment with corporate goals and compliance with all regulatory require

The Director, Cell & Gene Quality, International will support defining the strategy for the international expansion of Cell & Genetic programs. The role will establish the quality risk management plans, work closely with cross functional QA, CMC, External manufacturing, Supply Chain and Commercial teams to ensure QA oversight is maintained. Key activities include develop,

The objective of this position is to provide leadership and management oversight of cold (non radioactive) product manufacturing technical operations on the Billerica Campus, while ensuring compliance with all GMP, OSHA and other regulatory requirements. The Associate Director (AD) leads the manufacturing operations to deliver on time production of high quality pharmaceut