Past 24 hours
Boston, MA (603)
Cambridge, MA (298)
Watertown, MA (43)
Newton, MA (32)
Somerville, MA (19)
Years of Experience
0-4 years (492)
5-7 years (1,286)
8-10 years (696)
11-14 years (624)
15+ years (130)
Vice President (0)
Individual Contributor (0)
Raytheon Co (40)
Alexion Pharmaceuticals (29)
National Grid (26)
Thermo Fisher Scientific (24)
Easy Apply only
The Vice President will be involved in all stages of client management, including identification of prospective client opportunities, completion of industry and client research and assisting in the de...
They also must have a solid business understanding and be able to translate business process flows into technical use cases.
Analyses, prepare bidding documents, plans and specifications; as well as prepare material procurement and construction documents, and work with project planning, environmental, permitting, and constr...
Manage outsources biostatistics and programming deliverables associated with pharmacokinetic endpoints and analyses; provide input and review analyses specifications, review summary documents and tech...
Act as a quality reviewer for the development of functional group controlled documents and assist functional groups in management and processing of controlled documents...
Recruit and develop staff to execute department functions; ensure effective utilization of resources through strong people leadership including consistent performance management, robust employee devel...
Monitors, assesses, and maintains current awareness of evolving CMC regulations and guidance documents; apprises management of the impact of these changes...
Ability to facilitate the interface between the pharmaceutical company and the medical device vendor base.
Manages or works closely with architecture, engineering, product owners, and delivery functions to provide the end-to-end product experience to end user customers...
Collaborate with key stakeholders in the development and implementation of comprehensive internal (systems and procedures) and external (investigator sites and vendors) audit programs and plans...
Knowledge of the regulatory and compliance requirements of device/combination products design controls and manufacturing in US/EU/ROW.