To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data. Resp...
Our client is currently seeking an Analytical Chemist in the Pivotal Attribute Sciences Department in Cambridge, MA. This team plays a crucial role in pivotal phase analytical support, including product development support, testing of drug ...
The candidate will work as part of a collaborative, chemical process development team with a range of responsibilities including organic synthesis, reaction characterization & optimization, kinetics studies, distillations, crystallizations,...
Responsibilities: Execute QC second shift activities, working with the day and night shift team leads, including sample receipt, prioritization, and accurate entry into LIMS. Serve as a point of contact for Manufacturing during night shi...
As an individual contributor, this Instructional Designer position will have minimal supervision that will collaborate with subject matter experts to design, develop, and implement instructional materials. This role will be responsible fo...
With limited supervision, plans and conducts experiments, records and analyzes data, and ensures reliable results. Responsibilities: Develop and optimize bioassays to ensure successful implementation and routine execution, supporting hi...
Responsibilities: Execute QC activities, working with the day and night shift managers, including sample receipt, prioritization, and accurate entry into LIMS. Perform routine and complex analytical testing in chemistry, bioassay, and/or...
The Manufacturing Specialist is expected to own and execute under minor supervision all the processes related to deviations (minor and majors), Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verifications, Supplier Event Noti...
The Site Engineer is responsible for overseeing the maintenance, calibration, operational readiness of equipment, utilities, and facilities supporting cGMP manufacturing and laboratory areas. This role is integral to ensure the efficient, r...
The Senior Director of Medical Writing will have responsibility for executing a fit-for-purpose delivery model to produce a range of high quality clinical and regulatory documents to advance company goals across all investigational and mark...