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Your tasks and responsibilitiesThe primary responsibilities of this role, Associate Director, Global Regulatory Strategy - Oncology, are to: Act as t
The Quality Control Associate Scientist will lead or support the method technical transfer and/or validation activities for a cGMP biologics commercia
Summary:To perform microbiological testing on samples using defined methods in a cGMP compliant laboratory. Assures test results are accurately record
Summary:Individual will act as team lead for QC Microbiology area. Incumbent will be mentor to junior staff and point of contact for analyst in super
Provide quality oversight of the site investigations and CAPA programs and provide supervision of personnel approving investigations, change controls,
MAJOR DUTIES AND RESONSIBILITIES:Manage the QC Technical Support QC Services staff in developing and sustaining the following core programs: QC lab in
Summary:Provide Quality assistance and oversight during manufacturing of in-process intermediates and drug substance, and other GMP processes as requi
Responsibilities:Directs the daily operation of a biologics QC department testing and reporting of release and stability samples for drug substance an
Reporting to the Associate Director, QC Technical Support, the QCTS Bioassay Manager role will be responsible for leading a team of SMEs/analysts resp
Senior scientific operations leader responsible for planning and driving execution of in silico, in vivo and clinical sub-study workflows - across a d
ProteinSimple seeks a Field Applications Manager with strong leadership skills and expertise in protein analysis techniques
Amgen's Process Development organization is seeking a Scientist to join the Pivotal Drug Substance Technologies team responsible for developing innov
The Digital Plant 2nd Shift Engineer will be an integral part of the Digital Plant team within Bristol-Myers Squibb at Devens, MA. The role will serve
The Senior Medical Writing Scientist is responsible for preparing moderately complex clinical study documents and sections of regulatory submissions.
Vertex is seeking a talented individual to join our Drug Metabolism and Pharmacokinetics group in Boston, MA.
We are seeking a highly motivated scientist to join the cheminformatics group at Vertex.
The Sr. Manager is responsible for developing and implementing innovative regulatory strategies in support of various projects and sub-teams.
The manager/sr manager supports the execution of high quality, global, integrated cross-functional plans for one or more drug development program.
Scientific Experts (SEs) are individuals who are noted for their expertise in a therapeutic area and as a result have special needs...
The Lilly Innovation Center in Cambridge, Massachusetts allows Lilly to explore how next generation...