Job Search Results - Biospace
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Shire Pharmaceuticals Group
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Your search returned 24 jobs



2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleUnder the direction of the line manager, the Associate Director is responsible for supporting the oversight and management of the Global CMC Regulatory Submissions for Development submissions (IMPD/CTA/IND), Marketing Applications (NDA,...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary Duties: 1. Act as liaison between the in-country International RA Team and GRA in Lexington for any CMC and Quality/Regulatory compliance related issues and projects 2. Liaise between the CMC GRA team members and international regulatory...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary Role:1. Act as liaison between the in-country International RA Team and GRA in Lexington for any CMC and Quality/Regulatory compliance related issues and projects 2. Liaise between the CMC GRA team members and international regulatory leads...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleThe individual will be a key contributor within a group responsible for performing purification process development, including timely completion of small-scale experiments, scale-up, technology transfer and GMP floor support for programs...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary Role:* Work with the Global Medical Team leader , neuroscience to develop and execute multi-year global medical strategy for the specified Product/Disease Area, appropriately aligned with overall strategy and incorporating R&D functional...

2/8/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleThis position will provide technical support for the pharmaceutical development of Shire's pipelineproducts. Responsibilities include development of scalable and robust formulation for drug substance and drug product throughout their...

2/5/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleThe Regulatory Process Standards Lead will further the vision for Global Regulatory Affairs (GRA) in alignment with the One Shire business model to establish and document global process and standards. This position will collaborate with...

2/2/2016
Shire Pharmaceuticals Group
, MA

Primary Role Routine management & coordination of GMP compliance systems and policies for Alewife facility. Monitors policies, processes, procedures and controls ensuring that performance and quality of products conform to established standards...

1/29/2016
Shire Pharmaceuticals Group
, MA

Primary RoleManage team responsible for and function as an advisor of GMP/GDP Document Processing, including but not limited to Controlled Documents (SOPs, Work instructions, Forms, Master Batch Records, Specifications, Test Methods, Protocols and...

1/29/2016
Shire Pharmaceuticals Group
, MA

Primary RoleJob Summary:Primary duties of the position are focused around non-laboratory support of the QC functions. Primary activities would generally include but not limited to data analysis, data trending, project and testing coordination,...