- Merck & Co. (Rahway, NJ)
- …you enthusiastic and driven to create and lead execution of design verification testing strategies for innovative combination products?Join our company's Device ... & Process Development (DPPD) Team, which focuses on the design , development, and commercialization of novel biologic/drug/vaccine-device combination products for… more
- Cipla (Central Islip, NY)
- …finished drug products. Responsibilities include but are not limited to GMP documentation review and supporting other QA functions as needed. In this role, the ... associate II" include but are not limited to the following: Review documentation for manufacturing activities associated with commercial, development, and… more
- ValSource, Inc. (Worcester, MA)
- …Quality assessments (Development of CIP/SIP strategy, Automation development and GMP Design review ). Gather internal and external stakeholder requirements and ... these needs in User Requirements and Equipment Specifications to onboard a Vendor. Review vendor design specifications and submittals to ensure compliance with… more
- Merck & Co. (Rahway, NJ)
- …This individual will be expected to apply his/her knowledge of product design and development; manufacturing process development, qualification, and validation; and ... design control and risk management techniques to positively support...risks within our Company and with external suppliersAuthor and review relevant portions of the regulatory submissions (INDs, IMPDs,… more
- Insmed Incorporated (San Diego, CA)
- …teams, contract research organizations (CROs), and external vendors to prepare, review and finalize clinical study documents and plans Contribute to scientific ... aspects and stages of the protocol development and study execution, from study design planning through final reporting of results Provide scientific input and … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …quality compliance.Provide technical expertise in automation projects from user requirements, design evaluation, specification review through to testing and ... and process automation strategies through cell therapy manufacturing process design qualification, vendor evaluation, and enterprise system interface engineering… more
- Genscript USA Inc. (Piscataway, NJ)
- …Proven experience as an HVAC/MEP SME on large capital projects ( design review , field coordination, installation oversight, commissioning). Experience with ... Responsibilities: Serve as the HVAC/MEP technical lead for major capital projects, from design through commissioning. Review and validate design documents,… more
- Merck & Co. (MA)
- Job DescriptionAs a Senior Platform Engineer you will design , deploy, and maintain data platforms, predominantly concentrating on Databricks. - This role involves ... other engineers, product managers and technical leads,-you will help-to design systems, determine functional and non-functional-needs-requirements-and implement them accordingly.… more
- Syner-G BioPharma Group (Boston, MA)
- …and changed as necessary.) Assist with the requirements specifications, design , functional requirements, development, commissioning, and qualification of process ... ensure compliance with manufacturing requirements.Assist with the requirements specifications, design & development of process parameters, and the commissioning/validation… more
- Eisai, Inc (NJ)
- …role offers the opportunity to lead high-impact imaging strategies-from trial design and execution to data interpretation-while driving scientific innovation and ... and lead the strategic direction for Oncology Imaging, guiding protocol design -including modality selection, timing, and anatomical coverage-to ensure alignment with… more
