- Merck & Co. (Rahway, NJ)
- …candidate will focus on designing, implementing, and optimizing automated laboratory systems to accelerate pharmaceutical process development while ensuring ... regulatory compliance.This role will work collaboratively with process research and development scientists, automation scientists, and cross-functional teams to… more
- Merck & Co. (NC)
- …utility systems (eg USP water, HVAC, electrical distribution, Building Automation System , etc.) regarding functionality of equipment. - Deviation management, ... have opportunities across many diverse areas including Biological, Chemical, Automation , Capital Projects, Maintenance, Safety, Process Development , Technical… more
- Syner-G BioPharma Group (Boston, MA)
- … development , commissioning, and qualification of process equipment or systems for compliance with manufacturing requirements and facility fit.Lead start-up ... -- VALIDATION ENGINEER POSITION OVERVIEW: We are seeking a Validation Engineer to assist with the development and execution of validation protocols… more
- Syner-G BioPharma Group (Boston, MA)
- …upgrades.Serve as subject matter expert in cleanroom design, building automation systems , and energy management.Collaborate with internal stakeholders ... standards, and environmental regulations.Proficiency in AutoCAD, CMMS, and building automation systems .Maritime facilities background (preferred).Familiarity with GMP… more
- Cipla (Fall River, MA)
- Job Title : Mfg.Validation Engineer FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM (may vary ... is searching for experienced candidates for the position of Manufacturing Validation Engineer . The Manufacturing Validation Engineer is responsible for the… more
- Merck & Co. (TX)
- Job DescriptionAs a Senior Platform Engineer you will design, deploy, and maintain data platforms, predominantly concentrating on Databricks. - This role involves ... solutions. You will use your expertise in requirements analysis, programming languages, development methodologies, and tools to build and deliver platforms that meet… more
- ValSource, Inc. (Durham, NC)
- …addressed will include manufacturing equipment, critical and non-critical utilities, cleaning systems /processes, automation systems , filtration systems , ... Validation Specialist / Validation Engineer / CQV Engineer ValSource is...validation (CQV) of Pharmaceutical and Biotech GMP manufacturing facility systems and equipment. Responsibilities are expected to include but… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …documentation for the shopfloor including related problem-solving Participate in the development and implementation of procedural or automation improvement ... ready to realize your potential? The Position A process engineer on the cleaning team is a process ...Nordisk and FDA requirements. They are responsible for the development of cleaning processes, the validation of those processes,… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …DVs and other production documentation to the shopfloor Participate in the development and implementation of procedural or automation improvement changes ... and equipment start-ups from the laboratory through manufacturing scale. The Process Engineer will work alongside Process Associates and Process Scientists and may… more
- ValSource, Inc. (Worcester, MA)
- …lead teams through Safety assessments (PHA, HAZOP and LOPA) and Quality assessments ( Development of CIP/SIP strategy, Automation development and GMP Design ... within Pharmaceutical and Biotech GMP manufacturing facilities. This includes systems and equipment used in these environments. Responsibilities include, but… more
