Quality Management Jobs in Rahway, NJ

Job DescriptionRole Overview:The Sr. Specialist Regulatory Affairs Power Platform Solutions Specialist is a hands-on application support and configuration role supporting our system the business-built country regulatory requirements management platform within Global Regulatory Affairs and Clinical S...

Job DescriptionThe Senior Specialist Digital Process & Data Analysis (DPDA) serves as a strategic partner in advancing data-driven decision-making and digital capability adoption across the organization. Working closely with stakeholders this role leads requirements gathering alignment and implement...

Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance we ensure the safety and efficacy of our existing and pipeline products to produce safe effective innovative medicine.T...

Job DescriptionRole Summary:This position will be responsible for technical interrogation of the various drug delivery device technology platforms supporting our Company pipeline to identify risks and opportunities for improvement. They will utilize a wide variety of cutting-edge analytical instrume...

Global Development Quality Operations Drug Product (GDQ Ops)Education and Experience:Bachelor degree (B.S.) in an appropriate Science or Engineering discipline (engineering chemistry biology biochemistry microbiology).Minimum of 3 years experience preferred. Recent graduate may be considered if not...

Job DescriptionClinical Systems Implementation Team Lead within BEO manages the full range of activities related to the successful validation implementation and adoption of applications that support our companys clinical trials. These systems can be internally and/or externally facing large or small...

Job DescriptionUnder the direction of Therapeutic Area (TA) leadership the CDM (Clinical Data Management) Trial Lead is accountable for end-to-end delivery of data management activities for assigned studies ensuring quality integrity and compliance with GDMS standards and regulatory requirements. Th...

Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences) a distinguished department within our renowned Research and Development division quantitative scientists in partnership with other subject matter experts apply state-of-the art scientific methodologies and tools to enable the dis...

Job DescriptionThe Senior Director Biologics DP & Device Platform Lead Third Party Quality Management & Due Diligence (TPQM & DD) Global Development Quality is responsible for providing expert strategic scientific and operational leadership to teams. This position will lead strategic operational ini...

Job DescriptionJob DescriptionThe Senior Scientist Device Design Control Lead is a crucial member of our team responsible for spearheading design control efforts in combination product development commercialization and lifecycle management. This individual will oversee device design control activiti...

Job DescriptionJob Title: Senior Engineer - Device Technical OperationsJob SummaryThe Senior Engineer - Device Technical Operations position is a key engineering role within the Device Development and Technology Organization. This position is responsible for building strong engineering capabilities...

Job DescriptionPosition DescriptionOur Companys West Point PA site has an opening for an Operations Manager on 1st Shift within the Sterile Liquids Pilot Plant. This organization manufactures sterile drug products supporting our clinical pipeline in a highly regulated Good Manufacturing Practice env...

Job DescriptionThe position provides legal support and counseling to business clients on a wide range of manufacturing compliance issues (including cGMP) around the world. The position requires the ability to provide timely practical and compliant solutions while managing legal risks. The position r...

Job DescriptionThe Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in Clinical Operations can provide you with great development and a chance to see if we are the right company for your long-term goals.Our companys Global...

Job DescriptionThe Future Talent Program features internships that last up to 12 weeks and will include one or more opportunities in our Animal Health Division can provide you with great development and a chance to see if we are the right company for your long-term goals.Our Company is offering one...

Job DescriptionValidation Strategy Governance & ComplianceDefine and lead enterprise Business System Validation strategy across domains and platforms ensuring alignment with SDLC principles data integrity requirements regulatory expectations and Quality Management Systems (QMS).Oversee validation ri...

Job DescriptionThe Chemical Commercialization Technology (CCT) department which is part of our Manufacturing Division is seeking self-motivated individuals who are looking for an opportunity to work in a highly collaborative environment that provides substantial technical responsibility and leadersh...

Job DescriptionIt is critical that for all our company sponsored clinical trials patient safety high quality data and compliance with company requirements and regulations are delivered and sustained. The Country Clinical Quality Manager(CCQM) position has a significant impact in achieving those obje...

Job DescriptionSenior Scientist Combination Product CharacterizationOur companys Combination Product Characterization and Verification (CPCV) Team is seeking a hands-on device characterization and design focused scientist. This position will be responsible for technical interrogation of the various...

Job DescriptionThe Associate Director Standards & Execution is responsible for leading the planning execution and implementation of strategic initiatives that support the Global Regulatory and Clinical Safety (GRACS) Quality Management System (QMS). This role provides leadership and execution for ke...