- Novo Nordisk Inc. (Plainsboro, NJ)
- …Maintain learning management systems and track training completion rates to ensure compliance with safety and regulatory requirements Lead the development and ... for purpose learning Evaluate training curricula and make adjustments based on feedback, compliance audits, and evolving regulatory standards Key Area #2 Lead… more
- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you. The Associate Director, Compliance Operations will be a key member of Eisai's US Ethics & ... including vendor selection and onboarding Present updates to senior leadership on compliance trends, regulatory changes, and program enhancements C ontribute to… more
- Merck & Co. (Rahway, NJ)
- …Programs, FDA Regulations, IT Coordination, IT Operation, Pharmacovigilance, Policy Implementation, Regulatory Compliance , Regulatory Labeling, Regulatory ... 10 years of industry experience, at least 6 of those in a regulatory and/or compliance area and experience with technical systems in a regulated environment OR a… more
- Insmed Incorporated (NJ)
- …deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs and ... the future of science, we're in. Are you?About the Role:The Associate Director, Programming provides technical leadership and ensures adequate programming support… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director, Patient Services Quality & Process leads quality assurance and process ... improvement initiatives to ensure compliance , consistency, and operational excellence across Insmed's patient services programs. This role oversees a team that… more
- Merck & Co. (Durham, NC)
- Job DescriptionQuality Assurance Associate SpecialistOur Quality Assurance group ensures every single material inside our products is manufactured, processed, ... our incredibly high standards of quality and meets all regulatory requirements. Partnering across our-internal manufacturing facilities, external contract… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe USDA Compliance Subject Matter Expert (SME) - Associate Director, will report to the Animal Health Global Quality Compliance and Technical ... authority (particularly USDA-APHIS-CVB-IC and/or -PEL) as an inspector, product reviewer, compliance officer, other GMP/ regulatory role or Site Quality Head… more
- Merck & Co. (Rahway, NJ)
- …in alignment with the company's business goals, and quality and regulatory compliance .Essential Duties and Responsibilities:Program Leadership and Technical ... Job DescriptionThe Associate Director- Device Tech Transfer is a leadership...conducted with the highest regard for safety, quality, and regulatory compliance , aligning with the company's divisional… more
- Merck & Co. (Rahway, NJ)
- …in alignment with the company's business goals, and quality and regulatory compliance .-Essential Duties and Responsibilities:Utilize extensive experience in ... Job DescriptionJob Summary: -The Associate Director of Device Technology is a key...conducted with the highest regard for safety, quality, and regulatory compliance , aligning with the company's divisional… more
- Merck & Co. (Rahway, NJ)
- …DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is ... and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires… more
- Merck & Co. (Rahway, NJ)
- …construction and campus planning?- Have you advised on design standards, project scope, and regulatory compliance as well as act as a liaison with internal ... and building design standards, open space and site planning guidelines, and regulatory compliance such as ADA, environmental, and building codes.Ensure quality… more
- Insmed Incorporated (San Diego, CA)
- …we're in. Are you?About the Role:Insmed is seeking a Senior Research Associate - Lab Technician with specialized expertise in supporting preclinical and ... and interpret experimental data, contributing to reports, presentations, and regulatory documentation.Maintain accurate electronic laboratory notebooks and ensure adherence… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …language in associated contractual templates. Ensures Good Pharmacovigilance Practice and regulatory compliance in such arrangements. Oversees the management of ... reporting for DSI products, both investigational and marketed. Maintains compliance with Global PV regulations for individual case safety...PV Regulatory Intelligence (PVRI) and dissemination across CSPV stakeholders for… more
- Merck & Co. (Lower Gwynedd, PA)
- …trusted insights.- The PDMB Regulated Bioanalytics Department is seeking a Data Management Associate to join our LIMS & Data Management group. This role will support ... utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. As the Advance facility will not be fully constructed and… more
- Cipla (Hauppauge, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate (Reviewer) Location: 7 Oser Avenue Hauppauge, NY (Onsite) Employment Type: ... benefits. Shift: Second Shift - 3:00pm - 11:30pm Job Overview: The QA Associate (Reviewer) is responsible for review of batch production records, ensuring that all… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... Company and with external partners.Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs… more
- Merck & Co. (Rahway, NJ)
- …Logistics, Multiple Therapeutic Areas, Process Optimization, Publications Management, Regulatory Compliance , Risk Management, Sourcing and Procurement, ... (as a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines, strategies and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …we work together to change lives for the better. The Position The Associate Director, Consumer Social Media Strategy is a high-impact, hands-on leadership role ... deep expertise in consumer social media strategy, planning and execution. This Associate Director Consumer Social Media Strategy is accountable for creating and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …major programs or initiatives, and may function in a project leadership role Regulatory Compliance : Ensures compliance with all Federal regulations, ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...tasks performed by suppliers and business partners to ensure compliance with SDEA requirements. Relationships This position reports to… more
- Novo Nordisk Inc. (Boulder, CO)
- …of technical teams required Experience working to standards required for regulatory compliance of Aseptic Processing facilities required Understanding of ... of both worlds to develop new medicines for patients. The Position The Associate Director of Drug Product Manufacturing is accountable for all clinical drug product… more
