- Merck & Co. (Rahway, NJ)
- …Mindset - Demonstrated ability to deliver compliant supply and achieve highest quality , lowest cost, and shortest lead -time. Strategic Thinking - Ability ... Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director).-This role serves as a Virtual Plant Manager - responsible… more
- Merck & Co. (Rahway, NJ)
- …technology transfer to internal and external manufacturing sites, manufacturing investigations , process validation, and authoring of regulatory submissions. -Under ... the general scientific and administrative direction of Associate Principal Scientist, and working in conjunction with internal and external partners, this individual… more
- Merck & Co. (Rahway, NJ)
- …Automation, Safety, Technical Services, Process Development, Analytical, Regulatory, and Quality .As part of Our Company's Manufacturing Division, within the ... technology transfer to internal and external manufacturing sites, manufacturing investigations , process validation, and authoring of regulatory submissions. -Under… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …background. **Job Description** We are seeking an exceptional investigator to join us as Lead Associate , Quality Investigations in our Princeton, NJ ... This role will report to Lead Quality Systems. The Lead Associate , Quality Investigations is responsible for conducting thorough … more
- BeOne Medicines (Pennington, NJ)
- …study data to identify data anomalies, out-of-trends, and out-of-specifications. + Lead laboratory investigations for data anomalies, out-of-trends, and ... **_General Description:_** Establish a stability program in Quality Control for clinical and commercial phase biologics products in accordance to FDA/EU regulations,… more
- Merck (Rahway, NJ)
- …Mindset** - Demonstrated ability to deliver compliant supply and achieve highest quality , lowest cost, and shortest lead -time. . **Strategic Thinking** - ... Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director). This role serves as a Virtual Plant...Vaccine Products. Our team works with a "Safety First, Quality Always" mindset. As the primary point of contact… more
- Bristol Myers Squibb (Summit, NJ)
- …assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. Start and end ... here at BMS with our Cell Therapy team. The **Manufacturing Associate , Liso-cel CAR-T, Manufacturing Operations** Manufactures human blood derived components per… more
- Bristol Myers Squibb (Summit, NJ)
- …schedule. Communication and initiation of production deviations and assistance with quality investigations are required, as applicable. **Shifts Available:** ... no better place than here at BMS with our Cell Therapy team. The ** Lead Material Handler, CAR T Warehouse Operations** m anages material needs/requirements for CAR-T… more
- Capgemini (Bridgewater, NJ)
- …for junior SOC Analysts. You will also provide guidance related to investigations , peer review, process documentation, with the potential for interacting with ... + US Citizenship or Green Card: Required + Education: Associate 's Degree or higher preferred + Experience: 3 Years...and more effectively while maintaining a laser focus on quality ). **About Capgemini** Capgemini is a global leader in… more
- CSL Plasma (Clifton, NJ)
- …and change management. + You will recruit, hire, conduct performance reviews, lead investigations and deviations, enact corrective actions, and termination. + ... **The Opportunity** The Assistant Manager Quality (AMQ) reports to the Associate Director Quality . This position is located on site at our center in Clifton,… more
- dsm-firmenich (Princeton, NJ)
- …project timelines. + Method development and GCMS knowledge. + Participate in non-conformance investigations and lead or support root cause analysis efforts. + ... for the department performance in the areas of safety, health, environment, quality , and production. Provides technical support for other areas as needed. At… more
- Walmart (Westampton, NJ)
- …business problems. You will work closely with stakeholders to ensure data quality , develop business cases, and implement technological changes to enhance processes. ... in maintaining a secure and compliant environment. Additionally, you will lead efforts to improve employee health and safety, coordinate emergency responses,… more
- Merck (Rahway, NJ)
- …technology transfer to internal and external manufacturing sites, manufacturing investigations , process validation, and authoring of regulatory submissions. Under ... the general scientific and administrative direction of Associate Principal Scientist, and working in conjunction with internal and external partners, this individual… more
- Merck (Rahway, NJ)
- …Automation, Safety, Technical Services, Process Development, Analytical, Regulatory, and Quality . As part of Our Company's Manufacturing Division, within the ... technology transfer to internal and external manufacturing sites, manufacturing investigations , process validation, and authoring of regulatory submissions. Under… more
- Unilever (Englewood Cliffs, NJ)
- …Level: 1C Scope: Ice Cream US & Canada GTM Reports to: Alexandra Stein, Associate Director - HR, Ice Cream Location: Englewood Cliffs, NJ (Hybrid) Terms & ... Cream enthusiasts through an exciting business transformation. As the People Experience Lead , you'll be the key HR contact for Customer Development, Marketing,… more
- Burlington (Burlington, NJ)
- …Great Place to Work! Burlington Stores is a nationally recognized retailer of high quality , branded merchandise at everyday low prices, with over 1200 stores in 45 ... branded instance of the ThinkLP case management platform (Salesforce-based) and lead the development and expansion of the platform to support evolving… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …or medical device product candidates. + Interprets and communicates results of Phase I-IV investigations in preparation for a new drug. + Acts as the signatory on ... and provides clinical input into their governance committees. + Will help lead and support regulatory filing activities and documents. Providing strategic direction… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …or medical device product candidates. + Interpret and communicate results of Phase I-IV investigations in preparation for a new drug. + Be the signatory on NDA ... and provide clinical input into their governance committees. + Will help lead regulatory filing activities and documents. Providing strategic direction and editing… more
