- 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 (West Point, PA)
- …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
- CBRE (Trenton, NJ)
- Associate HR/People Business Partner (Remote PST/MST) Job ID 222836 Posted 04-Jun-2025 Service line GWS Segment Role type Full-time Areas of Interest People/Human ... the Role:** We are transforming, growing, and evolving. We're looking to add an Associate People Business Partner (PBP) to our team during this exciting phase of… 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
- Merck (West Point, PA)
- …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 (West Point, PA)
- …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
- PCI Pharma Services (Philadelphia, PA)
- …of our premises and assets. Additionally, the Security Specialist will lead incident response efforts, including investigation, documentation, and resolution of ... proactive security measures and situational awareness. + Conduct thorough investigations into security incidents, breaches, and other matters requiring detailed… more
- CenterWell (Trenton, NJ)
- …Drug Trend and Pipeline Forecasting will be the leader of Forecasting and would lead the team responsible for the process that forecasts $8 Billion in drug spend ... key stakeholders enterprise-wide to identify potential trend benders **Responsibilities** + Lead our medical and pharmacy drug trend and pipeline forecasting process… more
- PCI Pharma Services (Philadelphia, PA)
- …areas of process improvement, equipment modification and optimization, safety and quality improvement, and increasing throughput. This is achieved through individual ... interaction + Equipment Safety + Equipment Reliability + Equipment Performance + Lead the field activities for Process Line Trials (PLT's) and Engineering trials… 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