- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process ... the clinical , regulatory, formulation, commercial and other key company functions. Lead the Device Development Engineering Core teams focused on development of… more
- Merck & Co. (North Wales, PA)
- …have a proud legacy of scientific innovation and are accelerating the clinical development and commercial launch preparation for 2 novel products for certain ... (nAMD), and retinal vein occlusion (RVO)).-We are currently recruiting for an Associate Director US Marketing, HCP Strategy - Ophthalmology. This is an exciting… more
- Aequor (Aliquippa, PA)
- On- site in Easton, PA This is a 3PL warehouse environment, owned/operated by Langham Logistics. Schedule: Monday-Friday, 8am-5pm Overtime: Occasional, approx. ... documentation habits, and bring a positive, resilient, team-first attitude. On- site reliability is essential for this execution-heavy, hands-on role.… more
- Merck & Co. (Rahway, NJ)
- …data-driven decision-making. Under the broad guidance of the DSCS Digital Program Mgmt Lead , the Associate Director, DSCS Digital Project Manager, will be ... Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS)… more
- Merck & Co. (Rahway, NJ)
- …Pharm Sciences colleagues.-Recommends and executes programs of value to the Company which lead to availability of Clinical Supplies and Development Batches to ... and Skills:-The candidate should be able to work independently and lead or facilitate tasks successfully.Strong knowledge of business impacts and prioritization… more
- Bristol Myers Squibb (Devens, MA)
- …our Cell Therapy team. BMS Cell Therapy Manufacturing is seeking a Specialist, Lead Clinical Manufacturing Associate , Cell Therapy that bring enthusiasm, ... Therapy. This role is key to start up of Clinical Trials at Devens in a multi-product Cell Therapy...experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …activities involving but not limited to supplier qualification program, CMC audit, clinical /IMP vendor audits and overall GMP vendor audit program. Establish lessons ... collaboration with other QA functions and/or applicable stakeholders. Support/ lead and or co lead due- diligence...order to ensure the inspection readiness level of each site and maintain a capacitation program for GMP staff… more
- ACROBiosystems Inc. (San Jose, CA)
- …and encouraging cross-functional collaboration and continuous learning. Job Summary The Associate Regional Manager will lead commercial activities across ... proteins and critical reagents/assays to support drug development and clinical applications from target discovery and validation, candidate drug screening… more
- Aequor (Thousand Oaks, CA)
- …supporting daily routine tasks. This engagement requires conformance with site policies, safety, quality, and data-integrity requirements. The successful candidate ... focus on closed-system multi-layer vessels (HYPERStack®) for adherent cell lines. Lead process development and automation projects that increase throughput, reduce… more
- Genmab (NJ)
- …Then we would love to have you join us!Overview:The Director, Feasibility Lead , will drive the implementation of strategic, data-driven feasibility practices that ... optimize the design and delivery of clinical trials across Genmab's development portfolio. This role balances operational ownership of high-impact feasibility work… more
