- PCI Pharma Services (Bedford, NH)
- Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an ... testing the following sample types R&D, in-process, finished product, stability , as well as raw materials. Job duties may...or aberrant results and process changes** **.** **Act as lead in projects within the QC group and the… more
- Catalent Pharma Solutions (San Diego, CA)
- …**State** : CA **JOB DESCRIPTION** : + Review of analytical release and stability data, involving review of Potency tests of investigational new tablets and capsules ... master batch records, and specifications for analytical testing. + Lead role in onboarding new compounds to the site...train the direct report on analytical data review of stability and release data. + Perform Line Clearance activities… more
- Pfizer (New York, NY)
- **ROLE SUMMARY** Pfizer's Biopharma , Patient and Centre for Digital Innovation (BPC) team are responsible for the creation, configuration, launch, and support of all ... business objectives. Using influence more than authority, you will lead teams of engineers on the implementation of the...risks to achieve the desired results, balancing risks to stability and current norms versus the need for constant… more
- J&J Family of Companies (San Diego, CA)
- …based on La Jolla, California with a requirement to be on site. Ambrx Biopharma , Inc. **,** a Johnson & Johnson company, is a clinical-stage biologics company ... testing and set stage-appropriate systems suitability and acceptance criteria. + Lead CRO/CMOs to transfer and qualify/validate potency methods within bold… more
- Catalent Pharma Solutions (Kansas City, MO)
- …Department. The data may be used for submission in regulatory packages, release and stability testing of clinical and animal trial dose forms and in support of ... and Division/site performance standards and metrics. Sample types include in-process, release or stability for CMC support. Techniques may include any or all of the… more
- Bristol Myers Squibb (Cambridge, MA)
- …innovative ideas while advancing professionally alongside some of the brightest minds in biopharma . At Bristol Myers Squibb, we are inspired by a single vision - ... external) to progress an innovative biologics pipeline is key. **Responsibilities:** + Lead and drive innovation in protein engineering and core platform processes.… more
- Catalent Pharma Solutions (San Diego, CA)
- …analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing as well as Clinical Supply Services. ... safety of every patient, consumer, and Catalent employee.** **The Role:** + Lead the development of site Quality Objectives, site Quality Plans, Quality Management… more
- Catalent Pharma Solutions (San Diego, CA)
- …II clinical trials. Under the direction of the Manufacturing Supervisor or Team Lead , the Manufacturing Technician will work hands on, in their designated production ... analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing as well as Clinical Supply Services.… more
- Catalent Pharma Solutions (San Diego, CA)
- …testing, formulation development, GMP (Good Manufacturing Practices) manufacturing and stability storage and testing as well as Clinical Supply Services. ... Role:** + Establish project timelines and ensure milestones are met. Organize and lead meetings with client and internal teams to facilitate project completion, set… more
- Catalent Pharma Solutions (Morrisville, NC)
- …group. An individual in this role functions as a microbiology technical lead , interacts with external and internal customers for project support, and mentors ... (sterility, microbial limits, endotoxin testing, etc.) for API, Finished Product, Stability , Raw Materials and Components. The Environmental Monitoring team performs… more
- Catalent Pharma Solutions (San Diego, CA)
- …**City:** San Diego **State** : CA **JOB DESCRIPTION** : + Develop stability -indicating methods for peptide and small molecule API, intermediates, and drug products ... externally through oral and written updates and formal reports as necessary. Lead discussions with clients on technical topics relating to their project. Supervisor… more
- Catalent Pharma Solutions (Greendale, IN)
- …formulation and process development, optimization studies, and informal and formal stability studies. Complex formulations and process parameters will be solved by ... at local, technical, governance, executive and customer meetings. + Lead Catalent's strategies, initiatives, expectations, processes, and portfolio commitments +… more