- Merck & Co. (Rahway, NJ)
- …for sterile operations under the remit of Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group (Pharm Ops ... Sterile Pharm Ops Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the… more
- Merck & Co. (North Wales, PA)
- …Skills:Hematology, Medical Affairs, Medical Communications, Medical Knowledge, Medical Review , Medical Writing, Pharmaceutical Medical Affairs, Project ... into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the V&I… more
- Merck & Co. (Rahway, NJ)
- …This research opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development ... our Research & Development Division - - in particular Discovery Pharmaceutical Sciences, Biologics Analytical Research and Development (BAR&D), Bioprocess research… more
- Merck & Co. (Upper Gwynedd, PA)
- …to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC ... regulatory strategies for our company's pharmaceutical pipeline products in accordance with global regulations and guidances, and is-responsible for the preparation… more
- Merck & Co. (Rahway, NJ)
- …interface between our company and our External Partners (EP) for Active Pharmaceutical Ingredients (API) and intermediates. You will be responsible for providing ... diligence assessments and provide expert consultation on chemical manufacturing matters. Review process change requests and deviation reports while ensuring… more
- AUROBINDO (Dayton, OH)
- …group of companies that has a long history of excelling in generic pharmaceutical prouct development and manufacturing. Aurolife has a 10 year history of ... organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management… more
- Merck & Co. (North Wales, PA)
- …trial objectives.Liaises with partners, vendors, and vendor management team . Review and provide clinical operations input into relevant clinical documents such ... (Excel, PowerPoint, Word, Outlook, etc.)Education/ExperienceBachelor's Degree +9 years of pharmaceutical , clinical drug development, project management, and/or medical field… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... strategic plan for assigned therapeutic area(s). These deliverables include development and review of compliant scientific exchange materials to be used in external… more
- Merck & Co. (North Wales, PA)
- …scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with ... technical writing, and presentation skillsEducation/ExperienceBachelor's Degree +5 years of pharmaceutical , clinical drug development, project management, and/or medical field… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... government price reporting, patient support, as well as other pharmaceutical regulatory counseling. Essential Functions: Provides proactive and day-to-day legal… more
- Tris Pharma (Nashville, TN)
- …live within territory.The selected candidate handles all operational aspects of pharmaceutical sales and service including, but not limited to: generating sales, ... - Bachelors degree and minimum 1 year sales experience in a pharmaceutical , biotechnology, business to business (B2B), capital equipment, medical device and/or… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... inspection readiness and actively support regulatory inspections.Lead facility operating review meetings and sponsor various department projects to drive continuous… more
- Merck & Co. (Rahway, NJ)
- …11 ComplianceSupport standardization activities for System Development Life CyclePrepare, review , and approve documentation such as master inventory lists, ... for a common goal-Experience in Auditing and Compliance within pharmaceutical industry, including change management and deviation management.Experience supporting… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... and MSL managers. Develop congress abstract tracker, assign MSL coverage, review MSL reporting responsibilities, collate and distribute Congress Report, execute pre-… more
- Merck & Co. (Durham, NC)
- …DescriptionAre you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!The Associate ... to support investigations and develop appropriate CAPAs which lead to program improvements. Review and approve out of tolerance (OOT) records and ensure quality… more
- Merck & Co. (Rahway, NJ)
- …on the clinical trial team. Leading medical monitoring team in review and interpretation -of clinical data/medical protocol deviations in collaborations with ... and presentation skills - Education/Experience Bachelor's Degree +5 years of pharmaceutical , clinical drug development, project management , and/or medical field… more
- Tris Pharma (Monmouth Junction, NJ)
- …responsible for multiple facets of the Procurement function within a pharmaceutical manufacturing environment including, but not limited to, purchasing, sourcing, ... related positions of increasing technical and strategic responsibility in pharmaceutical or biotechnology manufacturing. Proven track record of strategic sourcing,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... processes globally. This role will be responsible for coordinating the authoring, review and approval of new or updated procedural documentation. In addition, this… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... disciplines and cultures. Must have technical knowledge on integrated data review and derivation/interpretation of metrics that can dynamically interface with… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... and oversees JReview and SAS program development for clinical data processing, data review reports and listings. This includes but is not limited to: Program design… more
