- Merck & Co. (North Wales, PA)
- …practices. The main objective for the Resource Capabilities and Label Operations (RCLO) team is to help the organization with the mission to achieve business ... ongoing support to job owners and agency partners on promotional review processes and systems, help job owners navigate complex situations, conduct… more
- Merck & Co. (Rahway, NJ)
- …to achieve new milestones in global healthcare. The Biologics and Biopharmaceutics team is responsible for the research and development of sterile & parenteral ... Director will influence the strategy, lead activities, and develop a team whose roles include design and development of formulation, manufacturing process,… more
- Merck & Co. (Durham, NC)
- …leadership skills to empower teams, solve complex technical challenges, and ensure compliance with industry standards while making a tangible impact on our ... Engineer is a member of the Engineering, Maintenance and Site Services (EMSS) team providing support to the Durham sites.- This includes Energy Center, Vaccine Bulk… more
- Merck & Co. (Durham, NC)
- …Calibration is a member of the Engineering, Maintenance and Site Services (EMSS) team providing support to the Durham sites.- This includes Energy Center, Vaccine ... 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. (Durham, NC)
- Job DescriptionThe Associate Specialist, is a member of the Site Automation team responsible for the assigned process control systems in support of manufacturing ... of process control, data collection techniques, and troubleshooting in compliance with SDLC, GMP, safety, and environmental regulations.- Actively support,… more
- Merck & Co. (Rahway, NJ)
- …clinical scientist on the clinical trial team . Leading medical monitoring team in review and interpretation -of clinical data/medical protocol deviations in ... and scientific acumen as part of a global, cross-functional team . - Job Responsibilities - Responsible for leading...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Merck & Co. (Durham, NC)
- …culture by reducing waste and constantly driving continuous improvement. -Responsible to review and approve compliance documents, as per procedures or ... and area cleaning. AccountabilityFirst line operations supervisor with a team of individual contributor production direct reports including safety, quality,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …myeloma.Legend Biotech is seeking QA Validation Specialist III as part of the Quality team based in Raritan, NJ. Role OverviewThe QA Validation Specialist role is an ... oversight of technical, qualification, and validation activities including data or document review and approval as needed. This role will be responsible for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …FMA Program at Novo Nordisk Inc (NNI). Accountable for ensuring that they and their team act in complete and total compliance with all laws, regulations and ... information Acts and is accountable for others in his/her team , acting in complete and total compliance ...exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Development Of People Supervisory.… more
- Merck & Co. (South San Francisco, CA)
- …assessment of drug candidates. The successful candidate will join a dynamic Data Science team focused on bringing AI/ML approaches to bear to improve the speed and ... AI (GenAI) to enhance document authoring processes, thereby improving efficiency and compliance in regulatory submissions.The candidate will play a key role in… more
- Repligen (Waltham, MA)
- …and Compile Quality metrics as inputs for monthly KPI's and management review meetings with the Senior Management team .Facilitate operational excellence ... This leader will be responsible for managing the site quality assurance team which includes all day-to-day activities for product manufacture, test and release… more
- Merck & Co. (Upper Gwynedd, PA)
- …of potential risks.Lead the development, communication, lifecycle management and review of the CMC Regulatory Strategy Document for assigned projects.Provide ... regulatory leadership as needed in product in-license/due diligence review and product transition to the Post-Approval Pharm CMC team .Manage execution of CMC… more
- Insmed Incorporated (San Diego, CA)
- …do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the ... Science's Top EmployerInsmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science… more
- Eisai, Inc (Nutley, NJ)
- …strategic plan for assigned therapeutic area(s). These deliverables include development and review of compliant scientific exchange materials to be used in external ... will work cross-functionally as a strategic partner with the broader Medical Affairs team as well as the Publications & Scientific Communications teams and other… more
- Tris Pharma (Monmouth Junction, NJ)
- …our proprietary science and technology.Our science and technology make us unique, but our team members set us apart; they are the engine fueling Tris' passion and ... pride in the company's success. Equally importance to each team member is how we interact with one another...systems thinking and a holistic systems-based approach to drive compliance and assess operational needs and activities in to… more
- Tris Pharma (Monmouth Junction, NJ)
- …our proprietary science and technology.Our science and technology make us unique, but our team members set us apart; they are the engine fueling Tris' passion and ... a successful business and take pride in the company's success. Equally importance to each team member is how we interact with one another on a daily basis. We… more
- Merck & Co. (North Wales, PA)
- …into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the V&I ... efficiently, focusing on delivering high-quality work and contributing to team goals.Required Qualifications, Skills and Experience MinimumMD/PharmD/PhD, plus minimum… more
- Genmab (NJ)
- …an exciting opportunity of a passionate, high profile, high-impact Global Medical Affairs team , and work in a dynamic and collaborative setting.The MSL/Sr. MSL is a ... member of a field-based team of advanced degree specialists who function as an...all aspects of investigator sponsored trials (ISTs), from submission, review and approval, through study activation/completionCollaborate effectively and proactively… more
- Aequor (Thousand Oaks, CA)
- …12 AM NIGHT: 7 PM - 8 AM Will change based on the manufacturing team they are supporting(Upstream/Downstream) and rotate every 6 months. The ideal candidate f will ... manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering areas/staff in the… more
- AUROBINDO (Durham, NC)
- …portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control ... training, on-boarding, orientation, policy implementation, compensation, and employment law compliance .Manage and conduct the new hire orientation and exit interview… more
