- 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
- Ascension (Wichita, KS)
- …with healthcare team members. May prepare statistical analysis and utilization review reports as necessary. Oversee and coordinate compliance to federally ... with healthcare team members. May prepare statistical analysis and utilization review reports as necessary. Oversee and coordinate compliance to federally… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …specifically for specialty pharmacy, REMS, co-partners and affiliates. Liaise with Audit and Compliance team to ensure that Global Medical Affairs audits are ... data quality and proactive detection and resolution of issues.External Engagement:Continuously review compliance metrics trends from regulators/ industry experts… 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. (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)
- 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. (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
- 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
- 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
- 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
- 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
- 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Biotech is seeking Director of Operations as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe Director of Operations is an exempt ... management of staff in a growing operation in terms of volume/output and team size.Responsible for multiple work centers within the facility to ensure high quality… more
- Merck & Co. (Rahway, NJ)
- …the key quality representative attending and contributing to oversight and business review meetings with our company and contractor personnel to discuss projects, ... for project planning and activities of self and indirect reports associated with team activities.Makes decisions and acts with authority to carry out actions as… 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
