- Merck & Co. (Rahway, NJ)
- …Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research facility.- The ... Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab… more
- Merck & Co. (Rahway, NJ)
- …Our team is looking for a strong candidate for the position of Principal Scientist (R5) within the Biologics product development group. Primary duties: Be a seasoned ... packaging, compatibility characterization for processing and administration, and supporting regulatory filings. Have deep fundamental knowledge around large molecule… more
- Merck & Co. (Rahway, NJ)
- …that enable us to create breakthrough science changing the way we approach animal health challenges.-The Senior Scientist within our company's Animal Health ... Job DescriptionOur Animal Health Research Laboratories team work tirelessly to invent...of development.- -The successful candidate will be a self-motivated scientist with an outstanding scientific track-record and passion for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and leads technical team in preparation of submission documents; authors regulatory documents where necessary with supervision. Health Authority Interactions: ... contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC...this position acts as the company liaison with the Health Authority (eg, US FDA and EU EMA) for… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the benefit of patients and global human health . Education and Minimum Requirement: PhD or equivalent degree in statistics/biostatistics or related discipline with a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small ... for working on cross-functional teams, developing and executing post-approval Regulatory CMC strategies, reviewing CMC information and data, authoring CMC… more
- Merck & Co. (Rahway, NJ)
- Job Description Senior Scientist , Process Cell Sciences (PCS) at Rahway, NJ The Biologics Process Research & Development organization within our company's Research ... energetic individual to join our Process Cell Sciences (PCS) group as Senior Scientist .-In this role, the successful candidate will work closely with team members of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Senior Scientist , Microbiology (Lab Lead) - Analytical Research & Development (Onsite) Small Molecule Analytical Research and ... Development (SMARD) is seeking a highly motivated Senior Scientist -Microbiologist to join the growing Microbiology Center of Excellence (COE).- This position is… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionAt our company, we are committed to improving the health and well-being of people around the world. As a leading global pharmaceutical company, we ... company's Research Laboratories in South San Francisco is seeking a Principal Scientist of In vivo Pharmacology with strong experience in cardiovascular and… more
- Merck & Co. (North Wales, PA)
- …or more clinical trials in the lung cancer program. Assists the Lead Clinical Scientist and study team with the scientific conduct of clinical studies. In this ... preferred.Required experience and skills: Working knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage multiple competing… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the benefit of patients and global human health . Responsibilities :Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, ... adjudication committee setupStudy outputs: Draft responses to IRBs and Health Authorities; Collaborates with Translational Medicine and Clinical Pharmacology to… more
- Merck & Co. (Rahway, NJ)
- …clinical assays.Author and review detailed statistical reports suitable for submission to health regulatory authorities, including the US FDA and international ... detailed statistical reports, as well as respond to inquiries from health regulatory authorities.Education Minimum Requirement:Ph.D. or equivalent degree in… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Today, we ... colleagues while developing and expanding your career.The Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical… more
- Merck & Co. (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for a Senior Scientist position available at its Rahway , New Jersey research facility . The ... Senior Scientist is a laboratory-based scientific role tasked with solving...- Authoring and reviewing internal technical reports, sections of regulatory filings ( eg, IND, BLA) and external scientific… more
- Merck & Co. (Rahway, NJ)
- …in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise in Liquid Chromatography and Mass ... validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.… more
- Merck & Co. (Rahway, NJ)
- …Development, Cell Based Sciences team in Rahway, NJ is seeking a motivated scientist with technical expertise in Biologics Potency assays in drug Development. More ... data in context of broader process and product development.-Working knowledge of regulatory guidance and quality standards, with experience authoring and reviewing … more
- Merck & Co. (North Wales, PA)
- …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on a clinical trial team.Leading medical monitoring team in review and ... to other clinical scientists.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage multiple competing… more
- Merck & Co. (South San Francisco, CA)
- …data generation, analysis, and reporting to project teams, governance bodies, and regulatory agencies, and manage key timelines and milestonesLead and develop a ... the right to require COVID-19 vaccinations for positions, such as in Global Employee Health , where the Company determines in its discretion that the nature of the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPrincipal Scientist , Late Stage Analytical Program LeadAbout the roleYou will join our Large Molecule Analytical Validation team to serve as an ... Quality, Upstream/Downstream Process Development, Formulations, Global Clinical Supply, CMC Regulatory , Quality, and Commercial-facing Partner Groups to support commercialization… more
