- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... Degree Life science preferred and- PhD Life science preferred Experience Qualifications- 7 or More Years 8+ years in...7 or More Years 8+ years in pharmaceutical/biopharmaceutical industry experience with a focus on small molecules and monoclonal… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as RA CMC representative supporting company initiatives. Qualifications:Education and Experience :Bachelor's Degree in Life Science required.M.S./PhD. preferred in a ... scientific discipline. MS Degree with 8-10 years pharmaceutical industry experience with 4+ years direct or related CMC regulatory experience orPhD. with 6-8… more
- Aequor (Thousand Oaks, CA)
- …degree. Nice to have: documentation practices, GMP, previous lab experience .Responsibilities: 1) Receive, clean, and evaluate product complaint return samples ... Life Sciences or related field or the equivalent combination of education and/or experience . Typically 2 plus years of related quality assurance or manufacturing … more
- Merck & Co. (Washington, DC)
- Job DescriptionPosition Description: Associate Director, Policy Advocacy The Associate Director, Policy Advocacy serves as the senior expert in the Global ... in advancing policy change in support of the company's business objectives. The Associate Director will proactively research and stay abreast of new strategies and… more
- Aequor (West Greenwich, RI)
- …completed Preferred Qualifications: Bachelor's Degree & 4 year of Quality/Manufacturing experience cGMP Experience Excellent written and verbal communication ... skills Experience with decision making more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director, Program Management is a senior position responsible for ... programs they manage. Program level responsibilities start with proactively partnering with senior leadership of the IT and the business community to identify and… more
- Aequor (Thousand Oaks, CA)
- …HOUR (SUPPLIER MAX SUBMITTAL RATE IS )Ideal candidate: Must have Smartsheet experience , Must have Agile project management and Agile frameworks (Scrum, Kanban, SAFE, ... etc.), BA/BS in Computer Science, IT, Engineering, Mathematics, life sciences, or other technical discipline; Advanced degree preferred. Demonstrated capability to influence without authority, drive detailed project planning, and lead projects execution,… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... DNREC, etc.) of animal facilities and program reviews is required.PurposeThe Associate Director/Attending Veterinarian will report to the Site Quality Head/Director… more
- Merck & Co. (Durham, NC)
- Job Description- The Associate Director of Quality Systems provides leadership, focus, and governance to the Hilleman site in the following Quality Systems: ... Product Review Authoring, Quality Risk Management, and Quality Council), the Associate Director will be responsible for comprehensive management of all activities… more
- Merck & Co. (Washington, DC)
- Job DescriptionPosition Description: Associate Director, Policy Strategy and Capabilities The Associate Director, Policy Strategy and Capabilities is ... team, reporting to the Executive Director, Policy Development & Strategy.The Associate Director will develop and maintain the strategic planning digital platform,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing Clinical ... global study and project team members, and to a limited extent with senior management, and outside vendors; works independently for all phases of studies… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe L3 Activation Oncology Associate Director role is responsible for liaising with Oncology brand teams to understand their brand-specific strategies ... required to execute them.Capture the comprehensive needs of One our Company's Experience to activate Oncology brands' desired "Learn" strategy to accelerate OME… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …analysis, supplier analysis, supplier management, supplier diversity required- Proven experience working with senior leadership, including C-suite executives ... for developing and continually growing strong relationships with DS internal senior stakeholders to assess, develop, implement and drive execution of Strategic… more
- Aequor (San Diego, CA)
- …ligases for targeted protein degradation. We are seeking a highly driven Research Associate / Senior Research Associate to assist in the identification and ... Job Description: Job Title: Research Associate Location: San Diego, CA* ONSITE Top Skills:...CA* ONSITE Top Skills: Expertise in mammalian cell culture Experience with plate-based cellular assays Immunoblotting, lentiviral infection, cellular… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed ... drugs for oncology indications. The Associate Vice President will manage and oversee the entire...Leaders or Team Members that could include Executive Director, Senior Director, or Director level personnel responsible for oncology… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …quality and stakeholder satisfactions. Responsible to communicate and escalate to Senior CMC Lead regarding the activity status and potential critical issues, ... pharmaceutical/biotechnology sciences with at least 7 years of industry experience required- Master's Degree Master's degree in chemistry, biochemistry,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as ... a member of the Global Project Team (GPT) utilizing precedent and experience to develop innovative and flexible approaches to achieve development goals, advise on… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …between CRO / vendors / AROAdditional non-study related activities: Occasional senior management interactions at FIHC, WDC; Initiates contact w/KOL and prepares ... or More Years with PharmD, PhD and relevant clinical experience preferred7 or More Years with Master's degree and...or More Years with Master's degree and relevant clinical experience preferred TravelAbility to travel up to 30%. In-house… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and supports PV Operations' medical review function. This position supports a senior physician in evaluating and mitigating safety signals as they arise. ... (from an accredited college or university)MD with board eligibility preferred Experience Qualifications1 or More Years of clinical experience preferred… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Ophthalmology will focus on driving strategy, development, and ... the late development of ophthalmology assets.May serve as a senior therapeutic area content expert within the company, providing...MD or MD/Ph.D. - Board Certified in Ophthalmology Required Experience and Skills:Minimum of 8+ years' experience … more
