109 associate scientist jobs found

Merck Job Description At our company, we are inspired by the belief that a research-driven enterprise dedicated to scientific excellence can create medicines and vaccines that save and improve lives. Every employee is building on our proud legacy of scientific breakthrough. Our ability to impact the lives of patients worldwide depends on the integrity, creativity, humility, and scientific acumen of our team. We are creating a diverse organization that is inspired by invention and founded on a culture of respect and collaboration. At our company's Research Labs, you'll have the opportunity to expand your knowledge and skills through collaboration with talented and dedicated colleagues while advancing your career. Our Company is currently seeking exceptional Associate Scientists to join our Research and Development Division's-WP's highly collaborative Discovery Chemistry Department. The successful candidates will contribute to multidisciplinary discovery teams by applying...

Repligen Overview Repligen is seeking an Associate Scientist to join our expanding Quality team. Responsibilities The qualified candidate will: Perform routine testing of raw materials for releasing following test instructions. Perform routine testing of in-process and final product samples following test instructions. Performing analytical Routinely use and reference the electronic document management system implemented at Avitide. Accurately compile and present results to support release of materials, products, and aid in root cause investigations. Be an active contributor to process improvements Qualifications Candidates should have most or all of the following qualifications: Minimum of Bachelor's Degree with experience in a scientific environment or equivalent industry experience. 1-3 years of experience preferred. Experience operating under ISO 9001:2015 quality systems preferred. Experience with modern analytical Experience...

A career in Boston - main video - YouTube Associate Scientist, Protein Biochemistry At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. The US Structural Biology Center of Excellence (CoE) at GSK, a new joint Vaccines and Pharma Center, will be established in Cambridge, MA in 2025. The mission of the CoE is to apply the full range of structural biology, protein biochemistry, and computational tools to design vaccine antigens, RNAs, delivery systems, and formulations for vaccines as well as to design antibodies, biologics, and small molecules. We are looking for a passionate and highly motivated associate scientist to join the CoE. As a crucial member of our team, you will be at the center of our protein expression and purification operations and you will find...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Dec 20 2024 We are currently looking for highly motivated , entry-level organic chemist to join our Medicinal Chemistry team in suburban Philadelphia. Our department partners with program teams across GSK’s research units to deliver high quality small molecules, from hit generation through late-stage lead optimization to address increasingly complex disease areas . The purpose of the role is to provide a high level of scientific and technical contributions to projects within the Medicinal Chemistry portfolio ( including but no t limited to: small molecules, PROTAC s , degraders, oligonucleotides, covalents , and antibody -drug conjugates ) with a primary responsibility of driving efficiencies , applying novel synthetic methods and techniques to design, synthesize, and purify candidate molecules. The successful applicant will become fluent in all areas of medicinal chemistry while working as part of a highly...

Merck Job Description Our Scientists are our Inventors. We deliver robust scientific data and interpretation that drives the commercialization of breakthrough therapeutics using innovative thinking, state-of-the-art facilities and modern equipment. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing your career. The Analytical Research and Development Mass Spectrometry -group in Rahway, NJ is seeking a motivated scientist with technical expertise in mass spectrometry-based protein characterization. This position has the opportunity to impact the analytical strategy for characterization of peptides, therapeutic proteins, antibody-drug conjugates, and vaccines. The ideal candidate will...

The Metropolitan Museum of Art GENERAL STATEMENT OF RESPONSIBILITIES & DUTIES: As the Associate Research Scientist, you will conduct analysis, research, and documentation to improve the Museum and wider preventative conservation field's understanding of how indoor temperatures and humidity parameters affect works of art. Working within the Preventative Conservation Science Laboratory, you will develop a detailed report on the fields current state of knowledge. You will help identify gaps, risks, potential impacts and propose further research opportunities to advise the museum on gallery condition best practices. This is a position with an established end-date or time frame. PRIMARY RESPONSIBILITIES & DUTIES: Collect, research, evaluate and review existing documentation and research on the effects of temperature or humidity variation on all types of artworks. Collaborate with internal and external stakeholders to research, develop, and advise on improving the...

PointClickCare PointClickCare is a leading North American healthcare technology platform enabling meaningful care collaboration and realtime patient insights. For over 20 years, the company has been focused on realizing its vision: to help create a world in which providers and plans can confidently deliver frictionless care. Since its inception, PointClickCare has grown exponentially, with over 2,200 employees working to impact millions across North America. Recognized by Forbes as one of the top 100 private cloud companies and acknowledged by Waterstone Human Capital as Canada's Most Admired Corporate Cultures, PointClickCare leads the way in creating cloud-based healthcare software. At PointClickCare, we offer a wealth of opportunities and a vibrant culture that empowers our employees. Our dynamic environment is the perfect place to advance your career while engaging in meaningful work alongside incredible colleagues. Here, you'll discover a space where your talents can thrive,...

Biogen Job Description About This Role This role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director, Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs, DSURs, PADERs and local reports. The Associate Director will be the subject matter expert on Aggregate Reports safety requirements worldwide and lead independently all aspects of the production of an Aggregate Safety Report, including responses to safety questions from health authorities. This role leads independently initiatives for process improvement and efficiencies, and collaborates with stakeholders to develop, implement and maintain processes that are compliant with global PV regulations for Aggregate Safety Reports. There will be close collaboration with vendors, SSA vendor oversight team, and with the SSA Quality Management team to ensure high quality standards...

Legend Biotech USA Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK) cell-based immunotherapy. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director, Clinical Research Scientist as part of the Clinical Development team based Remote. Role Overview The Clinical Research...

Biogen Company Description Biogen's West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey. Job Description HI-Bio, Inc., a Biogen company, is seeking a highly motivated Principal Scientist in Experimental Immunology to drive the discovery and validation of novel therapeutic targets in autoimmune and inflammatory diseases. The successful candidate will have the opportunity to drive forward multiple discovery programs that encompass target identification and validation, followed by development and application of in vitro and in vivo assays to evaluate therapeutic hypotheses. What You'll Do Drive novel target discovery and validation for immune-mediated diseases both as an individual contributor and in collaboration with...

Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross-functional team, you are recognized internally as a technical expert in an area of importance to the R&D function. You identify, define and solve complex business problems by applying your broad and in-depth technical knowledge. As an expert in your technical specialty, this leadership role requires you to interact with senior management and cross-functional teams to meet current and future strategic demands of the business. How you will contribute You will plan, lead and manage complex technically focused projects while using your technical expertise to guide, direct and influence activities lead by others. To ensure the right solutions are developed, you will use consumer knowledge and your technical expertise to identify future opportunities and to execute programs with technical rigor. This...

Site Name: Cambridge MA, GSK HQ, USA - Pennsylvania - Upper Providence Posted Date: Dec 19 2024 This role within Global Clinical Oncology R&D will serve as a clinical sciences leader on global oncology studies and contribute to program-level activities. Responsible for the delivery of quality study strategy and design, understanding the analysis and interpretation of data throughout the study, including leading clinical data review ongoing throughout study conduct. Responsible for the end to end of writing protocols (protocol concept to final study report) delivery. Contributor to informed consent forms development and other study related documents. Clinical Development Oncology Key Responsibilities: Review and/or enhance the technical and scientific robustness of project level clinical development plans. May support regulatory interactions, including contributing to briefing documents, presentations, addressing questions and responses. Ensure compliance with...

Site Name: Cambridge MA, GSK HQ, USA - Pennsylvania - Upper Providence Posted Date: Dec 19 2024 This role within Global Clinical Oncology R&D will serve as a clinical sciences leader on global oncology studies and contribute to program-level activities. Responsible for the delivery of quality study strategy and design, understanding the analysis and interpretation of data throughout the study, including leading clinical data review ongoing throughout study conduct. Responsible for the end to end of writing protocols (protocol concept to final study report) delivery. Contributor to informed consent forms development and other study related documents. Clinical Development Oncology Key Responsibilities: Review and/or enhance the technical and scientific robustness of project level clinical development plans. May support regulatory interactions, including contributing to briefing documents, presentations, addressing questions and responses. Ensure compliance with...

Merck Job Description The Biologics and Biopharmaceutics team is responsible for the research and development of sterile & parenteral drug products for biologics including monoclonal antibodies (mAbs), di- & tri-specific antibodies, and fusion proteins as well as the biopharmaceutic support for the oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team whose roles include design and development of formulation, manufacturing process, and primary packaging to enable phase appropriate regulatory filings for large molecule sterile products. These sterile products include those administered via intravenous, subcutaneous, or intramuscular routes of administration. This research opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions, processes...

This role qualifies for an enhanced Employee Referral Bonus in the amount of $3,500. Please refer to these process and eligibility requirements prior to submitting your referral. A career in Boston - main video (youtube.com) At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. We believe the Greater Boston area is an important hub for the biotech and pharma industry, which is why we’ve invested in growing our footprint and expanding our R&D space in Cambridge, with a primary focus on additional state-of-the-art lab space. Here, we will bring together talent and expertise, building upon GSK’s long history of vaccine development, to create globally leading viral capabilities and cutting-edge vaccines technologies, as we add to our robust portfolio targeting...

This role qualifies for an enhanced Employee Referral Bonus in the amount of $3,500. Please refer to these process and eligibility requirements prior to submitting your referral. A career in Boston - main video (youtube.com) At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. We believe the Greater Boston area is an important hub for the biotech and pharma industry, which is why we’ve invested in growing our footprint and expanding our R&D space in Cambridge, with a primary focus on additional state-of-the-art lab space. Here, we will bring together talent and expertise, building upon GSK’s long history of vaccine development, to create globally leading viral capabilities and cutting-edge vaccines technologies, as we add to our robust portfolio targeting...

Merck Job Description Job Title: Associate Principal Scientist, Cell Culture and Fermentation Sciences Level: R4 (Research Path) Level: P4 (Research Path) As part of Our Company's Manufacturing Division, within the Bioprocess Drug Substance Commercialization (BDSC), the Cell Culture and Fermentation Sciences (CCFS) department provides the technical process leadership and laboratory capabilities in support of late-stage pipeline and post-market commercial manufacturing processes for vaccines and biologics. CCFS supports various commercialization activities, including process characterization, technology transfer to internal and external manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction of Director in the CCFS group and working in conjunction with internal and external partners, this individual will support late stage and commercial program...

CareFirst BlueCross BlueShield Resp & Qualifications PURPOSE The Sr. Data Scientist is responsible for managing health equity data governance and advancing data initiatives across the enterprise. This role plays a critical part in supporting and advancing health equity and public health initiatives by acting as the liaison between various data system leads across the organization. The position also involves providing operational governance oversight, offering advisory support in identifying control improvements and governance opportunities, and coordinating internal audits. Additionally, the Sr. Data Scientist utilizes numerical techniques, algorithms, and models in statistical modeling, machine learning, and data mining to address business challenges and support enterprise-wide data science initiatives. ESSENTIAL FUNCTIONS: Manage Health Equity Data Governance: Oversee the development and implementation of data governance frameworks that support health equity....

CareFirst BlueCross BlueShield Resp & Qualifications PURPOSE: Purpose of the Data Analytics Manager is to execute business objectives with data and ensure alignment with the vision of the company. Individual will organize the technology, processes and financial resources necessary to address the current and future analytics needs of the business. Provides thought leadership and acts as a subject matter expert in the designing and recommending of appropriate analytical approaches and methodologies. Provides management responsibility into data-driven insights that inform the business's strategic direction. ESSENTIAL FUNCTIONS: Manage a team with a focus on the development of analytics capabilities across the company, including self-service capabilities through technology implementation, best practices and training. Ensure team members serve as a trusted advisor to clients on analytics and data. Interpret statistical analyses and help clients derive meaning from...

CareFirst BlueCross BlueShield Resp & Qualifications PURPOSE: Leads and manages the digital product team acting as the day-to-day manager; first point of escalation and day to day approval for implementing strategies designed to improve the digital customer experience and conversion. Ensures that the Digital Experience team develops and/or converts organization and departmental business strategies and translate those strategies into actional able roadmaps to ensure the digital product team delivers high-quality digital customer experiences. Advises stakeholders and the broader organization on aspects of the digital customer experience by ensuring knowledge, support, and training to enhance members' digital journeys. ESSENTIAL FUNCTIONS: Leads the day-to-day management of the Digital Product team members. Works closely with business units and product managers to translate business strategy into digital product roadmaps that drive digital capabilities that meet...