58 associate jobs found

Capital One Principal Associate, Data Scientist - Financial Services Data is at the center of everything we do. As a startup, we disrupted the credit card industry by individually personalizing every credit card offer using statistical modeling and the relational database, cutting edge technology in 1988! Fast-forward a few years, and this little innovation and our passion for data has skyrocketed us to a Fortune 200 company and a leader in the world of data-driven decision-making. As a Data Scientist at Capital One, you'll be part of a team that's leading the next wave of disruption at a whole new scale, using the latest in computing and machine learning technologies and operating across billions of customer records to unlock the big opportunities that help everyday people save money, time and agony in their financial lives. As a Data Scientist at Capital One's Auto Finance business, you'll be part of a high performing modeling and analytics team that's leading the...

Merck Job Description Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to use innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. As an Associate Principal Scientist in the multiscale separations team within the Separations Sciences team of Analytical Enabling Capabilities, you will work within a highly collaborative team to enable the advancement of the development pipeline. You will be primarily responsible for chromatographic isolation of pharmaceutical API and impurities from analytical scale to semi-prep scale and prep scale, covering the space of small molecules, peptides, conjugate-based modalities as well as emerging modalities in our portfolio. To accelerate the development of new medicines and vaccines, you will partner with process chemists and analytical scientists...

University of Michigan How to Apply A cover letter is required for consideration of this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position. Please label your job application file as follows: last name, first name. To be considered for this position, the applicant must have met or will have met all the required qualifications before the start date of employment. Job Summary The Michigan Alzheimer?s Disease Center (MADC) is an NIH-funded research center focused on conducting and supporting Alzheimer?s disease and related dementia research. A key aim of the center?s research is to work with communities to address disparities in Alzheimer?s disease and related dementias. The center also spans beyond research by promoting state-of-the-art care and wellness for individuals and families affected by dementia and increasing...

Repligen Overview Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key part in shaping some of the most innovative and life-changing therapies in the world. We foster a culture of purpose, collaboration, and shared success-where every voice matters and every contribution drives progress. Join us! Repligen is a global, publicly traded company seeking an Associate Scientist to join our dynamic team. The ideal candidate will support our team in testing affinity resins derived from Avitide's proprietary affinity ligand discovery platform, with emphasis on developing and optimizing downstream processes for the purification of biopharmaceutical products. This position offers an exciting opportunity to contribute to the advancement of novel therapies and medicines that impact...

Merck Job Description Associate Specialist - Process Engineer (P1) Job Description: The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) drug product development and clinical manufacturing facility in Rahway, New Jersey. The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products (spray-dried intermediates, tablets and capsules), leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating. We are part of our company's research division, focused on development and clinical deliveries in a GMP pilot facility supporting partners in Oral Formulation Sciences and Pharmaceutical Commercialization Technology to enable faster delivery of new medicines to clinical trials. The Non-Sterile (Oral Solids Dosage) team at the FLEx Center in Rahway is...

Merck Job Description Job Description: The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) drug product development and clinical manufacturing facility in Rahway, New Jersey. The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products (spray-dried intermediates, tablets and capsules), leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating. We are part of our Company's research division, focused on development and clinical deliveries in a GMP pilot facility supporting partners in Oral Formulation Sciences and Pharmaceutical Commercialization Technology to enable faster delivery of new medicines to clinical trials. The Non-Sterile (Oral Solids Dosage) team at the FLEx Center in Rahway is looking for an Associate Director - Process Engineering...

Merck Job Description Associate Specialist - Process Engineer (P1) Job Description: The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) drug product development and clinical manufacturing facility in Rahway, New Jersey. The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products (spray-dried intermediates, tablets and capsules), leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating. We are part of our company's research division, focused on development and clinical deliveries in a GMP pilot facility supporting partners in Oral Formulation Sciences and Pharmaceutical Commercialization Technology to enable faster delivery of new medicines to clinical trials. The Non-Sterile (Oral Solids Dosage) team at the FLEx Center in Rahway is...

E.L.F. BEAUTY About the Company e.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l.f. Cosmetics since 2004 and driven our portfolio expansion. Today, our multi-brand portfolio includes e.l.f. Cosmetics, e.l.f. SKIN, pioneering clean beauty brand Well People, Keys Soulcare, a groundbreaking lifestyle beauty brand created with Alicia Keys, Naturium, high-performance, biocompatible, clinically-effective and accessible skin care, and our newest brand, rhode, a line of curated skincare essentials, formulated for a variety of skin types and needs with high performance ingredients, it's a daily routine that nourishes your skin barrier over time. In our Fiscal year 25, we had net sales of $1 Billion and our business performance has been nothing short of extraordinary with 28 consecutive quarters of net sales growth. We are the #2 mass cosmetics brand in...

E.L.F. BEAUTY About the Company e.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l.f. Cosmetics since 2004 and driven our portfolio expansion. Today, our multi-brand portfolio includes e.l.f. Cosmetics, e.l.f. SKIN, pioneering clean beauty brand Well People, Keys Soulcare, a groundbreaking lifestyle beauty brand created with Alicia Keys, Naturium, high-performance, biocompatible, clinically-effective and accessible skin care, and our newest brand, rhode, a line of curated skincare essentials, formulated for a variety of skin types and needs with high performance ingredients, it's a daily routine that nourishes your skin barrier over time. In our Fiscal year 25, we had net sales of $1 Billion and our business performance has been nothing short of extraordinary with 28 consecutive quarters of net sales growth. We are the #2 mass cosmetics brand in...

University of Michigan Job Summary Yunlu Zhu Laboratory with Kresge Hearing Research Institute is looking for a Research Lab Specialist Intermediate. The research goal of the lab is to understand how the brain turns gravity signals into stable movement. The lab uses the model organism zebrafish (Danio rerio), combining genetics, imaging, behavior, and modeling. For more information on our research, please visit https://www.zhulab.fish The successful candidate will work under the supervision of the principal investigator and will play an integral role in daily research. Responsibilities* Responsibilities include, but are not limited to: Maintain transgenic zebrafish lines. Perform fluorescent screening and confocal imaging of transgenic zebrafish larvae. Conduct experiments and assist with data collection, organization, and quality control. Maintain documentation for experiments and assist with the development and implementation of laboratory protocols....

The Nature Conservancy What We Can Achieve Together: The Nature Conservancy in New Hampshire is seeking a motivated policy strategist and relationship builder who is eager to help develop and deliver high-impact conservation strategies that advance the Nature Conservancy's mission in the Granite State and across the U.S. The Policy Associate serves as a liaison and informational contact between the organization, elected officials, state agencies and partner organizations. They are responsible for leading strategic policy initiatives that advance TNC's science-driven goals for land and natural resource protection, freshwater and coastal restoration, and climate resilience. They will excel at building and sustaining relationships with internal staff, volunteers as well as key partners to achieve conservation outcomes. We're Looking for You: The Policy Associate reports to the Deputy State Director and works to develop and execute collaborative and integrated...

Revvity Overview: Join our team in a role that makes a real difference in workplace safety and environmental stewardship. As an Associate Physicist, you'll be an essential part of our Radiation Protection Program, helping ensure our employees work safely, our environment stays protected, and we maintain full compliance with Massachusetts Department of Public Health (MDPH) regulations and our radioactive materials license. This is hands-on work where your attention to detail and commitment to safety directly impact the well-being of your colleagues and our community. Location: Onsite, five days a week at our South End Boston facility Core Duties and Responsibilities: Perform radiation surveys in restricted and unrestricted areas using radiation/contamination instrumentation and associated equipment. Conduct periodic audits and assessment, including identification of ancillary hazards, remediation of hazards, and survey documentation for radiological conditions....

Conagra Brands Reporting to the Manager, Scientific Affairs, you will analyze the composition of food products, conduct experiments, gather data and findings, and prepare written reports to ensure compliance with nutritional labeling specifications, regulatory guidance, and food safety standards. You will also support the development of new analytical methods under direct supervision. A Taste of Your Responsibilities Develop project objectives, technical work plans, and complete assigned work on time with direct guidance. Perform chemical analysis on products to identify problems and opportunities supporting product development, nutritional labeling, quality initiatives, and applied research. Calculate and interpret data generated from laboratory instrumentation; isolate nonconforming work and make necessary corrections. Write, review, and identify improvements for test methods and technical procedures and initiate action plans. Conduct external research to stay current...

Alkermes, Inc. The primary responsibilities of an Associate Director in the Nonclinical Safety Evaluation (NSE) organization are to (1) design and implement nonclinical safety assessment strategies to support the nomination and development of Alkermes' diverse small molecule drug candidates and (2) communicate strategies and findings internally and to regulatory authorities globally. The Associate Director is the single point of accountability within NSE for all strategic, scientific, study-related, and regulatory aspects of the programs he/she manages. The Associate Director in NSE has a broad understanding of toxicology and regulatory requirements to progress candidates through clinical development and is recognized by internal peers for his/her scientific contributions and deliverables (within discipline) to Discovery and Development programs. The individual has specific expertise in one or more areas relevant to nonclinical safety evaluation, shows competency in all aspects,...

Acushnet Company Where Performance Meets Purpose Join a team that values excellence and innovation, at a company known for its iconic golf brands. At Acushnet Company, your background and experience contribute to creating the best products for dedicated golfers worldwide. Here, your performance has purpose. What You Will Be Doing As an Associate Manager, Human Resources, you will serve as a strategic and trusted partner to the Clubs Operations team, leading a broad range of HR responsibilities with a service-oriented and business-focused mindset. In this role, you will proactively support leaders and associates by providing expert guidance on employee relations, performance management, leadership development, compensation, staffing, and organizational effectiveness. You will manage complex employee relations matters, conduct investigations, and ensure consistent application of company policies and employment laws while maintaining the highest standards of...

Alkermes, Inc. This position is an integral part of the CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs by conducting clinical site, vendor qualification, internal systems and document audits to ensure compliance with cGCPs. The CQA Manager supports the department initiatives by leading CQA projects and assists with management of department resources. This position must be able to quickly identify critical and high risk business and compliance issues and report immediately to CQA management and assist/lead investigations and/or corrections of such issues. Travel requirement of 40% - 60% Responsibilities This position will : Schedule, personally conduct and/or supervise Good Clinical Practice (GCP) audit services by an external vendor/consultant and/or internal resources (auditors) which will support Clinical Development activities including but not limited to: Audits of clinical vendors, clinical sites...

Alkermes, Inc. The Associate Director, Regulatory Operations will be responsible for submission management across the development pipeline and support the commercial portfolio. This hands-on position will also assist with regulatory affairs systems, applications, and tools including supporting system implementations, maintenance, updates, and releases. You'll work closely with Regulatory Affairs and cross-functional partners to manage timelines, ensure submission readiness, and strengthen operational excellence across the organization. Key Responsibilities: Lead end-to-end management of regulatory submissions, ensuring timely, compliant, and high-quality deliverables. This role interfaces with external publishing vendor(s) for the preparation of submissions, and internal stakeholders to provide operational oversight and support for eCTD regulatory submission activities. Serve as submission manager and primary contact for publishing vendors and internal stakeholders....

Merck Job Description The Business Practices and Privacy Officer leads the strategy behind the implementation of Compliance and Privacy frameworks across the Puerto Rico, Central America & Caribbean Cluster by partnering with Global, Regional, and Local stakeholders while supporting markets strategy and providing cluster-level compliance guidance to drive consistency and execution on cluster priorities with operational excellence. This role ensures that business practices align with internal policies, external regulations, and ethical standards while facilitating commercial success. Reporting to the Associate Vice President, Managing Director of the Cluster role will focus on driving the pillar, Fostering Innovation, Simplification & Risk Evaluation, to continue reinforcing our strong Culture of Compliance & Collaboration. This is an exciting time to join the team and play a key role in advancing strategic initiatives and cluster projects that support our...

Merck Job Description The Business Practices and Privacy Officer leads the strategy behind the implementation of Compliance and Privacy frameworks across the Puerto Rico, Central America & Caribbean Cluster by partnering with Global, Regional, and Local stakeholders while supporting markets strategy and providing cluster-level compliance guidance to drive consistency and execution on cluster priorities with operational excellence. This role ensures that business practices align with internal policies, external regulations, and ethical standards while facilitating commercial success. Reporting to the Associate Vice President, Managing Director of the Cluster role will focus on driving the pillar, Fostering Innovation, Simplification & Risk Evaluation, to continue reinforcing our strong Culture of Compliance & Collaboration. This is an exciting time to join the team and play a key role in advancing strategic initiatives and cluster projects that support our...

University of Michigan Mission Statement Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society. Why Join Michigan Medicine? Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every...