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30 multi office jobs found

Mondelez International
Mar 14, 2026  
Sr. Consumer Scientist I Featured
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. Under the indirect supervision of a manager, you plan and organize cross-functional projects and develop consumer-centric objectives and strategies in response to business needs. You also interact independently with senior management and stakeholders. How you will contribute You will deliver on single or multi-stage complex projects, meeting standards and time frames by designing research and producing quality, actionable data. You will lead all aspects of qualitative and quantitative consumer research and ensure that the data gleaned is translated into a cohesive story. To that end, you will interpret results, report and present findings, and make recommendations that contribute to decision making. In this role, you may also lead descriptive panels, training, data analysis, reporting and assess panelist’s...
Mondelez International East Hanover, NJ, USA Full-Time
ACRT Services
Nov 14, 2025  
Environmental Compliance Senior Scientist Featured
EnviroScience, Inc. Full time Regular The Environmental Compliance Senior Scientist will assist and coordinate the Environmental Compliance group in multi-media sampling, subsurface investigations, sediment and waste characterization, ESA activities, NEPA, and permitting. They will take an active role in developing and executing technical scopes of work and budgets for proposals and reports. This role involves collaborating with various teams to deliver innovative solutions in environmental sciences, developing a strategic approach to operational efficiency and quality control while working closely with clients, regulatory bodies, and internal departments. The ideal candidate will have a background in environmental or related science, management experience, leadership, client communications and a thorough understanding of environmental laws and regulations. Essential Duties & Responsibilities Project Oversight and Operations Produce high-quality documentation that...
ACRT Services Stow, OH, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network West Point, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Associate Principal Scientist, Synthetic Purification AR&D
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...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Principal Scientist, Combination Products - Inhalation Devices
Merck Job Description This position will be responsible for leading and implementing medical device and combination product design controls for both new products and inline products from early design concept definition through commercialization to support regulatory filing, product launch, and post-market surveillance. This position will interact with cross-functional development teams within and external to Device Development. The incumbent must be able to work well with all levels of employees and be able to effectively coordinate the execution of device development strategies. This individual will be expected to apply his/her knowledge of product development and design control principles to positively support and influence clinical and commercial combination product development and launches to ensure they are developed and manufactured in accordance with regulatory, company, and customer requirements. Principal Responsibilities Lead/contribute to device...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network West Point, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
Director, Quality Control
Merck Job Description Ov erview The Director, Biologic Critical Reagents is a senior scientific leader responsible for the strategy, sourcing, development, quality, and lifecycle management of critical biological reagents used across discovery, development, analytical testing, manufacturing, and quality. This role ensures reagent reliability, traceability, and regulatory compliance while driving innovation through robust platforms, process excellence, and strategic partnerships. The Director will lead a multidisciplinary, global team (including first-line managers and scientists) and collaborate extensively across inline and pipeline large molecule product initiatives. Key Responsibilities Reagent Strategy, Governance & Lifecycle Management Define and execute a global strategy for biologic critical reagents (e.g., reference standards, controls, cell banks, antibodies, viral stocks, enzymes, media, assay reagents) across the Large Molecule product...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 14, 2026  
MADC Clinical Research Coordinator Associate
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...
Professional Diversity Network Ann Arbor, MI, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Associate Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)
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...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Associate Director, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)
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...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Sr. Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)
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 a Sr. Specialist - Process Engineer to lead...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)
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 Specialist - Process Engineer to lead...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Associate Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)
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...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Business Practices and Privacy Officer
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...
Professional Diversity Network Panama City, FL, USA Full-Time
Professional Diversity Network
Mar 13, 2026  
Business Practices and Privacy Officer
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...
Professional Diversity Network Guaynabo, Puerto Rico Full-Time
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