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R & D Jobs

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Join our Team Monolith invents, develops, and perfects process technologies that produce chemicals and materials that billions of people use every day. We’re builders. Innovators. Pragmatists. We believe that technology holds the solutions to climate change. That cleaner technology is better technology. At Monolith we apply scientific principles, engineering practices and a lot of hard work to s...

QA LAB SUPERVISOR Ft. Atkinson, WI Since 1909, the OSI Group has been a leader in the food processing industry. Our organization is committed to quality and excellence. OSI produces private label products, including the On-Cor Frozen Foods brand, out of our facility in Ft. Atkinson, WI. We welcome you to explore our world of food solutions and to discover more of what OSI can do for your career....

SUMMARY: The Analytical Chemist reporting to R&D Director. The Analytical Chemist is responsible for performing development and validation of analytical process. NOTE: Only the most qualified applicants will be interviewed. RESPONSIBILITIES: The Analytical Chemist will be responsible for maintaining all existing and new chemical instrumentation by performing routine maintenance and working wit...

TechData Service Company is a staffing firm for clinical professionals. Our clients are most of the major pharmaceutical companies and many other CROs, pharmaceutical and Biotechnology companies. We can often submit your resume to multiple companies and for multiple positions with multiple clients. If you are interested in these positions please contact Lu Cheng at ***** or...

Overview This individual will be responsible for the daily administration of a global LabWare LIMS instance for site. Will work closely with end-users to develop, troubleshoot, and support system based on business needs. Ability to work across sites and disciplines on maintenance and continuous improvement activities. Responsibilities Must be familiar with laboratory processes and workflows, an...

Overview The incumbent will be an experienced medical writer with specialization in clinical pharmacology. He/she will manage and oversee the preparation of clinical study protocols, clinical study reports, Investigator's Brochures, clinical pharmacology sections of US and EU clinical trial applications and marketing applications, and other high-level summary, briefing, and response documents in ...

Responsibilities We are seeking a highly motivated individual with experience in anti-drug antibodies assay development, validation and implementation in support of immunogenicity assessment of biological therapeutics. You will be a member of Global Bioassays and Technology, which plays a critical role in development of biological therapeutics from late stage of research, IND enabling GLP studies...

Overview Teva's innovative global R&D is hiring a Personalized Medicine and Pharmacogenomics (PMP) Expert, for a dynamic position responsible and accountable for devising and executing the PMP strategy, serving as the point person for scientific advice on portfolio compounds and new business development opportunities. The PMP Expert will work collaboratively with interfaces across the entire comp...

ASSOCIATE SCIENTIST II FOR BIOMARKER DETECTION REQUIREMENT # 15-01159 RECRUITER: TROY SANDERS JOB LOCATION: MOUNTAIN VIEW, CA AUGUST 14, 2015 Project Description: Major Duties and Responsibilities: Develop and validate immunoassays to detect soluble biomarkers. Perform sample testing. Possibly develop and/or conduct flow cytometry and/or fluorescence imaging cell-based assays using primar...

Overview: To ensure the quality of raw materials, formulations and finished product. Two shifts currently available: Tuesday - Saturday, 2 pm - 10:30 pm and Monday - Friday, 10 pm - 6:30 am Qualifications: Must have High School Diploma or GED. Must have college chemistry and/or quality laboratory experience. Must have a positive team building attitude with references to verify. Must be able...

Seeking a Clinical Manager for a consulting position at a pharmaceutical client. Skills: - ≥ 3 years technical and operational experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organization. - Proven ability to work independently and ability to collaborate and work effectively in teams. - Demonstrated ability to suppor...

Job ID: 39746 Position Description: Clean Harbors is the leading provider of environmental, energy and industrial services throughout North America. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean ...

Job ID: 39825 Position Description: Safety-Kleen Systems, a Clean Harbors Co., has a commitment to excellence deeply rooted in a strong sense of tradition. Our entire business model revolves around keeping North American businesses green. We generate more than $1.2 billion in annual revenue as a world-class environmental service organization and market leader in industrial hazardous waste manage...

Responsibilities We are seeking highly motivated individuals to join our team which is responsible for immunogenicity assessment of biologics by developing and implementing anti-drug antibodies assays. You will also be a member of Global Bioassays and Technology, which plays a critical role in development of biological therapeutics from late stage of research, IND enabling GLP studies, clinical t...

Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...

ADMINISTRATIVE ASSISTANT MUST HAVE PHARMACEUTICAL INDUSTRY EXPERIENCE REQUIREMENT #15-01152 RECRUITER: ANITA JORDAN JOB LOCATION: JERSEY CITY, NJ AUGUST 13, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The increase to both size and scope of the MCCM group has led to a need for incremental administrative support in order to provide for the increase...

Theradex® is an international contract research organization providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic test in the areas of oncology and life-threatening diseases for over 30 years. Theradex® conducts studies which lead to marketing approval of significant advances; and has built a reputation on as...

Our Company Akorn, Inc. is a niche pharmaceutical company that develops, manufactures and markets generic and branded prescription pharmaceuticals as well as animal and consumer health products. We specialize in difficult-to-manufacture sterile and non-sterile dosage forms including: ophthalmics, injectables, oral liquids, OTC’s, topicals, inhalants, and nasal sprays. Akorn markets its products t...

Our Company Akorn, Inc. is a niche pharmaceutical company that develops, manufactures and markets generic and branded prescription pharmaceuticals as well as animal and consumer health products. We specialize in difficult-to-manufacture sterile and non-sterile dosage forms including: ophthalmics, injectables, oral liquids, OTC’s, topicals, inhalants, and nasal sprays. Akorn markets its products t...

At Navitas we are domain experts in the areas of Clinical, Regulatory, Safety and Compliance. We pride ourselves on our industry insight, our simplification approach and our pragmatic solutions. Our capabilities cover; industry leading networks, strategic and change management consulting, technology and BPO. We are motivated by the success of our clients; improving outcomes, ensuring compliance an...