Scientist. Location: RTP, NC. We are seeking an experienced upstream/midstream scientist to support the development and scale-up of biological production processes used within the biopharmaceutical industry. This role involves working onsite in a modern facility and contributing to the production of biological materials that enable effective testing, optimization, and characterization of product performance. Responsibilities. Produce and characte...
Our client is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious or life-threatening medical conditions. They are among the world's leading biotech companies, with multiple products on the market and a promising development pipeline. Overview. The Animal Genetic Technologies department seeks a motivated laboratory researcher who will assist in the discovery of groundb...
Our biotechnology client is seeking a motivated Research Associate to assist in the discovery of groundbreaking therapeutics by supporting the primary research of several hundred internal customers. This is a 12-month contract based in Dixon, California. Responsibilities. Processing high volume samples in the laboratory (both manually and via laboratory robotics). Analyzing and performing quality control of genetic data. Helping to evaluate and i...
Our client, a leading organization in the scientific and healthcare industry, is seeking a Scientist I to join their team. As a Scientist I, you will be part of the Post Market Safety department supporting safety evaluation and regulatory compliance. Job Title. Scientist I. Location. Clark, New Jersey. Pay Range. $29.41 per hour. What's the Job. Prioritize workload for US OTC/Medical Devices & Hospital visit cases, data entry, MedDRA coding, and ...
R&D Partners is seeking to hire a. Research Associate, Analytical Development I. in. Newark, CA. Your main responsibilities as a. Research Associate, Analytical Development I. Perform and assist principal investigators with animal studies that may include. Dose administration – IP (intraperitoneal), intradermal, subcutaneous (SQ), intramuscular (IM), and oral gavage. Daily mice weighing, daily scoring after dosing completion. Assist team with dai...
Piper Companies. is seeking a. Validation Engineer (CQV – LCMS). in. Titusville, NJ. to support an industry-leading pharmaceutical organization. This role focuses on commissioning, qualification, and validation of LCMS and analytical laboratory equipment in a GMP environment. Responsibilities for the Validation Engineer (CQV – LCMS). Execute IQ/OQ/PQ for LCMS and other analytical instruments. Develop and maintain CQV documentation (URS, protocols...
Sr. Validation Engineer – Wilson, NC (Onsite Only). Long Term Contract. We’re seeking an experienced. Sr. Validation Engineer. to support ongoing commissioning, qualification, and validation activities at a large-scale pharmaceutical manufacturing site in. Wilson, NC. This role requires strong hands-on experience with equipment and automation system qualification, excellent documentation discipline, and the ability to work cross-functionally in a...
Job Description. We're seeking a CQV Validation Specialist to perform commissioning, qualification, and validation (CQV) of process equipment, utilities, and facilities for a regulated pharmaceutical manufacturing site. The ideal candidate will have hands-on experience with IQ/OQ/PQ, cleaning validation, and temperature mapping in GMP environments. Responsibilities. Execute and author IQ/OQ/PQ protocols for equipment, utilities, and facilities pe...
Job Description. We're seeking a CQV Validation Specialist to perform commissioning, qualification, and validation (CQV) of process equipment, utilities, and facilities for a regulated pharmaceutical manufacturing site. The ideal candidate will have hands-on experience with IQ/OQ/PQ, cleaning validation, and temperature mapping in GMP environments. Responsibilities. Execute and author IQ/OQ/PQ protocols for equipment, utilities, and facilities pe...
Research Technician Title: Research Technician Location: Chicago, ILReports to: Supervisor of Toxicology Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manuf...
About The Job CQV Engineer. Position: CQV Engineer. Company Overview. PharmEng Technology is a leading global provider of engineering and consulting services to the pharmaceutical and biotechnology industries. We specialize in providing innovative solutions to our clients to help them achieve their goals in drug development, manufacturing, and compliance. Job Summary. We are seeking a highly motivated and experienced CQV Engineer to join our team...
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career tha...
