At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.
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sgs-job-4093
Contract - 12 Months
Location (mandatory): Vacaville CA The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
location : Groton, CT 06340 We are seeking a Lab Technician to support necropsy and histology activities for rodent and non-rodent safety studies. This role is responsible for laboratory support functions, specimen handling, equipment maintenance, and ensuring compliance with GLP, SOPs, EHS standards, and animal welfare regulations. Candidates with a background in Histology or Animal Science are encouraged to apply, including entry-level professionals with relevant education
Location : Cambridge, MA 02140 Seeking a Comparative Medicine Trainer to provide hands-on training in laboratory animal techniques, coordinate training programs, support vivarium operations, and ensure compliance with animal welfare regulations. The ideal candidate will have experience working with rodents, laboratory animal training, and regulatory standards in a research environment.
Location (mandatory): Pearl River, NY 10965 (On-site) Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products. This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of highly regulated products. The successful candidate will work in a collaborative team environment while maintaining compliance with cGMP requirements and established laboratory procedures.
Location (mandatory): Tucson, AZ 85755 (Onsite) This is an onsite position for a Research Associate II in Research & Early Development supporting Ventana projects. The role is responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities. The primary focus is on slide imaging and image acquisition using systems such as the DP600s, 200s, VS200, and multispectral flash instruments. The individual will perform repetitive, well-defined tasks including virtual staining and assembling slide cohorts to enable the development of AI algorithms while ensuring compliance with GMP, GLP, Design Control, and company procedures.
Location (mandatory): San Diego, CA 92121 The Bioinformatics RA III or Scientist I (AI/ML – Assay Design) is responsible for developing AI and machine learning solutions to optimize assay and primer design for diagnostic platforms. This role combines bioinformatics, molecular biology, and data science to build intelligent pipelines that analyze high-throughput PCR and sequencing data, enabling data-driven assay development and improved diagnostic performance.
Location (mandatory): Vacaville CA We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.
Small Description: The Quality Control Biochemistry Associate II is responsible for contributing to key functional, tactical, strategic and operational aspects of the large molecule testing for Biochemistry group. This includes performing in-process, release testing, method transfer, validation testing and related activities associated with this testing.
Location : Cambridge, MA 02142 (Onsite) The Analytical Development team is seeking a highly creative and self-motivated candidate to join for a 6-month contract. This role will support the development of small molecule drug substances and drug products by developing innovative analytical technologies and establishing control strategies. The position will be responsible for chromatographic method development using supercritical fluid chromatography (SFC) and requires knowledge of organic chemistry, analytical chemistry, and experience working in a laboratory environment. Experience with analytical techniques such as UV, HPLC/UPLC, and LCMS is required.
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.