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_2145
Contract - 12 Months (possible extension)
Location - South San Francisco, CA 94080. Cell Line Development Research Associate is involved in the creation of stable cell lines for the recombinant adeno-associated viral vector (rAAV) production processes. He/she executes experiments, produces relevant documentation, and works under supervision. He/she will be responsible for: Culturing mammalian cells for viral production in shake flasks, spinner flasks, spin tubes, deep well and automation platforms. Performing experiments in the development, optimization and scale-up of AAV producer cell lines. Preparing process development protocols, data analysis summaries, technical reports, and other relevant process documentation. Optimization of transfection and transduction protocols for newly engineered cell lines. Maintaining an accurate laboratory notebook. Ensuring work conforms to applicable quality and safety standards. Participating on project teams (as needed). Must be able to lift 25 pounds. Due to the inherent nature of cell culture, some weekend work and/or work on holidays may be needed. On occasion, long work hours may be required depending upon the experiment schedule. Handling large volumes of cell culture or related materials, such as tens of liters, may be required. Also, several viral materials, including AAV, may be involved in the work.
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 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 (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.
Location: Research Triangle Park, NC 27709 (Onsite) Responsible for performing testing and sampling of bulk gases, monitoring utility parameters, inspecting raw materials, and collaborating with cross-functional teams including Microbiology and Manufacturing to ensure quality and compliance in research and production activities.
Location : Portsmouth NH 03801. The Dispensing Technician Level 1 supports the manufacturing of therapeutic proteins (API) by dispensing raw materials, including liquids, powders, acids, and bases, under cGMP conditions. This night-shift role requires attention to detail, adherence to cGMP and SOPs, and active participation in safety and quality processes within a controlled Class C environment.
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.