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_2959
Contract - 12 Months (possible extension)
Location (mandatory): Carlsbad, CA 92008. We are seeking an experienced Composite Technician to join our team. The ideal candidate will be a U.S. citizen with at least 5 years of hands-on experience in composite manufacturing processes such as prepregs, wet layup, and vacuum resin infusion. The role requires strong technical skills, including the ability to read blueprints, use precision measuring tools, and follow aerospace/defense quality standards like AS9100 and NADCAP. Candidates should be detail-oriented, physically capable of handling up to 50 lbs., and possess strong communication and teamwork skills. Experience with autoclave curing, composite repair, and process improvement (Six Sigma preferred) is highly desirable. Role Definition: The Carlsbad, CA site is looking for a skilled Composites Technician to join our advanced manufacturing team. The successful candidate will be responsible for fabricating, assembling, and repairing composite components. This role requires precision, attention to detail, and the ability to follow strict process controls in support of aerospace, defense, and high-performance product manufacturing.
This position for employment is in the Andover Quality Control Microbiology Laboratory working first shift supporting Laboratory operations Monday through Friday with occasional weekend and holiday coverage. The candidate should be flexible to support both assays performed in the Laboratory, as well as office-based work as needed to support the business. Non-Standard Work Schedule, Travel Or Environment Requirements Some rotational weekend and Holiday coverage is required to support the commercial manufacturing schedule. Adhere to safe work practices and procedures, including aseptic gowning procedures
Location: - Westborough, MA 01581 (On-site) The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines, address excursions and conduct investigations.
Location (mandatory): Portsmouth NH USA 03801 Small Description: The QC Specialist II will join the Quality Control department and assist with technical transfer activities, contributing to the testing and analysis of in-process samples, final product testing, and stability studies. This role requires familiarity with GMP (Good Manufacturing Practices) systems, quality records, and testing methodologies. The individual will work collaboratively to complete complex tasks while ensuring adherence to industry regulations, contributing to method transfers, instrument qualifications, and validation activities.
Location (mandatory): Pleasanton, CA 94588 The Product Manager / Product Evaluator II supports food product development by managing product samples, documentation, testing, and evaluations across multiple categories. This role plays a key part in new product demonstrations, sensory evaluations, and finished product specifications while ensuring food safety, quality, and accurate reporting—enabling product development teams to focus on strategic initiatives.
Location (mandatory): Vacaville California With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.
Location : Cambridge, MA 02141. The CMC Synthetics Platform within the Client R&D organization is responsible for the process development of small molecule drug substances undergoing clinical studies. We are seeking a hands-on laboratory manager with excellent organizational skills to support our activities. The person will provide services to Client at the Cambridge Crossing (CX), Cambridge, MA site. • Provide on-site service to the Client for both laboratory functions and laboratory equipment and instrumentation maintenance and upkeep • Perform experimental protocols to support the Client’s technology platforms • Ensure compliance with health and safety teams and training as required for Client lab operations • Support inventory management, purchasing, and shipping of chemical compounds and laboratory supplies
Location - 11202 El Camino Real San Diego CA USA 92131 The Structural Biology and Protein Sciences group is seeking a highly motivated contractor to support recombinant protein production efforts, primarily utilizing insect cell expression systems. The successful candidate will be responsible for maintaining eukaryotic cell cultures, generating and managing high-titer baculovirus stocks, and performing multi-liter scale protein expression and harvest workflows. Additional responsibilities include executing plate-based expression and purification profiling to enable rapid screening of construct and condition variants. This role requires strong organizational skills, attention to detail, and the ability to operate efficiently in a fast-paced research environment.
Location : Princeton, NJ 08540. Experienced Regulatory Affairs professional responsible for supporting global regulatory operations, ensuring compliance, maintaining regulatory data accuracy in RIMS, and enabling timely market access across multiple jurisdictions. The role requires 5 days a week onsite presence in Princeton, NJ during normal business hours.
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.