At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.
2025. All right reserved.
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): 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 (mandatory): Houston TX The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.
Location : Remote We are seeking a detail-oriented and innovative Marketing Healthcare Writer to join our team. This role focuses on creating accurate, engaging, and compliant digital content for diverse promotional channels within the healthcare sector. The ideal candidate will collaborate closely with the marketing team and leverage AI-driven tools to streamline content development while ensuring quality and compliance
Location : Portsmouth NH Validation Engineer II responsible for Computer System Validation (CSV) in a regulated biotech/pharma manufacturing environment, ensuring GMP compliance for automation, process control, and MES systems while supporting site and process improvement initiatives.
Location : Cambridge MA, USA 02142 The Analytical Development team is seeking a highly self-motivated analytical chemist to join us for a 12-month contract. This role will support analytical method development for small molecule and oligonucleotide programs. This position requires expertise in analytical chemistry and extensive experience in analytical techniques such as LC, LC-MS, GC, and GC-MS. The position also requires adequate knowledge of organic chemistry or pharmaceutical science. Hands-on experience with high resolution mass spectroscopy (HRMS) and prep LC would be a plus.
Location: Rockford, IL 61103 Performs a variety of laboratory tasks under the supervision of a Scientist/Researcher. The technician will use both standard procedures and adapted processes to support specific projects and routine operations, while collaborating with maintenance staff to ensure smooth equipment functioning.
Location : Sanford, NC. The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation.
M-F, 8am - 5pm. Full time, No OT... 100% Remote, Needed for at least one year, high possibility to extend for the full two years, No specific area/degree but must have a Bachelors Degree minimum... Candidate must be willing to participate/lead meetings and team calls occasionally. Manager values a candidate that is highly driven to learn to skills and take on new projects voluntarily. Manager likes candidates that are inquisitive. Need someone who is HIGHLY analytical. They'll be searching various systems, if they see something wrong they'll need to "go down the rabbit hole" to find out "why?" Need strong critical thinking skills to know when to search system to system for various bits of info. Must have experience working with multiple large data management systems, contracts and pricing, and/or contract development and analytics. Must have very strong writing/grammar and communication skills. Needs to have high attention to detail and accuracy. Interviews will be one with manager and then a panel interview. Must be able to perform high level Excel functions, formulas, vlook-ups. BONUS - manager would like to see Excel test scores. Resolve membership affiliation and inquiries from account management teams. Monitor Revenue Manager platform and boundary systems to confirm data accuracy. Responsibility for managing daily business tasks and processes with internal/external key stakeholders. Access and process data within reporting tools, including Revenue Manager, MicroStrategy, and boundary systems. Communicate and resolve membership discrepancies with internal and external customers; resolve inquires, maintain synchronization and integrity of membership. Create, maintain, and support a collaborative environment with external customers and internal business partners. Responsible and accountable for data compliance activities within membership and the oversight and execution of applicable processes and business decisions to achieve compliance. Ensure accurate and up-
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.