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_2108
Contract - 12 Months
Location : Belvidere, NJ 07823. • The QC Analyst is responsible for analyzing and testing raw materials, intermediates, stability samples, and finished products under cGMP guidelines using validated or compendial methods. • The role involves performing laboratory analysis with minimal supervision, preparing reagents and standards, calibrating and operating instruments (HPLC, GC, ICP, etc.), and maintaining accurate documentation. • The analyst supports product release testing, investigates out-of-specification results, and ensures compliance with safety, quality, and regulatory standards. • Candidates should hold a degree in a relevant scientific discipline, have 0–3 years of laboratory experience, and demonstrate knowledge of quality control techniques, GMP, and safety practices. • Flexibility to work shifts, overtime, and weekends is required. • 0-3 years of lab experience • Experience in Microsoft Office (outlook, word, and excel) • The schedule may be structured with a required overtime component built in. • Candidates must be able to work shifts, weekends, overtime (including coverage) and holidays as required. • All candidates, both internal and external, applying for this position understand that overtime may be required and adjusted based on business needs and to ensure continued safe operations. Position content- • Key areas of accountability/responsibility • Performs analysis in the laboratory with minimal supervision. • Prepares standards, mobile phases, and reagents. • Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.) • Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods. • Performs calculations, collects and prepares data for evaluation. • Keeps supervisor informed of work status • Investigation of OOS results under guidance of senior staff • Maintains good documentation practices.
Location : Plainsboro, NJ 08536. Panelists will participate in sensory evaluations of food, beverages, and odorant samples, both individually and in groups, under the guidance of a panel leader. Responsibilities include following detailed instructions, completing evaluations using ballots or digital devices, and contributing to group discussions. Applicants must complete sensory screening tests prior to panel admission, with compensation provided for participation. Requirements: No experience required. Must be able to commit to at least 1 year of testing. Sensory evaluations will occur every Wednesday from 9:30am to 12:30pm. Please note: the panel runs during business hours. Must be free of major food allergies and dietary restrictions. Should have good communication skills, willingness to take direction from panel leaders and work well within a team of other sensory panelists. Applicants should have an excellent sense of smell and of taste, as well as the ability to accurately describe what they taste and smell. Applicants should be free of aversions to nearly all common foods and beverages.
Location: Cincinnati, OH (Onsite) The Lab Technician performs a variety of chemical, biological, and physical tests required for research, development or quality control. This position compiles data for reports and assists in special studies in the laboratory and in the field.
Location : San Diego CA The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw materials, in-process, and finished goods for the Molecular Diagnostics Division. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products.
Location : 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.
Location (mandatory): Portsmouth NH • We are seeking a QC Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed.
Location - Marana, AZ The global sub-chapter Production Engineering - Change Services is part of the global Engineering Chapter responsible for cost efficient, reliable and lean Change Control Management (ECRs). The scope of this team is mainly on Product Care topics for established products and introduction of new products from pilot phase to commercial production. The sub-chapter brings in technical expertise to deliver successful material, system, process and product changes.
The Data Assurance Associate (GPV) plays a vital role in ensuring the accuracy, compliance, and quality of case processing activities within Pharmacovigilance. This role involves active communication with internal teams, external partners, and vendors to address case-related queries, oversee case corrections, and support training initiatives. The associate will contribute to maintaining the highest standards in pharmacovigilance operations while driving process improvements and compliance with global regulatory requirements.
Location : Vacaville CA Under moderate supervision, QC Specialist is expected to support planning, managing, and executing projects related to the product portfolio for Vacaville Quality Control. These projects include analytical transfers, control system updates, regulatory filings and other activities associated with the life-cycle of a product.
Location - Vacaville California Responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Roche/Genentech corporate principals, quality policies, standards and core values. Maintains company’s right to operate, supply to patients, and cost effectiveness by actively participating in continuous improvement projects
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.