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 (mandatory): Chicago, IL The Video team is responsible for designing, implementing, and supporting video solutions across the City. The team partners with multiple city agencies to define requirements and deliver solutions that increase situational awareness for mission critical first responders.
Location (mandatory): 3340 Enterprise Way, Miramar, FL 33025 The Laboratory Technician is responsible for ensuring timely, accurate, and comprehensive processing during screening, admission, study conduct, and discharge procedures. The role supports clinical and laboratory operations while ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory standards.
Location (mandatory): Pearl River, NY 10965. This is a laboratory-based position within the Vaccines Early BioProcess Analytical Development group. The role supports early vaccine development through routine sample testing, analytical method development, and assay qualification studies. The position is highly hands-on, fast-paced, and focused on supporting high-visibility vaccine projects through extensive bench work.
Location: 4745 Wiley Post Way Salt Lake City, UT 84116 Small Description: This is an entry level position. Shift Schedule: Monday - Friday 8:00am - 5:00pm. Job ID: TEVAJP00009751. Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. Focus on candidates who have hands-on bench and laboratory experience (including academic or internship lab work), with exposure to sample preparation, routine testing, and documentation in a lab setting. Prioritize early-career profiles, such as associate-degree level candidates or students currently in school or taking a short break.
Location (mandatory): 66 Hudson Yards Blvd East, New York, NY 10001 (Hybrid) Small Description: This is a full-time, 12-month Contractor/Research Associate (RA) position on the HTA, Value & Evidence (HV&E) Thoracic & Precision Medicine Oncology team within the Global Access & Value (GAV) organization. The Research Associate will provide technical support, analysis, and reporting for assets at various stages of development within the Economics and Outcomes Research (HEOR) function. Interview Schedule: Two rounds of interviews will be conducted: an initial screening interview followed by a team interview.
Health Care Copywriter (Digital & Media Content) This fully remote role is for a Health Care Copywriter who creates compliant, engaging digital and media content for both HCP and consumer audiences. You’ll translate clinical data and approved claims into clear messaging across ads, social, emails, video scripts, and partner platforms, while working closely with designers, marketers, and regulatory teams. The job requires 3+ years of healthcare copywriting experience, comfort with MLR processes, attention to detail, and the ability to leverage GenAI tools to accelerate content without compromising accuracy or compliance.
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): 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): Houston TX The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be responsible for maintaining, stocking, and set-up of clean room environment.
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.