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_2480
Contract - 12+ Months (possible extension)
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 (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.