A fast-growing biotechnology company is expanding their team in Salt Lake City, and they are in immediate need of an. Equipment Qualification Specialist. to support them fully onsite for. 6 months. The Quality Control (QC) team is seeking an equipment qualification and Empower integration specialist to support the onboarding, qualification, and performance verification of new analytical laboratory equipment in preparation for GMP commercial readi...
A fast-growing biotechnology company is expanding their team in Salt Lake City, and they are in immediate need of a. Stability Coordinator. to support them fully onsite for. 12 months. This specialist will support the QC team by planning, executing, and maintaining cGMP stability programs from Phase 1 through Commercial. Depending on team needs, this role may also support Environmental Monitoring (EM) trending in partnership with QC Microbiology,...
A fast-growing startup Biotechnology company is in need of a. QA Specialist for 12 months. This is a. fully remote. position scheduled for. 30 hours/week although this could fluctuate depending on the client's workload. This consultant will report to the Head of Quality. Target start date is January 12th, 2026. The Quality team is small and they need a QA Specialist who will be focused primarily on batch record review. This consultant needs to ha...
A large pharmaceutical company in Los Angeles is in immediate need of a. CQV Engineer for a 12-month project. this is an onsite position and is 40 hours/week. The client needs. someone with. Facilities CQV experience including EMPQ, Vessel IOV and IOPQ including mixing and temp mapping. They have personnel assigned to Utilities (WFI, Alcohol, N2, Compressed Air, etc.), CIP, Filter Press, Centrifuge, CIP skids and Cleaning Validation. this experie...
A fast-growing biotechnology company is expanding their team in Salt Lake City, and they are in immediate need of a. Sr. Validation Engineer. to support them fully onsite for. 12 months. The Sr. Validation Engineer will serve as a key contributor to process validation and equipment qualification initiatives, supporting GMP biologics manufacturing. This position is responsible for developing and executing validation strategies, authoring protocols...
A fast-growing biotechnology company is expanding their team in Salt Lake City, and they are in immediate need of a. Sr. Validation Engineer. to support them fully onsite for. 12 months. The Sr. Validation Engineer will serve as a key contributor to process validation and equipment qualification initiatives, supporting GMP biologics manufacturing. This position is responsible for developing and executing validation strategies, authoring protocols...
CANDIDATES CURRNETLY WORKING UNDER F1 OPT/F1 OPT STEM/H1-B WILL NOT BE CONSIDERED. W2 CANDIDATES ONLY. MDR Principal R&D Engineer (Through April 2026, with strong potential for extension // Tempe, AZ). Top 3 Required Skills. Process development (i.e. process characterization and validation – DOE, PCR, TMV, IQ, OQ, PQ). Statistics. Strong problem-solving skills. Education Required. Advanced degree in Physics, Mechanical Engineering, Materials Scie...
Job Title. Senior Human Factors Design Engineer (Exempt). Location. Boston, MA (Onsite 4 days/week). Contract Duration. 1 year. Product Line. Surgical OU products. Overview. We’re seeking a Senior Human Factors Design Engineer to apply human factors principles to the design and evaluation of medical devices. This role involves usability testing, risk analysis, and study execution to ensure products are safe, effective, and user-friendly. You’ll w...
Job Title. Supplier Quality Engineer II (Contract – Boulder, CO). Employment Type. Contract through November 2026. W2 only. Location. Boulder, CO. About the Role. Medtronic is seeking a. Supplier Quality Engineer II. to join our team in Boulder, CO. This role focuses on supplier quality management, compliance, and continuous improvement across multiple product lines. You’ll ensure suppliers meet rigorous quality standards, lead audits, support ne...
Supplier Quality Engineer II (Contract through November 2026 // Boulder, CO). Play a key role in client’s quality and compliance by maintaining and updating the Approved Supplier List, supporting supplier-related compliance projects, and ensuring our suppliers meet rigorous quality standards. You’ll qualify new suppliers, lead audits to uphold GMP and regulatory requirements, and work closely with engineering teams to resolve issues and implement...
GMP QUALITY CONSULTANT (6-9 months, Possibility of Extension). SUMMARY. Consultant needed for remote assignment providing senior-level GMP Quality Operations oversight and SME guidance in support of therapeutic production. DUTIES & RESPONSIBILITIES. Review and evaluate compliance of GMP-related documents such as master batch records, executed batch records, deviations, non-conformance, change controls, etc. Quality evaluation for outsourced GMP o...
Duties. Develops, coordinates, and conducts technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE) constructs. Recommends design or test methods and statistical process control procedures for achieving required levels of product reliability. Completes risk analysis studies of new design and processes. Compiles and analyzes performance reports and process control statistics. investigates and an...
