Qualifications and Skills. Prior experience with hand tools and equipment maintenance is essential. Basic electrical and pneumatic system understanding is necessary. Proficient written and oral communication skills are required. Familiarity with computer systems and software is preferred. Ability to work independently and as part of a team is crucial.
Job Details. Job Title: Quality Engineer-Medical Device. Job Location: Lafayette, Colorado (On-site). Type: W2 Contract. Duration: Position is 6 months from the start date of the candidate. Job Description. Responsibilities may include the following and other duties may be assigned. Drawing and specification reviews. Manufacturing process control plan reviews. Measurement System Analysis (MSA), Test Method Validation (TMV) reviews. Manufacturing ...
Job Responsibilities. Responsibilities include, but are not limited to, the following. Engage with both Corporate IT and IOPS IT to ensure IT processes and procedures meet Regeneron’s Quality System requirements. Participate in and support Quality Risk Management (QRM) principles during formal and informal risk assessment initiatives. Provide support and guidance for quality system record activities such as change controls, corrective and prevent...
Job Details. Job Title. Sr Electrical Engineer. Job Location. Mounds View, Minnesota. TECHNICAL SKILLS. Must Have. BS ELECTRICAL ENGINEER. FPGA design and development. Nice To Have. AMD / Xilinx FPGA. Preference for individuals with experience implementing video subsystems in a FPGA design. Vivado Design Suite. Top 3 skills sets required. . Less focus on video subsystem design, FPGA lab, FPGA build process, FPGA simulation. Can you please confirm...
Job Title. Quality Compliance & Risk Analyst. Location. Fully onsite in St. Louis. Start Date. ASAP. Job description. We are looking for a Quality Compliance & Risk Analyst to lead risk identification, assessment, and mitigation efforts related to manufacturing processes, product quality, and regulatory compliance. This role will be responsible for ensuring adherence to industry regulations and implementing risk management strategies to enhance o...
Role. GxP Document Control Senior Specialist. Location. Andover, MA (Hybrid - 3 Days Onsite). Duration. 3 Months (With high possibility of Extension). Rate. Competitive - Only USC or GC on W2 or 1099. Position Overview. One of my Customer is seeking a detail-oriented and highly organized GxP Document Control Sr. Specialist (Contractor) to support our Quality Control (QC) and compliance functions. This role is responsible for managing both physica...
Role. CSV Professional. Duration. 6 Months. Onsite / Hybrid / Remote : Fully Onsite. Rate : Open. My Client is seeking a skilled CSV professional with 8-10 years of experience in Computer System Validation (CSV) within biotechnology, along with some project management experience. This role is key in driving projects to successful completion. Responsibilities. Manage CSV processes, including CAPAs, investigations, and deviations. Lead projects fro...
Role. IT Project Manager. Location. St. Paul, MN or St. Louis, MO (Onsite). Duration. 6 months with potential for extension. Open for C2C / W2. Locals Only. About the Opportunity. Join our client, a global leader in drug delivery systems, as an IT Project Manager. This is a dynamic, high-impact role supporting critical SaaS implementation projects in collaboration with implementation partners and internal stakeholders. Key Deliverables. Act as th...
