Job Title Administrative Assistant I \ Lab Assistant Location Santa Rosa, CA, 95403 Duration 6 Months Timings 8AM 4 30 PM Roles and responsibilities Enter analytical test data that is received from Tech I's and Tech II's into the lab database. Collect and compile data for review by Certifying Scientist(s). Accurately document and record information for the Scientists to r

Title Regulatory Affairs Project Leader Location Santa Clara, CA, 95054 USA Duration 12 Months Job Description Education Bachelor's degree required, Masters degree preferred Experience Minimum of 3 years experience Skills Knowledge of US and/or Canadian regulation relating to product and/or device clearance (FDA) Duties Assists in definition/implementation of regulatory s

Position Title Financial Analyst Location Pleasanton CA USA 94588 Duration 06 months. The Financial Analyst will be an FP&A professional supporting Heart Failure Operations. This position will be partnering with various levels of business teams to drive financial ownership, cost efficiency, and business excellence. Scope of responsibilities include supporting the Operatio

Title Phlebotomist I Location Fremont CA 94538 Duration 8 Months Shift 7 am 4 pm Monday Friday with rotating Saturdays The Patient Services Representative I (PSR I) represents the face of the company to patients who come in, both as part of their health routine or for insights into life defining health decisions. The PSR I draws quality blood samples from patients and pre

Title Phlebotomist I Location North Hollywood, CA (91607) Duration 6 Months Shift Central zone. 8AM 5PM PST Hrs/Wk 40.00 Summary The Patient Services Representative I PSR I represents the face of the company to patients who come in, both as part of their health routine or for insights into lifedefining health decisions. The PSR I draws quality blood samples from patients

Seeking candidate with experience with international (outside of EU and US) product registrations; experience working with medical device operations on control of product release; experience working with electronic change management/document control systems. Duties Responsible for implementing and maintaining the effectiveness of the quality system. Supports manufacturing

Job Title Regulatory Specialist II Location Alameda, CA (94502) Duration 12 Months Shift 8 AM to 5 PM Experience Background (Any) Medical Device, Pharmaceutical, Regulatory Affairs, Quality Assurance, SW Engineering, APAC regulatory submission, or APAC related work under Quality Assurance/Engineering. Job Description (Expectation) Responsible for regulatory activities, in

Perform general maintenance, installation, and repair duties and perform a variety of duties relative to facilities maintenance areas of responsibility. Ensures all appropriate building standards are maintained at a high level of quality. Works independently (i.e. with minimal supervision) as well as within the context of a team. Other duties as assigned by the Manager or

Read, understand, and follow written Standard Operating Procedures Correctly identify analyzed samples and verify the accuracy of sequence for each batch Process acquired instrument data and generate appropriate reports Conduct the first review of GC/MS and/or LC/MS/MS analytical data by each assay SOP Transcribe or upload results to the LIS for final review and certifica

Perform routine tasks such as media/buffer preparation, thawing of cryopreserved cells, cell culture passaging, aseptic sampling and banking competently and independently to support ongoing projects in cell culture lab Take routine analytical measurements for cell growth, gas content analysis, pH, osmolality, nutrient and metabolite measurements and HPLC analysis of monoc