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Production Chemist 3

Job Overview

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Compensation

Hourly
Range $26.50 - $39.25
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Benefits

Health Insurance
Dental Insurance
Vision Insurance
Paid Time Off
401(k) Plan
Tuition Reimbursement
Career development opportunities

Job Description

Dexcom Corporation, listed on NASDAQ under the symbol DXCM, stands as a trailblazer and global frontrunner in continuous glucose monitoring (CGM) technology. Since its inception, Dexcom has been driven by an ambitious mission to revolutionize diabetes management and unlock critical insights that enhance health outcomes. With over 25 years of pioneering change, Dexcom has shaped the CGM industry and continues to expand its vision beyond diabetes. The company now focuses on empowering individuals to take control of their overall health by leveraging personalized, actionable data aimed at addressing significant health challenges. Dexcom is committed to a broader goal of improving human health worldwide through innovative biosensing technologies.

The company boasts a dedicated workforce of passionate professionals who embrace a warrior mentality toward earning customer trust, operating with integrity, thinking innovatively, and demonstrating reliability. Having already transformed millions of lives, Dexcom aspires to reach millions more across the globe. Their growth strategy involves evolving into a leading consumer health technology company, while maintaining a focus on developing solutions for serious medical conditions. Constant innovation in biosensing technology remains the cornerstone of the company’s ongoing success and ambitious future.

Joining Dexcom means becoming part of the San Diego Pilot Operations team, a dynamic group focused on the critical frontiers of continuous glucose monitoring device development and testing. The Production Chemist 3 role at Dexcom involves leading analytical testing efforts for materials and parts that underpin both current and next-generation biosensor designs. This includes close collaboration with interdisciplinary teams such as research and development scientists, sustaining quality engineers, and process development engineers. The role demands maintaining current Good Manufacturing Practice (cGMP) compliance, developing and refining test methods, and providing technical guidance and training to team members, including new hires. The position also includes responsibilities related to the installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) processes for new analytical instruments introduced to the laboratory.

The ideal candidate thrives in a fast-paced, evolving environment and approaches challenges with a positive, solution-oriented mindset. The role plays a pivotal part in ensuring samples are accurately tested using sophisticated analytical equipment and techniques, and results are precisely analyzed, reviewed, and reported. The chemist will contribute to method development, validation, and improvements as necessary to support quality and innovation. Prioritizing safety and adherence to 6S principles within the laboratory environment is essential. Additionally, maintaining meticulous documentation—including test reports, deviations, and analytical data—is critical to operational excellence. The Production Chemist 3 will further lead or support investigations related to deviations or out-of-specification results and partake in regular maintenance of critical analytical instruments.

With a salary range from $100,700 to $167,900, this full-time opportunity not only offers an exciting role within a cutting-edge biotechnology company but also opens doors to substantial career growth and skill development in analytical chemistry within highly regulated industries. Candidates with backgrounds in pharmaceuticals, medical devices, or polymer industries, and proficiency in advanced analytical techniques such as High-Performance Liquid Chromatography (HPLC) and Gel Permeation Chromatography (GPC), statistical data analysis, and regulatory compliance stand to thrive and drive significant impact at Dexcom.

Job Requirements

  • Typically requires a Bachelor’s degree in a technical discipline
  • Minimum of 5-8 years related experience or a Master’s degree and 2-5 years equivalent industry experience or a PhD and 0-2 years experience
  • Experience in analytical chemistry and quality control in regulated industries
  • Proficiency in HPLC and GPC techniques
  • Ability to perform statistical data analysis
  • Strong problem-solving abilities
  • Willingness to maintain safety standards and 6S practices
  • Ability to conduct method validation and improvements
  • Effective communication and teamwork skills

Job Qualifications

  • Bachelor’s degree in a technical discipline such as analytical chemistry
  • Several years of experience in analytical quality control within pharmaceutical, medical device, or polymer industries
  • Proficiency in complex analytical techniques and instruments including GPC and HPLC
  • Experience defining and executing test method validation
  • Experience conducting statistical analysis of laboratory results
  • Experience reviewing and taking corrective action in response to technical or operational issues related to analytics and instrumentation
  • Excellent problem-solving skills and attention to detail
  • Knowledge of regulatory requirements for medical devices or pharmaceuticals (Part 11 compliance) is a plus
  • Knowledge of lean manufacturing and testing principles is a plus

Job Duties

  • Provide technical leadership for the analytical chemical and material analysis for pilot test and chemistry labs
  • Perform chemical analysis of samples following ASTM standard methods and internally developed methods including HPLC, GPC, glucose concentration analysis, DSC, SEM, Karl Fischer titration, DLS, and UV-Vis spectroscopy
  • Perform data analysis on results and statistical analysis on data and secondary data review when required
  • Ensure samples are processed in a timely and efficient manner and provide regular reports on the status of sample analysis
  • Assist in method development, method validation or method improvement as needed
  • Maintain a safe working environment and adhere to safety protocols and 6S practices
  • Maintain accurate records for all laboratory activities including test results, deviations, and reports
  • Lead or support investigations of deviations or results that are out-of-specification
  • Maintain analytical instruments and perform minor routine maintenance on instruments as required

Job Criteria

Experience

Mid Level (3-7 years)


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