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Manufacturing & QC Associate I

CareDxBrisbane, Australia | California, United StatesOnsite
This job is no longer open

Title: Manufacturing & QC Associate I 
CareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients. The Manufacturing & QC Associate I will be an integral part of the Lab Services team, responsible for producing high-quality reagents to support patient testing in our Clinical Lab.

This role includes participation in routine manufacturing and process development activities and provides support in troubleshooting and process improvement efforts. The Manufacturing & QC Associate I reports directly to the Supervisor, Manufacturing & QC. This is a full-time onsite position based in our Brisbane, CA Clinical Lab. 

Responsibilities:


  • Participate in the routine manufacturing and quality control of reagents required for diagnostic assays, including inspection of raw materials and consumables.
  • Assistin resolving routine problems that arise in the manufacturing process and escalate issues as needed.
  • Assistin scheduling and prioritizing production tasks to meet customer demand and ensure efficient operation of the Manufacturing department.
  • Support process development, product transfer, and validation activities, as needed.
  • Workcollaboratively with various departments (e.g., CLIA Lab, Quality Assurance, Supply Chain, R&D, Automation and Process Engineering) on cross-functional projects and activities.
  • Utilize established SOPs and QC testing procedures, maintainaccurate records, and assist in developing new documentation as needed.
  • Work with Supply Chain to ensure adequate supply and material replenishment, maintainingaccurate inventory records.
  • Support Quality Management System guidelines, participate in internal audits, and ensure compliance with cGMP standards.
  • Promotea safe work environment and adhere to all EH&S regulations and requirements.
  • Perform other related duties and assignments as required. 

Qualifications:


  • BA/BS in Biological or Life Sciences with at least 0-3 years of related experience in a Manufacturing or Clinical Laboratory environment.
  • Knowledge and hands-on experience in molecular biology concepts and techniques. Familiarity with reagent manufacturing, real-time PCR and/or NGS workflows is preferred.
  • Good problem-solvingskills and escalate quality issues in a timely manner. 
  • Ability to work as part of a high performing team and collaborate effectively with staff.
  • Ability to follow instructions and learn new things quickly.
  • Good time management skills and ability to multitask effectively.
  • Ability to work independently, but also within a team environment.  
  • Self-motivated, well organized withgood attention to detail.  
  • Ability to adapt and work in a dynamic environment.
  • Highly organized with the ability to multi-task and adapt to changing priorities and deadlines.
  • Strong interpersonal, verbal, and written communication skills. Ability to effectively communicate in one-on-one or group settings.
  • Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook. 

Additional Details:


Every individual at CareDx has a direct impact on our collective mission to improve the lives of organ transplant patients worldwide. We believe in taking great care of our people, so they take even greater care of our patients.  Our competitive Total Rewards package includes: 

  • Competitive base salary and incentive compensation
  • Health and welfare benefits including a gym reimbursement program
  • 401(k) savings plan match
  • Employee Stock Purchase Plan
  • Pre-tax commuter benefits
  • And more!

In addition, we have a Living Donor Employee Recovery Policy that allows up to 30 days of paid leave annually to a full-time employee who makes the selfless act of donating an organ or bone marrow. With products that are making a difference in the lives of transplant patients today and a promising pipeline for the future, it’s an exciting time to be part of the CareDx team. Join us in partnering with transplant patients to transform our future together. CareDx, Inc. is an Equal Opportunity Employer and participates in the E-Verify program. By proceeding with our application and submitting your information, you acknowledge that you have read our U.S.

Personnel Privacy Noticeand consent to receive email communication from CareDx. ******** We do not accept resumes from headhunters, placement agencies, or other suppliers that have not signed a formal agreement with us. #LI-Hybrid #LI-In Office 

This job is no longer open

Life at CareDx

CareDx: Transforming Transplant Patient Care Through Novel Surveillance Management Solutions CareDx, Inc. is dedicated to improving the lives of organ transplant patients through non-invasive diagnostics. By combining the latest advances in genomics and bioinformatics technology, with a commitment to generating high quality clinical evidence through trials and registries, CareDx is at the forefront of organ transplant surveillance and pre-transplant HLA typing solutions. NASDAQ:CDNA About AlloSure® AlloSure is the first and only non-invasive blood test that directly measures allograft injury and identifies the probability of active rejection to better manage kidney transplant patients. AlloSure is a clinical-grade, proprietary Next-Generation Sequencing (NGS) based test to detect donor-derived cell-free DNA (dd-cfDNA) in order to identify organ injury in kidney transplant recipients. AlloSure is analytically validated as a sensitive, specific, and precise measurement of dd-cfDNA. AlloSure detects active rejection (acute active ABMR, chronic active ABMR, or TCMR) with high accuracy, outperforms serum creatinine in kidney transplant recipients, and is highly sensitive in distinguishing ABMR from no ABMR. AlloSure is performed in the CareDx CLIA-certified laboratory. http://www.allosure.com/ About AlloMap® AlloMap Molecular Expression Testing is a non-invasive blood test used to aid in the identification of heart transplant recipients with stable allograft function who have a low probability of moderate/severe acute cellular rejection at the time of testing in conjunction with standard clinical assessment. AlloMap testing measures the expression levels of 20 genes from a blood sample. The combined expression of these genes is represented as an AlloMap test score. AlloMap is performed in the CareDx CLIA-certified laboratory and has been commercially available in the United States since 2005. AlloMap was cleared by the U.S. Food and Drug Administration in 2008 and was CE marked for the European Union in 2011. Use of AlloMap is also included in the International Society for Heart and Lung Transplantation (ISHLT) Practice Guidelines, published in August 2010, the worldwide standard for the care of heart transplant patients. http://www.allomap.com/
Thrive Here & What We Value1. Focus on improving the lives of organ transplant patients worldwide2. Taking great care of our people, so they take even greater care of our patients3. CareDx offers products, testing services, and digital healthcare solutions along the pre and post-transplant patient journey4. CareDx is the leading provider of genomics-based information for transplant patients5. Competitive Total Rewards package including: Competitive base salary and incentive compensation, Health and welfayer benefits, 401(k) savings plan match, Employee Stock Purchase Plan, Pretax commuter benefits
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