Quality Control Specialist II
Quality Control Specialist II
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Roche fosters diversity equity and inclusion representing the communities we serve. When dealing with healthcare on a global scale diversity is an essential ingredient to success. We believe that inclusion is key to understanding peoples varied healthcare needs. Together we embrace individuality and share a passion for exceptional care. Join Roche where every voice matters.
The Position
Listening and responding to the everchanging needs of people aroundthe world.
The Opportunity
2nd Shift / MonFri 4:00 pm12:30 am Saturdays mandatory during Flu Season Saturdays may be mandatory during Flu Season.
As a Quality Control Specialist II you will conduct incoming inprocess and finalrelease QC testing in a controlled manufacturing environment. You may also implement validation studies and test protocols generate analytical reports investigate NonConformances evaluate processes & procedures apply statistical techniques review specifications and inspect & test equipment. You are collaborating with R&D Manufacturing Quality and Supply Chain within the company and when appropriate with customers and suppliers on qualityrelated issues. Also you are:
- Preparing/formulating QC test solutions including aqueous solutions containing salts organics acids bases and/or modified DNA and organic solutions
- Performing validation and stability studies implementing protocols analyzing data and initiating nonconformances for MRB
- Completing batch records while maintaining good documentation practices cGMP and ISO standards.
- Responsible for timely completion of scheduled work orders and monitoring inventory levels
- Participating in departmental projectsworks with QC members on OOS/NCR/CAPA investigations as needed. Performs complex data analysis and communicates these results to the supervisor and coordinating departments
- Monitoring 5S and inventory levels daily
- Trains new employees on procedures
Who you are
- B.S. degree required in basic sciences life sciences or engineering with five 5 years of relevant experience in a QC capacity
Behaviors competencies and qualities of the ideal applicant.
Technical knowledge of molecular biology including principles of nucleic acid hybridization probe and primer design and enzymatic amplification of specific gene sequences
Safety precautions required for working with biohazards and bloodborne pathogens knowledge
Knowledge of the Quality System; able to implement change orders
Basic statistics relevant to the interpretation and analysis of scientific data. Understanding of molecular techniques (DNA extraction PCR Amplification)
The expected salary range for this position based in California is 48000..00 USD Annual. Actual pay will be determined based on experience qualifications geographic location and other jobrelated factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Relocation benefits are not available for this posting.
Who we are
GenMark is now a proud member of the Roche Group more than 100000 people across 100 countries are pushing back the frontiers of healthcare. As a global leader in healthcare Roche Diagnostics offers a broad portfolio of products tools and services that help in the prevention diagnosis and management of diseases like HPV HIV hepatitis and diabetes as well as other medical conditions such as fertility and blood coagulation. With the addition of GenMark to the Roche Group syndromic infectious disease diagnostics is now added to the long list of disease states and conditions that the Roche Group addresses. GenMarks ePlex true sampletoanswer system offers unique solutions to address the most significant challenges facing clinical laboratories while supporting hospital systems to deliver patientcentered valuebased care. ePlex streamlines the diagnostic workflow from physician order entry to the final test report and is the true sampletoanswer solution designed to improve patient care reduce costs and increase lab efficiency. GenMark is headquartered in Carlsbad California.
GenMark is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individuals race color religion gender sexual orientation gender identity/expression national origin/ancestry age mental/physical disability medical condition marital status veteran status or any other characteristic protected by law.
Required Experience:
Unclear Seniority
Employment Type
Full-Time
