Manufacturing Technician II
About The Position
The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Manufacturing Technician II. Under general supervisor, the scope of this position is responsible for a variety of moderately complex assembly and non-assembly functions in support of manufacturing goals. This position will be onsite in San Diego, CA.
Requirements
- High school diploma or equivalent required
- Two to four years of related experience required
- This position is not currently eligible for visa sponsorship.
Nice To Haves
- Knowledgeable of federal and other regulations, e.g. QSR’s, ISO, ISO 13485, CMDR
- Computer operated experience required
- Knowledge of MS Office and manufacturing systems required
- Experience with working with semi-automated equipment required
- Basic knowledge of GMP, Documentation Practices required
- Demonstrates commitment to the development, implementation and effectiveness of Quidel Quality Management System per ISO, FDA and other regulatory agencies
- Understands and is aware of the quality consequences which may occur from the improper performance of their specific job.
- Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities
Responsibilities
- Responsible for completing set-up operations for one or multiple of the following: assembly, packaging and prep operations in compliance with approved documentation and QSR
- Responsible for the completion and accuracy of moderately complex documentation associated with the manufacturing processes
- Responsible for cleaning, performing and documenting routine equipment maintenance and minor repair
- Assists in Lean Initiatives, e.g. Kaizen team, metric tracking
- Responsible for record keeping
- Responsible for supporting new equipment installation and validation
- Carries out duties in compliance with established business policies.
- May be required to successfully complete cross-training in other areas
- May be required to assist in training of temporary and manufacturing personnel
- May be required to conduct area clearance signoffs
- May be required to comprehensively review documents and sign for review check
- Perform other duties & projects as assigned
Benefits
- QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays.
- All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
