CPT Clinical Operations Lead Jobs
Clinical Operations Lead roles sit at the intersection of healthcare delivery and project management, making them a strong CPT fit for graduate programs in public health, health informatics, or healthcare administration. Your DSO must confirm the role directly advances your degree requirements before CPT authorization is granted.
See All Clinical Operations Lead JobsOverview
Showing 4 of 4+ Clinical Operations Lead jobs
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
See all Clinical Operations Lead jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Operations Lead roles.
Get Access To All JobsINTRODUCTION
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 Associate Operator. Under close supervision, this position is responsible for a variety of assembly and non-assembly functions in support of manufacturing goals.
This position will be onsite in Carlsbad, CA.
THE RESPONSIBILITIES
- Operates equipment used to manufacture products.
- Checks and inspects products against departmental procedures.
- Responsible for recognizing product or equipment problems that arise during the manufacturing process.
- May be required to assist with the set-up and clean-up of manufacturing equipment.
- Responsible for Lean Initiatives.
- Carries out duties in compliance with established business policies.
- Performs other duties and projects assigned.
THE INDIVIDUAL
Required:
- 0 - 2 years of related experience required.
- Basic knowledge of regulations (FDA, ISO, OSHA, etc.).
- 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.
- This position is not currently eligible for visa sponsorship.
Preferred:
- High school diploma or equivalent.
- Experience in medical device manufacturing.
- MS Office and manufacturing systems.
THE KEY WORKING RELATIONSHIPS
Internal Partners:
Mechanics, Engineers and Management
External Partners:
Vendors and Contractors
THE WORK ENVIRONMENT
The work environment characteristics are representative of a manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Works on assignments that are routine in nature.
THE PHYSICAL DEMANDS
Position requires ability to lift up to 50 lbs. on a regular basis. May be required to perform repetitive manufacturing processes (e.g., manual lamination, manual cassette assembly, pouch inspection, etc.) up to 90% of workday. Walking, standing, and/or sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted.
SALARY TRANSPARENCY
The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $41,365.59 - $52,741.13 and is bonus eligible. 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.
EQUAL OPPORTUNITY
QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.
INTRODUCTION
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 Associate Operator. Under close supervision, this position is responsible for a variety of assembly and non-assembly functions in support of manufacturing goals.
This position will be onsite in Carlsbad, CA.
THE RESPONSIBILITIES
- Operates equipment used to manufacture products.
- Checks and inspects products against departmental procedures.
- Responsible for recognizing product or equipment problems that arise during the manufacturing process.
- May be required to assist with the set-up and clean-up of manufacturing equipment.
- Responsible for Lean Initiatives.
- Carries out duties in compliance with established business policies.
- Performs other duties and projects assigned.
THE INDIVIDUAL
Required:
- 0 - 2 years of related experience required.
- Basic knowledge of regulations (FDA, ISO, OSHA, etc.).
- 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.
- This position is not currently eligible for visa sponsorship.
Preferred:
- High school diploma or equivalent.
- Experience in medical device manufacturing.
- MS Office and manufacturing systems.
THE KEY WORKING RELATIONSHIPS
Internal Partners:
Mechanics, Engineers and Management
External Partners:
Vendors and Contractors
THE WORK ENVIRONMENT
The work environment characteristics are representative of a manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Works on assignments that are routine in nature.
THE PHYSICAL DEMANDS
Position requires ability to lift up to 50 lbs. on a regular basis. May be required to perform repetitive manufacturing processes (e.g., manual lamination, manual cassette assembly, pouch inspection, etc.) up to 90% of workday. Walking, standing, and/or sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted.
SALARY TRANSPARENCY
The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $41,365.59 - $52,741.13 and is bonus eligible. 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.
EQUAL OPPORTUNITY
QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.
See all Clinical Operations Lead jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Operations Lead roles.
Get Access To All JobsClinical Operations Lead CPT: Frequently Asked Questions
Does a Clinical Operations Lead role qualify for CPT authorization?
CPT eligibility depends on whether the role is an integral part of your curriculum, not the job title itself. A Clinical Operations Lead position typically qualifies for students in public health, health informatics, or healthcare administration programs when duties include project oversight, cross-functional coordination, and quality improvement work that maps to your coursework. Your DSO makes the final determination based on your specific program requirements.
Can I work full-time as a Clinical Operations Lead on CPT?
Full-time CPT authorization, meaning 20 or more hours per week, is allowed but has consequences. Twelve months of full-time CPT eliminates your OPT eligibility entirely, which removes your post-graduation work authorization window. Most students in clinical operations programs choose part-time CPT during the academic year and reserve full-time authorization for internship semesters where the credit is built into their degree plan.
What documents do employers need to hire me on CPT?
Your employer needs your I-20 with the CPT authorization endorsed on page two, showing the employer's name, role description, and authorized dates. They'll also need your I-94 arrival record and passport. For I-9 verification, CPT is documented under List A using your foreign passport plus I-20. Some compliance teams also request a letter from your DSO confirming the authorization, so carry one to your first day.
How do I find Clinical Operations Lead roles open to CPT students?
Search Migrate Mate for Clinical Operations Lead postings filtered for international students. Clinical operations hiring is concentrated in hospital systems, contract research organizations, and health technology companies, and many of those employers have prior experience with CPT authorization. Narrowing to employers with LCA filing history through the OFLC Wage Search also helps identify organizations already comfortable with international student work authorization requirements.
Does CPT for a Clinical Operations Lead role count toward H-1B eligibility later?
CPT itself doesn't affect H-1B eligibility, but the work experience you build in clinical operations strengthens your specialty occupation case when your employer later files an H-1B petition. USCIS evaluates whether the role requires a degree in a specific field, and clinical operations work in healthcare administration or public health typically supports that determination when tied to your degree. Your employer's attorney will reference your CPT experience as part of the specialty occupation argument.
See which Clinical Operations Lead employers are hiring and sponsoring visas right now.
Search Clinical Operations Lead Jobs