OUR TEAM: The IVD Production team consists of expert manufacturing scientists delivering high ... 3. A self-directed individual to work efficiently & accurately with strong customer service.
OUR TEAM: The IVD Production team consists of expert manufacturing scientists delivering high ... 3. A self-directed individual to work efficiently & accurately with strong customer service.
OUR TEAM: The IVD Production team consists of expert manufacturing scientists delivering high ... 3. A self-directed individual to work efficiently & accurately with strong customer service.
OUR TEAM: The IVD Production team consists of expert manufacturing scientists delivering high ... 3. A self-directed individual to work efficiently & accurately with strong customer service.
Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry
Monmouth Junction, NJ · On-site
$93K - $127K/yr
Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry | Lab-on-Spin-Disk ... Direct experience with L ab-on-Spin-Disk, Lab-on-Disk, centrifugal microfluidics, or similar POC ...
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Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry
Monmouth Junction, NJ · On-site
$93K - $127K/yr
Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry | Lab-on-Spin-Disk ... Direct experience with L ab-on-Spin-Disk, Lab-on-Disk, centrifugal microfluidics, or similar POC ...
Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch ...
Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch ...
Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch ...
Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch ...
Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch ...
Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch ...
Program Director
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
San Diego, CA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
San Diego, CA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
San Diego, CA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
San Diego, CA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Exec Director, Regulatory Affairs
$174K - $230K/yr
The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and ... Provides IVD regulatory input during clinical development to ensure compliance of diagnostics used ...
Exec Director, Regulatory Affairs
$174K - $230K/yr
The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and ... Provides IVD regulatory input during clinical development to ensure compliance of diagnostics used ...
Exec Director, Regulatory Affairs
Parsippany, NJ · On-site
$150K - $199K/yr
The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and ... Provides IVD regulatory input during clinical development to ensure compliance of diagnostics used ...
Exec Director, Regulatory Affairs
Parsippany, NJ · On-site
$150K - $199K/yr
The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and ... Provides IVD regulatory input during clinical development to ensure compliance of diagnostics used ...
Exec Director, Regulatory Affairs
Foster City, CA · On-site
$174K - $230K/yr
The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and ... Provides IVD regulatory input during clinical development to ensure compliance of diagnostics used ...
Exec Director, Regulatory Affairs
Foster City, CA · On-site
$174K - $230K/yr
The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and ... Provides IVD regulatory input during clinical development to ensure compliance of diagnostics used ...
Program Director (Atlanta)
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Program Director (Atlanta)
Atlanta, GA · On-site
We are seeking a highly skilled and experienced Program Director to lead cross-functional programs within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This role will oversee ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$125 - $225/hr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$125 - $225/hr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$160 - $230/hr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$160 - $230/hr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$180 - $240/hr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$180 - $240/hr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
$125K - $225K/yr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
$125K - $225K/yr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$125K - $225K/yr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Senior Director of Regulatory Affairs
Cleveland, OH · On-site
$125K - $225K/yr
The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well ...
Director Ivd information
What is a Director IVD?
What are the key skills and qualifications needed to thrive as a Director IVD?
What are some common challenges faced by a Director IVD when leading cross-functional teams?
What is the difference between Director Ivd vs Medical Laboratory Director?
| Aspect | Director Ivd | Medical Laboratory Director |
|---|---|---|
| Credentials | Typically requires CLS/MT certification, relevant degree, and managerial experience | Requires medical director certification, medical degree, and clinical laboratory experience |
| Work Environment | Oversees in vitro diagnostic device development and manufacturing | Manages clinical laboratory operations and compliance |
| Industry Usage | Used mainly in biotech and diagnostics companies | Common in hospital, clinical, and reference labs |
The main difference is that a Director Ivd focuses on in vitro diagnostic products, including development and regulatory compliance, while a Medical Laboratory Director oversees clinical laboratory operations and patient testing. Both roles require relevant certifications and industry experience but serve different functions within the healthcare and diagnostics sectors.
What cities are hiring for Director Ivd jobs?
Cities with the most Director Ivd job openings:
What are the most commonly searched types of Ivd jobs?
The most popular types of Ivd jobs are:
What states have the most Director Ivd jobs?
States with the most job openings for Director Ivd jobs include:
What job categories do people searching Director Ivd jobs look for?
The top searched job categories for Director Ivd jobs are:

Promega rating
8.9
Based on 8 frontline employees who took The Breakroom Quiz
Job description
YOUR ROLE: As an IVD Operations Support Technician on the IVD Production team, you will be primarily responsible for washing and autoclaving labware, staging raw materials for production, and maintaining lab and gowning supply inventory, along with other lab support duties as needed to keep our manufacturing lab running efficiently. This role is physically demanding, you can expect to be on your feet and in the lab most of each day and to be moving materials as part of routine tasks. You will have to be comfortable with the physicality of the role and with working in a cGMP-regulated, gowned, environmentally controlled lab space. You will operate equipment including industrial parts washers, autoclaves, and pumps, supporting scientists who manufacture products used in diagnostic testing, forensic investigations, and cutting-edge medical research.
CORE DUTIES:
1. Operate labware wash machines and autoclaves according to departmental operation and safety guidelines.
2. Plan and maintain stockroom supplies, stock all items used in area of responsibility.
3. Staging of raw materials according to process orders.
4. Maintain accurate daily activity logs and batch records.
5. Keep work areas clean and free from clutter.
6. Ability to identify needs or problems and to communicate proper courses of action on various cleaning issues and follows through to ensure completion.
7. Operate pH meters, conductivity meters, balances, autoclaves, peristaltic pumps, vacuum pumps, filtering apparatus and laboratory mixing equipment.
8. Plan daily schedule according to incoming requests.
9. Identify unsafe situations, processes or procedures and report them as appropriate.
10. Meet customers' needs in a professional manner.
11. Provides backup in several areas of department.
12. Process Special Request from IVD Production, IVD Product Finishing and/or Engineering staff as needed.
13. Assist in compiling information and data for special reports.
14. Assist in specific projects as required and assigned.
15. Assist with training of others in the proper and safe use of all equipment.
16. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others.
17. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work.
18. Understands and complies with ethical, legal and regulatory requirements applicable to our business.
KEY QUALIFICATIONS:
1. High School diploma or proven work experience that ensures you are ready to be successful in this role.
2. Punctuality and ability to maintain a good attendance record are essential.
3. Demonstrate a continuous willingness to be flexible with regard to job activities and associated scheduling.
4. Excellent communication skills.
5. Clean production areas and equipment.
6. Competency in general math.
7. Works independently with moderate supervision and with other team members.
8. Must be able to use in-house software (Microsoft Office and ERP) to perform general duties.
9. Ability to maintain a positive attitude toward work activities and show a willingness to accept direction and advice and be a team player.
10. Strong attention to detail.
11. Demonstrated proficiency in digital tools and technology, including Microsoft applications and mobile platforms, with the ability to adapt and leverage emerging technologies, such as artificial intelligence, to improve efficiency, automation, and collaboration.
PREFERRED QUALIFICATIONS:
1. Previous work experience in glassware preparation within a laboratory setting.
2. Knowledge and/or coursework in biological sciences or chemistry.
3. A self-directed individual to work efficiently & accurately with strong customer service.
PHYSICAL DEMANDS:
1. Standing, walking and bending on a continuous basis as well as going up and down stairs.
2. Ability to work in limited space areas.
3. Ability to operate washing and drying labware equipment.
4. Ability to move up to 300 lbs. on a dolly and 500 lbs. on a pallet jack occasionally.
5. Ability to safely handle and transport glassware and labware items up to 300 liters in size and weighing up to 50 pounds for several hours per week.
At Promega, we value diversity and strive to create an inclusive workplace. We are proud to be an Equal Opportunity Employer, making employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.