Associate Laboratory Technologist

About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.

Find your future at Revvity 

Overivew:

EUROIMMUN US (a Revvity Company) is one of the leading manufacturers of medical laboratory diagnostics worldwide. EUROIMMUN stands for innovation and is dedicated to improving the science of diagnostics and people's lives worldwide. Our extensive product portfolio and innovative technologies are designed to provide quick, accurate, and reliable diagnoses. More than 3,300 employees in 17 countries develop, produce, and sell test systems to support the diagnosis of diseases, as well as software and automation solutions for the performance and evaluation of these tests. Laboratories in over 140 countries use our assays and automation for autoimmune, infectious disease, allergy, antigen, and molecular testing. EUROIMMUN U.S. proudly prioritizes a people-centered culture, securing a spot among New Jersey's 2023 Top Places to Work.

EUROIMMUN US Quality Control Department aims to be a full-service Quality Control and reference laboratory offering product testing to ensure they meet predetermined quality standards, complaint testing, and customer support. The Laboratory Technologist will be a valuable addition to the Quality Control laboratory. Under the guidance of the laboratory manager, the Laboratory Technologist will be responsible for ensuring the highest standards of product quality through comprehensive testing and analysis in our state-of-the-art laboratory facilities. The Laboratory Technologist will report to the Quality Control Manager.

Key Responsibilities:

Essential responsibilities include, but are not limited to,

• Adhering to all company policies, procedures and complying with all safety and regulatory requirements.
• Perform routine and non-routine qualification of raw material, in-process samples, and finished products using a variety of analytical techniques and instrumentation.
• Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting, and maintaining records of test results.
• Interpret test results accurately and promptly, identifying any deviations from specifications or quality standards.
• Adhere to the laboratory's quality control policies and document all quality control activities, instrument and equipment verifications, procedural calibrations, and maintenance performed.
• Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.
• Collaborate with cross-functional teams to investigate and resolve quality-related issues.

• Ensuring other assigned tasks are completed as necessary.
• Perform other delegated tasks, as required

Basic Qualifications:

• Bachelor’s degree in Chemistry, Biology, Physics, or a related field.
• 0-2 years of Quality Control experience in a regulated industry.

Preferred Qualifications:

• Excellent organizational skills with the ability to prioritize tasks and manage multiple projects simultaneously.
• Effective communication and interpersonal skills, with the ability to work collaboratively in a team environment.
• Detail-oriented mindset with a commitment to accuracy and precision in all work activities.
• Computer proficiency, including Word, Excel, and PowerPoint.
• Manual dexterity is required to operate and manipulate equipment.
• Frequent standing and walking around the lab.
• Long hours of sitting on the computer might be required.
• Experience in ELISA, IFT, Blot, and other Microbiology & Immunology testing principles & techniques
• Previous experience working in a quality control laboratory within a manufacturing environment.
• Understanding of quality assurance principles, GMP/GLP guidelines, and regulatory requirements (e.g. FDA, ISO).

The base salary range for this full-time position is $22/hr - $27.88/hr.

This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.

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What do we offer?

We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits:

• Medical, Dental, and Vision Insurance Options

• Life and Disability Insurance  

• Paid Time-Off

• Parental Benefits

• Compassionate Care Leave

• 401k with Company Match

• Employee Stock Purchase Plan

Learn more about Revvity’s benefits by visiting our Bswift page. Log-In instructions are provided towards the bottom of the Bswift page.

*For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information.

Revvity is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to any characteristic or status protected by applicable federal, state, and/or local laws. If you are an applicant with a disability that requires reasonable accommodation to complete any part of the application process or are limited in the ability—or unable to use—the online application system and need an alternative method for applying, you may contact [email protected].