Quality Control Scientist I

QuidelOrtho; Raritan (NJ, IL); On-site; USD 67,000 - 80,000; Full time

Job summary

An established industry player is seeking a QC Scientist I to ensure the quality and compliance of diagnostic products. This role involves testing stability and final product release, participating in investigations, and ensuring adherence to regulatory standards. Join a forward-thinking company dedicated to transforming diagnostics for a healthier future. This position offers a collaborative environment where your contributions can make a significant impact on patient care and quality assurance. If you are passionate about quality control and laboratory science, this is the perfect opportunity for you.

Benefits

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) plan

Employee assistance program

Employee Stock Purchase Plan

Paid time off

Paid Holidays

Qualifications

• Bachelor's degree in Medical Technology or related field required.
• Knowledge of GMP and quality control processes essential.

Responsibilities

• Perform product release and stability testing under supervision.
• Document results clearly and maintain compliance with regulations.

Skills

Pipetting

Indirect Antiglobulin Testing (IAT)

Direct Antiglobulin Testing (DAT)

Grading Blood Bank reactions

Instrument maintenance

Titrations

Quality Control

Reverse Blood grouping

Good Manufacturing Practices (GMP)

Microsoft Office Suite

Good Documentation Practices (GDP)

Education

Bachelor's degree in Medical Technology

Bachelor's degree in Clinical laboratory Science

Bachelor's degree in Biology

Bachelor's degree in Chemistry

Job description

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

The QC Scientist I will be responsible for testing stability and final product release of all OCD products. This person will assure compliance with company standards and applicable regulatory agencies. The QC Scientist I will participate in failure investigations to help determine root cause, track and trend data, identify and suggest process improvements to improve business measures.

This position will be located in Raritan, NJ.

The Responsibilities

• Organizes and performs product release, stability and raw material testing under direct supervision. Performs testing within established timelines and in accordance with current specifications.

• Documents results clearly and accurately. Interprets results by complying to appropriate specification requirements. Perform data trending of critical product, process information and release test results to be used in SPC/ trend analysis

• Maintains sufficient inventories off reagents and supplies

• Assures compliance to company procedures, GMP, FDA, Safety and ISO regulations in all functions.

• Participate in laboratory investigations, technology transfer, validation and R&D projects

• Perform other work-related duties as assigned

The Individual

Required:

• Bachelor's degree in Medical Technology, Clinical laboratory Science, Biology, Chemistry or related field of study

• Pipetting

• Perform Indirect Antiglobulin Testing (IAT)

• Perform Direct Antiglobulin Testing (DAT)

• Grading Blood Bank reactions

• Perform Instrument maintenance

• Perform titrations

• Quality Control

• Reverse Blood grouping

• Knowledge and experience with Good Manufacturing Practices (GMP)

• Proficiency with Microsoft Office Suite of products

• Knowledge and experience with Good Documentation Practices (GDP)

• This position is not currently eligible for visa sponsorship.

Preferred:

• Blood Bank Tube Testing

• Blood Bank Instrument Testing

The Key Working Relationships

Internal Partners:

Planning, Quality Engineering, Product Support, Operations

External Partners:

Instrument Support Personnel

The Work Environment

The work environment characteristics are representative of a laboratory.

The Physical Demands

Physical and work condition demands of the position include: Manual dexterity to handle lab equipment, Repetitive motions, Standing for long periods of time

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 $67,000 - $80,000 annually. 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 Employment 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 their 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 [e-mail].

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