QC Inspector II

As we continue to grow as QuidelOrtho, we are seeking a Quality Inspector II. The Quality Inspector II will support personnel and will work under general supervision and follow established procedures. Also included at this level, are Senior level Inspector positions that perform under strict procedures. Frequent use and application of procedures, technical standards, principles, theories, concepts, and techniques. Ability to identify defects and/or other functional attributes as listed in the inspection documents. Provides solutions to a variety of problems of moderate scope and complexity. Exactly follows established processes and procedures. Work is reviewed for soundness of technical judgement, overall adequacy, and accuracy. Applies acquired job skills, on the job training, and company policies and procedures to complete all assigned tasks.

This position is in Raritan, NJ.

Schedule: 11:00pm – 7:30pm (Monday – Friday)

The Responsibilities

• Ability to prioritize daily workloads in a fast-paced, high energy work environment.

• work cohesively within a team environment.

• Proficiently read, remember, and consistently/accurately apply on the job training and knowledge of written procedures.

• Must have a strong sense of urgency, customer service, communication & time management skills.

• Inspect, sample, & disposition Incoming components, raw materials, chemicals, and biologics and support other inspections as required.

• Identify discrepancies related to specifications & procedures during inspection process.

• Initiate quality events including nonconformances and assist with root cause investigations, and/or product disposition.

• Execute transactions for material movement in the current ERP database and ensure appropriate material status control is maintained.

• Contributes as a team member to department-specific continuous improvement projects

• Ensure testing and related equipment is appropriate and calibrated.

• Ensure quality documents are filed and archived in a retrievable and timely manner.

• Proactively maintain robust cGMP guidelines and compliance with all internal and external procedures.

• Maintain training binder, ensure all training is completed in a timely manner.

• Perform other work-related duties as assigned.

The Individual

Required:

• High School Diploma or GED equivalent

• 2 years of relevant technical experience in a similar industry

Preferred:

• Associate degree in a technical discipline

The Key Working Relationships

• Internal Partners: Coordinate with such groups as Operations, Procurement, Supplier Quality, Quality Engineers, Engineering, etc.as required during inspections, investigations, and validation activities.

• External Partners: Interaction with regulators and customers during audits. Communicate with suppliers when appropriate for requests for documentation, corrections, and/or additional information as required.

The Work Environment

The work environment characteristics are representative of a manufacturing, laboratory, and/or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples.

Physical Requirements

Up to 15% of the time at desk, and 85% of the time spent standing, walking, moving (pushing, pulling, etc.), or sitting for inspections. Must be able to safely lift 50 pounds and or push/slide pallet jacks, boxes, etc.; forklift operation when necessary. Ability to successfully pass a vision and color test (use of corrective lens like contacts/glasses acceptable). Flexible work hours to meet project deadlines as required.

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 $21.00 to $26.00/hour 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 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 orthorecruiting@orthoclinicaldiagnostics.com