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Formulation Technician II

Ortho Clinical Diagnostics

Rochester, NY

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JOB DETAILS
SKILLS
Assemblers Technology, Chemistry, Clinical Laboratory, Communication Skills, Component Assembly, Computer Skills, Current Good Manufacturing Practice (cGMP), Diagnostics Solutions/Software, Documentation, English Language, Establish Priorities, FDA Requirements, Film, GMP (Good Manufacturing Practices), Genetics, Geography, High School Diploma, Hospital, ISO (International Organization for Standardization), Identify Issues, Immunoassays, Industrial Coating, Information Technology & Information Systems, Lift/Move 35 Pounds, Manual Dexterity, Manufacturing, Mechanical Assembly, Medicine, Microsoft Excel, Microsoft Office, Microsoft Outlook, Microsoft Word, OSHA, Production Schedule, Regulations, Regulatory Requirements, SAP, Safety Process, Schedule Development, Standard Operating Procedures (SOP), Team Player, Testing, Time Management, Warehousing
LOCATION
Rochester, NY
POSTED
Today
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 aremore 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

As we continue to grow as QuidelOrtho, we are seeking a Formulation Technician II to perform operations as described by our Standard Operating Procedures (SOPs) under Good Manufacturing Practices (GMPs) in our Film manufacturing Department located in Rochester, NY. You will prepare sets-up and assemble components needed for production, visually inspect components for defects, operate and troubleshoot equipment issues while strictly following all regulations and requirements including cGMP's, OSHA, FDA, and ISO regulations.

This opportunity is located in Rochester, NY.

Work Schedule: Ability to work a varying schedule of shifts (combination A-B-C) is required.

The ideal candidate will prepare solutions following preparation instructions using raw materials, chemical additions, testing, and finishing of solutions to coat diagnostic film. Work with, operate and troubleshoot equipment issues while strictly following all regulations and requirements including cGMP's, OSHA, FDA, and ISO regulations.

The Responsibilities

  • Effectively communicates verbally and in writing.
  • Demonstrates a sense of urgency to complete production schedule on time.
  • Accepts personal responsibility for the quality and timeliness of work.
  • Accurately and timely completes all required reporting functions using an SAP/ERP computer system.
  • Uses computer-based documentation system to find, view and print specifications and procedures.
  • Prepare solutions used in Film/Coating manufacturing, while following safety procedures and practices and maintaining a clean orderly work environment.
  • Follow a recipe driven process with precise accuracy, operates machinery and interacts with computer-controlled equipment and processes.
  • Disposes of scrap/rejected material in appropriate manner and according to safety regulations.
  • Ability to work in a team environment.
The Individual
  • A High School Diploma or GED is required. Vocational education would be preferred
  • Knowledgeable in the areas of chemical and solution preparation, recipe driven processes, solvent/aqueous coating, film coating technology, and mechanical assembly. 2-3 years of experience is preferred in one or all disciplines.
  • Must have basic computer skills i.e., Microsoft Office (Word, Excel, Outlook).
  • The ability to read and write in English is required.
  • Knowledge and experience with GMP/ISO regulations is preferred.
  • Strong mechanical aptitude, troubleshooting of process and equipment is required.
  • Physical work condition demands for the position include standing, bending, and stooping -some lifting not to exceed 45 pounds.
  • Manual dexterity for manipulating parts and repetitive motions is required.
  • Ability to work a varying schedule of A and B shifts and C shifts. Shifts are 8 hours M-Fri with occasional Overtime shifts.
Preferred:
  • Experience with quality information systems (i.e. SAP).
  • Knowledge and experience with GMP/ISO regulations.


Key Working Relationships

Internal Partners: Maintenance, Engineering, Quality

External Partners: Suppliers

Work Environment

The work environment characteristics are representative of a manufacturing, laboratory, 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. Up to 75% of the time you will be, standing, walking or sitting, bending and stooping for extended periods of time. Ability to lift up to 35 lbs. Manual dexterity for manipulating parts and repetitive motions are required. Flexible work hours to meet project deadlines.

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 $20.75 to $23.38 hourly 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 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 recruiting@quidelortho.com.

About the Company

O

Ortho Clinical Diagnostics

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