Perrigo Company is dedicated to making lives better by bringing Quality, Affordable Self-care products that consumers trust everywhere they are sold.  Help us do it.

External applicants please note:  To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.)  Thank you.

Description Overview

Provides primary Quality Assurance review and approval for deviations, change controls, and other cGMP documentation and studies and ensures that all information and documentation conforms to company policy, cGMP’s and all other applicable FDA guidance’s.  Assists with monitoring of cGMPs throughout the facility and is a first responder to quality events on the shop floor.  Assists with validation and verification activities for enhancements in the facility from a food safety and quality perspective.  Assists with the assembly of Annual Management Review materials.

Scope of the Role

• Responsible for reviewing and approving documents such as deviations, management reviews, non-routine batch status change requests, planned deviations, calibration non-conformances, etc.  First responder to quality events on the shop floor and provides initial risk assessment.
• Works with operations, laboratory, engineering, and maintenance managers and staff to develop, evaluate and implement action plans which maintain or improve product and process quality.
• Develops and implements procedures, processes and documentation that are used to ensure the Company’s quality standards are met and maintained.
• Participates in quality driven initiatives in the continuous support of Quality Improvement.  
• Entering data into a CAPA system that will be used to identify trends and/or root causes; they shall also be responsible for participating in comprehensive investigations as necessary.  
• Completes internal audits to ensure compliance to cGMPs and codes company is certified to.
   

Experience Required

• Bachelor’s degree in food science, microbiology, or closely aligned field
• Minimum three years’ experience in and knowledge of manufacturing in infant formula, food or beverage industry is preferred. 
• Demonstrated understanding of and ability to apply cGMPs and US FDA laws and requirements in an FDA regulated industry.  
• Demonstrated ability to organize multiple tasks and change priorities to meet project deadlines. 
• Excellent analytical skills are essential, including well developed interpersonal skills. Prior professional experience in inspection, quality control, and release in infant formula, food or beverage industry is preferred.  Computer literacy is required.
   

External applicants please note:  To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.)  Thank you.

We are an equal opportunity employer.  All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities. #DIV

Ferrero  

Colgate-Palmolive