In this role you will validate/qualify cleaning processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures.
As a Assoc QA Validation Specialist a typical day might include, but is not limited to, the following:
Generate, execute and/or review master and completed cleaning validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria
Lead all aspects of cleaning validation for program to ensure program adherence in accordance with approved schedules
Analyze the results of testing and determine the acceptability of results against pre-determined criteria
Investigate and troubleshoot problems which occur and determines solutions or recommendations for changes and/or improvements
Review, edit and approve deviation notifications, deviation investigations, and corrective actions
Effectively communicate to key partners on cleaning validation programs (program adherence, success rate, issues / roadblock
Review, edit and approve change controls, SOPs, reports and other documentation
Coordinate with other departments or outside contractors/vendors to complete validation tasks
Train/advise less experienced Specialists
Lead projects and prepares status reports
May be required to supervise contingent workers
Other duties assigned by management
This role might be for you if:
You have the ability to maintain integrity and honesty at all times
You have the ability to work independently or as part of a team
You have the ability to communicate with transparency
You have the ability to continuously drive processes for improved performance
You demonstrate supportive behavior at all times
You have a basic solid understanding of Microsoft Suite (Word, Excel, Powerpoint)
You have the ability to meet commitments on time
You have effective time management skills
You have the ability to identify continuous improvement needs
To be considered for this position you must hold a BS/BA in Engineering, Chemistry, or Life Sciences with 1+ years of related experience within the field preferred; may substitute relevant experience for education.
#IREADV #JOBSIEST #LI-Onsite #REGNIEQA
Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.