Job Description
In this role you will apply functional knowledge in quality to validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures.
In this role a typical day might include, but is not limited to, the following:
Generate, execute and/or review master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria
Analyze the results of testing and determines 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
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 prepare status reports
May be required to supervise contingent workers
Other duties assigned by management
Flexibility to travel globally as required
This role might be for you if you demonstrate the following:
Ability to maintain integrity and honesty at all times
Ability to work independently or as part of a team
Ability to communicate with transparency
Continuously drive to improve processes for improved performance
Demonstrate respectful & supportive behaviour at all times
Basic working knowledge of Microsoft Suite (Word, Excel, PowerPoint)
Meets commitments on time
Effective time management skills
Ability to identify continuous improvement needs
To be considered for this role you must hold a BS/BA in Engineering, Chemistry, or Life Sciences.
Assoc level requires 0-2 years of related experience within the field preferred.
Specialist leve requires 2-5 years of related experience
Sr Specialist requires 6+ years of related experience
Principal requires 7+ years of related experience
#REGNIEQA #JOBSIEPR #LI-Onsite
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.