We are currently looking to fill a Sr QA Project Specialist role supporting our Change Control Business Process Management team. This position supports the achievement of Quality Assurance (QA) objectives by planning, coordinating and leading project activities. This position manages cross-functional projects as both a facilitator and organizer, using knowledge within the pharmaceutical industry and project management techniques.
In this role, a typical day might include the following:
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Lead cross-functional projects and develop project timelines.
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Identify and lead project priorities and cross-project dependencies.
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Collaborate with functional leads/subject matter experts in driving execution and removing constraints that prevent advancement of efforts/projects.
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Proactively engage in activities to meet schedules and resolve issues.
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Identify skills needed for project management and deploy and maintain trainings and/or tools.
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Develop and manage content by obtaining relevant information through research and/or collaboration with subject matter experts.
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Helps maintain alignment across IOPS through ensuring robust global communications of projects.
This role may be for you if you:
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High computer literacy with capability in email, SharePoint, Microsoft 365, and related project, business, and communication tools.
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Familiarity with Agile, Scrum, Kanban, and other project methodologies.
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Excellent time and project management skills with the ability to manage many diverse assignments simultaneously and changing priorities.
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Motivated, independent, self-sufficient, and able to receive an assigned task and see it through to completion with minimal direction.
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High level of professionalism and confidence to work effectively with employees from all levels of the organization.
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Skilled in motivating, presenting with and teaching/training others, using both technical and non-technical language to explain sophisticated subjects and processes.
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Strong collaborative skills with the ability to seek and value input.
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Sound judgment, initiative, and interest in creative problem-solving.
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Excellent written, oral, and interpersonal communication skills for a variety of audiences.
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Ability to consistently achieve high quality and compliant deliverables.
To be considered for this role you must hold a Bachelor’s degree in a related field and the following minimum amounts of relevant experience for each level:
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Specialist – 2+ years
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Sr Specialist – 5+ years
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Principal Specialist – 8+ years
PMP certification preferred. May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.
#REGNQA
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, 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. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
$65,100.00 - $145,500.00
What We Do
At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.
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