Quality Control Scientist (Change Control)
Regeneron Pharmaceuticals, Inc, Troy, NY, United States
Position Summary
We are currently looking to fill a Technical Resources Specialist part of our QC Technical Resources Chemistry Team. This position will be supporting change control of validation and qualification activities, with some project management activities. Regeneron has successfully commercialized numerous products and in this fast-paced environment with a strong pipeline, QC Technical Resources Specialists have the opportunity to develop scientifically and also gain insight into other areas of the business.
Responsibilities
Execute and manage change controls within the QC TR Chemistry group
Collaborate with internal and external teams to coordinate change control activities
Coordinate and participate in weekly project update meetings
Communicate to management any delay in validation/transfer timelines
Raise discrepancies to management as needed
Execute some project management activities involving transfer of analytical methods to contract and partner labs
Qualifications
To be considered for the QC Technical Resources Specialist position you must have a BS/BA in Chemistry, Biochemistry, Biology or related field with 2+ years of experience. Experience with project management and experience in a GMP setting is preferred.
Level is determined based on qualifications relevant to the role.
Enjoy working in a fast-paced environment
Are able to multi-task, prioritize and execute projects independently
Are able to write and review transfer documents such as protocols and reports
Enjoy and are able to communicate cross-functionally to business units
Can take on new and sometimes ambiguous challenges and learn quickly
Develop and drive scientific and/or business-related improvement ideas
Possess effective time management skills, and the drive to meet deadlines
Have working knowledge of Microsoft Suite (Word, Excel, Powerpoint)
Benefits
Regeneron offers comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leave (e.g., military and parental leave) for eligible employees at all levels.
Salary
Salary Range (annually)
$67,400.00 - $110,000.00
Equal Opportunity Statement
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.
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We are currently looking to fill a Technical Resources Specialist part of our QC Technical Resources Chemistry Team. This position will be supporting change control of validation and qualification activities, with some project management activities. Regeneron has successfully commercialized numerous products and in this fast-paced environment with a strong pipeline, QC Technical Resources Specialists have the opportunity to develop scientifically and also gain insight into other areas of the business.
Responsibilities
Execute and manage change controls within the QC TR Chemistry group
Collaborate with internal and external teams to coordinate change control activities
Coordinate and participate in weekly project update meetings
Communicate to management any delay in validation/transfer timelines
Raise discrepancies to management as needed
Execute some project management activities involving transfer of analytical methods to contract and partner labs
Qualifications
To be considered for the QC Technical Resources Specialist position you must have a BS/BA in Chemistry, Biochemistry, Biology or related field with 2+ years of experience. Experience with project management and experience in a GMP setting is preferred.
Level is determined based on qualifications relevant to the role.
Enjoy working in a fast-paced environment
Are able to multi-task, prioritize and execute projects independently
Are able to write and review transfer documents such as protocols and reports
Enjoy and are able to communicate cross-functionally to business units
Can take on new and sometimes ambiguous challenges and learn quickly
Develop and drive scientific and/or business-related improvement ideas
Possess effective time management skills, and the drive to meet deadlines
Have working knowledge of Microsoft Suite (Word, Excel, Powerpoint)
Benefits
Regeneron offers comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leave (e.g., military and parental leave) for eligible employees at all levels.
Salary
Salary Range (annually)
$67,400.00 - $110,000.00
Equal Opportunity Statement
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.
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