Quality Control Scientist

Location
Rensselaer, NY, United States
Posted
Oct 26, 2020
Ref
18521BR
Required Education
Doctorate/PHD/MD
Position Type
Full time
Summary:
Perform assay development, characterization, optimization, transfer, validation and investigation for the Quality Control (QC) chemistry group. Provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.

Essential Duties and Responsibilities include, but are not limited to, the following:
• Performs assay development/validation for Quality Control (QC) Chemistry group.
• Reviews new test procedures and assays.
• May evaluates and bring in new methodologies/techniques when needed.
• Facilitate assay transfer from R&D and to business partners.
• Organize analytical assay transfer internally and externally.
• Set product specifications.
• Participates in technical troubleshooting and problem investigation.
• Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.
• Participates in training programs for analysts.

Knowledge, Skills & Abilities:
• Ability to work independently or in a team.
• Ability to prioritize, manage multiple tasks, and meet deadlines.
• Ability to interpret and apply cGMPs, USP, EP, JP, BP, ICH regulatory requirements and industry best practices.
• Ability to maintain integrity and honesty at all times.
• Ability to communicate with transparency.
• Continuously drive to improve processes for improved performance.
• Demonstrate respectful behavior at all times.
• Ability to multi-task.
• Ability to analyze and identify trends.
• Develops and delivers effective presentations.
• Problem-solving skills.
• Ability to train others on basic systems and processes.
• Strong written communication.
• Ability to work in an ever-changing environment.
• Critical thinking skills.

Education and Experience:
• Requires Ph.D in Biochemistry, Chemistry, Biology, Pharmaceutical Sciences or related field, and a minimum 1 year experience in the pharmaceutical or biotechnology industries.

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 amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity 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.

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