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Biotech Production Compliance Coordinator, Rensselaer, NY

Regeneron
27 May 2020 Years
692
Section: Medicine and Pharmacy
Vacant position: Biotech Production Compliance Coordinator, Rensselaer, NY
Organization: Regeneron
District: Brooklyn
Education: Incomplete schooling
Work experience: Without experience
Work schedule: Full time work day
Requirements for applicants:

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 behavior at all times.

Ability to learn and follow routine procedures independently.

Basic troubleshooting skills.

Identify and communicate continuous improvement ideas.

Ability to work in an every-changing environment.

Build and maintain working relationships.

Goes above and beyond by demonstrating proficiencies with assigned tasks.

Ability to gather, generate, and interpret data.

Participates in projects.

Education and Experience:

Bachelor’s degree, preferably in Life Sciences or a related field, or

AS/AAS Degree in Biotechnology/Biological Science and 2 years of relevant work experience.

Relevant biotech or pharmaceutical industry experience may be substituted in lieu of educational requirement.

Duties:

Performs all compliance related administrative tasks necessary for supporting commercial manufacturing operations.
Level to be determined based on qualifications relevant to the role.

Performs administrative tasks in all areas of production as needed in accordance with cGMP standards and in compliance with written procedures.

Reviews completed batch records and logbooks in accordance with cGMP standards to ensure compliance with written procedure.

Reviews, edits, and revises controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures.

Monitors production processes to obtain necessary data in support of investigations and track effectiveness of changes.

Participates in cross-functional study teams to support and/or author investigations.

Gathers, trends, and analyzes process related data to drive consistency and timeliness.

Documents all training.

Assists with training of new employees.

Ensures all tasks are performed in a manner consistent with safety standards.

Working conditions:

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media. We do not interview candidates on Google Hangouts. We also do not hire for "at-home data entry" positions.

e-mail: candidatesupport@regeneron.com
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