Supervisor QC Data Review

Location
Rensselaer, New York, US
Posted
Nov 21, 2018
Ref
14117BR
Discipline
Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases . Summary . Supervise the daily review of analytical data of Routine Testing activities for Early phase, Pre-Clinical molecules in the QC Analytical Sciences laboratories as well as perform laboratory investigations Schedule is Sat-Wed . Essential Duties and Responsibilities include, but are not limited to, the following . Supervises Early Phase molecules routine testing review of analytical data. Testing encompasses ELISAs, DNA by PCR, Gel Electrophoresis, HPLC assays and Isoelectric focusing . Schedules work assignment and monitors direct reports progress . Reviews test results, revises testing procedures, authors compliance records . Responsible for ensuring deadlines are met for group so product can be released on time . Performs laboratory investigations for unexpected results working with cross functional teams to identify root cause and corrective actions . Ensures compliance of the group, documents any deviations identified . Answers questions from various customers to help interpret analytical data . Attends meetings to keep informed of manufacturing and clinical development needs and priorities, and provides analytical information and expertise . Ensures direct reports receive proper and prompt training . Ensures that lab safety standards are maintained . Ensures lab compliance with applicable cGMP regulations and SOPs . Performs personnel management functions including monthly meeting with direct reports, weekly time sheet approval, scheduling of vacations, personnel development, and performance evaluations . Knowledge, Skills & Abilities . Solid supervision and leadership skills . Ability to interpret and communicate information . Ability to prioritize, manage multiple tasks, and meet deadlines . Ability to organize and maintain data or information #LI-KS1. Education and Experience . BS in Chemistry, Biochemistry, or Biology, and 5+ years of relevant, progressive biotech or pharmaceutical laboratory experience. Previous supervisory experience required . This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business . To all agencies . Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid . 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.