Qa Senior Specialist

Location
Cambridge, MA, United States
Posted
Aug 20, 2018
Ref
R-00577
Hotbed
Genetown
Required Education
Bachelors Degree
Position Type
Full time
Title:
Qa Senior Specialist

Company:
Ipsen Bioscience, Inc.

Job Description:

Core Responsibilities:
  • Support day to day operations, including: batch release.
  • Participate in internal and external meetings and site visits to ensure compliance cGMPs.
  • Support in maintaining and adhering to compliance requirements for established quality systems programs.
  • Interact with project teams as they impact the quality operation.
  • Ability to work independent and under supervision in a timely manner.
  • Support compliance requirements and time frames.
  • Interact with internal personnel on matters often requiring coordination between departments.
  • Participate in internal and external audits to ensure compliance to cGMPs (and GxP) requirements.

Core Competencies:
  • Effectively demonstrate an understanding of cGMPs and how it applies to specific responsibilities.
  • Work independently under general supervision and direction.
  • Practice safe work habits and adheres to safety procedures and guidelines.
  • Core Responsibilities:
  • Support day to day operations, including: batch release.
  • Participate in internal and external meetings and site visits to ensure compliance cGMPs.
  • Support in maintaining and adhering to compliance requirements for established quality systems programs.
  • Interact with project teams as they impact the quality operation.
  • Ability to work independent and under supervision in a timely manner.
  • Support compliance requirements and time frames.
  • Interact with internal personnel on matters often requiring coordination between departments.
  • Participate in internal and external audits to ensure compliance to cGMPs (and GxP) requirements.
  • Core Competencies:
  • Effectively demonstrate an understanding of cGMPs and how it applies to specific responsibilities.
  • Work independently under general supervision and direction.
  • Practice safe work habits and adheres to safety procedures and guidelines.
  • Core Responsibilities:
  • Support day to day operations, including: batch release.
  • Participate in internal and external meetings and site visits to ensure compliance cGMPs.
  • Support in maintaining and adhering to compliance requirements for established quality systems programs.
  • Interact with project teams as they impact the quality operation.
  • Core Competencies:
  • Effectively demonstrate an understanding of cGMPs and how it applies to specific responsibilities.
  • Work independently under general supervision and direction.
  • Practice safe work habits and adheres to safety procedures and guidelines.
  • Ability to work independent and under supervision in a timely manner.
  • Support compliance requirements and time frames.


IPSEN is an equal opportunity employer that strictly prohibits unlawful discrimination. We recruit, employ, train, compensate, and promote without regard to an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.