Pharmaceutical Quality Deviation Specialist at Freyr

Qualifications: 

• B.S./M.S. degree in appropriate engineering/scientific field. Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry.
• Previous experience in writing investigations for a typical events in a manufacturing environment. 

Responsibilities:

•  Primary responsibilities include day-to-day technical support to manufacturing operations, including resolution and reduction of process deviations, development and implementation of corrective/preventative actions, and leading manufacturing and laboratory investigations.
• This Individual will also develop working relationships with counterparts in other areas supporting aseptic manufacturing, testing, planning, and release and is required to utilize sound scientific and engineering principles to investigate process deviations.

Regards,

Kriti S
Recruiter, Staffing Dept. (US Region)     
 +1 (609)681-2343      
  kriti.shukla@freyrsolutions.com 
Regional office Address : 150 College Road West, Suite 102, Princeton, NJ 08540
Website:  www.freyrsolutions.com