US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…
ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Deviation Management Specialist:
-
Employment Type:
Contractor
-
Location:
West Point, PA (Onsite)
Do you meet the requirements for this job?
Deviation Management Specialist
Careers Integrated Resources Inc
West Point, PA (Onsite)
Contractor
Job Title: Deviation Management Specialist
Job Location: West Point, PA
Job Duration: 12+ months (Possibilities of Extension)
Work Shift: 8 A.M. – 5 P.M.
Pay Range: $41.50/hr. on W2
Job Description:
Qualification:
Job Location: West Point, PA
Job Duration: 12+ months (Possibilities of Extension)
Work Shift: 8 A.M. – 5 P.M.
Pay Range: $41.50/hr. on W2
Job Description:
- 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 be responsible for providing scientific support for manufacturing areas within Client’s Manufacturing Division (MMD).
- 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.
- Troubleshooting and root cause analysis of laboratory test failures and manufacturing atypical events, development of corrective/preventative actions is required.
- Analysis of complex problems through critical analytical thinking and the design/execution of laboratory/pilot scale experiments is required.
- Off-shift work may be required.
Qualification:
- B.S./M.S. degree in appropriate engineering/scientific field.
- Minimum of 0-3 years post-bachelor’s 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 atypical events in a manufacturing environment.
- Familiar with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities.
- Demonstrated ability to work both independently and as a part of a cross-functional team.
- Excellent written and verbal communication skills.
Get job alerts by email.
Sign up now!
Join Our Talent Network!