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Deviation Management Specialist - I (Assistant)

Primary Talent Partners

Durham, NC

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JOB DETAILS
SALARY
$41 Per Hour
SKILLS
Analysis Skills, Asepsis, Audio Engineering, Biotech and Pharmaceutical, Communication Skills, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Identify Issues, Lean Manufacturing, Lean Six Sigma, Manufacturing, Manufacturing Analysis, Manufacturing Operations, On Site Support, Presentation/Verbal Skills, Problem Solving Skills, Process Engineering, Root Cause Analysis, Scientific Principles, Technical Support, Testing, Writing Skills
LOCATION
Durham, NC
POSTED
1 day ago
Primary Talent Partners has a new contract opening for a Deviation Management Specialist - I (Assistant) to join our pharmaceutical client in Durham, NC. This is a 12-month contract to start with the potential for extensions. 


Pay:$41.00/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.


Description
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 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 manufacturing atypical events, development of corrective/preventative actions is required
  • Analysis of complex problems through critical analytical thinking
  • Off-shift work may be required.


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 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.
  • Ideal candidate with some co-op/internshi and 1-2 yrs real world experience.
  • Mostly deviation incidents and will ultimately train/work on investigations


Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at info@primarytalentpartners.com

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