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Sr Quality Control Chemist
Ref No.: 17-21183
Location: Rocky Mount, North Carolina
Immediate need for a Sr Quality Control Chemist  with experience in the Pharma  Industry. This is a 18 months  contract opportunity with long-term potential located in Rocky Mount,NC . Please review the job description below:

Job ID: 17-21183

 Key Responsibilities/Key Requirements and Technology Experience:
  • The Sr. Quality Specialist shall independently conduct and write complex formal investigation reports with input from area SMEs.
  • The candidate will function as an independent reviewer of drafted investigations providing constructive feedback and in some instances act as a coach to the investigator.
  • This position will also perform impact risk assessment as well as assist in root cause determination and plans appropriate corrective action and preventative action.
  • The incumbent will assist in the tracking and trending of corrective and preventative action to assure timely closure.
  • This person will also perform reviews and evaluate sensitive, confidential information and develops recommendations for use by the plant quality assurance department. 
  •  In order of importance, list the primary responsibilities critical to the performance of the position.
  • Please include actual tasks and/or essential responsibilities that highlight accountability and level of judgment required.
  • 2-5 years experience in pharmaceutical quality environment required Experience in sterile manufacturing and an understanding of the sterilization process and its impact to products.
  • Working knowledge of environmental monitoring and aseptic manufacturing.
  • Understanding of process validation requirements.
  • American Society for Quality (ASQ) certification is an asset.
  • Pharmaceutical operations experience and/or knowledge.
  • Experience in a solutions facility preferred. Working knowledge of FDA regulations.
  • Knowledge of various quality tools such as root cause analysis, DMAIC process, fishbone analysis, etc. Prior investigation writing experience (with determination of product impact).
  • Strong oral and written communication presentation, interpersonal skills and adept at communication with employees at all levels within the organization.
  • Excellent facilitation skills and ability to facilitate strategy meetings.
  • Superior technical writing and problem solving skills.
  • Organize data, extract key information and write technical summary reports.
  • Expertise with word-processing, spreadsheet, and presentation software.
  • TrackWise experience a plus. 
  • Provide the primary groups or key positions that this position will have interaction with as a regular part of the position responsibilities.
  • Include any external interactions as appropriate.
  • Ability to interface with multiple levels of people in the organization, including plant personnel and senior management.   
  • Indicate the formal education, certification or license(s) required and/or preferred.
  • Include the minimum number of years of relevant experience required for the position (where legally permissible).
  • Bachelor's degree (science preferred) with 3-5 years experience in the FDA regulated industry.   
  • 3-5 years' experience in pharmaceutical quality environment required

Our client is a leading Pharma  Industry and we are currently interviewing to fill this and other similar contract positions. Qualified candidates should apply online for immediate consideration.