Integrated Resources Inc

Quality Control Chemist

Contract · Rocky Mount, NC
✓ Verified live on the employer's own system · added 3284 days ago
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Mid-level · 3+ yrs exp

Requirements

Education: Bachelor's degree

Experience: 3+ years

Skills & tools

CoachingRoot Cause AnalysisQuality AssuranceOperationsWritingTechnical WritingExcelManagement
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Full job description

Job Title: Sr. Quality Specialist/ Quality Control Chemist Location: Rocky Mount - NC Duration: 18 Months Job Description:

  • 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. POSITION

RESPONSIBILITIES :

  • In order of importance, list the primary responsibilities critical to the performance of the position.
  • 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. ORGANIZATIONAL RELATIONSHIPS:
  • Ability to interface with multiple levels of people in the organization, including plant personnel and senior management. EDUCATION AND EXPERIENCE:
  • Bachelor’s degree with 3-5 years experience in the FDA regulated industry. All your information will be kep t confidential according to EEO guidelines. With Regards, Abhishek Singh 650-399-0881 Clinical Recruiter Integrated Resources, Inc.

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This posting was published by Integrated Resources Inc on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.