Deviations Investigator at Insight Global in Rocky Mount, North Carolina

Posted in Other about 5 hours ago.

Type: full-time





Job Description:

Insight Global is seeking an Investigator for a Pharmaceutical client in the greater Raleigh area. This is an onsite role, that requires heavy technical writing. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients. You will help us in investigation of our quality issues in manufacturing and quality laboratories. You will investigate deviations and out-of-specification results and atypical result investigations. Your problem solving skills will help to identify root cause and suggest appropriate corrective action plan. Your attention to detail will help us ensure that the reports are aligned to regulatory requirements and company policies.

You will:

- Perform impact risk assessment as well as assist in root cause determination and plans appropriate corrective action and preventative action.

- Ensure Quality Management System for the investigations department are followed and maintained.

- Conduct and write formal investigation reports with varying degrees of complexity with the assistance of plant personnel and oversight from Lead/Manager

- Frequently enters the production area wearing appropriate gowning as necessary, to collaborate with colleagues and gather information for each investigation.

- Prior investigation writing experience (with determination of product impact).

- Plans appropriate corrective action and preventative action (CAPA).

- Perform reviews and evaluate sensitive, confidential information and develops recommendations for use by the plant quality assurance department.

- Defining and recommending corrective and/or preventive actions identified through the investigation process.

- Facilitates strategy meetings.

REQUIRED SKILLS AND EXPERIENCE

- 3-5 years of experience in a GMP/Pharma manufacturing environment

- Prior experience utilizing various investigation tools (5 Whys, Fishbone, 6 Ms, DMAIC method, etc.)

- Prior experience with technical writing (such as deviations, etc.)

- Proficiency with MS Office Suite (specifically Word, Excel, and PowerPoint)

- Strong written and verbal communication skills; ability to effectively communicate with employees at all levels within the organization, including plant colleagues and senior management. - Excellent facilitation skills and ability to facilitate strategy meetings.

- Ability to effectively organize data, extract key information, and write technical summary reports
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