Scientific and Clinical Careers

Job Title

Scientific & Clinical Job Details

Scientific Technical Writer

Job Code: #568
Job Type: Contract
Salary: $32.00 - $37.00/hour
Job Location: Wilson, NC
Posted 2 days ago

Job Description

Job Title:  Technical Writer

Pay:  $32.00 - $37.00 per hour 

POSITION SUMMARY:  The Technical Writer is responsible for independently investigating and reporting on deviations to the
manufacturing process, customer complaints on finished product, and other manufacturing problems as assigned.

PRINCIPAL ACTIVITIES:
• Responsible for describing problems, identifying possible causes, collecting and organizing existing data, comparing causes to facts, identifying probable root causes, and determining the best solutions in
order to control the manufacturing process.
• Responsible for managing multiple deviation investigations simultaneously.
• Provides follow up and scheduling to ensure batch release process is not impacted by outstanding deviations.
• Ensures investigations will withstand regulatory scrutiny and are compliant with cGMP regulations.
• Works with process experts and production personnel to fully understand and solve problems, provides technical expertise and recommends improvements.
• Writes Impact Assessments and Investigation Reports, works within TrackWise.
• Assigns corrective/preventive actions (CAPAs) as necessary in order to resolve problems.
• Performs continuous review and follow-up on investigations to minimize overall product impact and ensure the timely disposition of product that is directly affected.
• Informs Management on the progress of on-going investigations, provides information to and takes direction from the Deviation Review Board.
• Utilizes Word, Excel, Documentum and other electronic systems to complete tasks.
• Maintains compliance with company policies, training requirements, cGMPs and safety standards.

REQUIREMENTS:
• BS/BA degree (experience may be considered in lieu of degree), with prior experience of root cause analysis and investigation of deviation events.
• Must have at least three years of experience in a GMP manufacturing environment, writing standard operating procedures and protocols and/or reports.
• Requires advanced critical thinking skills.
• Must be familiar with regulatory (FDA) requirements, working in a pharmaceutical environment.
• Good organizational, communication, and interpersonal skills are necessary.