CAPA Investigator Owner(CAPA/NCR writer)
2 days ago
Description:
12 months contract ; May extend ;
Onsite
CAPA/NCR writers
HM Notes:
The candidate should have worked on CAPAs/root cause analysis/change control/audits in the past
The position includes writing deviations/NCRs
Manager prefers bachelors, but it's more about experience
Manager wants to see 3-5 years of experience- open to more
Example job titles include Tech Writer or Quality Investigator
Role will be 5 days onsite
Interview: First interview will be virtual with camera on, then second interview onsite
They must be comfortable in PPE
They will be working on an average of 5 active investigations at a time
Description:
Essential Duties and Responsibilities:
Perform non-conformance (NCR) investigations within the Track Wise 8 Management System.
Execute implementation of CAPAs associated with NCR investigations.
Maintains a high level of expertise in current regulatory requirements, and serve as a plant resource for compliance to these requirements. Maintains audit ready status for assigned areas and assists other areas within the facility in maintaining compliance with local procedures as well as US & International Regulatory and corporate quality requirements.
Provide guidance and coaching on performance of DMAIC problem solving and process improvement projects for less experienced individuals within the plant.
Qualifications:
Candidate must not be allergic to Penicillins or Cephalosporins
Understanding of the product's intended use and manufacturing process
Ability to prioritize multiple tasks to ensure compliance with regulations and standard operating procedures.
Strong problem solving and analytical skills.
Consultation and facilitation skills.
Understanding of statistics in support of fact based decision making.
Excellent written/verbal communication and organizational skills
Ability to make independent decisions with minimum oversight
Customer sensitivity / acumen and ability to interact with all levels of management.
Experienced user of TrackWise preferred.
Working knowledge of FDA Regulations and International Regulatory requirements.
Understanding of risk management tools.
Available to work during off-shift or weekends as appropriate to support investigations and training
Education and/or Experience:
• BS/BA (4 years of university level education) in science, engineering or related field.
•2-4 years relevant work experience in cGMP related industry or in a clinical setting.
• Greenbelt certification or equivalent experience using Six Sigma or other Lean Manufacturing tools is a plus.
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