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CAPA Investigator
CAPA InvestigatorGandiva Insights • IL, United States
CAPA Investigator

CAPA Investigator

Gandiva Insights • IL, United States
1 day ago
Job type
  • Full-time
  • Quick Apply
Job description

Job Title : CAPA Investigator Owner

Location : Round Lake IL

Duration : 12 Months

Description : CAPA / NCR writers

Description : CAPA / NCR writers

1. Perform non-conformance (NCR) investigations within the Track Wise 8 Management System.

2. Execute implementation of CAPAs associated with NCR investigations.

3. 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 client corporate quality requirements.

4. Provide guidance and coaching on performance of DMAIC problem solving and process improvement projects for less experienced individuals within the plant.

Qualifications :

1. Candidate must not be allergic to Penicillins or Cephalosporins

2. Understanding of the product's intended use and manufacturing process

3. Ability to prioritize multiple tasks to ensure compliance with regulations and standard operating procedures.

4. Strong problem solving and analytical skills.

5. Consultation and facilitation skills.

6. Understanding of statistics in support of fact based decision making.

7. Excellent written / verbal communication and organizational skills

8. Ability to make independent decisions with minimum oversight

9. Customer sensitivity / acumen and ability to interact with all levels of management.

10. Experienced user of TrackWise preferred.

11. Working knowledge of FDA Regulations and International Regulatory requirements.

12. Understanding of risk management tools.

13. 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.

Thanks & Regards,

Anupam Das

Manager- Recruitment & Sales

Direct Number : 346-658-2825 / 360-614-3032

115 Gemini St. Suite# 173 Houston, TX 77058

anupam@gandivainsights.com

www.gandivainsights.com

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Investigator • IL, United States