Carrer

Hi,

Hope you doing Well !!!

Here is our Implementing partner Requirement. Kindly share suitable resumes ASAP to neha.g@nityo.com

Role:  Quality Engineer With Certification in Regulatory Compliance & Standards

Location: Naples, FL 34108

Duration of contract: 6 months

Interview: Phone/ Skype

Required start date: Immediately

Technical Skills:-

1. Thorough knowledge of CAPA(Corrective Actions and Preventive Actions), Nonconformance and Deviation workflows, Experience in medical devices or pharmaceutical companies

2. Knowledge of Trackwise or Quality Management System Nice to have skills (Top 2 only)

1.            Excellent  communication and Inter-Personal skills

2.            Knowledge on regulatory standards

Desired years of experience : 5

Education/ Certifications (Required) : Certification in Regulatory Compliance & Standards

Top 3 responsibilities you would expect the subcon to shoulder and execute:

1.     Coordinate and assist Coordinators with regular review meetings held with business owners who participate on the CAPA teams.

2.    Coordinate and assist Coordinators with reviews of CAPA responses with QA staff to assure completeness and compliance to internal and external standards.

3.     Monitor and support activities related to the processing of Nonconformance and Deviation records.

Assist with the organization, documentation, and coordination of ongoing tasks within the Quest Quality Management System as directed by Supervisor.  

What is the team size, make up, culture, soft skills, and dress code, Hours? 3-4 team members need to be handled by Subcon . Excellent verbal and written communication needed. 8 hours working

I may miss to check voice messages but never miss to reply Emails. Please do email me If I miss your call.

Thanks & Regards,