QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations.

• Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation and maintenance of the procedures, actions and documentation necessary to assure compliance according to the appropriate federal and international regulations which govern the user's applications.

• Reports on the status of validation activities to fulfill regulatory requirements.

• Performs system administration and configuration of quality information technology systems.

• Performs investigation non-conformance events

• Availability to work overtime and weekends when necessary

• Good problem-solving skills

• Initiates, recommends, and provides solutions to the Non-Conforming Product as per procedures

• Verifies the implementation and effectiveness of non-conforming CAPA

• Executes job responsibilities as established in the procedures

• Follows the documentation procedures Non- Conformance Resolution

• Evaluating, Investigating & Completion of Non- Conformance

• Investigation (Data gathering of Quality issue)

• Identify Corrective/Preventive Actions

• Implementing Corrective/Preventive Actions

• Lead complaint activities with the Operating Units members

Qualifications:

• Bachelor Degree in Engineering

• Two or three (2 - 3) years of previous experience 

• Basic knowledge in quality manufacturing operations Nonconforming product, Yield, Pareto defect, Bounding.

• Basic knowledge in Statistical Process Control.

• Basic Process Validation knowledge in Process Validation.

• Availability for 2nd or 3rd shift 

  Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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