Deviation Investigators​/Senior Quality Specialist

Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

• Quality Record Initiation:
  Initiate quality records promptly and accurately for identified deviations, ensuring alignment with both industry and Client expectations.
• Deviation Investigations:
  Conduct thorough investigations for identified deviations, employing root cause analysis methodologies.
• Assess the impact on product quality with input from various departments.
• CAPA Identification and Implementation:
  Identify and recommend Corrective and Preventive Actions (CAPA) based on investigation findings.
• Collaborate with stakeholders to ensure the effective implementation of CAPA measures.
• Comments Resolution:
  Timely resolution of internal and client comments related to investigations.
• Collaborate with relevant parties to address and close out comments effectively.
• Document Retrieval and Operator Interviews:
  Retrieve necessary supporting documents to substantiate investigation findings.
• Conduct interviews with manufacturing operators to gather relevant information.

• Timely initiation and completion of quality records.
• Thoroughness and accuracy in deviation investigations.
• Meeting the minimum requirement of closing deviations per week.
• Effectiveness in identifying and implementing CAPA measures.
• Possible availability and responsiveness during weekends.
• Efficient resolution of internal and client comments.