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Process Specialist-CDM/PV @ Cognizant

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 Process Specialist-CDM/PV

Job Description



Job Summary

The Process Specialist-CDM/PV role involves managing and optimizing processes within Pharma Research & Development. The candidate will contribute to enhancing safety operations and pharmacovigilance case processing. With a hybrid work model and rotational shifts the role demands adaptability and technical expertise. The position does not require travel.


Responsibilities

  • Oversee the management and optimization of processes within Pharma Research & Development to ensure efficiency and compliance.
  • Provide support in pharmacovigilance case processing ensuring accurate and timely documentation of safety data.
  • Collaborate with cross-functional teams to enhance safety operations and improve overall process effectiveness.
  • Analyze data and generate reports to support decision-making and strategic planning in pharmacovigilance activities.
  • Implement best practices and innovative solutions to streamline processes and improve productivity.
  • Ensure adherence to regulatory requirements and industry standards in all aspects of pharmacovigilance and safety operations.
  • Facilitate communication and coordination between different departments to achieve seamless workflow and process integration.
  • Monitor and evaluate process performance identifying areas for improvement and implementing corrective actions.
  • Assist in the development and maintenance of standard operating procedures to ensure consistency and quality in process execution.
  • Support training and development initiatives to enhance team capabilities and knowledge in pharmacovigilance and safety operations.
  • Utilize technical skills to troubleshoot and resolve process-related issues minimizing disruptions and ensuring smooth operations.
  • Contribute to the continuous improvement of processes by providing insights and recommendations based on data analysis.
  • Engage in rotational shifts to provide consistent support and coverage across different time zones.

  • Qualifications

  • Possess a strong background in Pharma Research & Development with experience in pharmacovigilance case processing.
  • Demonstrate proficiency in safety operations and regulatory compliance within the pharmaceutical industry.
  • Exhibit excellent analytical skills and the ability to interpret complex data sets for informed decision-making.
  • Show adaptability to work in a hybrid model and manage rotational shifts effectively.
  • Have a keen eye for detail and a commitment to maintaining high standards of quality and accuracy.
  • Display effective communication skills to collaborate with cross-functional teams and stakeholders.
  • Be proactive in identifying process improvements and implementing innovative solutions.
  • Hold a relevant degree in pharmaceutical sciences or a related field.
  • Have a minimum of 2 years and a maximum of 4 years of experience in the pharmaceutical industry.
  • Experience in PV Case Processing and Safety Ops is considered a valuable asset.
  • Demonstrate the ability to work independently and as part of a team to achieve organizational goals.
  • Show commitment to continuous learning and professional development in pharmacovigilance and safety operations.
  • Be familiar with industry-standard software and tools used in pharmacovigilance and process management.
  • Job Classification

    Industry: IT Services & Consulting
    Functional Area / Department: Production, Manufacturing & Engineering
    Role Category: Operations, Maintenance & Support
    Role: Operations, Maintenance & Support - Other
    Employement Type: Full time

    Contact Details:

    Company: Cognizant
    Location(s): Mumbai

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    Keyskills:   development data analysis analytical workflow continuous development pv regulatory compliance monitoring research process improvements operations ops process management s continuous improvement case processing safety operations safety compliance communication skills

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    Company DetailsCognizant Technologies Ltd