ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- Kochi, India
- Type
- Full-time
- Posted
- Jun 15, 2026
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Sr Production Assoc
at ACUTA
Job Profile - Sr Production Assoc (120 Grade)
Job Overview:
Perform variety of production execution activities for 80 plus countries
globally on their critical deliverables with its highest accuracy and quality.
Also need to implement various process enhancements and automations for global
offerings in IQVIA worldwide. Involves quality assurance, production of
reports, answering queries from Local Offices for the EMEA & LATAM regions.
Principal Accountabilities:
• Executing, Monitoring, 1st level fixing and 2nd level escalating
• Reporting and rerunning production processes as defined in Schedule
• First & Second level break-fix support for Mainframe-Infrastructure and its
components.
• Participate in Root Cause Analysis as appropriate.
• Ensure daily process & procedures remain accurate and up to date. Ensure
account checklist items are completed and signed off.
• Diagnose, troubleshoot and report/resolve interruptions or problems in
system processing and or hardware anomalies.
• Providing Production support 24X7 which involves escalation of abend.
• Provide immediate fixes to the production abends. Solving production abends
as per the abend document.
• Monitor batch cycles for daily, weekly, monthly, quarterly, yearly jobs and
report statistics to client.
• Ensure timely completion of the batch cycles as per the schedule.
• Check for long running jobs and investigate in case there are any loop back
issues with batch jobs.
Job Skill Requirements:
• Basic knowledge on Mainframe, JCL, COBOL, ESP, REXX.
• Strong analytical skills and problem-solving ability.
• Excellent written and good oral communication skills.
• Creative thinker and an eye for detail and quality.
• Fair knowledge in MS Excel, MS Power Point, Power BI etc.
Qualifications
• Master’s degree MSc, MCA etc.
• 0-1 years of experience in Mainframe Development or Support function.
• Pharmaceutical industry knowledge will be an added advantage but is not a
pre-requisite.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.