At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Areas Of Responsibility
Own end-to-end delivery of LIMS (CaliberLIMS Preferred) implementation programs, ensuring alignment with laboratory operations, business goals, and regulatory requirements.
Lead requirement gathering, solution design, and system configuration including workflows, and user roles/permissions.
Manage project planning, timelines, risks, & resource allocation to ensure successful and timely delivery.
Drive integration of LIMS with Lab Instrument including Port based, File based and CDS (Empower) and enterprise systems (such as SAP and TrackWise) ensuring data integrity and system performance.
Ensure compliance with GxP standards (GMP, GLP, FDA, 21 CFR Part 11) and lead Computer System Validation (CSV) activities.
Act as the primary liaison between business stakeholders, IT teams, QA, and external vendors, ensuring clear communication and alignment.
Lead user enablement including training strategy, SOP development, documentation, and change management for successful adoption.
Establish post-go-live support, continuous improvement initiatives, and system enhancements to optimize performance and user experience.
Travel Estimate
Don't want to miss the next one?
Subscribe to daily email alerts for roles matching your interests.
Financial Accountability (cost/revenue with exclusive authority)
NA
Job Requirements
Educational Qualification
Bachelor’s degree in Information Technology, Computer Science,
Specific Certification
Experience
7-10 Years
Skill (Functional & Behavioural):
7–10 years of experience in LIMS implementation, with exposure to regulated environments such as pharmaceuticals or biotechnology.
Strong expertise in LIMS platforms (CaliberLIMS preferred) and understanding of laboratory workflows (QC/R&D).
Proven experience in system integration (instruments and enterprise applications) and basic understanding of data architecture.
In-depth knowledge of regulatory compliance (GxP, FDA, GMP, GLP, 21 CFR Part 11) and Computer System Validation (CSV).
Strong leadership, stakeholder management, communication, and problem-solving skills with the ability to manage multiple priorities.
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).
Similar roles you might like
More openings like this one — take a look before you go.
