MSD
Website:
msd.com
Job details:
Job Description
Material Management, Specialist Business Analyst
The Opportunity
- Based in Hyderabad, join a global healthcare biopharma company and be part of a 130-year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
- Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.
- Drive innovation and execution excellence. Join a team that is passionate about using data, analytics, and insights to drive decision-making and create custom software, allowing us to tackle some of the world's greatest health threats.
Our Technology Centres focus on creating a space where teams can come together to deliver business solutions that save and improve lives. An integral part of our company's IT operating model, Tech Centres are globally distributed locations where each IT division has employees to enable our digital transformation journey and drive business outcomes. These locations, in addition to the other sites, are essential to supporting our business and strategy.
A focused group of leaders in each Tech Centre helps ensure we can manage and improve each location, from investing in the growth, success, and well-being of our people to making sure colleagues from each IT division feel a sense of belonging, to managing critical emergencies. Together, we must leverage the strength of our team to collaborate globally to optimize connections and share best practices across the Tech Centres.
Role Overview
As part of our global Lab Transformation effort, we are seeking an IT Business Analyst to support SDLC development and GMP validation of the Biovia OneLab platform for Quality Control labs. This role will support the creation, editing, and maintenance of documentation such as SOPs, work instructions, and validation records. Working under the guidance of the Lead IT Business Analyst, this role ensures that documents align with GxP and data integrity requirements while assisting with formatting, version control, and document management processes. The IT Business Analyst will collaborate with technical teams to gather information, incorporate feedback, and build foundational knowledge of Biovia CIS Pro and regulated documentation practices.
What Will You Do In This Role
- Elicit and document business requirements for lab materials management.
- Conduct stakeholder interviews and working sessions to gather insights and clarify needs.
- Analyze and translate business requirements into functional and technical specifications for the selected technology.
- Collaborate with project teams to ensure alignment in the design and implementation of systems and processes.
- Develop and maintain comprehensive project documentation, including requirement specifications, use cases, and design documents.
- Facilitate discussions to ensure stakeholder understanding and agreement on requirements and design.
- Conduct gap analysis to identify discrepancies between current processes and desired outcomes.
- Support the design and implementation of solutions that comply with regulatory standards in the GxP environment.
- Assist in user acceptance testing (UAT) to ensure that solutions meet business requirements and operational needs.
- Provide training and ongoing support to end-users on new systems and processes.
- Perform light coding, database querying, and system configurations as needed to support project goals.
- Draft SDLC documents (Process Maps, Workflows, RS, UAT, SOPs, etc.)
What Should You Have
- 3-7 years, Proven experience as a Business Analyst / Technical Analyst in the regulated GxP pharma lab environment.
- Strong understanding of regulatory requirements and compliance in the pharmaceutical industry.
- Experience with the Laboratory Information Systems (LIMS) or Laboratory Execution System (LES).
- Experience with system-system integrations and instrument integrations.
- Experience supporting large-scale, global, complex projects, associated with digital transformation/optimization initiatives.
- Familiarity with testing tools and methods e.g. JIRA, Microsoft Teams, etc.
- Technical skills in light coding, database querying (e.g., SQL), and system configurations.
- Excellent analytical and problem-solving skills.
- Strong communication and interpersonal skills to effectively engage with stakeholders.
- Ability to work independently and as part of a cross-functional team and manage multiple priorities in a dynamic environment.
- Experience supporting large-scale, global, complex projects, associated with digital transformation/optimization initiatives.
Nice to haves
- Bachelor’s degree in a relevant field (e.g., Life Sciences, Information Technology).
- Experience with Agile methodologies and project management tools.
- Experience with the Biovia CISPro.
- Experience with MODA, Scitara, LabWare, or LabX.
- Experience with Appian.
- Knowledge of data analysis and visualization tools.
Who We Are
We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
What We Look For
Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.
Required Skills
Asset Management, Benefits Management, Management System Development, Product Management, Requirements Management, Stakeholder Relationship Management, Strategic Planning, System Designs
Preferred Skills
Current Employees apply HERE
Current Contingent Workers apply HERE
Secondary Language(s) Job Description
#MSDHYDIT
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status
Regular
Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Hybrid
Shift
Valid Driving License
Hazardous Material(s)
Job Posting End Date
08/21/2026
- A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID R401697
Click on Apply to know more.
