Job Description
Specialist, Material Management Tester
The Opportunity
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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.
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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.
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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 a Tester to support SDLC development and GMP validation of the Biovia OneLab- Biovia CISPro platform for Quality Control labs. This role works under the direction of the Lead Tester to develop and execute test scripts that ensure the platform meets business, compliance, and validation requirements in a regulated environment. The Tester supports efforts to ensure compliance with FDA 21 CFR Part 11 and data integrity standards, and collaborates with QA, IT, business, and laboratory teams to support system changes and updates.
What will you do in this role:
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Create test plans, scenarios and test scripts.
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Implement software testing, using either manual or automated programs and exploratory testing, and evaluate results.
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Document and report defects or problems with software.
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Provide feedback to software developers and stakeholders regarding usability and functionality
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Support the design and implementation of solutions that comply with regulatory standards in the GxP environment.
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Develop SDLC documents (SIT, UAT, test summaries, etc.).
What Should you have:
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Proven experience as a Tester in the regulated GxP pharma lab environment (3-7 years).
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Understanding of regulatory requirements and compliance in the pharmaceutical industry.
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Excellent analytical and problem-solving skills.
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Ability to work independently and as part of a cross-functional team and manage multiple priorities in a dynamic environment.
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Experience developing test scripts in a regulated environment.
Nice to haves:
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Bachelor’s degree in a relevant field (e.g., Life Sciences, Information Technology)
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Experience with Agile methodologies and project management tools.
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Experience with Computer System Assurance (CSA).
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Experience with the Laboratory Information Systems (LIMS) or Laboratory Execution System (LES).
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Experience with Biovia CISPro.
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.
#HYDIT2025
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
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:
06/23/2026
- 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:R401696
