Specialist, Product Analyst- Quality

• 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. Be a part of a team with passion for using data, analytics, and insights to drive decision-making, and which creates custom software, allowing us to tackle some of the world's greatest health threats.

As a  Specialist, Product Analyst – Quality, you will be responsible for driving solution design, implementation, and continuous improvement of the different QMS tools with specific alignment to the Quality business processes. Essential skills include a strong technical as well as business background, proficiency in project management methodologies (Agile, Scrum), and excellent organizational abilities.

This role is positioned within the company , will have advanced experience in the life sciences industry, specifically Quality Management Systems and technology landscapes; specifically, Veeva Vault Quality; will have knowledge of GxP and will play a critical role during the solution design to satisfy business needs and assuring adoptability to future system scalability.

Veeva Config specialist, GXP

• Apply a structured approach to discover, document, and manage business process, user and stakeholder needs, including opportunity statements, use cases, insights, and requirements.
• Gather insight into user journey, behavior, motivation, and pain points. Expose unarticulated problems and unmet needs.
• Document business process, business, and user needs in the form of problem statements to make up the backlog. Facilitate the “how” with the Development team.
• Gain expertise in the business area.
• Manage business analysis per agreed priority backlog items in JIRA.
• Participating in impact assessment activities, reviewing proposed changes and ensuring impact is understood.
• Deliver product enhancements through agreed backlog process to ensure Quality solutions evolve to meet business needs.
• Ensure Quality solutions remain compliant as a Validated Solution through verification testing, documentation, and validation efforts.
• Provide overall leadership, guidance, and management of all aspects of a given solution, including requirements gathering, enhancements delivery plan, and implementation.
• Initiate projects including defining a scope/charter, identifying stakeholders, and establishing governance.
• Act as a bridge between Business SMEs, technical teams, and non-technical stakeholders. Communicate delivery status, solution health, risks, and issues to all parties involved and ensure that everyone is aligned and informed.
• Conduct product status meetings and present updates to stakeholders and senior management. Evaluate delivery performance and implement continuous improvement practices.
• Understand the technical aspects as well as business process impacts to make informed decisions, provide guidance, and communicate effectively with the development team. This includes having a deep understanding of the QMS business processes, technology stack, architecture, and potential technical challenges.
• Work closely with the Product Owner to prioritize and refine the product backlog, ensuring that the team focuses on delivering the most valuable features.
• Identify potential risks and develop mitigation strategies. Proactively address issues that could impact project success.

• Minimum Level of Education Required: Bachelor’s Degree in Computer Science, Engineering, MIS, and Science OR in a related field. The job requires a solid academic background on how Information Technology supports the delivery of business objectives.
• Preferred Level of Education: Veeva Certifications (Veeva Vault/Vault Quality Suite/ QMS). The role holder has completed the Certified Vault Training and is up to date.
• 3+ years of experience in technical project management, with a strong understanding of project management methodologies (Agile, Scrum, Waterfall).
• Understanding of Quality Management System Capabilities (Audit/Inspection management, CAPA management, Deviations management, Complaint management).
• Experience in solution delivery with GMP systems.
• Experience with architecture, integration, interfaces, portals, and/or analytics.
• Understanding of Systems Development Life Cycle (SDLC), and current Good Manufacturing Practice (cGMP) processes.
• Knowledge and experience with QMS relevant tools like Veeva Vault Quality, TrackWise.
• Proven experience in leading complex technical projects in a fast-paced environment.
• Strong technical background with knowledge of software development, systems integration, or related areas.
• Excellent organizational, leadership, and decision-making skills.
• Strong analytical and problem-solving abilities.
• Effective communication and interpersonal skills to liaise with cross-functional teams.
• Ability to manage multiple projects simultaneously and adapt to changing priorities

Our technology teams operate as business partners, proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate internationally to deliver services and solutions that help everyone be more productive and enable innovation.

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.

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.

Current Employees apply HERE

Current Contingent Workers apply HERE