Vault Quality DevOps - Perform technical analysis SDLC Release Testing activities Current Employees apply HERE Current Contingent Workers apply HERE Secondary Language s R3 Senior Manager Vault Quality Technical 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 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 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 Center helps to ensure we can manage and improve each location from investing in 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 And 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 Act as a liaison between Quality Operations IT and business stakeholders to gather analyze and document requirements related to Veeva Vault Quality applications Drive process improvements and system enhancements to optimize the use of Veeva Vault for Quality Management Support the implementation and ongoing maintenance of Veeva Vault Quality modules aligned with regulatory and business needs What will you do in this role Responsibilities Collaborate with Quality Compliance and IT teams to understand business processes and translate them into system requirements for Veeva Vault Quality Operations Gather analyze document and validate comprehensive business and functional requirements to support system enhancements upgrades and new implementations Analyze current Quality Operations workflows e g QualityDocs QMS Audit Issues Inspections Complaints Change Control and identify opportunities for automation or process improvement using Veeva Vault Support configuration and testing activities by creating test plans test cases and coordinating User Acceptance Testing UAT Facilitate communication between technical teams developers administrators and business users to ensure clear understanding of requirements and solutions Assist in change management activities including training material development user guides and conducting training sessions Monitor system performance and user feedback to recommend continuous improvements Ensure compliance with regulatory standards FDA 21 CFR Part 11 GxP in all system-related processes Maintain documentation such as business process maps requirement specifications and SOPs related to Veeva Vault Quality Operations What should you have 4 years of Technical Analyst experience with Vault Quality Systems QualityDocs QMS Strong understanding of Quality processes including CAPA Change Control Document Management Complaints and Audits Experience gathering and documenting business and functional requirements Familiarity with system validation lifecycle and testing methodologies Experience using JIRA XRAY for test case management test execution reporting defect management within Agile environments Excellent communication and stakeholder management skills Ability to translate complex business needs into clear technical requirements Knowledge of regulatory requirements in pharmaceutical biotech or medical device industries Proficiency with process mapping and documentation tools Detail-oriented with strong analytical and problem-solving skills However we will be happy if you also have Experience working directly with Veeva Vault or other cloud-based QMS platforms Veeva Certifications Veeva Vault Vault Quality Suite QMS The role holder has completed the Certified Vault Training and is up to date Background in regulated environments pharma biotech medical devices Experience with Agile or other software development methodologies Familiarity with reporting and data analysis 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 for life 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 chance 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 HYDIT 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 RegularRelocation VISA Sponsorship Travel Requirements Flexible Work Arrangements HybridShift Valid Driving License Hazardous Material s Required Skills Asset Management Benefits Management Management System Development Product Management Requirements Management Stakeholder Relationship Management Strategic Planning System Designs Preferred Skills Job Posting End Date 10 28 2025A 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 R366259