Specialist, Supplier Quality Systems & Data (SQMS) – Global Shared Services
Job Summary
Job Description
Specialist Supplier Quality Systems & Data (SQMS) Global Shared Services
About the Role
We are looking for a detail-oriented Quality professional to join our global Supplier Quality Management (SQM) team within a shared services organization supporting Human Health manufacturing sites worldwide.
As a Specialist you will focus on execution and maintenance of Supplier Quality Management Systems (SQMS) with a strong emphasis on data quality accuracy and system-driven processes. You will support global supplier quality activities through consistent system usage data governance and process compliance.
What Youll Do
- Execute day-to-day SQMS activities including data entry workflow management and record maintenance within systems such as Veeva Vault and SAP.
- Ensure high-quality accurate and complete supplier data in SQMS (e.g. Approved Supplier List supplier records change controls and performance data).
- Support supplier lifecycle processes including onboarding qualification change notifications SCAR tracking and supplier performance monitoring through system execution.
- Perform data quality checks identify discrepancies and drive corrections to ensure Right-First-Time (RFT) data integrity.
- Support global SQMS intake and workflow routing ensuring timely and compliant processing of requests.
- Generate and maintain standard reports dashboards and metrics related to supplier quality processes (cycle times compliance status data completeness).
- Collaborate with sites procurement supply chain and suppliers to clarify data requirements and resolve system/data issues.
- Assist in audit and inspection readiness by ensuring documentation and system records are complete accurate and readily retrievable.
- Contribute to continuous improvement initiatives focused on enhancing SQMS usability automation and data governance.
What Youll Bring
- 7 years of experience in the pharmaceutical/biologics industry within Quality Assurance or Supplier Quality.
- Working knowledge of cGMP and basic regulatory expectations (ICH FDA EMA).
- Hands-on experience with electronic Quality Management Systems (e.g. Veeva Vault SAP) preferred.
- Strong focus on data quality accuracy and attention to detail.
- Experience working with structured data reporting and dashboards (Excel Power BI or similar tools).
- Ability to follow defined processes and procedures while managing multiple tasks with high accuracy.
- Good collaboration and communication skills to work across global teams and functions.
- Problem-solving mindset with ability to identify data issues and propose practical solutions.
- Proficiency in Microsoft Office tools (Excel Power BI PowerPoint Word).
Why Join Us
- Gain hands-on experience with global SQMS platforms and supplier quality processes.
- Build expertise in data-driven quality systems and digital quality transformation.
- Work in a collaborative global environment supporting critical supplier quality operations.
- Contribute to improving data integrity compliance and process efficiency at scale.
Location and Travel
- Based in Pune within a global shared services organization (hybrid model: 3 days onsite/week).
- Minimal travel may be required.
Required Skills:
Aseptic Manufacturing Audits Compliance Corrective and Preventive Action (CAPA) Detail-Oriented Documentation Review Driving Continuous Improvement GMP Compliance Quality Assurance Tools Quality Auditing Quality Management Systems (QMS) Quality Standards Root Cause Analysis (RCA) Supplier Quality Management TroubleshootingPreferred 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:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
HybridShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
05/27/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
IC
About Company
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more