Senior Specialist Job At Bristol Myers Squibb | Pharmaceutical Sciences Apply Now

Senior Specialist Job At Bristol Myers Squibb

Bristol Myers Squibb (BMS) is hiring a Senior Specialist – APMC Data Management in Hyderabad, Telangana. This Pharmacy Job role is ideal for professionals with experience in regulatory systems, quality compliance, supply chain data, and CMC operations, offering exposure to global product lifecycle management in a highly regulated biopharmaceutical environment. Graduates seeking Pharmacy Jobs and want to start their career with Pharmacy Careers can apply now.

Job Details

• Job Title: Senior Specialist – APMC Data Management
• Location: Hyderabad, Telangana, India

About the Company

Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to transforming patients’ lives through science™. BMS offers meaningful, high-impact careers with a strong focus on innovation, compliance, diversity, inclusion, and employee well-being, supported by world-class benefits and career development opportunities. This Pharmacy Job role plays a significant role in the company.

Educational Requirements

• Bachelor’s degree in Pharmaceutical Sciences

Experience Required for this Pharmacy Job

• Minimum 3 years of experience in:

  • Technical, Quality, or Regulatory roles

  • Biopharmaceutical or pharmaceutical industry

• Experience in Quality Compliance or Operations preferred

Key Responsibilities for this Pharmacy Job 

• Execute daily operations in regulatory and quality systems, including:

  1. Veeva Vault RIM

  2. Veeva Quality Systems

  3. Regulatory Content Repositories

• Configuring and managing activities in SAP Batch Release Hub is essential for this Pharmacy Job
• Support Change Control Restriction Management, including CMC assessments and document management
• Perform operations within Authorized Supply Chain Maps
• Manage Document Data Extraction, including configuration and exception handling
• Review and assess data from eCTD and CTD Module 3 for accuracy and consistency
• Collaborate with CMC, Quality, and Supply Chain teams
• Escalate risks, deficiencies, and unresolved issues proactively
• Support timely product release activities
• Identify and recommend process improvement opportunities
• Ensure compliance with GMP standards and BMS policies
• Provide support across additional systems, including:

  1. Change Controls

  2. Deviations

  3. SAP and regulatory platforms

Skills Required for this Pharmacy Job

• Strong understanding of:

1. Biologics, pharmaceuticals, or cell therapy operations
2. Product release processes (DS, DP, finished products)
3. Global post-approval submissions and lifecycle changes

• Experience with:

1. SAP
2. eCTD / CTD Module 3
3. Veeva RIM and Veeva QMS (preferred)

• Knowledge of:

1. Bills of Materials (BOM)
2. GMP compliance
3. 21 CFR Part 11, EU Annex 11, Data Integrity principles

• Strong analytical, documentation, and organizational skills
• Ability to balance speed, quality, and risk
• Collaborative and cross-functional working mindset
• Fluent professional English communication skills

Why This Job Role?

This Pharmacy Job role offers exposure to global regulatory systems, quality compliance, and supply chain data management within a world-class biopharmaceutical organization. It is ideal for professionals seeking to strengthen their expertise in product lifecycle management, regulatory operations, and GMP-driven systems while working on impactful medicines that change patients’ lives. Graduates seeking Pharmacy Jobs and want to start their career with Pharmacy Careers can apply now.

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