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Analytical Quality Assurance-2

Bristol Myers Squibb
Bristol Myers Squibb
5+ years
Not Disclosed
Hyderabad
9 May 6, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Analytical Quality Assurance – 2

Company

Bristol Myers Squibb

Location

Hyderabad, Telangana, India

Employment Type

Full-time

Requisition ID

R1602024


Position Summary

The Analytical Quality Assurance (AQA) role is responsible for the timely review, evaluation, and approval of qualification activities for analytical reference standards and critical reagents (RS-CR) used in GMP analytical testing.

The role ensures compliance, data integrity, and regulatory alignment while supporting fast-paced quality operations across a global pharmaceutical network. It requires close collaboration with analytical operations, quality teams, and compliance stakeholders to ensure availability of qualified materials for clinical and commercial testing.


Key Responsibilities

Quality Review and Approval

  • Perform accurate and timely QA review, evaluation, and approval of RS-CR qualification documentation.

  • Ensure deliverables are completed within defined timelines (typically ~3 days per cycle).

  • Manage multiple concurrent review assignments in a high-volume environment.


Compliance and Technical Understanding

  • Maintain strong knowledge of GMP requirements related to analytical testing and RS-CR qualification.

  • Ensure adherence to applicable procedures, quality standards, and regulatory expectations.

  • Apply critical thinking to evaluate risk and urgency in documentation review.


Stakeholder Collaboration

  • Collaborate with RS-CR operations, Analytical Quality & Compliance (AQ&C), and other global stakeholders.

  • Participate in discussions to understand workload, timelines, and documentation status.

  • Communicate proactively using appropriate channels (e.g., MS Teams for urgent issues).


Issue Resolution and Continuous Improvement

  • Escalate and resolve quality and compliance issues in collaboration with stakeholders.

  • Participate in meetings to support resolution of documentation or compliance concerns.

  • Contribute to process improvements and consistency in RS-CR qualification standards.

  • Provide feedback to improve quality systems and ensure right-first-time approvals.


Systems and Documentation Management

  • Use enterprise systems to review and approve qualification documentation.

  • Work across platforms such as Veeva, LIMS, SharePoint, Outlook, and internal document systems.

  • Ensure accurate tracking, documentation, and record maintenance.


Qualifications

Education

  • Bachelor of Science in Life Sciences, Pharmacy, Nursing, Chemical Engineering, Bioengineering, or related field.


Experience

  • Minimum 5 years of experience in a pharmaceutical, biotechnology, or medical device organization in a Quality role.

  • Experience in GMP analytical testing environments is preferred.

  • Experience in reference standard or critical reagent qualification is an advantage.


Skills and Competencies

Technical Skills

  • Strong understanding of GMP analytical testing processes.

  • Familiarity with quality systems and documentation workflows.

  • Proficiency in electronic quality and document management systems (e.g., Veeva, LIMS).


Analytical and Cognitive Skills

  • Strong critical thinking and risk assessment ability.

  • Ability to manage urgent tasks with strict timelines.

  • High attention to detail and accuracy in documentation review.


Organizational Skills

  • Ability to prioritize multiple tasks in a fast-paced environment.

  • Strong time management and workload coordination skills.


Communication and Collaboration

  • Strong written and verbal communication skills in English.

  • Ability to collaborate across global teams and time zones.

  • Ability to incorporate feedback and maintain strong stakeholder relationships.


Work Environment

  • High-volume, fast-paced quality assurance environment.

  • Strong emphasis on compliance, urgency, and precision.

  • Cross-functional global collaboration.