Experience: Master’s degree in chemistry/ pharmacy with 8-10 years of experience in Analytical Method Transfer / Validation executions in Quality control Laboratory and Quality Review of sterile dosage manufacturing facility.

Core Competencies

• Analytical Method Validation/Transfers/Verification
• Change Management process
• Risk assessments principles and tools
• Qualification of lab equipment’s
• Regulatory requirements & Compendial Changes
• Stability Management

Technical Skills

• Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography),GC,IC, ICP-MS techniques
• Qualified in multiple analytical techniques(HPLC-with Empower, GC, IC, ICP-MS, Potentiometry, UV‑Vis, FTIR, Karl Fischer, AAS, XRF, NIR and pH meters)
• Demonstrated technical skills in method validation and testing
• Having Capability to understand the Compendial methods and Conduct analytical method validation in accordance with ICH Q2 (R1/R2), USP, and EP standards.
• Interpretation of analytical systems generates data against the procedure requirements.
• Having capability to assess the test method requirements against USP, EP, BP, and JP requirements for New Product Introduction (NPI).
• Review of document analytical method verification and method transfer activities.
• Demonstrate knowledge of ICH Q9 (Quality Risk Management) and apply risk‑based principles for identifying, assessing, controlling, communicating, and reviewing quality risks throughout the product lifecycle.
• Perform identification, assay, purity, and related analytical tests using validated methods.
• Having Knowledge on assessment of Elemental Impurities, Nitrosamine impurities, Extractable & Leachable and its guideline requirements.

• Knowledge in validation principles and practices related to the Process validation, cleaning validation, Analytical Method validation, Water system, HVAC system, Equipment & Utility Qualifications.
• Knowledge of various Quality tools required for investigations
• Technical Writing- Ability to create documentation that is accurate, complete, unambiguous, and as concise as possible aimed to be understood by any level of organization
• Knowledge in change control assessment
• Basic idea on manufacturing operations, validation and engineering functions
• Experience in handling Regulatory agency inspections

Behavioral/Any Other Skills

• Interpersonal Skills: Effective communication with all colleagues from different levels and builds constructive and effective relationship
• Managerial Skills: Persistent approach to resolving issues, Effective situation handling capabilities, strong time management skills.
• Acts Decisively: Makes decision in a timely manner based on available information
• Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives
• Self-accountable & Proactive approach

• Strong scientific and analytical thinking

• Excellent review and documentation skills

• Regulatory and GMP compliance mindset

• Investigation and problem-solving capabilities

• Cross-functional collaboration

• Leadership and mentoring skills

• Attention to detail and data integrity focus

• Effective communication and stakeholder management

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.