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Technical Lead

2+ years
Not Disclosed
10 July 26, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Analytical Method Development and Validation Specialist

Key Responsibilities:

  • Analytical Method Development: Develop and validate analytical methods for all pharmaceutical dosage forms in accordance with current compendial pharmacopoeias, ICH guidelines, and global regulatory requirements.

  • Method Transfer: Execute the transfer of analytical methods for pharmaceutical dosage forms, ensuring smooth integration and consistency across various platforms.

  • Technical Support: Provide technical assistance to Abbott manufacturing facilities and Third-Party Manufacturers (TPMs) worldwide, facilitating optimal performance and compliance.

  • Collaborative Meetings: Engage in multidisciplinary team meetings (including Manufacturing, Supply Chain, Commercial, Quality Assurance, and Regulatory Affairs) to offer scientific support for Product Evaluation, Formulation, and Process Development.

  • Literature Search: Conduct literature searches related to drug substances and create detailed analytical profiles to support development efforts.

  • Sample Analysis: Perform routine analyses of samples including product development batches, stability study samples, and raw materials.

  • Instrument Operation and Calibration: Operate and calibrate analytical instruments and equipment, ensuring accuracy and reliability in results.

  • Lab Investigations: Conduct investigations for Out of Specification (OOS) and Out of Trend (OOT) results, implementing corrective actions as necessary.

  • Data Review and Release: Review and release data as assigned, ensuring compliance with quality standards.

  • Documentation: Document analytical activities following Good Documentation Practices (GDP), including the preparation of Standard Operating Procedures (SOPs), Standard Test Procedures (STPs), Specifications, Certificates of Analysis (COAs), and stability reports.

  • Data Review: Review analytical development and stability data, ensuring adherence to regulatory and quality standards.

  • Compliance: Ensure adherence to all compliance programs, including Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environmental policies, and HR policies.

  • Additional Duties: Perform all other relevant duties as assigned to support the overall objectives of the department.