Validation and Life Cycle Management Specialist

3 days ago

Hyderabad, Telangana, India beBeeProcess Full time ₹ 18,00,000 - ₹ 24,00,000
Job Overview

We are seeking a highly skilled Validation and Life Cycle Management Professional to join our team. The ideal candidate will possess expertise in preparing process and cleaning validation documentation, executing change tasks, and ensuring compliance with cGMP requirements.

">Key Responsibilities:
  • Prepare process and cleaning validation documentation as well as change evaluations.
  • Execute change tasks to meet cGMP requirements on time and with quality.
  • Ensure site validation programs meet global regulatory expectations.
(preparation of process and cleaning validation documentation as well as change evaluations, executing change tasks to meet cGMP requirements on time and with quality)
(Preparation of process and cleaning validation documentation as well as change evaluations, executing change tasks to meet cGMP requirements on time and with quality)Support process validation lifecycle activities.Create local templates for the respective validation documentation.Participate in pre-validation activities and risk assessments to ensure the success of commercial process validation.Provide technical expertise and facilitate the creation of a quality risk assessment.Have a profound background in organic chemistry to support physico-chemical buffer stability risk assessments, evaluation of corrosive agents as part of facility comparability assessments.Prepare Nitrosamine, raw material risk assessments and declarations for residual solvents and elemental impurities.Support in Extractable and Leachable (E&L) risk assessments, gathering E&L data from suppliers, coordinating E&L studies, calculating AET threshold and maintaining accountability for the site during audits.Support in preparation and updation of Hazard Analysis Critical Control Point (HACCP), Control strategies.Support OPV/CPV preparation and assessment of process performance to support site MS&T team.Ensure project tracking documentation/tools are updated according to plan.Collaborate closely with the development organization (or sending site) for technical transfers and new product launches to ensure knowledge transfer, appropriate control strategies, risk analysis and control, and readiness for commercial process validation.Coordinate prerequisites for PPQ batches (Qualification status, Status of the analytical methods, raw materials, consumables), update of Risk Assessments for Microbio buffer hold validation, and generates deviation lists for PPQ batches.Prepare, approve and life cycle management of Gxp documents.Ensure that data integrity checks are conducted to verify that all the data is complete, consistent, and free from errors before proceeding with any further analysis or reporting.Coordinate of documentation review with the site MS&T, QA, and QC, also Reg CMC where applicable.

 

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