Novartis Pharmacy Specialist MS&T Post – Apply Online
Novartis hiring candidates with bachelor’s degree in pharma for the post of Specialist MS&T. M Pharma job opening, Pharma job opening 2023, Pharmacy job opening 2023, Novartis job opening 2023. Interested and eligible candidates may check out all the details
Job Title: Specialist MS&T
Job Id: 367729BR
Work Location
Hyderabad, AP
Eligbility Criteria & Experience:
Bachelor’s degree in Pharmacy, Pharmaceutical Technology, Chemical Engineering, Chemistry or equivalent science streams. Desirable M.Sc./MS. or equivalent experience.
• Min 3 years of experience in MS&T, Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substance or drug products. Hands on experience in ongoing process validation or continued process verification.
• Minimum of 3 years of pharmaceutical process validation and cleaning validation. Should have the experience in pharmaceutical process validation protocol/report writing, cleaning validation protocol and report writing, in sterile manufacturing setups, biologics.
• Should be familiar and able to perform basic statistical evaluations using Minitab or other statistical analysis tools. Basic knowledge on deviation handling, incident investigations, root cause analysis, and CAPA management
• Knowledge of risk assessment and risk management programs. Should be familiar with regulatory guidance on validation, product filing and post approval
changes. Basic knowledge of statistical analysis, results interpretation, and usage of statistical tools (Example: Minitab, Statistics etc.)• Good communication, presentation and interpersonal skills. Fluent in English (oral and written).
Your key responsibilities:
Your responsibilities include, but not limited to:
• The Technical specialist supports MS&T team on sites by collecting data, reviewing or writing technical documents related to validation (e.g. process validation, ongoing process verification, cleaning validation, packaging), APR PQR, technical files, product risk assessment procedures and maintaining a product oversight throughout the lifecycle. The scope includes all drug products bulk (DP), finished products (FP) and all chemical intermediates/APIs under Novartis responsibility. For that purpose, technical specialist collects data from the Novartis Business Units, act in accordance with legislation, internal rules, good practices and business objectives.
• Support Validation program including process validation, ongoing process verification (OPV), risk assessment, cleaning validation, ongoing cleaning verification for Novartis drug product and drug substance manufacturing sites. Create validation documentation including process validation protocol/reports, risk assessment, ongoing process verification (OPV) plans/ reports, cleaning validation protocol/reports based on alignment with Site Validation Lead.
• Using monitoring tool such as OPV Monitor or Discoverant perform, OPV evaluations, assess process performance and provide insight, recommendation, and conclusion to the site MS&T Lead/Product Steward.
Create and review GxP documents including SOPs, working procedures, trend reports, and technical investigations, as and when needed
• Support tasks related to technical changes, incident investigations for the product and process. Provide active support during internal and external audits by collecting and presenting the requested process/ data and reports. Coordinate & manage project for a smooth knowledge transfer activity from site/ function to Operations Center. Act as single point of contact for the services delivered to sites/ functions by the respective team, including the review of feedback and timely completion of identified actions.
• Coordinates with Global MS&T team, IT team for the ongoing data management, evaluation and reporting in the OPV Monitor OR Discoverant tool. Coordination of documents preparation in the right formats (eg. Novstyle for Subway, ESOPS etc) and ensure timely review and approval of the documents. Ensure services are delivered on time and in line with partner and Novartis MS&T requirements
• Coordinates documentation review with the site MS&T, QA, and QC, also Reg CMC where applicable. Obtains deviation reports from relevant systems in support to validation to enable conclusions. Coordinates and owns DI check with Data integrity manager where applicable. Coordinates inputs from respective functions (QA, QC, MS&T), to create the validation documents and decide on the study strategy. Coordinates the execution of the study with respective functions. Collects results and creates reports.
Apply Online
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