Jobs at Vitely

Reviews method development, validation, study data, calibration records, logbooks, and scientific reports for accuracy, completeness, compliance, and consistency. Performs QC checks, verifies GLP, GDP, and GCP practices, reviews environmental monitoring data, supports laboratory cleanliness and safety, and collaborates with scientists, analysts, statisticians, and quality assurance teams.

Prepare and review quality management documents, plan and conduct system and study audits for IVRT, IVPT, and in-vitro studies, review protocols and analytical records, assess deviations, OOS, CAPA, change controls, and validation documents, deliver training, control documentation, verify computerized system compliance, support regulatory and sponsor audits, and manage sample retention activities.

Manage financial operations, accounting, tax compliance, audits, budgeting, reporting, banking, cash flow, risk management, and internal controls. Prepare financial statements, forecasts, variance analyses, and regulatory filings while optimizing costs, working capital, and accounting processes. Coordinate with auditors, tax consultants, regulators, and stakeholders, ensuring compliance with Ind-AS, IFRS, GAAP, GST, TDS, and income tax requirements.

Supports bioanalytical laboratory activities, including sample preparation and processing for pharmacokinetic studies. Follows GLP, SOPs, protocols, and laboratory procedures while assisting senior analysts. Maintains accurate, complete, correct, and traceable records according to ALCOA+ principles and regulated documentation requirements. Applies chromatography knowledge, troubleshoots laboratory issues, and ensures timely documentation with strong attention to detail.

Designs and analyzes in vitro experiments for pharmaceutical and life sciences research. Applies statistical models, validates data, develops statistical analysis plans and technical reports, supports regulatory submissions, and collaborates with scientists and researchers. Uses SAS, R, JMP, or Python for analysis, visualization, and reporting while ensuring compliance with FDA, ICH, and GLP requirements.

Develop and maintain full-stack web applications using C#, .NET Core, Angular, SQL Server, HTML, CSS, JavaScript, and jQuery. Build APIs and microservices, optimize databases, integrate frontend and backend services, write maintainable code, participate in Agile ceremonies and code reviews, and troubleshoot production issues and performance bottlenecks.

Designs and executes manual and automated tests across web, mobile, and desktop platforms. Develops automation frameworks and scripts, performs API testing, manages defects, analyzes results, documents test plans and reports, reviews requirements, and supports root cause analysis. Collaborates with developers, product owners, and business analysts to improve software quality and testing processes.

Conduct analytical method development and validation, prepare protocols and reports, and operate HPLC, LCMS, ICPMS, and OES instruments. Support extractable and leachable studies, preferably in pharmaceutical or CRO environments. Ensure compliance with GLP, GDP, data integrity, timelines, and quality standards while collaborating effectively with team members.