India

Provide strategic guidance and expertise in oncology for the development and execution of medical affairs plans focusing on Lung Cancer, GU Cancers and Hematology portfolio. Collaborate with cross-functional teams to support the successful launch and commercialization of oncology products.

Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality.

Ensure on time analysis of Finished products and raw materials for required product and projects. Review of analytical data, raw data, daily usage logbooks and Lab notebooks for routine operations for analytical development function. Preparation and review of critical documents like Analytical Method validation protocol, reports, Analytical method transfer protocols and reports.

Bachelors degree in life sciences or business. Experience in consulting management in the life sciences, pharmaceutical/ biotech consulting industry or equivalent industry role

Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical regulatory documents. Writers and edits clinical regulatory documents, including submission summaries and other complex documents.

First class in M.PHARM or M.S in Pharmaceutics, drug delivery, Pharmacology, Pharm-Biotechnology, Nanomedicines, or equivalent from a recognized University. As per BITS RMIT PHD program eligibility.

The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.

Project Managers provide business and technical leadership for one or more projects within a business unit, leading project teams through the identification, justification, prioritization, initiation, development and implementation processes. This Sr. Specialist position will act as a Project Manager leading commercial launches in US and Global markets within the Pharmaceutical Business segment.

Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies