Require Research Associate at Baxter - M.Pharm Apply

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries.

Post : Research Associate II - SPO

Job Description
• Actively supports launch and sustenance of Baxter commercial product globally.
• Support all commercialized project related requirements related to Baxter manufacturing sites and CMOs Globally.
• Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of product design governance documents for a particular product family.
• Make sure the relevant documents for various product families are available to support risk management, change control processes and design integrity.
• A very good understanding of Quality Risk Management for pharmaceutical products is required per ICH Q9 and ensure sustenance of Baxter commercial products globally by following Baxter Quality Management Systems.
• Respond to customer queries regarding safety aspects of the product after consultation with Clinical affairs and other relevant functions.
• Manage Platform core team performance, product life cycle, project schedule, execution, budget commitments and spend.
• Review weekly, monthly/yearly progress of the projects and send report to the governance team to implement the improvements suggested by the governance.
• Drive the discussion and ensure the implementation of VIP/ MIP projects, alternative vendor projects.
• Own supplier notification of change (SNC) or change control to support the implementation of change on time.

Candidate Profile
Postgraduate degree with at least 7 years of experience in the pharmaceutical industry, with a focus on formulation development and project management. Preferably, experience in managing generic product development portfolios and/or product life cycle management for various dosage forms in regulated and semi-regulated markets.

• Educational Qualification : Master’s in Pharmaceutics or equivalent
• Data Analysis and Good communication skills for effective liaison and teamwork
• Problem-solving skills, analytical skills and attention to detail
• Excellent organizational skills and the ability to work on several tasks or projects concurrently
• Presentation skills - for presenting ideas and findings to colleagues and customers
• Ability to work well independently, with minimum supervision
• Drive, enthusiasm and self-motivation
• An aptitude for mathematics and statistics and highly developed IT and technical skill
• Project management skills and having knowledge of MS office and project management tracking software (Microsoft project, primavera and Planisware) to track and monitor the project progress will be an added benefit.

Additional Information
Experience : 7 years
Qualification : M.Pharm
Location : Ahmedabad, Gujarat
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : SPO
End Date : 20th August 2025