RA II - SPO

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Essential Duties and Responsibilities

• 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.

Qualifications:

• 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.

Education and/or Experience:

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.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

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