Baxter Hiring Analytical Lab Research Associates in Ahmedabad

Baxter GPRD (Global Product Research & Development) in Ahmedabad, where innovation meets excellence. Baxter is a global leader in healthcare, committed to advancing healthcare through a diverse range of life-changing medical products. Our Analytical Lab (Stability) team is at the forefront of ensuring the quality and safety of our injectable products. Join us in our mission to make a meaningful impact on healthcare around the world.

Company Vacancies List

Position Title: Baxter Analytical Lab Research Associates

Company Name: Baxter GPRD, Ahmedabad

Role: Research Associate in Analytical Lab (Stability)

Job Location: Ahmedabad
Education: M.Pharm/MSc/Ph.D
Experience: 6 to 11 Years
Job Description:
1) Develop stability study designs
2) Technical feasibility analysis of complex research and design concepts.
3) Analytical trouble shooting and Investigations

Key Skills

• Stability Study Design, Analytical Method Development, Regulatory Compliance, Collaboration, Problem Solving, Innovation

Analytical Lab (Stability) Department & Responsibilities

The Analytical Lab (Stability) at Baxter GPRD, Ahmedabad, plays a crucial role in ensuring the stability and quality of injectable products. As a Research Associate, you will:

• To provide support to the Stability Team in day to day technical and operational activities.
• Develop stability study designs for new product development and sustaining product projects.
• Without assistance, make sound technical recommendations regarding stability study designs for new product development and sustaining product projects that are more routine than not. Provide some analysis/redesign of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility.
• Employ appropriate techniques/methods to successfully and independently execute routine assignments related to stability study design and development within negotiated deadlines. Identify alternative methods and technologies for improving existing or new products/processes.
• Maintain current/working knowledge of relevant QSRs and other regulatory requirements, such as the stability related ICH guidelines, for R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities.
• Recommend appropriate study designs, techniques, and processes for a specified sequence of tasks where needed, including the use of LIMS systems for electronic stability protocols.
• Contribute to technical feasibility analysis of complex products.
• Demonstrate ability to apply technical theories and principles to projects within area of Expertise for nonroutine tasks. Analyse and determine best solutions to non-routine experimental design or research problems with minimal assistance. Accurately assess results for validity and conformance to specifications
• Evaluate results relative to product requirements, definitions and/or program goals.
• Providing technical rationale for expiration dating and label storage statement recommendations, preparing regulatory submissions, responding to regulatory communications.
• Ensuring compliance related deliverables are completed on schedule and per plan
• Independently plan and execute a series of stability study designs and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines.
• Play a lead role in the evaluation, selection and adaptation of various techniques/strategies, which accomplish business objectives such as quality and cycle time.
• Displays a solid understanding of theories/practices utilized by other disciplines outside the primary area of expertise.
• In addition to having an in-depth knowledge and understanding of cGxP and related regulations and guidance, can be able to provide expert advice and/or is an active participant in the generation, review, adoption, and interpretation of such regulations.
• Maintain focus on meeting both external and internal customer expectations.
• Develop stability study designs for new product development and sustaining product projects.
• Contribute to technical feasibility analysis of complex research and design concepts.
• Evaluate results relative to product requirements, definitions and/or program goals.
• Providing technical rationale for expiration dating and label storage statement recommendations, preparing regulatory submissions, responding to regulatory communications.
• Ensuring compliance related deliverables are completed on schedule and per plan.
• Collaboration with cross functional teams such as QA, M&Q, Regulatory, Quality control, and all the projects.
• Coordinate stake holders to progress the projects and internal activities in a right direction to achieve the organizational requirement.
• To follow all the relevant cGxP and related regulations.
• Lead the analytical problem-solving efforts to meet urgent business needs.
• Focus on innovation, process improvement, and/or operational excellence initiatives.
• Independently plan, execute, and manage projects/programs that both span multiple disciplines and utilize established methods, techniques, or approaches.
• Implement new or improved techniques and procedures around specific tasks; write and implement SOP’s. Implement research outlines for large scientific projects. Apply state of-the-art techniques in expertise to develop new or improved products
• Able to handle the NCR/sNCR and Change controls.

Apply online