Baxter Hiring Analytical Lab Research Associates in Ahmedabad
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- Company Vacancies List
- Position Title: Baxter Analytical Lab Research Associates
- Company Name: Baxter GPRD, Ahmedabad
- Analytical Lab (Stability) Department & Responsibilities
- Apply online
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/M.Sc/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
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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
To apply for this job please visit baxter.wd1.myworkdayjobs.com.