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Research Associate I – R&D (Analytical Development Laboratory)

2+ years
not specified
10 Sept. 3, 2025
Job Description
Job Type: Full Time Education: Not specified Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Research Associate I – R&D (Analytical Development Laboratory)

Job Requisition Number: JR - 178471
Location: Ahmedabad, Gujarat, India
Department: Research & Development (R&D)
Category: Analytical Development Laboratory (ADL)
Posting Date:


About Baxter

At Baxter, we are committed to creating a world where every individual—regardless of who they are or where they come from—has the opportunity to live a healthy life. Since 1931, this belief has driven our mission to Save and Sustain Lives.

Our global teams are united by this mission and operate in a culture built on trust, courage, and collaboration. We encourage ownership, innovation, and accountability—ensuring that every employee's work makes a difference.


Position Summary

As a Research Associate I in the Analytical Development Laboratory (ADL), you will be responsible for conducting analytical testing, instrument operation and calibration, data recording, and supporting regulatory and method validation work. The role requires a strong foundation in laboratory practices, instrument handling, and documentation compliance aligned with regulatory standards.


Key Responsibilities

Analytical Testing & Documentation

  • Conduct testing and data recording for various samples, including:

    • API samples

    • Development product samples

    • Validation and stability samples

    • PDR, RLD, and bulk hold samples

  • Follow draft/approved Method of Analysis (MOA) or current Pharmacopoeia guidelines.

  • Ensure adherence to ALCOA++ principles, Good Documentation Practices (GDP), and Good Laboratory Practices (GLP).

Instrument Operation & Calibration

  • Operate laboratory instruments such as:

    • HPLC, GC, Auto Titrator, Karl Fischer Titrator, pH Meter, Balance

  • Perform daily or scheduled instrument calibration per Standard Operating Procedures (SOPs).

  • Verify instruments after preventive or breakdown maintenance.

Compliance & Protocol Adherence

  • Follow instructions and approved protocols for assigned activities.

  • Check the shelf life of chemicals/reagents before use.

  • Track and report preventive and breakdown maintenance activities.

Project Execution & Reporting

  • Complete planned activities (method validation, submission studies, regulatory queries) within assigned timelines.

  • Communicate project issues to the sub-department manager and contribute to resolution plans.

  • Monitor and analyze result trends before reporting.

  • Maintain daily work status updates and reports.

Documentation & SOP Management

  • Prepare and maintain SOPs and standard documentation formats.

  • Implement new or improved procedures and write corresponding SOPs.

  • Support innovation, continuous improvement, and operational excellence in lab processes.

Training & Knowledge Development

  • Complete training as per the quality matrix requirements.

  • Maintain up-to-date knowledge of:

    • cGxP regulations

    • Regulatory compliance requirements relevant to R&D activities

Team Collaboration & Compliance

  • Collaborate with cross-functional teams.

  • Escalate any abnormal results, deviations, or non-compliance events to the manager.

  • Support procurement by tracking and communicating routine lab needs.


Required Skills & Qualifications

  • In-depth understanding of cGxP, ICH guidelines, and regulatory expectations.

  • Proficient in the use of analytical instruments and methods.

  • Strong attention to detail and documentation accuracy.

  • Ability to work independently and collaboratively in a team environment.

  • Problem-solving mindset for analytical issues.


Location

Baxter (India) Pvt. Ltd.
Navratna Corporate Park

  • Tower A, Ground Floor

  • Tower B, 21st and 22nd Floor
    Ahmedabad, Gujarat – 380058
    India


Employee Benefits

  • Support for parents

  • Continuing education & professional development

  • Health & well-being benefits

  • Paid time off

  • 2 days of paid volunteering leave per year


Equal Opportunity Employer

Baxter is an equal opportunity employer and does not discriminate on the basis of:

  • Race, color, religion, gender

  • Age, sexual orientation, gender identity or expression

  • National origin, veteran status, or disability


Reasonable Accommodations

If you need a reasonable accommodation due to a medical condition or disability during the application process, click here to submit your request.


Recruitment Fraud Notice

Beware of employment scams. Baxter does not request personal or financial information via unofficial channels. Refer to our Recruitment Fraud Notice for details.


How to Apply

Click the "Apply Now" button on the job posting page.