Research Associate

Bjain Pharmaceuticals

5 - 10 years

3 - 7 Lacs

Noida

Posted:7 hours ago| Platform:

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Skills Required

Computer science ERP Data analysis Healthcare Clinical research Navision Troubleshooting Information technology STP Data entry

Work Mode

Work from Office

Job Type

Full Time

Job Description

JD for Research Associate

Job Overview:

We are looking for a passionate and dedicated

BHMS fresher

to join our research team as a

Research Associate

. The ideal candidate should have a strong foundation in homeopathy, a keen interest in clinical or pharmaceutical research, and a willingness to learn and grow in a dynamic environment.

Key Responsibilities:

Assist in planning and conducting clinical and non-clinical research related to homeopathic medicines.

Review and summarize scientific literature related to ongoing or upcoming projects.

Support data collection, data entry, and preliminary data analysis.

Maintain accurate and up-to-date documentation for for . The ideal candidate will assist in designing, developing, and maintaining solutions within Microsoft Dynamics NAV/Business Central. This is an excellent opportunity for a junior developer to grow their skills in ERP development and support.Key Responsibilities:
Development and Customization:
Assist in the development and customization of Microsoft Dynamics NAV/Business Central solutions to meet business needs.Write clean, efficient, and maintainable AL, C/AL, and C/SIDE code.

System Maintenance and Troubleshooting:
Diagnose and resolve technical issues within NAV/Business Central environments. Provide system support and maintenance for for Regulatory and Quality Manager Preferred for Female Candidate.
- Responsible for implementation of Quality Management System as per regulatory requirements.
- Regulatory Documentation.
- Management of the Continual Improvement of the Systems, Product Quality Review Process for the Corrective and Preventive Action System.
- Accountable for the Data integrity and implementation of the SOP and policy.
- Evaluate & approval of master documents pertaining to various departments.
- Responsible for preparation and approval of all master documents like BMR, SOP, STP, SPEC, formats and checklist.
- Accountable for Control Sample Management and Stability Management.
- Responsible for implementation of QA systems for ensuring that compliance as per sops.
- Responsible for external & internal audits.
- Review, evaluation, and approval of Document on behalf of factory department in guidance of technical head.
- To follow cGMP practices and implementation of the information recorded.
- Responsible for review and approval of equipment qualification/requalification/ validation protocols, a compilation of summary reports of the products.

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