Synergen Bio, a growing name in bio-research and quality compliance, is inviting applications for the position of Research Associate (BR-QC) at its Pune (Shivajinagar, Wakadewadi) facility. This opportunity is ideal for candidates with a background in Quality Control, Bio-Research (BR), GLP, and regulatory compliance, looking to strengthen their careers in analytical review and quality systems.
With increasing demand for regulatory-compliant bioanalytical research, this role offers hands-on exposure to method validation, audits, SOP governance, and sponsor interactions, making it a strong career move for early-career professionals.
📌 Job Overview
- Position: Research Associate (BR-QC)
- Company: Synergen Bio
- Number of Vacancies: 02
- Job Location: Shivajinagar, Wakadewadi, Pune, Maharashtra
- Experience Required: 1 to 2+ years
- Qualification: MSc / B.Pharm / M.Pharm
- Department: Bio-Research – Quality Control (BR-QC)
🧪 Key Roles & Responsibilities
As a Research Associate – BR-QC, the selected candidate will be responsible for ensuring data integrity, regulatory compliance, and quality excellence across bioanalytical research activities:
- Review of raw data forms and chromatograms related to method development, method validation, and project sample analysis
- Review of bulk spiking checklists, Excel worksheets, and concentration data
- Review and compliance check of SOPs, study protocols, and analytical procedures
- Review of method validation reports and analytical study reports
- Monitoring and review of temperature and humidity records in the BR department
- Preparation and maintenance of training matrix, training plans, and job descriptions
- Conducting SOP and GLP training for new and existing employees
- Effective implementation of GLP and regulatory guidelines within the BR department
- Review and maintenance of IQ/OQ/PQ documentation
- Review of instrument calibration reports and preventive maintenance records
- Review of daily calibration logs and equipment logbooks
- Participation in and execution of internal system audits
- Review and management of CAPA, Deviations, and OOS investigations
- Handling query responses from Sponsors and Regulatory authorities
- Providing regulatory and SOP guidance to BR personnel
🎓 Eligibility Criteria
- Educational Qualification:
- MSc (Life Sciences / Chemistry / Biotechnology)
- B.Pharm or M.Pharm
- Experience:
- Minimum 1 year experience in BR-QC, Bioanalytical QC, or regulated laboratory environments
- Key Skills:
- GLP & regulatory compliance
- Data integrity and audit readiness
- SOP management and training
- Bioanalytical documentation review
- Regulatory query handling
💼 Why Join Synergen Bio?
- Exposure to regulated bio-research and QC operations
- Strong learning curve in GLP, audits, and regulatory documentation
- Opportunity to work closely with Sponsors and Regulatory bodies
- Structured quality systems and professional work culture
- Ideal role for building a long-term career in BR-QC and regulatory science
📧 How to Apply
Interested and eligible candidates should share their updated CV via email:
📩 Email: careers@synergenbio.com