Development Quality Assurance Formulations Hiring at Aizant Drug Research Solutions
- Development Quality Assurance (DQA – Formulations) Jobs for B Pharm/M.Pharm Graduates in Hyderabad
- Why Join Aizant?
- Job Role: Development Quality Assurance (DQA – Formulations)
- Location:
- Required Qualification:
- Experience:
- Key Responsibilities
- Core Responsibilities in DQA Role
- Skills Required
- Who Should Apply?
- How to Apply
- Job Overview Table
B Pharm/M.Pharm Openings: DQA Formulations Jobs in Hyderabad (2–7 Yrs Exp)
Apply now for Development Quality Assurance (DQA) – Formulations vacancies in Hyderabad. Qualification: B Pharm/M.Pharm. Experience: 2–7 years.
Development Quality Assurance (DQA – Formulations) Jobs for B Pharm/M.Pharm Graduates in Hyderabad
Looking to boost your pharma career with a reputed organization? Aizant Drug Research Solutions invites experienced professionals for the role of Development Quality Assurance (DQA – Formulations) at its Hyderabad (Dulapally) facility. This is a rewarding opportunity for qualified candidates with a passion for pharmaceutical quality standards and regulatory compliance.
Why Join Aizant?
Aizant is a leading pharmaceutical services company recognized for its integrated drug development capabilities. With a focus on innovation, compliance, and quality, it offers a work culture that supports learning, growth, and impactful contributions in the pharmaceutical field.
Job Role: Development Quality Assurance (DQA – Formulations)
Location:
Hyderabad – Dulapally
Required Qualification:
B Pharm / M.Pharm
Experience:
2 to 7 years in Development Quality Assurance / Formulations / Pharmaceutical Quality Assurance
Key Responsibilities
Core Responsibilities in DQA Role
SOP & Documentation
- Prepare and review departmental SOPs
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
Quality Checks and Process Monitoring
- Conduct in-process checks during manufacturing and packaging
- Perform line clearance activities and inspections of process intermediates
- Monitor and check pilot bio batches
Sampling & Validation
- Collect and maintain reserve/reference samples
- Conduct sampling of residue, stability, and finished products
Protocol Development & Reporting
- Execute and review the following:
- Process validation / performance qualification protocols
- Cleaning validation protocols
- Continuous process verification reports
- Hold time study protocols and reports
- Instrument/equipment qualification activities
Skills Required
- Strong understanding of GMP and regulatory compliance
- Documentation proficiency
- Attention to detail
- Familiarity with pharmaceutical formulations and analytical methodologies
Who Should Apply?
This role is ideal for B Pharm or M.Pharm professionals with a solid background in Quality Assurance in a formulations or development setting. Professionals with hands-on experience in DQA protocols and documentation will be preferred.
How to Apply
Interested and qualified candidates may send their updated resume to:
Note: Immediate joiners will be given priority.
Job Overview Table
| Company Name | Aizant Drug Research Solutions |
|---|---|
| Current Vacancies | Development Quality Assurance (Formulations) |
| Required Education | B Pharm / M.Pharm |
| Experience Required | 2 to 7 Years |
| Location | Hyderabad (Dulapally) |
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