Sushen Medicaments Hiring Quality Assurance Officer
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience Criteria
- Location & Salary
- Application Process
- Career Growth & Learning Opportunity
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What type of manufacturing exposure does this role provide?
- Is GMP knowledge mandatory?
- Where is the job located?
- How can I apply?
- Summary Table
DQA Officer – BSc/BPharm – Ahmedabad Vacancy
DQA Development Quality Assurance Officer hiring in Ahmedabad. BSc, MSc, BPharm freshers eligible. 1 vacancy. Apply now.
A promising entry-level opportunity has opened for freshers and early-career professionals in pharmaceutical quality assurance with the hiring of a Development Quality Assurance (DQA) Officer – OSD at Changodar, Ahmedabad. This role is designed for candidates who want hands-on exposure to IPQA activities, quality management systems, and GMP-compliant solid oral dosage manufacturing.
The position offers direct involvement in development-stage manufacturing and quality oversight, making it an excellent starting point for graduates aiming to build long-term careers in pharmaceutical quality assurance, regulatory compliance, and GMP operations.
Company Overview
Sushen Medicaments is a growing pharmaceutical organization engaged in formulation development and manufacturing with a strong focus on quality, compliance, and process excellence. The company operates in regulated manufacturing environments and follows GMP-driven systems to ensure consistent product quality and patient safety.
With an emphasis on structured documentation, quality culture, and hands-on learning, Sushen Medicaments provides a solid foundation for young professionals entering pharmaceutical quality and manufacturing functions.
Job Role & Responsibilities
As a Development Quality Assurance Officer (OSD), the selected candidate will support quality assurance activities during formulation development and manufacturing stages.
Key Responsibilities
- Perform In-Process Quality Assurance (IPQA) activities for solid oral dosage (OSD) formulations
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
- Monitor in-process checks and ensure compliance with approved procedures
- Support Quality Management System (QMS) documentation and data handling
- Ensure adherence to current Good Manufacturing Practices (cGMP) during development and manufacturing
- Assist in maintaining GMP documentation, logs, and records
- Coordinate with production and development teams to support quality objectives
This role provides practical exposure to real-time GMP operations and development quality systems.
Eligibility / Qualifications
Required Education
B.Sc, M.Sc, B.Pharm
Experience Criteria
- Freshers or candidates with up to 1 year of experience in QA or IPQA
- Basic understanding of IPQA activities and QMS documentation is preferred
- Willingness to work in a regulated pharmaceutical manufacturing environment
Male candidates are preferred as per operational requirements.
Location & Salary
- Job Location: Changodar, Ahmedabad, Gujarat
- Salary: Competitive entry-level package, aligned with industry standards. Compensation will be based on qualifications and any prior exposure.
Application Process
Interested and eligible candidates can apply through either of the following options:
- Apply directly via LinkedIn
- Email your updated CV to: careers@sushenmed.com
Shortlisted candidates will be contacted for further selection steps.
Career Growth & Learning Opportunity
This DQA role offers a strong learning curve for fresh graduates. Exposure to IPQA, QMS documentation, GMP audits, and development-stage manufacturing builds a solid foundation for future roles in Quality Assurance, Regulatory Affairs, and Compliance functions across the pharmaceutical industry.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes. Freshers and candidates with up to 1 year of experience are eligible.
What type of manufacturing exposure does this role provide?
The role focuses on solid oral dosage (OSD) formulation development and manufacturing quality assurance.
Is GMP knowledge mandatory?
Basic awareness of GMP is preferred, but detailed training will be provided on the job.
Where is the job located?
The position is based at Changodar, Ahmedabad, Gujarat.
How can I apply?
You can apply via LinkedIn or send your CV to careers@sushenmed.com.
Summary Table
| Company | Sushen Medicaments |
|---|---|
| Vacancies | 1 |
| Required Education | B.Sc, M.Sc, B.Pharm |
| Experience | 0–1 year |
To apply for this job email your details to careers@sushenmed.com
