Company Description Sushen Medicamentos Pvt. Ltd. is an EU-GMP certified engineering and formulation partner for global pharmaceutical companies, delivering end-to-end product management from plant design to commercial batch execution.

The company specializes in designing and implementing pharmaceutical manufacturing facilities compliant with WHO-GMP, USFDA, UKMHRA, and other international regulatory standards, including full equipment procurement, qualification, and engineering services. Sushen also provides formulation and development services for oral solid dosage forms, stability and dissolution studies, and tech transfer support as a CDMO. Its state-of-the-art, WHO-GMP certified laboratory and scale-up facility are DSIR-approved and built to USFDA and EU GMP norms.

With a multidisciplinary team and over two decades of experience, Sushen has successfully executed more than 40 projects for pharma clients across the US, Europe, CIS, Middle East, Latin America, Africa, South East Asia, and India.

Position: Officer / Executive – Quality Assurance

Department: Quality Assurance

Location: Changodar, Ahmedabad

Experience: 0–4 Years

Industry: Pharmaceutical – Oral Solid Dosage (OSD) preferred

Qualification: B.Pharm / M.Pharm / M.Sc. or relevant pharmaceutical qualification

Job Summary:

You will be responsible for supporting Quality Assurance activities to ensure that manufacturing and quality processes comply with GMP, SOPs, and applicable regulatory requirements. The role involves documentation, in-process quality oversight, compliance monitoring, and coordination with cross-functional teams.





Key Responsibilities:

- Review and maintain GMP and quality-related documentation.
- Perform and monitor line clearance and in-process quality checks.
- Ensure compliance with SOPs, GMP requirements, and established quality procedures.
- Support review of Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and related documents.
- Assist in handling deviations, CAPA, change controls, and other quality events.
- Support investigation of quality-related incidents and implementation of corrective actions.
- Monitor compliance with Good Documentation Practices (GDP).
- Coordinate with Production, QC, Engineering, and other departments for quality-related activities.
- Participate in internal audits, inspections, and other QA compliance activities.
- Ensure proper documentation and timely closure of assigned quality-related activities.

Required Skills:

- Knowledge of GMP and pharmaceutical quality systems.
- Understanding of QA documentation and GDP.
- Good analytical and problem-solving skills.
- Good communication and interpersonal skills.
- Attention to detail and strong documentation skills.
- Ability to work effectively in a team and pharmaceutical manufacturing setting.

Preferred:

- Candidates with 0–4 years of experience in the pharmaceutical industry , preferably in OSD manufacturing .
- Candidates with exposure to QA operations, documentation, deviations, CAPA, change control, and GMP compliance will be preferred.

? Interested candidates can apply directly or share their updated CV at [email protected] for consideration.

📌 Quality Assurance Officer / Executive (Ahmedabad)
🏢 Sushen Medicamentos
📍 Ahmedabad