Openings For Formulation DQA - Trainee

MSN Group; Hyderabad; On-site; INR 240,000 - 420,000; Full time

Job summary

MSN Group is seeking a Trainee Formulation DQA in the R&D Center. The role focuses on supporting QA activities across formulation processes, ensuring GMP/GDP standards and robust documentation.

Fresher candidates with M.Pharm (Pharmaceutics) will be trained to review quality documents, assist in line clearance, CAPA, and change control while coordinating with production and QC teams.

Qualifications

• M.Pharm in Pharmaceutics is required.
• Fresher candidates preferred; training provided.
• Knowledge of GMP, GDP, SOPs, BMR, and BPR is essential.
• Strong documentation and data integrity mindset.

Responsibilities

• Assist in reviewing and maintaining Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Support in-process quality checks during tablet, capsule, liquid, and other dosage-form manufacturing.
• Verify compliance with GMP and GDP.
• Assist in reviewing SOPs, protocols, and other quality documents.
• Support line clearance activities before manufacturing and packaging operations.
• Help review deviations, OOS results, and CAPA under supervision.
• Assist in change control and document control activities.
• Ensure proper documentation, traceability, and data integrity.
• Coordinate with Production, Quality Control (QC), and other departments to support product quality.
• Participate in internal audits, training, and regulatory compliance activities as assigned.

Skills

Basic knowledge of pharmaceutical Form

GMP GDP SOPs BMR BPR

Pharmaceutical manufacturing processes

Deviations CAPA change control and doc

Communication observation analytical

MS Word Excel basic computer skills

Attention to detail and learning

Education

M.Pharm (Pharmaceutics)

Job description

Role & responsibilities

Job Title: Trainee Formulation DQA

Department: Quality Assurance (QA) / Formulation

Qualification: M.Pharm (Pharmaceutics)

Experience: Fresher

Job Location: R&D Center

Employment: Full-time

Job Responsibilities

• Assist in reviewing and maintaining Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).


• Support in-process quality checks during tablet, capsule, liquid, and other dosage-form manufacturing.


• Verify compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).


• Assist in reviewing Standard Operating Procedures (SOPs), protocols, and other quality documents.


• Support line clearance activities before manufacturing and packaging operations.


• Help review deviations, Out of Specification (OOS) results, and Corrective and Preventive Actions (CAPA) under supervision.


• Assist in change control and document control activities.


• Ensure proper documentation, traceability, and data integrity.


• Coordinate with Production, Quality Control (QC), and other departments to support product quality.


• Participate in internal audits, training, and regulatory compliance activities as assigned.

Skills Required

• Basic knowledge of pharmaceutical formulation and dosage forms.


• Understanding of GMP, GDP, SOPs, BMR, and BPR.


• Knowledge of pharmaceutical manufacturing processes.


• Basic understanding of deviations, CAPA, change control, and documentation.


• Good communication, observation, and analytical skills.


• Basic computer knowledge, including MS Word and Excel.


• Attention to detail and willingness to learn pharmaceutical quality systems