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 Positive Manufacturing Practices (GMP) and Positive 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

📌 Openings For Formulation Dqa Trainee Hyderabad
🏢 MSN Group
📍 Hyderabad