The candidate must have experience in OSD IPQA / DOC. / Validation

Exp.- 0 to 04 (OSD Formulation)

Key Responsibilities:

In-Process Quality Assurance (IPQA):

- Perform line clearance, in-process checks, and monitoring during manufacturing and packaging.
- Ensure adherence to Standard Operating Procedures (SOPs), Good Documentation Practices (GDP), and cGMP guidelines.
- Monitor critical process parameters during production to ensure consistent product quality.
- Handle deviation, change control, incident reports, and CAPA documentation.

Documentation (DOC.):

- Preparation, review, and control of SOPs, protocols, batch records, logbooks, and other quality-related documents.
- Ensure compliance with regulatory and internal documentation requirements.
- Maintain controlled copies and support document issuance and retrieval.

Validation:





- Assist in preparation and execution of validation protocols (process validation, cleaning validation, equipment qualification, etc.).
- Support validation documentation, reports, and related activities.
- Coordinate with cross-functional teams for validation and requalification programs.

Desired Skills & Competencies:

- Solid knowledge of cGMP, GDP, and regulatory requirements (USFDA, MHRA, WHO).
- Good analytical, documentation, and problem-solving skills.
- Ability to work effectively in cross-functional teams.
- Willingness to work in shifts (if required).
- Freshers with good academic background and strong interest in Quality Assurance are encouraged to apply.

📌 QA - Trainee Officer / Officer (Ahmedabad)
🏢 Aneta Pharmaceuticals
📍 Ahmedabad