Lactose (India) Limited, a leading pharmaceutical excipient manufacturer, is inviting applications from qualified candidates for the Quality Assurance (Dispatch) department at its Poicha (Rania), Taluka Savli, District Vadodara, Gujarat facility. This opportunity is ideal for candidates with 1–2 years of pharmaceutical QA experience who are looking to build their career in a GMP-regulated manufacturing environment.

Job Overview

Particular Details

Company

Lactose (India) Limited

Department

Quality Assurance (Dispatch)

Position

Jr. Officer / Officer

Job Location

Poicha (Rania), Tal. Savli, Dist. Vadodara, Gujarat

Experience

1–2 Years

Qualification

B.Sc. / B.Pharm / M.Sc.

Industry

Pharmaceutical Manufacturing

Application Mode

Email

Educational Qualification

Candidates should possess any of the following qualifications:

B.Sc.

B.Pharm

M.Sc.

Applicants should have 1–2 years of relevant experience in Quality Assurance, Dispatch QA, or IPQA activities within a pharmaceutical manufacturing company.

Job Responsibilities

Selected candidates will be responsible for:

Monitoring all dispatch activities according to approved SOPs.

Verifying dispatch orders against actual dispatched materials.

Executing dispatch quality checklists.

Inspecting the physical condition of bags, labels, and shipment batches.

Performing IPQA rounds throughout the manufacturing plant.

Verifying transport vehicles for cleanliness before dispatch.

Maintaining dispatch-related documentation and records as per GMP procedures.

Ensuring compliance with quality standards and regulatory guidelines.

Required Skills

Knowledge of GMP, GDP, and SOP compliance.

Experience in pharmaceutical dispatch documentation.

Understanding of IPQA practices.

Documentation and record management skills.

Attention to detail and problem-solving ability.

Good communication and teamwork.

Why Join Lactose (India) Limited?

Work with a reputed pharmaceutical manufacturer.

Exposure to regulated Quality Assurance systems.

Career growth opportunities.

Professional and compliance-driven work environment.

Opportunity to strengthen GMP and dispatch quality expertise.

How to Apply

Interested and eligible candidates can send their updated CV to:

Email: vinayak@lactoseindialimited.com

Ensure your resume includes your educational qualifications, work experience, current CTC (if applicable), notice period, and contact details.

Technical FAQs

1. What is the role of Quality Assurance (Dispatch) in pharmaceutical manufacturing?

Quality Assurance (Dispatch) ensures that products are dispatched according to approved SOPs, GMP requirements, and customer specifications while maintaining product quality and documentation accuracy.

2. Why are dispatch SOPs important?

Dispatch SOPs standardize the dispatch process, reduce errors, maintain product integrity, ensure regulatory compliance, and improve traceability during transportation.

3. What is IPQA and why are IPQA rounds conducted?

In-Process Quality Assurance (IPQA) involves monitoring manufacturing and dispatch operations to ensure compliance with GMP standards, identify deviations, and maintain consistent product quality.

4. Why is vehicle cleanliness verification mandatory before dispatch?

Vehicle inspection prevents contamination, protects product quality during transportation, and ensures compliance with GMP and customer quality requirements.

5. What documents are typically maintained in pharmaceutical dispatch?

Common dispatch documents include dispatch checklists, batch release documents, invoices, packing lists, transport records, vehicle inspection records, delivery challans, and quality verification records.