Puerto Life Sciences Pvt. Ltd. has announced an excellent career opportunity for experienced pharmaceutical professionals. The company is hiring Manager and Assistant Manager – Quality Assurance for its Sterile Injectable Manufacturing Facility located in Neemrana, Rajasthan.

If you have experience in Quality Assurance (QA), Sterile Injectable (SVP/LVP) manufacturing, cGMP, GDP, QMS, and regulatory compliance, this is a great opportunity to join a fast-growing pharmaceutical organization operating with global quality standards.

Puerto Life Sciences Recruitment– Overview

Particular Details

Company Name

Puerto Life Sciences Pvt. Ltd.

Job Role

Manager / Assistant Manager – Quality Assurance

Department

Quality Assurance (QA)

Job Location

Neemrana, Rajasthan

Qualification

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

Experience

Manager: 10–15 Years, Assistant Manager: 6–8 Years

Industry

Sterile Injectable Manufacturing

Employment Type

Full-Time

Email ID

hr@puerto.in

Official Website

www.puertolifesciences.com

About Puerto Life Sciences

Puerto Life Sciences Pvt. Ltd. is a rapidly growing pharmaceutical company specializing in Sterile Injectable Manufacturing, including SVP (Small Volume Parenterals) and LVP (Large Volume Parenterals). The company operates according to international cGMP standards and focuses on delivering safe, reliable, and high-quality injectable products to global markets.

Position Details

Manager – Quality Assurance

Experience Required: 10–15 Years

Assistant Manager – Quality Assurance

Experience Required: 6–8 Years

Educational Qualification

Applicants should possess any of the following qualifications:

B.Pharm

M.Pharm

M.Sc.

Candidates with experience in sterile injectable manufacturing and pharmaceutical quality systems will be preferred.

Key Responsibilities

Selected candidates will be responsible for:

Managing Quality Management Systems (QMS)

Ensuring cGMP and GDP compliance

Batch Review and Batch Release

Handling Deviations, CAPA and Change Control

Regulatory Compliance and Internal Audits

Validation and Documentation Review

Risk Assessment and Quality Improvement

Data Integrity Compliance

Root Cause Investigation

Leading QA teams and continuous improvement initiatives

Required Technical Skills

Candidates should have knowledge of:

Sterile Injectable Manufacturing (SVP/LVP)

cGMP Guidelines

Good Documentation Practices (GDP)

Quality Management System (QMS)

CAPA Management

Change Control

Batch Record Review

Data Integrity

Validation Documentation

Root Cause Analysis (RCA)

Risk Assessment

Leadership & Team Management

Why Join Puerto Life Sciences?

Opportunity to work in a global-standard sterile injectable manufacturing facility.

Exposure to international regulatory practices.

Career growth in Quality Assurance leadership roles.

Collaborative work environment with continuous learning opportunities.

Competitive salary and benefits based on experience.

How to Apply

Interested and eligible candidates can send the following documents:

Updated CV/Resume

Current CTC

Notice Period Details

Email: hr@puerto.in

Official Website: https://www.puertolifesciences.com

5 Technical FAQs

1. What is the role of Quality Assurance in sterile injectable manufacturing?

Quality Assurance ensures that sterile injectable products are manufactured according to cGMP guidelines, regulatory requirements, and internal quality standards to maintain product safety, sterility, and efficacy.

2. What is CAPA in pharmaceutical Quality Assurance?

CAPA (Corrective and Preventive Action) is a systematic process used to investigate deviations, identify root causes, implement corrective actions, and prevent recurrence to improve product quality.

3. Why is Data Integrity important in pharmaceutical manufacturing?

Data Integrity ensures that all manufacturing, testing, and quality records are complete, accurate, consistent, and traceable throughout the product lifecycle, supporting regulatory compliance.

4. What are SVP and LVP in sterile manufacturing?

SVP (Small Volume Parenterals) are injectable products typically packaged in containers of up to 100 mL, while LVP (Large Volume Parenterals) are sterile infusion products packaged in containers larger than 100 mL.

5. What is Batch Review and Batch Release?

Batch Review involves verifying manufacturing records, quality control results, and compliance documentation. Batch Release is the formal approval by Quality Assurance to distribute a finished pharmaceutical batch after confirming it meets all quality specifications.