Elysium Pharmaceuticals Ltd., a rapidly growing pharmaceutical company based in Vadodara, Gujarat, has announced exciting career opportunities for qualified and experienced professionals in Quality Assurance, Production, and Quality Control functions. The organization is seeking motivated candidates who possess strong GMP knowledge, regulatory compliance awareness, and a commitment to pharmaceutical quality standards.

This recruitment drive offers opportunities for both fresh and experienced candidates across multiple departments, making it an excellent career move for professionals looking to grow in the pharmaceutical manufacturing industry.

Company Overview

Elysium Pharmaceuticals Ltd. is committed to delivering high-quality healthcare products while maintaining stringent quality and regulatory standards. The company focuses on innovation, compliance, and operational excellence, creating a professional environment for career development.

Available Positions

1. IPQA Officer

Experience Required: 1–3 Years

Key Responsibilities:

In-process quality checks

Line clearance activities

GMP documentation review

Compliance monitoring during manufacturing operations

Ensuring adherence to quality systems

2. Production Officer (Softgel & Parenteral)

Experience Required: 0–3 Years

Key Responsibilities:

Production process execution

Equipment operation and monitoring

In-process control (IPC) activities

Maintaining production quality standards

Compliance with SOPs and GMP guidelines

3. QC Officer (RM, HPLC & Finished Product)

Experience Required: 1–3 Years

Key Responsibilities:

Analysis of raw materials and finished products

HPLC operation and testing

In-process sample analysis

Data integrity compliance

Laboratory documentation and reporting

4. Senior Production Officer (Tablet)

Experience Required: 4–6 Years

Key Responsibilities:

Tablet manufacturing operations

Batch Manufacturing Record (BMR) handling

Logbook and documentation management

Production planning and execution

Regulatory and GMP compliance

Desired Candidate Profile

The company is looking for professionals with:

Relevant pharmaceutical industry experience

Strong knowledge of GMP requirements

Documentation and compliance expertise

Effective communication skills

Teamwork and problem-solving abilities

Proactive and quality-focused approach

Immediate joiners will be given preference.

Job Location

Vadodara, Gujarat

How to Apply

Interested candidates can share their updated resumes at:

Email: aman.kumar@elysiumpharma.com

Technical FAQs

1. What is the role of IPQA during pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) ensures manufacturing activities comply with GMP requirements through line clearance, process monitoring, documentation verification, and in-process quality checks.

2. Why is HPLC important in Quality Control laboratories?

High-Performance Liquid Chromatography (HPLC) is used to identify, quantify, and ensure the purity of pharmaceutical compounds, making it one of the most critical analytical techniques in QC.

3. What is the significance of Batch Manufacturing Records (BMR)?

BMR provides complete documentation of manufacturing activities, ensuring traceability, regulatory compliance, product consistency, and audit readiness.

4. What are In-Process Controls (IPC) in production?

IPC refers to quality checks performed during manufacturing to ensure product parameters remain within specified limits before proceeding to the next stage.

5. What is data integrity in pharmaceutical quality systems?

Data integrity ensures that all records are accurate, complete, consistent, attributable, and maintained throughout the product lifecycle in accordance with regulatory requirements such as ALCOA+ principles.