Eris Therapeutics has announced a recruitment drive for experienced Quality Control (QC) professionals. The company is inviting applications for Officer and Executive/Senior Executive positions in the Quality Control department. Candidates with 0–7 years of relevant pharmaceutical experience and hands-on knowledge of HPLC analysis, method validation, and laboratory instrumentation are encouraged to apply.

This is an excellent opportunity for B.Pharm, M.Pharm, M.Sc., or other eligible pharmaceutical professionals looking to build their careers with one of India’s leading pharmaceutical organizations.

Job Overview

Particular Details

Company Name

Eris Therapeutics

Department

Quality Control (QC)

Job Role

Officer, Executive, Senior Executive

Experience

0–7 Years

Employment Type

Full-Time

Industry

Pharmaceutical

Selection Process

Resume Screening, Technical Interview & HR Interview

Application Mode

Email

Open Positions

Quality Control Officer

Quality Control Executive

Quality Control Senior Executive

Roles & Responsibilities

Selected candidates will be responsible for:

Analysis of Raw Materials, In-Process Samples, and Finished Products using HPLC.

Calibration and routine maintenance of HPLC instruments.

Performing Method Validation as per regulatory requirements.

Stability sample analysis and documentation.

Following GMP, GLP, and laboratory SOPs.

Maintaining analytical records and ensuring data integrity.

Supporting regulatory audits and quality compliance activities.

Required Skills

Candidates should possess knowledge of:

High Performance Liquid Chromatography (HPLC)

Method Validation

Stability Testing

Calibration of Laboratory Instruments

Pharmaceutical Quality Control

Good Manufacturing Practices (GMP)

Good Laboratory Practices (GLP)

Documentation and Data Integrity

Analytical Chemistry

Preferred Qualification

Eligible candidates may include:

B.Pharm

M.Pharm

B.Sc.

M.Sc. (Chemistry/Analytical Chemistry or relevant discipline)

(Qualification should match company requirements.)

Experience Required

0 to 7 years of relevant experience in Pharmaceutical Quality Control.

Freshers meeting the eligibility criteria may also apply if considered by the company.

How to Apply

Interested candidates can send their updated CV to:

Email: recruitment@eristherapeutics.com

Contact Number: 9558001555

Ensure your resume highlights your analytical techniques, HPLC experience, and QC exposure before applying.

Why Join Eris Therapeutics?

Reputed pharmaceutical company

Career growth opportunities

Exposure to advanced analytical instruments

Professional working environment

Opportunity to work with experienced QC teams

Technical FAQs

1. What is HPLC and why is it important in Quality Control?

HPLC (High Performance Liquid Chromatography) is an analytical technique used to identify, separate, and quantify pharmaceutical compounds. It ensures that medicines meet quality, purity, and regulatory standards.

2. What is Method Validation?

Method Validation confirms that an analytical method consistently produces accurate, precise, specific, and reliable results according to ICH guidelines.

3. What is Stability Sample Analysis?

Stability testing evaluates how a pharmaceutical product maintains its quality, safety, and efficacy under different environmental conditions over time.

4. Why is HPLC calibration necessary?

Calibration verifies that the HPLC system provides accurate and reproducible results. Regular calibration ensures compliance with GMP and regulatory requirements.

5. What are GMP and GLP in pharmaceutical laboratories?

GMP (Good Manufacturing Practices) ensures products are consistently manufactured to quality standards, while GLP (Good Laboratory Practices) ensures laboratory testing is reliable, traceable, and properly documented.