Officer - Quality

Job Description

Title: Officer - Quality

Company Name: Nevian Lifescience PLC

Vacancy: --

Age: At least 25 years

Job Location: Gazipur (Tongi)

Salary: --

Experience:

• At most 2 years

BPharm/MPharm/M. Sc in Chemistry/Biochemistry/Applied Chemistry from a reputed university.

• At most 2 years

• Age At least 25 years

• Up to 2 years of experience in pharmaceutical GxP environment (e.g. Production, Quality, etc.).

• High integrity, attention to detail, accountability, and commitment to ethical practices in a GMP-regulated environment.

• Strong analytical, critical thinking, problem-solving, and effective written and verbal communication skills with the ability to work collaboratively.

• Self-motivated, adaptable, well-organized, and eager to learn, with the ability to manage time effectively.

• Physically fit to do analytical activities at chemical laboratory.

Nevian Lifescience PLC – formerly Novartis (Bangladesh) Limited – carries forward a 250-year global legacy and a 50-year local heritage in healthcare excellence. With its EU-GMP and ANVISA-certified facility, Nevian produces world-class medicines, including Novartis global brands under license, and serves as the importer and distributor of Novartis’ innovative therapies in Bangladesh.

At Nevian, we are a team of passionate professionals driven to make a real difference for patients. We foster a culture where talent is valued, collaboration thrives, and everyone is empowered to perform at their best. Join us and be part of a team making a lasting impact on millions of lives.

We are seeking for Officer, Quality to join our Quality team at Tongi Site.

Major Responsibilities:

Quality Operations

• Manage GxP documents – issuance, receipt, reconciliation, filing, and archiving.

• Assist in quality investigations, document non-conformances, and track CAPAs.

• Provide quality oversight in GMP areas, identify issues, and support improvements.

• Preparation of Product Quality Review as per annual plan.

Quality Compliance

• Monitor Key Quality Indicators (KQI) and ensure timely reporting

• Assist in handling change control and in third party management.

• Support internal self-inspections, regulatory inspections, and third-party audits

• Contribute in implementation of regulatory guidelines at site level

Quality Control

• Finished Product Analysis, Raw material Analysis, Stability Sample Analysis and Analytical Sample Preparation.

• Supporting in the development of raw and packaging material sources.

• Ensuring compliance of all activities aligning with SOP and official regulations.