Officer - Quality Operations

Job Description

Title: Officer - Quality Operations

Company Name: Nevian Lifescience PLC

Vacancy: --

Age: Na

Job Location: Gazipur (Tongi)

Salary: --

Experience:

• At most 1 year
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Healthcare/Lifestyle product
• Freshers are also encouraged to apply.

• Bachelor of Science (BSc) in Pharmacy
• Bachelor of Science (BSc) in Chemistry
• Bachelor of Science (BSc) in Biochemistry
• Bachelor of Science (BSc) in Applied Chemistry

• Minimum bachelor’s degree in Pharmacy, Chemistry, Biochemistry, or Applied Chemistry.

• At most 1 year
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Healthcare/Lifestyle product
• Freshers are also encouraged to apply.

• 0–1 year of relevant experience will be considered an added advantage.

• Strong technical skills, including operation of laboratory instruments, use of data management software, and preparation of technical reports for investigations.

• Excellent interpersonal, analytical, and communication skills in both Bengali and English.

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(s) to join our Quality Operations team at Tongi Site.

Major Responsibilities:

• Manage GMP documents and records, including maintenance of the central archive.

• Prepare Product Quality Review reports in alignment with regulatory and company requirements.

• Contribute to Quality Oversight activities to ensure ongoing compliance and continuous improvement.

• Support batch record review and ensure timely resolution of documentation gaps or deviations.

• Perform GxP document review and approval as per established procedures.

• Ensure all activities are conducted in compliance with SOPs, GMP, and applicable regulatory guidelines.