NIPRO JMI Pharma Ltd
Executive-Validation/QC at NIPRO JMI Pharma Ltd - Join a Leading Pharmaceutical Company!
Cumilla
Deadline: 2025-09-21
1 Positions
Job Overview
Company: NIPRO JMI Pharma Ltd
Location: Cumilla
Type: FullTime
Salary: Negotiable
Posted: 2025-09-15
Experience: 3 Years
Education Requirements
Master of Science (MSc) in Chemistry or Applied Chemistry, or Master of Pharmacy (M.Pharm).
Job Responsibilities
- Conduct sampling and testing of raw materials, packaging materials, bulk, and intermediate products.
- Prepare reagents and perform standardization in alignment with pharmacopeial compendia.
- Develop analytical methods for both new and existing products.
- Execute analytical method validation for finished products.
- Perform analysis of hold-time study samples to ensure product stability.
- Prepare and review departmental SOPs and finished product analytical methods.
- Manage QMS-related activities, including OOS, LIR, deviations, change controls, and non-conformities.
- Ensure proper documentation, compilation, and record-keeping of raw materials, packaging materials, and finished products.
Required Skills
- communication and interpersonal skills
- Microsoft Office
Benefits & Compensation
- Provident Fund
- Gratuity
- Festival Bonus:3
- Profit Share
- Weekly 2 Holidays
- Group Life Insurance
- Lunch Facility: Partially Subsidized
- Salary Review: Yearly
Job Description
NIPRO JMI Pharma Ltd is on the lookout for an enthusiastic and dedicated Executive-Validation/QC to join our dynamic team. As a key player in our quality assurance department, you will be responsible for ensuring that our products meet the highest standards of quality. The role entails a variety of responsibilities aimed at maintaining our reputation for excellence in pharmaceutical manufacturing.You will engage in diverse tasks including:Conducting sampling and testing of raw materials, packaging materials, bulk and intermediate products.Preparing reagents and performing standardization in alignment with pharmacopeial compendia.Developing analytical methods for both new and existing products.Executing analytical method validation for finished products.Performing analysis of hold-time study samples to ensure product stability.Preparing and reviewing departmental SOPs and finished product analytical methods.Managing QMS-related activities, including OOS, LIR, deviations, change controls, and non-conformities.Ensuring proper documentation, compilation, and record-keeping of raw materials, packaging materials, and finished products.The ideal candidate will be a committed team player and possess excellent skills in communication and interpersonal skills with proficiency in Microsoft Office.Qualifications Required:Master of Science (MSc) in Chemistry or Applied Chemistry, or Master of Pharmacy (M.Pharm).We have a competitive salary range that is negotiable based on experience and qualifications.This opportunity is based in Cumilla, Bangladesh, and we encourage all eligible applicants to apply before the deadline.If you're looking to advance your career in an energizing environment and make a real impact in the pharmaceutical industry, we want to hear from you!