Executive/ Sr. Executive, QC, Unit-2 (Mawna, Gazipur)

Job Description

Title: Executive/ Sr. Executive, QC, Unit-2 (Mawna, Gazipur)

Company Name: The IBN SINA Pharmaceutical Industry PLC

Vacancy: --

Age: 25 to 35 years

Job Location: Gazipur

Salary: Negotiable

Experience:

• 2 to 5 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• 2 to 5 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Age 25 to 35 years

• Candidates should be Sound health, self-motivated, capable of working under pressure, willing to work in three shifts and committed to maintaining quality, safety and regulatory compliance;

• 2-5 years of hands on experience in the ARD/ FR&D of reputed pharmaceutical Manufacturing company;

• Maximum age 35 years.

• Perform routine chemical analysis of Raw Materials (RM), in-process Samples, Finished Products (FP), stability samples and purified water according to approved specifications and test methods.

• Operate analytical instruments such as HPLC, GC, UV-visible Spectrophotometer, FTIR, Dissolution Tester ph Meter, conductivity Meter, TOC Analyzer, Karl Fischer Titrator, and other laboratory equipment.

• Record analytical data accurately and maintain laboratory notebooks, worksheets, logbooks, and electronic records in compliance with good documentation Practices (GDP) and ALCOA= data integrity principles.

• Coordinate installation, Qualification (IQ/OQ/PQ), calibration, preventive maintenance, and annual performance verification of laboratory instruments.

• Supervise the sampling. testing, review, and release of Raw Materials (RM) Packaging Materials (PM) Finished Products (FP), in Process samples water environmental monitoring samples, water, environmental monitoring samples, and cleaning validation samples.

• Supervise laboratory investigations related to Out-of-Specification (OOs) , Out-of-Trend (OOT), deviations laboratory incidents, and CAPA implementation.

• Ensure compliance with WHO GMP, PIC/S GMP, EU GMP, USP, BP, EP, and applicable regulatory guidelines.

• Maintain Good Documentation Practices (GDP), ALCOS+ data integrity principles, and electronic/physical laboratory records.

• Responsible to carry out any other duties as when assigned by Head of the Department.

• Medical allowance,Profit share,Provident fund,Gratuity,Mobile bill
• Salary Review: Yearly
• Lunch Facilities: Full Subsidize
• Festival Bonus: 2

• As per company rules.