Manager - QC

Job Description

Title: Manager - QC

Company Name: Sharif Pharmaceuticals Limited

Vacancy: --

Age: 35 to 45 years

Job Location: Narayanganj (Rupganj)

Salary: Negotiable

Experience:

• 10 to 15 years

• M.Pharm from any reputed university

• 10 to 15 years

• Age 35 to 45 years

• Analytical skills

• Self-motivated

• 10-15 years of working experience in reputed Pharmaceuticals Industry.

• Having at least 5 years working Experience in this same position.

• The applicants should have experience in the following area(s): Calibration, Cleanroom, Compliance, Compliance Audit, Pharma audit and International Regulatory Audit.

• Must know Advance Excel-like expert in a pivot table, PPT Leadership Capability & excellent communication skills Positive, Self-motivated, Honest, Dedicated, detail-oriented & possessing a good memory. Sincere, Honest & Accountable for the job

• Able to work in a team

• Possessing a positive attitude

SHARIF PHARMACEUTICALS LIMITED, an ISO certified company, having state-of-the-art plant, is committed to serve the country as a leading pharmaceutical company. We are looking for following position -

• Job Location: Factory (Barabo, Tarabo, Rupganj, Narayangonj)

Job Responsibilities

• Sampling and analysis of Raw material and packaging material including documentation

• Analysis of finished product, In process sample & Stability Sample including documentation Reagent & inventory management. Identifies and mitigates risks in QC lab oratories, processes, and systems that could negatively impact lab operations and QC performance.

• Preparation of WRS, TS, VS, indicator and Standardization of VS.

• To perform QC Instrument operation & Calibration HPLC (High Performance Liquid Chromatography) GC (Gas Chromatogra- phy). TOC (Total Organic Carbon), UV (Ultraviolet), FTIR (Fourier Transform Infrared Spectroscopy) & AAS (Atomic absorption spectrometry) etc.

• Sampling & Analysis of Raw materials, packaging materials, finished products and Physical & Chemical analysis of Raw, Potable, DM (Demineralize), PW (Purified Water), WFI (Water for Injection) and ETP (Effluent Treatment Plant) Water.

• To perform Analytical Method Validation and Verification

• Scheduling, Planning, performing and review of QC validation activities.

• Writing, reviewing and approving documentation e.g. technical reports, standard operating procedures, laboratory protocols, trend analyses.

• Facilitate the maintenance of the lab including routine housekeeping, lab inventory, and equipment

• Preparation and review of SOPs, Specifications and methods for raw material and Validation of analytical methods, cleaning & qualification of equipment.

• Carryout Microbiological analysis of sterile and non-sterile raw materials and products according to approved procedure in order to ensure that the product is free from specified microorganisms.

• Preparation and standardization of volumetric solution, secondary working standards from reference standard etc.

• Having the ability to manage and execute DGDA (Directorate General of Drug Administration) Bangladesh, audits successfully requires a comprehensive understanding of both local regulatory requirements and international best practices.

• Contribute to team building, training, and problem-solving initiatives

• Professionally develop analysts to improve on individual and overall performance

• Mobile bill

• Salary Review: Yearly

• Festival Bonus : 2

• Leave: As per company policy