Assistant Manager- R&D Department (Analytical)

Job Description

Title: Assistant Manager- R&D Department (Analytical)

Company Name: Sharif Pharmaceuticals Limited

Vacancy: --

Age: At most 38 years

Job Location: Narayanganj

Salary: --

Experience:

• 5 to 7 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• B.Pharm/M.Pharm from any reputed university

• 5 to 7 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Age At most 38 years

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: Assistant Manager- R&D Department (Analytical)
Job Location: Factory (Barabo, Tarabo, Rupgonj, Narayangonj)
Job Responsibilities

• To Perform analytical method development for both compendia & non-compendia method

• Assist with all aspects of analytical development, including new assay development, qualification and validation, and routine sample analysis.

• Conduct routine LC-MS sample analysis to support characterization, stability, formulation development, and comparability studies by following experimental design, protocols, and SOPs

• Contribute to the development of new analytical methods, such as HPLC and LC-MS-based assays, to augment our analytical capabilities for release, characterization, and stability testing.

• Prepare and review of method validation protocols and reports.

• To perform physical and chemical analysis of incoming Raw Materials (API

• & Excipients) for source Validation To perform physical and chemical analysis intermediate, and finished products.

• Develop and validate test methods for cleaning validation

• Collaborate with QC to support method transfer and validation.

• Generate and review laboratory investigation reports

• Contribute to analytical sections for regulatory submissions while ensuring high-quality data integrity and documentation

• Prepare specifications and test procedures for raw materials and finished dosage forms

• Prepare SOP, STP, and other documents as per requirements.

• Provide cross-functional support to upstream/downstream process development, formulation, and quality control teams

• Collaborate with multi-disciplinary teams, effectively communicate results in oral and written formats

• Demonstrate a willingness to quickly learn new skills and technologies and adapt to changes

• Mobile bill

• Salary Review: Yearly

• Festival Bonus: 2

• Leave: As per company policy