Sharif Pharmaceuticals Limited

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Summary

Vacancy: —
Age: 35 to 45 years
Location: Narayanganj (Rupganj)
Salary: Negotiable
Experience: 10 to 15 years
Published: 25 Nov 2024

Requirements

Education

M.Pharm from any reputed university

Experience

10 to 15 years

Additional Requirements

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

Responsibilities & Context

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

To Ensure, the quality of all manufactured products as per cGMP.
To Handle the QMS functions like Change Control, Deviation, non-conformities, out-of-specification, Market Complaints, Product Recall, and Risk Management.
To be responsible for the preparation, controlling, and archiving of different GMP documents like Site Master File, Training Manual & its Schedule, Internal and external audit schedule & maintain its Implementation, BMR, BPR, SOP, and all sorts of docu- ments of Plant.
To be responsible for all kinds of validation-related activities for the design, commissioning. qualification & continued valida- tion of all equipment, facility & utility and Conduct GMP-related training for respective personnel as per the training calendar.
To monitor the evaluation of any non-compliance observed during in process and implement corrective & preventive action against audit findings.
To the maintenance of documentation for audits & compliance activities of the QA Department.
To ensure in fulfilling questionnaire & necessary document as per the requirement of vendor audit, regulatory audit & other audits.
To Preparation of Technology Transfer Protocols & Reports and ensure the availability of all regulatory documents for Technol- ogy transfer of a product.
Perform Training Needs Assessments (TNA) to prepare & conduct training programs of employees.

Compensation & Other Benefits

Mobile bill
Salary Review: Yearly
Festival Bonus: 2
Leave: As per company policy

Employment Status

Full Time

Job Location

Narayanganj (Rupganj)

Source link

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