Manager - QA
Job Description
Title: Manager - QA
Company Name: Sharif Pharmaceuticals Limited
Vacancy: --
Age: 35 to 45 years
Job Location: Narayanganj (Rupganj)
Salary: Negotiable
Experience:
- 10 to 15 years
Published: 2024-11-25
Application Deadline: 2024-12-05
Education:
M.Pharm from any reputed university
Requirements:
- 10 to 15 years
Skills Required:
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.
Job Other Benifits:
Mobile bill
Salary Review: Yearly
Festival Bonus: 2
Leave: As per company policy
Employment Status: Full Time
Job Work Place:
Company Information:
Gender: Both Male and Female can apply
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Category: Pharmaceutical
