Asst. Manager/ Sr. Executive- Quality Control
Job Description
Title: Asst. Manager/ Sr. Executive- Quality Control
Company Name: Bengal Remedies Limited
Vacancy: --
Age: Na
Job Location: Gazipur (Tongi)
Salary: Negotiable
Experience:
- At least 5 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Published: 2024-09-02
Application Deadline: 2024-09-07
Education:
Master of Pharmacy (M. Pharm)/ Bachelor of Pharmacy (B. Pharm)/ Master of Science (MSc)
Requirements:
- At least 5 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Skills Required:
Additional Requirements:
Responsibilities & Context:
To run & maintain quality control activity as per GLP (Good Laboratory Practices) in Quality Control Department.
To check & follow the approved departmental SOPs & Procedure.
To ensure proper cleanliness & housekeeping Lab on daily basis.
To make plan for the analysis of daily samples and ensure that all necessary testing to be carried out carried out properly.
To monitor and ensure the timely sampling and analyze starting materials, packaging materials, intermediate, bulk and finished products in relation to their approved specifications.
In case of any abnormalities /out of specification observed, it should be informed to Head of Quality Assurance for following the appropriate procedure for investigation & corrective action.
To confirm volumetric solutions, reagents, buffer solutions and indicators has been Prepared according to approved standard procedure and to maintain their record and discard them after their valid self-life.
To follow approved specifications and test procedure for analysis.
To prepare working standards as per SOP and maintain its record and ensure availability of working standards & perform the qualification (Qualitative & Quantitative).
To perform calibration and validation of measuring and monitoring equipments, jointly with QA.
To perform source validation, cleaning validation, process validation, method validation etc. jointly with QA.
To develop and validate analytical method for new raw materials, intermediate and finished products jointly with QA.
To evaluate batch records and to check all necessary production and quality control documentation has been completed and endorsed by respective authorities.
To distribute the daily work plan and supervise the activities of the subordinates.
Monthly report preparation, for management evaluation.
To evaluate Batch Manufacturing Record (BMR) & Batch Packaging Record (BPR).
To perform regulatory affairs related work.
To participate in the training and internal audits or self-inspections.
To perform any other job assigned by the reporting authority.
Job Other Benifits:
- Mobile bill
- Salary Review: Yearly
- Lunch Facilities: Full Subsidize
- Festival Bonus: 2
Employment Status: Full Time
Job Work Place: Work at office
Company Information:
Gender: Male and Female can apply
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Category: Healthcare/Medical
