Arbro Pharmaceuticals Pvt. Ltd Urgent Openings in Manufacturing & Quality Assurance Departments
Openings @ Arbro Pharmaceuticals Pvt. Ltd
QA Executive
Experience: 1-3 yrs
Qualification: B.Pharm / M.Pharm
Location: Delhi NCR
Responsible for documentation and implementation of all QA & QC activities
Verification and technical support for all technical documents master formula, standard operating procedure, raw material, finished product specifications.
Responsible for handling various quality management systems like deviation, change control and market complaints.
Responsible for providing quality assurance support to the manufacturing operations
Internal auditing of QA/QC and other departments
Review of all QC/QA activities.
Art work control of labels, leaflets, visual aids, promotional materials of domestic and export.
Verification and implementation of new label matter design and promotional materials as per regulatory compliances,
Export related technical support-material safety data sheet, ingredient report etc.
Coordination with R&D and technology transfer group during Trial/Validation of batches.
Review and approval of records (ie: SOP, Batch record, master formulation, specification certificate of analysis, stability studies, labeling etc.
Manufacturing Chemist
Experience: 1-4 yrs
Qualification: B.Pharm / M.Pharm
Job description
1. Responsible for day to day activity
2. Issuance and receive of blank Batch Manufacturing Record
(BMR) from QA department.
3. Issuance of Raw Material from Raw Material store as per BMR.
4. Maintaining the process parameters as per BMR.
5. Keep the BMR updated for on-line production activity.
6. Maintaining Usage, Cleaning & Maintenance log book of
different equipment.
7. Daily calibration of electronic weighing balance.
8. To carry out the cleaning procedure of all the equipment.
9. To ensure timely preventive / breakdown maintenance of
equipment.
10. To plan all the resources needed for timely production
11. Monitoring and maintaining the GMP in production
12. Ensuring the quality of products
13. Responsible for stock keeping and inventory
2. Issuance and receive of blank Batch Manufacturing Record
(BMR) from QA department.
3. Issuance of Raw Material from Raw Material store as per BMR.
4. Maintaining the process parameters as per BMR.
5. Keep the BMR updated for on-line production activity.
6. Maintaining Usage, Cleaning & Maintenance log book of
different equipment.
7. Daily calibration of electronic weighing balance.
8. To carry out the cleaning procedure of all the equipment.
9. To ensure timely preventive / breakdown maintenance of
equipment.
10. To plan all the resources needed for timely production
11. Monitoring and maintaining the GMP in production
12. Ensuring the quality of products
13. Responsible for stock keeping and inventory
Send CV at jobs@arbropharma.com
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