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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