| Job Code |
40966
|
| Posting Date | 02 Mar 2010 |
| Closing Date | 13 Jul 2010 |
| Industry |
Pharma/Bio-tech/Clinical research
|
| Job Tenure |
Permanent
|
| Gender Requirement |
None
|
| Summary |
We are seeking an experienced, and motivated candidate, must have good communication skills and the ability to work both as part of a team and individually.
|
| City | Karachi |
| Country | Pakistan |
| Experience Required |
5-10 Year(s)
|
| Management Level |
Management (Manager, Director, etc)
|
| Availability |
|
| Work Location | Onsite |
| Location | Karachi |
|
Age Requirement |
30 - 40 Year(s) |
| Salary Offered |
Not provided by user
|
| Minimum Education |
Pharm.D/ B.Pharm / M. Pharm / M.Sc.
|
| Job Description |
Supervises the working of the Q.A. Department.
Co-ordinates the artwork preparation with Artist & Marketing.
Preparation & Reviewing of SOP’s.
Assists and co-ordinates the inspection of the plant and prepare the reports.
Prepare and issue monthly cGMP report.
Oversee stability testing program, market surveillance program and maintenance of record.
Issuance of protocol for validation.
Co-ordinate in IQ/OQ/PQ of QA equipments.
Co-ordinate with Production in performing IQ/OQ/PQ of Production equipment’s.
Co-ordinate in preparation of MO / PO.
Co-ordinate in the preparation of dossiers for New Products and Export Products.
Work on preparation of budget. Work on 90% of budget allocation.
Assist H. Q.O in routine Quality Operation activities an issuance of reports.
Oversee all inprocess activities including line clearance and inprocess checks performed by Q.A Auditors.
Oversee checking of all product BMR’s.
Oversee computer releases of finished products for onward dispatch to the market.
Oversee packaging components testing in accordance with the written specifications.
Supervise and co-ordinate all ISO documentation application & procedures.
|
| Candidate Ability |
Professional:
Hands on experience of inspection activities in a pharmaceutical.
Able to work in the Laboratory in an efficient manner.
Having knowledge of GLP, GMP and other ethical practices in Laboratories,
Able to supervise the working of Quality Assurance section based on Quality System elements viz. Change Control, Deviations, Documentation, Calibration and Maintenance, Stability, Validation, Audit, Training etc.
Able to organize relevant activities with the objective to increase productivity and smooth running of the department.
Able to maintain relevant records in an efficient manner.
Personal:
A contributing team player
Excellent Communication skills
Problem solving and decision making
Willing to learn, take up challenges and grow
|
| Career Path / Benefits / Perks Offered |
An attractive salary package with fringe benefits including Company car, Medical, PF, Group insurance, Gratuity, Congenial Working Environment and Career Growth opportunities await the selected candidate.
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