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Job Description and Requirements
1-To manage and control the daily activities in the quality assurance department.
2-To ensure the proper implementation of the international standards in manufacturing, laboratories, processing, packaging & warehousing .
3-To ensure that all operations performed in the department are in compliance with Jordanian legal & cGMP’s requirements .
4-To check & approve all active documents that has impact on product quality.
5-To prepare department budget & follow its implementation.
6-To maintain the department personnel in good moral.
7-Co-operate & Co-ordinate with Plant director and Managers for planning schedule & implementation of company works .
8-To Co-ordinate with R&D department and TQM about pharmaceutical formulations in case of changes and deviations.
9-To Co-ordinate & approve all validation activities & evaluation of results in co-operation with the related technical departments .
10-To ensure that products are produced according to approved procedures, records & documents .
11-To approve IQ/OQ & PQ documents for all production machines & Lab instruments & utilities.
12-To follow up the implementation of training program according to the approved system.
13-To maintain all the company documents in the department.
14-To monitor the suppliers of materials.
15-To ensure that the appropriate validations are done
16-To ensure that the department is fulfilling the company policy & targets.
17-To act as deputy of senior TQM Manager during his absence.
18-To manage QA employees affairs .
19-To organize QA program .
20-To inform senior TQM Manager when detects are found
21-To manage and control the daily activities in the dept.
22-To approve employee’s leaves and vacations.
23-To manage the auditing activities either internally or externally according to company plan and system
24-To ensure the proper implementation of the cGMP regulations in manufacturing, processing, packaging & warehousing
25-To establish good communications procedures with other departments
- B.Sc or M.Sc chemical engineering
- B.Sc or M.Sc pharmacy, Chemistry
- Current good manufacturing practices
- GMP Training
- ISO 9001 , ISO 14001
- Managerial & Supervisory Skills
-10 years in pharmaceutical industry, 5 years as QA Manager
-Computer literate, good command of English written and spoken,
organizational and leadership skills.
-Communication with managerial level.