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Quality Control Manager Job Vacancy

Our client, a very busy manufacturing company with its operations along Mombasa road, and which has been operating in Kenya for over five years requires the services of a Qualified Quality Control Manager
Job Description
1.    Responsible for ensuring that products processed are of the quality required for their intended use.
2.    Responsible for final release of products from one manufacturing stage to the other.
3.    Responsible for rejecting of products from proceeding to the next production process if it does not comply with the stated specifications.
4.    Responsible for all the production & QC documentation in the company.
5.    Ensuring that calibration and validation of production and laboratory equipments including balances, autoclaves, oven driers, mixing tanks, etc are done on schedule basis.
6.    Ensuring there is continuous training of production and Q.C personnel in act as a GMP administrator.
7.    Ensuring that the calibration and validation records are maintained and up-dated and validation of the air and water production systems, a septic filling and Q.C analytical procedures are performed.

8.    Ensuring that customer’s complaints related to the quality of the product are well handled and records maintained.
9.    Ensuring that monitoring and performing continuous stability studies of the products are done and records maintained.
10.  Ensuring that product recalls to the quality of the product are well handled.
11.  Responsible for follow-up of health and safety matters with relevant authorities.
12.  Responsible for co-ordinating medical examination of personnel with the company doctor and keeping personnel files.
13.  Ensuring that review of batch production records and investigations in any discrepancies in the data provided are done and records maintained.
14.  Responsible for co-ordinating self-inspection on regular basis.
15.  Ensuring that the isolation and destruction of obsolete printed packaging materials or rejected materials are done and records maintained.
16.  Ensuring that the set of analytical procedures for all the raw materials and finished products in the company are documented.
17.  Ensuring that the master production records (master formula) are well documented and detailed enough to include all the processes done during manufacturing.
18.  Ensuring that a set of specifications for testing all staring materials and packaging components are documented.
19.  Ensuring that a set of specifications for testing all finished products are documented.
20.  Responsible for ensuring all relevant sops are in place and reviewed periodically as per requirements.
21.  Ensuring that maintenance and testing of equipments like balances are done and records maintained.
22.  Ensuring that validation of analytical procedures used in quality control are performed.
23.  ensuring that procedures for monitoring of the environmental parameter in the sterile area including viable micro-organisms, air speeds, air changes and particle size are available and records maintained.
24.  ensuring that sterility tests for the sterile area in microbiology areas are done and records maintained
25.  Ensuring that laboratory microorganisms are well maintained to assure suitability for microbial testing. The micro-organisms should be identified and adequate records maintained showing history of their use
26.  Ensuring that products are designed and developed in a way that takes account of the requirement of c GMP.
27.  ensuring that laboratory records which include complete data derived from all tests necessary to assure compliance with established specifications and standards, including examinations, essays, etc are prepared and complied to.
28.  responsible for the pest control department and production departments are running their requirements and schedule as required
Ideal candidate
·         Must have  done a Degree in Pharmacy or
·         Must Have a Diploma in Pharmacy and with a hand-on the job experience of over 5yrs in the same field.
·         Concrete experience with a busy manufacturing company is an added advantage especially in the quality assurance department.
·         Must be very sharp and keen to details; analytically smart.
·         Good report writing skills required.
To apply for this position contact us through the following contacts:  email: or call 0726648869 or 0724689682 before 7th /10/10.
Any application after the stipulated time will not be considered.

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