Theres an urgent vacancy for the Post of A Quality Control Manager in a renowned Pharmaceutical company. Application closes two weeks from date of advertisement. Email - dairo.ayo@gmail.com

1. Job Responsibilities:
a. Manage the provision of analytical services (finished products, intermediate products, raw materials and packaging materials/components).
b. Have complete authority and responsibility for the sampling, testing, acceptance and rejection of all raw materials, packaging materials, intermediate materials being received into the company to ensure only materials of acceptable quality are received at all times.
c. Have complete authority and responsibility for the sampling, testing, acceptance and rejection of intermediate and finished products produced by the company.
d. Develop testing, manufacturing, packaging procedures and other critical quality documents, and manage their controls to ensure world-class Quality Management system.
e. Develop testing specifications, monographs and reports for all raw/packaging materials, finished and intermediate products.
f. Develop and manage the Standard Operation Procedure system through improved documentation activities to ensure all factory vital processes are adequately covered with relevant operational procedures.
g. Coordinate and effectively partake in the Qualifications, Validations and Calibrations programs of the factory processes to ensure accuracy/reliability and assured high product quality/integrity.
h. Organize the Good Manufacturing Practice programs through direct and scheduled internal and external training of staff and follow-up evaluation.
i. Manage the quality audits (and make corrections) for all internal processes and external suppliers of goods/services that have direct or indirect impact on quality of the final product.
j. Coordinate the Environment, Safety and Health (SHE) program of the system to ensure compliance with local regulatory agencies and global SHE standards with emphasis on the cleaning activities of the environment.
k. Coordinate the change control process for the factory to assure traceability.
l. Manage the deviation reporting system and ensure non conformances are promptly reported and corrected.
m. Develop monthly quality management report and reflect all relevant KPIs
n. Manage the stability program for marketed and web products to achieve desired regulatory and product improvement objectives.
o. Coordinate the environmental monitoring process to ensure products are manufactured only at the desired conditions.
p. Provide relevant quality documentation and Personal Protective Equipment (PPE) to operational processes to ensure compliance to GLP and safety conscious environment.
q. Provide periodic GMP training to all staff to ensure nobody works within the factory without first undergoing GMP and other relevant quality training.
r. Ensure preparation of Quality management department budget in relation with finance control management
s. Partake in the NPD team activities to ensure no undue delay in planned launch date.
t. Any other job related assignments that may be assigned from time to time by the supervisory manager.

2. QUALIFICATIONS:
a. B.Sc./HND applied Sciences, especially Chemistry, Biochemistry, Industrial chemistry,
b. Post graduate qualifications in science desirable.
c. Minimum of 5 years experience in Quality Management Process of a pharmaceutical company
d. Practical instrumentation method of analysis, a must.
e. Must be computer literate.

Anjelus:
Theres an urgent vacancy for the Post of A Quality Control Manager in a renowned Pharmaceutical company. Application closes two weeks from date of advertisement. Email - dairo.ayo@gmail.com

1. Job Responsibilities:
a. Manage the provision of analytical services (finished products, intermediate products, raw materials and packaging materials/components).
b. Have complete authority and responsibility for the sampling, testing, acceptance and rejection of all raw materials, packaging materials, intermediate materials being received into the company to ensure only materials of acceptable quality are received at all times.
c. Have complete authority and responsibility for the sampling, testing, acceptance and rejection of intermediate and finished products produced by the company.
d. Develop testing, manufacturing, packaging procedures and other critical quality documents, and manage their controls to ensure world-class Quality Management system.
e. Develop testing specifications, monographs and reports for all raw/packaging materials, finished and intermediate products.
f. Develop and manage the Standard Operation Procedure system through improved documentation activities to ensure all factory vital processes are adequately covered with relevant operational procedures.
g. Coordinate and effectively partake in the Qualifications, Validations and Calibrations programs of the factory processes to ensure accuracy/reliability and assured high product quality/integrity.
h. Organize the Good Manufacturing Practice programs through direct and scheduled internal and external training of staff and follow-up evaluation.
i. Manage the quality audits (and make corrections) for all internal processes and external suppliers of goods/services that have direct or indirect impact on quality of the final product.
j. Coordinate the Environment, Safety and Health (SHE) program of the system to ensure compliance with local regulatory agencies and global SHE standards with emphasis on the cleaning activities of the environment.
k. Coordinate the change control process for the factory to assure traceability.
l. Manage the deviation reporting system and ensure non conformances are promptly reported and corrected.
m. Develop monthly quality management report and reflect all relevant KPIs
n. Manage the stability program for marketed and web products to achieve desired regulatory and product improvement objectives.
o. Coordinate the environmental monitoring process to ensure products are manufactured only at the desired conditions.
p. Provide relevant quality documentation and Personal Protective Equipment (PPE) to operational processes to ensure compliance to GLP and safety conscious environment.
q. Provide periodic GMP training to all staff to ensure nobody works within the factory without first undergoing GMP and other relevant quality training.
r. Ensure preparation of Quality management department budget in relation with finance control management
s. Partake in the NPD team activities to ensure no undue delay in planned launch date.
t. Any other job related assignments that may be assigned from time to time by the supervisory manager.

2. QUALIFICATIONS:
a. B.Sc./HND applied Sciences, especially Chemistry, Biochemistry, Industrial chemistry,
b. Post graduate qualifications in science desirable.
c. Minimum of 5 years experience in Quality Management Process of a pharmaceutical company
d. Practical instrumentation method of analysis, a must.
e. Must be computer literate.

Still expecting applications...

.

Have sent my CV (abiodunoluwafemi4@gmail.com) I hold postgraduate degree in industrial chemistry