Q.A Manager

a) Responsible to maintain a satisfactory and good environment in between production,

b) Ware house, maintenance and marketing according to the GMP and GLP.

c) Responsible to manage the smooth working and technical activities in Q.C.

d) Authorized to release or reject the Raw Material, Packaging Material, In process

Product for further processing and finished product on valid ground.

e) QCM is responsible to review and monitor the objectives on regular basis and

Can revised whenever need.

f) QCM will evaluate the Laboratory and ensure that laboratory is capable

of doing the tests as per specifications and standards.

g) Responsible for all the purchases made in laboratory, raised requisition

Containing the specification of reagent, equipment, glass ware,

Chemicals and microbiological articles.

h) The bulk samples of chemicals and glass wares are being stored by material

Management department on storage condition to agreed and verified by QCM.

i) QCM will responsible for evaluation and approved to suppliers and vendors.

j) QCM assigns the complaint to the Laboratory staff for investigation for root

cause and proposed corrective action.

k) QCM ensures the competent and authorized persons for operational work of

Equipment, performance and calibration.

l) QCM authorize the activity to a person on the basis of his evaluation, experience

training are satisfactory knowledge of the testing, equipment and calibration.

m) QCM is responsible to prepare the Job description of each member of the laboratory.

n) QCM ensures that all facilities required to perform a test in standard manners like

energy resources, weighting and environmental conditions.

o) QCM review all environmental monitoring record on monthly basis.

p) QCM ensure the appropriate SOPs are available for all tests, performed

under the scope of accreditation.

q) QCM ensure that open hand instruments for all equipments are available

in laboratory and appropriate personnel are trained as them.

r) QCM is responsible to ensure that correct date is being transferred from

raw data to final report.

s) QCM ensure that reference materials are certified against traceable certificates

and theirs standards is also available of internal standard are used than

they are validated before use.

t) Any amended in test report, calibration date and other QC related documents

with Log books registers, formats and sheets can only executed after the approvals of QCM.

u) All SOPs and Methods preparations and approved.

v) Enforce GMP compliance in production QC and Warehouses.

w) Responsible of all documents such as IQ, OQ, PQ, validation and stabilities.

x) to supervise the maintenance of monthly log registers for Raw, Finished, Packaging and stability records.

y) To supervise the inventories and consumption records of Reagents and Glass wares.

Job Specification

a) Documentation, Clerical - Knowledge of administrative and clerical procedures and systems such as word processing, managing files and records, stenography and transcription, designing forms, and other office procedures and terminology.

b) Chemistry - Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations that they undergo. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods.

c) Mathematics - Knowledge of arithmetic, algebra, geometry, calculus, statistics, and their applications.

d) Production and Processing - Knowledge of raw materials, production processes, quality control, costs, and other techniques for maximizing the effective manufacture and distribution of goods.

e) Medicine - Knowledge of the information and techniques needed to diagnose and treat human injuries, diseases, and deformities. This includes symptoms, treatment alternatives, drug properties and interactions, and preventive health-care measures.

Quality management is focused on both quality assurance and control of processes to assure,

not only qualitative products, but also the methods to achieve it.

Measures the percentage of work processes that are mapped,

Measures the percentage of product improvement

Measures the percentage of production delays due to any reason

Measures the average number of defects per manufacturing

Skills

a) Critical Thinking - Using logic and reasoning to identify the

strengths and weaknesses of alternative solutions, conclusions

or approaches to problems.

b) Monitoring - Monitoring / Assessing self performance, other individuals,

or organizations to make improvements or take corrective action.

c) Systems Analysis - Determining how a system should work and

how changes in conditions, operations, and the environment will affect

outcomes.

d) Systems Evaluation - Identifying measures or indicators of system

performance and the actions needed to improve or correct performance,

relative to the goals of the system.

Information Technology and Services - Karachi, Pakistan

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