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Chemironcare Products Nigeria Limited - Jobs/Vacancies - Nairaland

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Chemironcare Products Nigeria Limited by AkajamesO: 1:56pm On May 11, 2020
Job vacancy

Company Information
Chemironcare Nigeria product Limited, formerly
known as Chemech Laboratories Nigeria
Limited, was established in 1987 and is a
household brand today.
Our commitment and business purpose is
clear; to provide a medium of healthcare,
which is quite simply, superior in quality
and delivers real health value to our
consumers.
We envision being an African market
leader in providing nutritional healthcare
supplements; with the demanding work
and lifestyle patterns today, we feel it is
crucial for supplemental drugs to deliver
noticeable differences to our consumers’
health, drive and quality of life. Our focus
always remains on prominent health
epidemics, such as anemia, with a view
to delivering a difference.
Our products are developed and
produced through extensive and careful
research on the physiological needs of our
customers base, using dedicated
manufacturing and logistical facilities.
Chemiron’s vision for the next five years
will revolve around expanding our
product base, by continuing research into
ongoing health issues, which affect a wide
range of people. Our success stems from
gaining extensive knowledge about a
condition, before proceeding to develop
formulas that make a visible impact,
quickly and effectively.




Industry: Pharmaceutical and Health care

Location: Agbara plant, Ogun state

Position: 1. production pharmacist

Duties
Co-ordinates in planning and organizing the manufacturing process of the company.

Implements Operational manuals, production plans and programs.

Ensures conformance of manufacturing processes with organizational objectives and polices with the coordination of Production Executive/ Asstt. Manager Production.

Checks the availability of adequate raw and packing materials, utilities, filters and machine size parts.

Fulfills the monthly and weekly production plans according to the schedule with the coordination of Production Executive/ Asstt. Manager Production.

Monitors drugs manufacturing activities in compliance with the requirements of cGMP.

Ensures that all standard yield are maintained by production lines.

Controls production process and production facilities.

Ensures the general cleanliness and hygienic conditions of the manufacturing areas.

Ensures that all production equipments are maintained in good working order.

Assists in pilot scale trials of products under development.

Ensures that there is discipline and good working culture among the staff.

Makes sure the on job training of production personnel.

Ensures the hygienic condition of production personnel.

Ensures production people wear mask, gloves and shoes before entering into production.

Prepares daily reports.

Performs other duties as assigned by Production Executive/ Asstt. Manager Production.

Responsibilities

Responsible for any delay during daily as well as weekly work schedule.

Decides either to reject or use by sorting non-conforming raw and packing materials discovered during the manufacturing process after discussing with Production Executive/ Asstt. Manager Production.

Takes decision about where engaging man power in absence of work.

Responsible for planning of work according to weekly program.

Mainly supervises duties of subordinates, operators and rest of workers.


Responsible for materials issued from warehouse for manufacturing.

Responsible to keep all confidential matters secret and protect the interest of the company.


2. Production Chemist

Responsibilities: includes but not limited to:
Investigated causes of failures and developed new procedures for problem solving to produce high quality product and maximize output.
Utilized protein purification HPLC, mass spectrometry, synthesis and cleavage of oligonucleotides, and polymerase chain reaction.
Worked independently performing troubleshooting, staff mentoring, and object-oriented research and analysis.
Reduced cost product development by 50%.
Maintained validation summaries and standard operation procedures to ensure compliance with cGMPs.

Qualification: Bsc or HND, MSc. With 3 years experience in the field.


Interested and qualified candidates should send their cv to akajames101@gmail.com use job title as your subject.

Deadline 30th June

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