Senior Quality Assurance/Control Officer at a Pharmaceutical Company

Posted on Tue 06th Aug, 2019 - hotnigerianjobs.com --- (0 comments)

A Pharmaceutical organisation in Nigeria with interest in business expansion is in search of an experienced personnel to occupy the vacant position below:

Job Title: Senior Quality Assurance/Control Officer

Location: Nigeria

Job Description and Profile

The Senior Quality Assurance/Control Officer will be a team member of Quality Assurance Department.
He/she is responsible for the implementation of quality management system.
He/she is responsible for all quality assurance Issues e.g. validation, documentation, quality control, etc, with the supervision of the Quality Assurance Manager

Duties and Responsibilities

Conducting a management review of the quality system
Following up on and closing pending preventive and corrective action requests
Ensuring that organizational systems and training is in place
Preparing organization for ISO 9001 audit
Ensuring that documentation and design controls are appropriate for the organization
Administering document control and configuration management system
Overseeing established calibration and testing program
Assisting the management team and provide quality assurance support as necessary
Physico-Chemical Analysis of Materials and Products using appropriate equipment e.g. HPLC
Qualification and validation of equipment, processes and products in the factory
Overseeing the in-process staff and activities
Enforcing Good Manufacturing Practices (GMP)
Reviewing and checking Batch Manufacturing Records (BMRs)
Calibrating of Equipments
Affixing status labels on finished products.

Education, Training and Qualification

Minimum of First Degree in Chemistry, Biochemistry or other related discipline
Minimum of 8 years working experience preferably in a similar position in a pharmaceutical Industry
Additional qualification(s) and/or a professional qualification will be an added advantage

Knowledge, Skills and Training:

Excellent knowledge of WHO documentation, Common Technical Documentation (CTD) for products registration.
Business skills as may be responsible for managing budgets, leading a team and liaising with suppliers
Good knowledge of physico-chemical analysis
Ability to use HPLC
Process enhancement and organizational skills
Excellent communications skills - effective verbal and written communication
Analytical and interpersonal skills and ability to strategize
Capable to manage the entire in-process staff and activities
Excellent IT skills - MS Words, Excel, Power-points are compulsory
Ability to work without supervision and under pressure to meet deadline
Good experience in validation
Ability to prepare protocols

Application Closing Date
30th August, 2019.

How to Apply
Interested and qualified candidates should send their detailed Resume to: cms4limited@gmail.com using the position applying for as the subject of the email.

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