PZ Cussons is a dynamic consumer products group and innovator of some of the world's best known and loved brands. Calling on over 130 years of expertise, we operate internationally in carefully selected developed and emerging markets that present the greatest strategic potential for future growth. Our world-class supply chain and distribution networks enable us to meet our global consumer needs and deliver quality brands that add value and enhance everyday lives.
We are recruiting to fill the position below:
Job Title: Laboratory Analyst
Job ID: JR003133
Location: Aba, Abia
Key Accountabilities, Responsibilities & Decision Making
List the main areas of responsibility. Think about what technical tasks the role covers and how much accountability it has when making decisions about strategy, budgets, and people.
Typically, 5 - 8, written in order of importance.
Key Accountability
Typical Activity / Output
% of Time (Optional)
e.g. Strategic Planning / Operational Delivery / Team Leadership
Develop annual business plans aligned to regional growth objectives / Manage daily operations ensuring quality, safety and efficiency / Coach and develop team members to build capability and engagement
20%
Dimensions:
Return on Investment
Customer Satisfaction
Turn Around Time
Strategic Alliances with different institutions
Shift coordination / supervision
Calibration of equipment.
Analysis of % concentration & SG of Concentrated HCl.
Reagent preparation and standardization.
Reagent/ stationery request.
Bulk liquid Analysis.
Ensure proper documentation.
Preparation of daily, weekly & monthly summaries
Attend to jobs assigned by Q.C. Supervisor, and QA manager.
Raising of work orders.
Assist in special analysis.
Weekly physiochemical evaluation of Semi & Finished Goods.
undefined
Principal Accountabilities:
The key outputs of the job
List in priority order, if possible, typically 8-10
NOT a task list
Any requirement for organizing & planning including own work and the allocation of resources
Typical decisions made and if they are advisory or directly responsible for the outcome
Ensure conclusion & documentation of subordinates’ daily tasks using SOPs.
Availability of calibrated data for all key measuring equipment and equipment efficiency and reliability when verified.
OTIF of all analyses. Reliable, authorized and effective documentation of results.
Reagent preparation should be done on or before 70% consumption of current stock in use (must never be at zero stock level).
Reagents’ Buffer stock update must be current and escalated when stock is 30% of buffer stock level. Same for stationery.
Min of three bulk liquid tallow tanker results to be released before 11am daily, if vehicle registration begins by 9am.
All data, results and information of tests/activities must be accessible, retrievable, readable, clear, without mutilations, signed as appropriate and stored in the right logs/files and file/logbook position.
OTIF of all summary reports (weekly review to be ready on or before 7am Monday of proceeding week).
Key Attributes:Occupational Health & Safety (OH&S):
To be aware of the hazards in the workplace within his control, and the control measures to reduce the risk associated with those hazards.
Achieve 85% of action closure arising from monthly HSE inspection.
Achieve 95% compliance with behaviour-based safety (BBS) walk around.
Train 65% of the workforce on safety awareness.
Environmental Management System (Ems) Objectives
Key Activities:Understand roles and responsibilities and the importance of conformity with the EMS requirements.
Implements and complies with EMS requirements relating to environmental aspects and impacts and other policies, procedures and /or regulations applicable to assigned jobs.
Quality And Plan Compliance Delivery: GMP
Key Accountability:To have a good knowledge of GMP requirements and application on site in line with GMP standard (PZC GMP standard/NAFDAC requirements)
Key Activities:Ensure that manufacturing operation meets stipulated GMP
Quality Management System (QMS) Objectives: (QMS)
Key Accountability:To ensure the effectiveness of the Quality Management System (QMS) and improve on the system.
Internal And External Relationships:To work with other staff continually to improve performance while adhering to legislative and company standards.
To work closely as a team with the line manager and other leaders as to deliver set objectives
undefined
Knowledge, Skills and Experience:
Outline the background and capabilities required to perform effectively. Describe the level of knowledge required (e.g. basic operational, advanced functional, cross-functional, strategic
Education / Qualifications
Required Qualifications:B.Sc., HND or OND in Physical Science: Chemistry, Industrial Chemistry, other related Laboratory Science courses, and Chemical Engineering.
Basic operational Software Knowledge in Computer.
Good Understanding of GMP (ISO 22716:2007) and QMS (ISO 9001:2015) standards.
Experience:(preferred level of experience or type of experiences e.g. entry, working, significant, deep professional)
undefined
Required Experience:
Minimum of 1 year work experience in a similar position.
Ability to work longer hours as the work may demand.
undefined
Technical and Professional Skills:(e.g. Specific systems, tools or expertise)
undefined
Laboratory Analytical skills
Problem solving skills
Effective time management skills.
Application Closing Date19th January, 2027.
How to Apply
Interested and qualified candidates should:Click Apply Now button to apply
How To Apply
-
Make sure you are logged in and your email is verified (Register if you dont have an account).
-
Click the Apply Now button above.
-
Your default email application or the application link will open.
-
Attach your Application letter, updated Curriculum Vitae (CV) and any supporting documents required.
-
Use a professional subject line such as Application for "Indicate Position"
-
Make sure to send your application before the closing date.
Note: Only shortlisted candidates are contacted.
