Job Description

Kenvue is currently recruiting for a:


Production Pharmacist

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S and BAND-AID that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours.

Role reports to:

Manufacturing Lead Excellence

Location:

Europe/Middle East/Africa, South Africa, Gauteng, Johannesburg

Work Location:

Fully Onsite

What you will do

Day-to-Day Support:

Ensure that procedures and processes within area of responsibility are performed in accordance with relevant Standard Operating Procedures, Work Instructions and current Good Manufacturing Practices. Drive and support close out of all relevant compliance related audit findings. Responsible for performing line-openings and in process checks according to legislative and company requirements. Update GMP documents (SOP, WI, PPI and PI etc), as required and train accordingly. Ensure effective communication to all relevant parties. Ensure all production documentation and processes are completed as per cGMP guidelines.

Process Knowledge

Understand process flow Understand process controls as well as risks Understand technically the product and its composition Understand process/product cost structure Support training to operators

Product Stewardship

GMP, EHS and Quality compliance during the execution of the Plan and all related tasks. Ensures compliance with work instructions according to the relevant SOP's Initiate, investigate and close out relevant GMP and SOP compliance related NC, CAPA, Change Controls,

Deviations and Customer Complaints.
Support process transfers (in or out) Perform in-process audits - both planned and ad hoc accordingly to ensure that GMP standards are met and maintained. Support regulatory with technical documents

Continuous Improvement:

Drive, contribute and support continuous improvement initiatives of GMP compliance and standards within the department accordingly and together with the management team. Analyze the process on a routine basis to identify risks or inefficiencies. Lead the execution of

Improvement Projects in the area of responsibility
Plan the implementation of improvement projects Perform internal assessments in production areas and develop corrective actions to strengthen

Job requirements

Registered with SAPC as a qualified Pharmacist. 2-3 years pharmaceutical manufacturing experience Supervisory experience/qualification will be an added advantage Good knowledge and understanding of the SA cGMP Guide Good planning and administrative competencies Good verbal and written communication Logical approach to problem solving and trouble shooting High work standards and business ethics Must be available to work shifts if required

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.