puestos de Quality Assurance en Sudáfrica

Location: Johannesburg, South Africa.

Reports To: Manufacturing Lead Excellence.

Work Location: Fully Onsite.

About Kenvue

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.

• Ensure that procedures and processes within area of responsibility are performed in accordance with relevant SOPs, WIs and current Good Manufacturing Practices.
• Drive and support close-out of all relevant compliance-related audit findings.
• Perform 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.
• Support process transfers (in or out).
• Perform in-process audits – both planned and ad‑hoc – to ensure that GMP standards are met and maintained.
• Support regulatory with technical documents.
• Drive continuous‑improvement initiatives of GMP compliance and standards within the department.
• Lead the execution of improvement projects in the area of responsibility.
• Plan the implementation of improvement projects and perform internal assessments in production areas, developing corrective actions to strengthen processes.

• Understand process flow, process controls, risks and product composition.
• Understand product and cost structure.
• Ensure GMP, EHS and Quality compliance during execution of the Plan and related tasks.
• Initiate, investigate and close out relevant GMP and SOP compliance‑related NC, CAPA, Change Controls and deviations.
• Handle customer complaints, ensuring timely resolution.

• Registered with SAPC as a qualified Pharmacist.
• 2–3 years of pharmaceutical manufacturing experience.
• Supervisory experience / qualification is 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 troubleshooting.
• 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.

Seniority Level: Mid-Senior level

Employment Type: Full-time

Job Function & Industries: Supply Chain; Personal Care Product Manufacturing

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