Production Pharmacist

Kenvue; Cape Town; On-site; ZAR 500 000 - 600 000; Full time

Job summary

A leading healthcare company based in Johannesburg seeks a Production Pharmacist to ensure that all procedures align with Good Manufacturing Practices. The ideal candidate will have 2-3 years of experience in pharmaceutical manufacturing. You will drive continuous improvement initiatives and ensure compliance across all processes. Strong communication skills and the ability to handle customer complaints are essential. This is a full-time role requiring shifts if necessary.

Qualifications

• 2–3 years of pharmaceutical manufacturing experience.
• Supervisory experience is an added advantage.
• High work standards and business ethics.

Responsibilities

• Ensure procedures are performed in accordance with relevant SOPs and Good Manufacturing Practices.
• Drive continuous-improvement initiatives of GMP compliance within the department.
• Handle customer complaints and ensure timely resolution.

Skills

Pharmaceutical manufacturing experience

Good verbal and written communication

Problem solving

Planning and administrative competencies

Knowledge of SA cGMP Guide

Education

Registered with SAPC as a qualified Pharmacist

Job description

Production Pharmacist

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.

Responsibilities

• 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.

Process Knowledge & Product Stewardship

• 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.

Job Requirements

• 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.

Legal & EEO Statement

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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