Production Pharmacist

Adcock Ingram Holdings Ltd; Johannesburg; Vor Ort; ZAR 350.000 - 550.000; Vollzeit

Zusammenfassung

Adcock Ingram Holdings Limited in Johannesburg is seeking a Production Pharmacist to ensure compliance with SAHPRA, PIC/S and GMP in pharmaceutical production. You will verify batch documentation, conduct line openings, resolve non-conformances and support audits.

The role trains staff, updates SOPs, maintains product quality and patient safety, and works to uphold regulatory standards across manufacturing operations.

Aufgaben

• Ensure compliance with GMP, PIC/S, and SAHPRA regulations.
• Oversee production line opening and line clearance checks.
• Review batch manufacturing records and packaging records for release.
• Verify calibration status of measuring equipment used in production.
• Investigate non-conformances, perform root cause analysis and implement CAPAs.
• Train staff on GMP, SOP compliance, and quality systems; maintain audit readiness.

Jobbeschreibung

Adcock Ingram Holdings Limited and its Subsidiaries(„we”, „us“) is committed to protecting and respecting your privacy. Our Privacy Notice sets out the basis on which personal information collected inter alia from you, social media, recruitment agencies and our website, will be processed by us. The Privacy notice is available on our website www.adcock.co.za.

One of the conditions under the Protection of Personal Information Act 4 of 2013 (POPIA) provides that candidates have the right to be informed about the collection and use of their personal information,

In the course of your application: we may

• collect personal information that may be used to identify potential professional opportunities other than the job you have applied for but of which we think might be of interest to you.
• use your Personal Information to confirm references or background checks you have provided us.
• request your consent to participate in aptitude tests or recruitment assessments.

We also use your personal information to respond to your inquiries, to verify your information and to share information with you.

Your personal information will be securely stored by the Human Capital Department and it will be retained for a period of up to 12 months as of the closure of the application procedure if your application is unsuccessful, and in case of a successful application and you are hired, your data will be transferred to your personal employee file.

By applying for this position, you consent to us processing your personal information.

We reserve the right to make an appointment. If you have not heard from us within 30 (thirty) days of the closing date, please accept that your application was unsuccessful. Correspondence will be entered into only with shortlisted candidates.

JOB PURPOSE:

The Production Pharmacist ensures compliance with SAHPRA, PIC/S, and GMP regulations by overseeing pharmaceutical production processes. The role involves verifying batch documentation, conducting line openings, resolving non-conformances, investigating customer complaints, and ensuring adherence to quality and regulatory standards. Additionally, the Production Pharmacist trains staff, updates SOPs, and supports internal and external audits to maintain product quality and patient safety.

MAIN TASKS / RESPONSIBILITIES:

Compliance with GMP, PIC/S, and SAHPRA Regulations

• Ensure all manufacturing processes comply with local and international pharmaceutical regulations.
• Conduct production line opening and line clearance checks as per SOPs.
• Monitor adherence to Standard Operating Procedures (SOPs) and Good Documentation Practices (GDP).
• Participate in regulatory audits and inspections, ensuring site readiness.

Batch Documentation Review & Product Release

• Review batch manufacturing records (BMRs) and packaging records to verify compliance.
• Ensure correct SOPs, specifications, Bill of Materials (BOMs), and process parameters are followed.
• Verify calibration status of measuring equipment used during production.
• Check for proper traceability of raw materials, intermediates, and finished products.
• Handle batch-related deviations and non-conformances, providing justifications where necessary.
• Investigate non-conforming products, ensuring proper root cause analysis (RCA) is performed.
• Implement corrective and preventive actions (CAPAs) for product defects.
• Conduct trend analysis on defects and recommend improvements.
• Investigate and respond to customer complaints, ensuring issues are addressed promptly.

Training & Development

• Develop and update training materials and lesson plans for production staff.
• Train operators and supervisors on GMP, SOP compliance, and quality standards.
• Assess staff competency and ensure training records are maintained.
• Conduct monthly GMP audits and report findings to management.
• Update SOPs to reflect current production and quality assurance practices.
• Participate in internal and external audits, ensuring audit findings are addressed.
• Work on continuous improvement initiatives to enhance product quality and compliance.