Production Pharmacist Assistant

2 weeks ago

Cape Town, South Africa Biovac Full time

**BIOVAC** is one of the leading sterile vaccine manufacturers rooted in Africa, with our core purpose being to "protect life". We are looking to hire a dynamic, passionate, confident, proactive and meticulous Production Pharmacist Assistant to join a goal-oriented team.

**QUALIFICATIONS NEEDED**:

- Pharmacist Assistant (Post-Basic).

**NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE**:

- At least 1 years experience working in a manufacturing environment.

**KEY DUTIES & RESPONSIBILITIES OF THE ROLE**:

- Accountable for the compliance to all relevant aspects outlined by the SA Pharmacy Act 53 of 1974 and its current amendments and the Medicines and Related Substances Control Act, No 101 of 1965 and its current amendments.
- Responsible to ensure that all operational activities and stages comply with company procedures, policies and regulatory GMP requirements.
- Responsible for a state of audit readiness within the department.
- Assists in delivering batch records and related documentation at a pharmaceutical acceptable standard.
- Responsible to ensure that all critical stages for which they are involved with, are executed to according to the quality standards set by the company and regulatory guides.
- Responsible to be involved in all critical stages of operation, predefined and agreed upon with the Responsible Pharmacist and relevant Quality Assurance and Department Managers.
- Assists with the creation and updating of SOPs and Work Instructions on a continuous basis and ensure the operational activities comply with Standard Operating Procedures.
- Assists with the creation and updating of batch records on a continuous basis and ensure the operational activities comply with Standard Operating Procedures.
- Assists in attainment of Quality targets set for the department.
- Assists in the timeously delivery of batch records to Quality Assurance.
- Responsible for the timeous execution of all activities defined by the SA Pharmacy Act 53 of 1974 and its current amendments and the Medicines and Related Substances Control Act, No 101 of 1965 and its current amendments.
- Assists in the timeous execution of all critical activities, predefined and agreed upon with the Responsible Pharmacist, Quality Assurance and Production departments. This includes, but not limited to:

- independently checking and signing each dispensed material and its mass or volume.
- checking and signing the addition of each material to the mix.
- checking and signing the identity of the bulk product and printed packaging material.
- checking and signing that each packaging line or station is clear of previous product, packaging components.
- records, or materials not required for the planned packaging operations, and that equipment is clean and suitable for use before any packaging is undertaken.
- other critical activities or stages as defined within each department as agreed upon the Responsible Pharmacist and relevant Quality Assurance and Department Manager.
- assist with the compounding, manipulation or preparation of a non-sterile or sterile medicine or scheduled substance according to a formula and Standard Operating Procedures approved by the responsible pharmacist.
- assist with the manufacturing of a non-sterile or sterile medicine or scheduled substance according to a formula and Standard Operating Procedures approved by the responsible pharmacist.
- the distribution and control of stock of Schedule 1 to Schedule 6 medicines or scheduled substances.
- Drives first time right execution in all relevant activities.
- Assists in the attainment of Operational targets set for the department. Participate and delivers in Departmental projects.

**Application Deadline: 15 August 2023**

**_Disclaimer: _**
- By submitting your CV and personal information, you agree that Biovac may utilise this information to conduct and complete our recruitment process, which entails distributing your information to all internal recruitment participants and service providers who forms part of the process._

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