Time Type : Full Time
Minimum Requirements : Grade 12, Bachelor of Pharmacy, Advanced Computer Literacy Level in MS Word, Excel, PowerPoint and Outlook
Job Related Requirements : Minimum of 1-year experience in the pharmacy sector post the completion of internship and community service.
Registered with the South African Pharmacy Council.
Added Advantages for the role
- GxP / ISO
- Certification related to warehousing / Distribution pharmacy
- Excellent communication and interpersonal skills
- High attention to detail, ethical, and deadline-driven
- Ability to perform under pressure and collaborate across departments
Main purpose of the role : The successful incumbent of this night shift Pharmacist role will be obligated to ensure adherence to statutory requirements as outlined in the Pharmacy Act, Medicines and Related Substances Control Act and all associated regulations.
The incumbent will also be required to portray a Pharmaceutical and Healthcare Quality representative role.
This particular portfolio is perceived as a part-time role mainly determined by the facility's assigned tier.
Commitment to quality in respect of pharmaceutical product integrity remains pivotal with the incumbent.
This is done in good faith and ensuring appeasement of regulatory authorities, whether domestic or foreign, as and when required.
Duties and Responsibilities
Assist in upholding all compliance obligations set forth in the Pharmacy Act, Medicines and Related Substances Act and all associated regulations on behalf of the DSV Solutions' business unit.Uphold GxP principles at the DSV Solutions Gauteng Park wholesale pharmacy.Support the Responsible Pharmacist through the communication of current issues ensuring ongoing HealthcareQMS compliance within the pharmaceutical instance.Active participation in audits whether internal, client, statutory or other.Active participation in non-conformance closure through appropriate implementation of remedial action, under the guidance of the Responsible Pharmacist and in support of the same.Active participation in procedures associated with product lifecycles including receiving, sampling, retention, returned / rejected, re-packing and other.Develop and implement operational processes, procedures, process flows and / or other written documentation in pursuit of pharmaceutical quality, as and when required.Active participation in the CAPA process to ensure successful closure of identified shortcomings.Document control, Site Master File, Quality Manual.#J-18808-Ljbffr