Responsibilities:
QC Final product against master sample
Conduct sensory and chemical
on internal system
Maintenance of supplier quality assurance program
Regularity compliance e
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Pharmacist Assistant, Brooklyn, Pretoria / Tshwane. Company Name: BGI CIVILS Key Outputs: The successful successful applicant will be responsible for but not limited to the following job functions: Accurate capturing with each new script under the supervision of a pharmacist. Ensure todays work is done today, that all silo’s time. Adhoc assistance to the Administration Pharmacist. An Important Announcement from (jobscoin.com) sharing jobs from multiple sources and we are not responsible for any type of scam.
Co- ordination of the quality relevant activities in the BU to reach Quality Objectives. Identify and improvement of BOS Take part in the definition of quality objectives in the business plan and strategic planning planning (qual objectives). Co- Ordinatore quality relateed activities in accordance to PLUS (Coordination) the COMPANY Quality standards. Support in setting up structures / processes in the quality area, to ensure Background in Quality Management field. Min 5 years experience of which 3 years on quality related activities
We are looking for a meticulous and experienced Quality Assurance Engineer to join our manufacturing team
candidate will be responsible for ensuring that our products meet all necessary quality standards before
understanding of quality assurance processes in manufacturing.
Key Responsibilities:
Tshwane Metro, Pretoria, Brooklyn
Tshwane Metro, Pretoria, Brooklyn
that, the role will involve general production pharmacist duties, as well as evolving into QA and QC functions
involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing, and Controls (CMC) up-to-date knowledge of regulatory guidelines. Key Responsibilities: 1. Regulatory Submissions: Prepare, compile Authority (SAHPRA) and other relevant authorities. Manage timelines for regulatory submissions and approvals schedules. 2. CMC Writing: Write and review high-quality CMC documentation for regulatory submissions, including with internal departments, including R&D, quality assurance, and manufacturing, to gather necessary
purpose of the job: To implement and maintain stock management at Project PrEP implementation sites, to support in all activities to both line manager and sub[1]district team manager and other ad hoc reports when required reproductive health including contraception, STI management, and pre-and post-exposure prophylaxis arena demonstrate effective self-management Follow through to ensure that quality and productivity standards training: Grade 12 Certificate as Post Basic Pharmacist Assistant Required minimum work experience: Full