ng>Product Registration:
processes
Duties and Responsibilities:
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE EE Key Responsibilities: Manage work streams for- and report on the assigned portfolio of products Conduct Sound project management capabilities Proven ability to consistently deliver to quality, time and cost role profile available on application) Apply to response "at" mvgrecruitment.co.za Subject: MP/SRA Supporting
Regulatory Affairs Pharmacist OTC POS24203
Based: Midrand project management capabilities
Key Job Outputs
and services industry as their next Credit Control Manager and lead the charge in ensuring the financial happy Commercial support quote-to-cash: engage and control payment terms and commercial payment terms, credit credit risk assessments Open new accounts and manage credit terms/limits on existing customers Assist team exposure monthly and inform managers Liaising with branch and regional managers on overdue customer amounts VAT laws Manage monthly reporting of bad debts under group policies Manage the credit control team, setting
Responsible for providing pharmaceutical care services (within scope of practice) and performing day-to-day standards of customer service and care Efficient stock control and administration, including repacking of medicine Council of South Africa for the various levels as a Pharmacist Assistant (Qualified, Post Basic and Learner
Senior Regulatory Affairs Pharmacist: OTC -POS24206
Area : project management capabilities
Key Job Outputs
looking for a Quality Systems Specialist to be based full time at our offices. The Quality Systems Specialist required to do the administration of the Quality management system ensuring compliance to ISO9001. Input Input into Environmental and OHS. Create and control documentation, records, action items, audits, meetings SharePoint administration Exposure to management of Quality Management Systems Training and presentation environment Key Performance Areas: Administration of all Quality Documents Drafting, checking, and collating of
degree in Quality Management or a related qualification at an NQF 6/7 level.
* 2 Years quality management
management or Quality Assurance and /or Business Process Redesign
* 1 Year Risk Management (advantageous)
Primary Responsibilities:
Maintain the Quality management System (QMS)
*
documents
* Develop, implement and validate quality standards, processes and procedures withing the
audit information
Monitor Compliance with Quality Standards:
* To audit business units'
Primary Responsibilities
Maintain The Quality Management System (QMS)
control and status, draw complex diagrams, attachments
documents.