changing constraints and the need to complete projects on time
Purpose:
- The Assistant Project Manager will support the Project Manager (PM) with all the
Contract.
- The Assistant Project Manager will also work closely with the Project Administrators and
the effective execution of the project.
- The Assistant Project Manager will also be responsible
dashboard of the project progress.
- The Assistant PM will support the Project Manager with Integration
Management, Procurement Management and also assist with all Project Communication (reporting and meetings)
the Project Manager (PM) with all PM-related tasks associated with the contract
The Assistant PM
PM will support the Project Manager with Integration, Scope analysis, Cost control, Quality Management
Management, Procurement Management and also assist with all Project Communication (reporting and meetings)
Collaborate
/>Collaborate closely with Project Administrators and Engineers to ensure effective project execution
Manage
/>Manage the project schedule during the design phases
Obtain updates from various disciplines
Maintain
Multi-National firm , is currently in search of an Assistant Project Manager who can join their team in Johannesburg soon as possible to support the Project Manager with all the Project Management tasks Requirements: Bachelor's engineering Professionally Registered with ECSA Project Management qualification Contract Management knowledge Minimum 5-10 years of Project Management experience in large multi-disciplinary projects RPO is a Specialist
Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services To ensure legal and regulatory compliance with the relevant medicine Regulatory Authorities (Country Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work of products: Assisting with internal product queries from relevant departments Assisting with external stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently
and external reports to ensure accuracy.
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable) Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned group of portfolios Assisting with internal product queries from relevant relevant departments Assisting with external product queries from the SAHPRA, other MRA's and third-party
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key coordinating response to the regulatory authority. Maintain regulatory knowledge of the various territories Effectively managing, auditing and implementation of Regulatory systems Key Requirements: BSc or equivalent Science field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): including database maintenance. Quality Assurance (QA): Assist QA Manager with artwork review and quality management notify the Responsible Pharmacist (RP) of findings. Assist with QA batch release of Act 101 products in the required. Prepare for inspections, renew licenses, and assist with GMP in-house training. Act as an authorized