Authority interactions To track and manage all GRP activities and report any non-compliances to the Responsible Ensure all post-approval product maintenance activities including CMC variations, package insert safety non-submission of critical variations Product labelling activities successfully completed within specified timelines diverse and harmonious working environment and actively encourage the development of the company culture Expertise in Information and document management technology and electronic/paper publishing software. Excellent
manufactures tailor-made technology and system solutions for applied surface technology. The products protect organisations Responsible Care management system activities as and if required. • Drive the 5 “S” program Chemistry (NQF level 7) or; • BTech (Bachelor of Technology) in Chemistry (NQF level 7) • Experience: A minimum
upheld by assisting with performance of scheduled activities, i.e., PTS/ILC/IP Calibration Maintenance Verifications SOP/Method Review Waste Management Ensure that activities are carried out and completed on or before the scheduled activities. Keep training record up to date at all times with all training activities completed equivalent) N. Dip. Biotechnology N. Dip. Food Science/Technology EXPERIENCE AND SKILLS REQUIRED: 0 - 3 Years experience
upheld by assisting with performance of scheduled activities, i.e., PTS/ILC/IP Calibration Maintenance Verifications SOP/Method Review Waste Management Ensure that activities are carried out and completed on or before the scheduled activities. Keep training record up to date at all times with all training activities completed equivalent) N. Dip. Biotechnology N. Dip. Food Science/Technology EXPERIENCE AND SKILLS REQUIRED: 0 - 3 Years experience
medical institutions. We are proud of our clean, technological advanced facility and we encourage our clients world-wide boundaries, according to sustainable technological innovation and processes, specifically those design experiments and develop new metal recovery technologies. Maintain accurate records of experiments, procedures advancements in metal recovery techniques and technologies. Provide technical support and guidance to other
regarding the status of specific project/ Client activities. Developing PV medical raining presentations regulatory inspection preparedness for PV systems and actively participating in PV inspections or audits. The aggregate/ ad hoc reports for product portfolio. Actively participating in the Signalling Meeting, Drug life cycle. Providing medical input for product activities relating to Investigator's Brochures, Clinical compliance metrics for PV and medical information activities. Develop/ educate employees. Support the growth
regarding the status of specific project/ Client activities. Developing PV medical raining presentations regulatory inspection preparedness for PV systems and actively participating in PV inspections or audits. The aggregate/ ad hoc reports for product portfolio. Actively participating in the Signalling Meeting, Drug life cycle. Providing medical input for product activities relating to Investigator's Brochures, Clinical compliance metrics for PV and medical information activities. Develop/ educate employees. Support the growth
staff, and distributors supporting regulatory activities on behalf of the company. Primary Responsibilities regulatory activities and relevant country business/commercial plans. Promote team spirit/activities in alignment progress of registration submission and approval activities, and ensure line management is advised of progress
process Suggest improvement to process Direct audit activities to production schedules Establish priorities resolve problems occurring during Quality Assurance activities Ensure that all routine test procedures are carried
degree in a relevant field such as Information Technology, or Engineering. • Proven experience in quality