with applicable laws, regulations, and industry standards. Conduct regular inspections and audits to identify industry trends, and ensure compliance with relevant standards. Conduct risk assessments and participate in the In-depth knowledge of health and safety regulations, standards, and best practices. Familiarity with conducting
consistently deliver to quality, time and cost standards Experience in use of CTD software builder and liaise and negotiate with others Ability to set standards and objectives and monitor progress Complex problem
consistently deliver to quality, time and cost standards Experience in use of CTD software builder and liaise and negotiate with others Ability to set standards and objectives and monitor progress Complex problem
inspections and audits to ensure adherence to SHEQ standards and regulations. Provide training and support updated on relevant regulations and industry standards to ensure ongoing compliance. Qualifications:
inspections and audits to ensure adherence to SHEQ standards and regulations. Provide training and support updated on relevant regulations and industry standards to ensure ongoing compliance. Qualifications:
Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) Experience with Regulatory Affairs actions. Document Control Reviewing and updating of Standard Operating Procedures and Quality Documents. General
Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) Experience with Regulatory Affairs actions. Document Control Reviewing and updating of Standard Operating Procedures and Quality Documents. General
safety of oneself and others. Adhere to ethical standards and regulations governing laboratory research
safety of oneself and others. Adhere to ethical standards and regulations governing laboratory research
strives for excellency through distinctly higher standards than the norm. We therefore urge only candidates