development and process characterisation, evaluate process improvements and resolve potential processing issues Communicate work through oral presentations and written documentation including technical reports and GMP documents to support regulatory filings Participate in cross-functional teams and interact with representatives from Process Development, Project Management, Manufacturing, and Quality to arrive at more »
abreast of technological and legislative advancements. 4. Engage with stakeholders to translate technical strategies into actionable plans, ensuring compliance with all relevant standards (eg. GMP, SHE, DI.) 5. Drive business growth through digital capabilities, collaborating with cross-functional teams to enhance the company's digital footprint. ROLE REQUIREMENTS: To be …/Data Scripting/Automation/Databasing Key Words: Senior Research Scientist/Digital Technologies/Technical Leadership/Data/SHE Compliance/GMP/Data Integrity/Continuous Improvement/Digital Projects/Cross-Functional Collaboration/Mentoring/Coaching Hyper Recruitment Solutions Ltd (HRS) is an Equal more »
Job summary Are you looking for a new challenge and passionate about developing pharmaceutical quality control services? We have an exciting and rare opportunity available for a registered scientist professional to join our team and specialise in this area. This more »
Proactively address stakeholder concerns, resolve conflicts, and facilitate effective communication channels throughout the project lifecycle. Quality Assurance and Compliance Ensure compliance with regulatory requirements, GMP, and other relevant standards within the pharmaceutical industry. Implement robust quality assurance processes to monitor and evaluate project deliverables, ensuring adherence to specified quality standards. more »
