Description:
Qualifications Required:
Degree or diploma in Engineering / Natural Sciences / Microbiology or equivalent.
Necessary Experience and Industry Accreditation
At least 5 years’ experience in pharmaceutical/ biotech manufacturing industry. At least 1 to 2 years’ experience at junior to Senior Management level. Experience in quality management systems within a cGMP facility. Good Engineering Practice and understanding of ISPE guide.
Key Duties and Responsibilities
Management and mentorship of Senior Validation Scientists, Validation Scientists and Validation Interns. Ensuring that Validation requirements are achieved at the required quality and regulatory levels (Company, SAHPRA, WHO, pharmacopoeia) and within the agreed timeframes. Conduct section planning and execute activities within own scope of accountability. Ensure adequate capacity planning and performance delivery in line with strategic, tactical and operational plans. Role profiling, goal setting and performance management of Validation staff within the section. Review and/or update high level validation and qualification guidance documents, such as VMP, VPs, SOPs. Attend and participate on technical and projects strategic meetings/discussions involving internal and external stakeholders. Ensure execution of routine qualification activities i.e. Equipment / Utility / Facility, Systems, CSV and Data Integrity. Review and approves protocols and reports for all qualification activities based on company standards/guidelines, procedures, and Industry current practices. Reporting on key operations, critical numbers and key performance indicators that impacts the section’s short, medium- and long-term objectives. Conduct effective and comprehensive costing, budgeting and expense management for own section, taking all overlapping site activities into consideration. Lead own section’s transition into commercial operations and mind-set as well as managing efficiencies, reducing wastage and contributing to overall profitability. Assist in Process Development activities including Process Validation, Cleaning Validation and Cold Chain. Participate in Process Automation and Data Management activities including Data Integrity and CSV. Ensure execution of qualification processes: FAT, Commissioning, SAT, DQ, CIA, SLIA, IQ, OQ, PQ and PRQ as per defined timelines and cGMP and report timeously on qualification progress and status to the Validation Manager. Ensure and or assist system/ equipment owners with identifying maintenance and calibration requirements. Ensure relevant OOS and OOT investigation non-conformances/ deviations, change controls and CAPA’s are initiated and completed. ...Additional Info:
5 to 7 years
Salary: RR750000 to R850000
Job Reference #: 913148560
18 Jul 2022;
from:
gumtree.co.za