manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement Initially, the primary functions will be to ensure GMP compliance across the small/medium size manufacturing especially pharma products). Implement thew SOPs, GMP structures, ISO 9001 and other ISO standards. After pharma production experience. Solid understanding of GMP requirements. ISO 9001 and other ISO experience an
manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement Initially, the primary functions will be to ensure GMP compliance across the small/medium size manufacturing especially pharma products). Implement thew SOPs, GMP structures, ISO 9001 and other ISO standards. After pharma production experience. Solid understanding of GMP requirements. ISO 9001 and other ISO experience an
manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement Initially, the primary functions will be to ensure GMP compliance across the small/medium size manufacturing especially pharma products). Implement thew SOPs, GMP structures, ISO 9001 and other ISO standards. After pharma production experience. Solid understanding of GMP requirements. ISO 9001 and other ISO experience an
can 'hit the ground running' - to start asap in a GMP environment, doing Analytical Validation, including Lead validation and calibration activities for a GMP pharmaceutical and API manufacturing facility.
can 'hit the ground running' - to start asap in a GMP environment, doing Analytical Validation, including Lead validation and calibration activities for a GMP pharmaceutical and API manufacturing facility.
can 'hit the ground running' - to start asap in a GMP environment, doing Analytical Validation, including Lead validation and calibration activities for a GMP pharmaceutical and API manufacturing facility.
can 'hit the ground running' - to start asap in a GMP environment, doing Analytical Validation, including Lead validation and calibration activities for a GMP pharmaceutical and API manufacturing facility.
Medicines and Related substances and regulations, GMP and any other QA/RA related guidelines. Salary is
Medicines and Related substances and regulations, GMP and any other QA/RA related guidelines. Salary is