An established pharmaceutical manufacturing company has an opportunity for two Validation Analysts to join their team. Ideally, one more experienced analyst (3 to 4 years' experience), and one more junior analyst (1 to 2 years of experience). This position will report to the QC (Quality Control) Man
to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products. Initially products, but want to be licenced for all - especially pharma products). Implement thew SOPs, GMP structures SAPC registered PRETORIA area. You need 3 years of pharma production experience. Solid understanding of GMP
to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products. Initially products, but want to be licenced for all - especially pharma products). Implement thew SOPs, GMP structures SAPC registered PRETORIA area. You need 3 years of pharma production experience. Solid understanding of GMP
to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products. Initially products, but want to be licenced for all - especially pharma products). Implement thew SOPs, GMP structures SAPC registered PRETORIA area. You need 3 years of pharma production experience. Solid understanding of GMP
for CAMs & Coismetics products, as opposed to pharma products Excellent references are a requirement
for CAMs & Coismetics products, as opposed to pharma products Excellent references are a requirement
Role requires The QHSE Lead to form part of the Pharma Quality & Compliance group which provides support
Role requires The QHSE Lead to form part of the Pharma Quality & Compliance group which provides support