Associate Quality Systems
Job DetailsJob Description
Responsibilities:
oUnder limited supervision, assists in carrying out production-related tests and inspections to control qualityoFollows established procedures to check, test and inspect raw materials, intermediates or finished productsoProperly documents test results in appropriate records and computer systemoSupports documentation and records, distributing, and filing all manufacturing procedures, deviations, etc.
oFollows Standard Operating Procedures (SOPs) and maintains compliance to current Good Manufacturing Practice (cGMP) regulatory guidelines
Qualifications:
oHigh School Diploma or equivalent vocational or technical training; Associate's degree in a relevant scientific discipline preferredo1-2 years' related pharmaceutical experience including experience in a regulated environmentoKnowledge of cGMP standardsoProficiency in Microsoft Office and QC systemsDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements.
Refer to local job documentation where applicable.
About UsOur BenefitsWe encourage you to make your well-being a priority.
It's important and so are you.
Learn more about how we care at CSL.
About CSL PlasmaCSL Plasma is one of the world's largest collectors of human plasma.
Our work helps to ensure that people with rare and serious diseases are able to live normal, healthy lives.
We are committed to our work because lives depend on us.
Learn more about CSL Plasma.
We want CSL to reflect the world around usAs a global organisation with employees in 35
countries, CSL embraces diversity, equity and inclusion.
Learn more about Diversity, Equity & Inclusion at CSL.
Do work that matters at CSL Plasma! Recommended Skills Filing Good Manufacturing Practices Microsoft Office Pharmaceuticals Standard Operating Procedure Certified Global Meeting Planner Estimated Salary: $20 to $28 per hour based on qualifications.
Responsibilities:
oUnder limited supervision, assists in carrying out production-related tests and inspections to control qualityoFollows established procedures to check, test and inspect raw materials, intermediates or finished productsoProperly documents test results in appropriate records and computer systemoSupports documentation and records, distributing, and filing all manufacturing procedures, deviations, etc.
oFollows Standard Operating Procedures (SOPs) and maintains compliance to current Good Manufacturing Practice (cGMP) regulatory guidelines
Qualifications:
oHigh School Diploma or equivalent vocational or technical training; Associate's degree in a relevant scientific discipline preferredo1-2 years' related pharmaceutical experience including experience in a regulated environmentoKnowledge of cGMP standardsoProficiency in Microsoft Office and QC systemsDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements.
Refer to local job documentation where applicable.
About UsOur BenefitsWe encourage you to make your well-being a priority.
It's important and so are you.
Learn more about how we care at CSL.
About CSL PlasmaCSL Plasma is one of the world's largest collectors of human plasma.
Our work helps to ensure that people with rare and serious diseases are able to live normal, healthy lives.
We are committed to our work because lives depend on us.
Learn more about CSL Plasma.
We want CSL to reflect the world around usAs a global organisation with employees in 35
countries, CSL embraces diversity, equity and inclusion.
Learn more about Diversity, Equity & Inclusion at CSL.
Do work that matters at CSL Plasma! Recommended Skills Filing Good Manufacturing Practices Microsoft Office Pharmaceuticals Standard Operating Procedure Certified Global Meeting Planner Estimated Salary: $20 to $28 per hour based on qualifications.
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