PLC Quality Coordinator Associate
Responsibilities:
• Under limited supervision, assists in carrying out production-related tests and inspections to control quality
• Follows established procedures to check, test and inspect raw materials, intermediates or finished products
• Properly documents test results in appropriate records and computer system
• Supports documentation and records, distributing, and filing all manufacturing procedures, deviations, etc.
• Follows Standard Operating Procedures (SOPs) and maintains compliance to current Good Manufacturing Practice (cGMP) regulatory guidelines
Qualifications:
• High School Diploma or equivalent vocational or technical training; Associate's degree in a relevant scientific discipline preferred
• 1-2 years' related pharmaceutical experience including experience in a regulated environment
• Knowledge of cGMP standards
• Proficiency in Microsoft Office and QC systems
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
CSL offers the following benefits for this full-time position: Options for health care benefits, including choices of plans for medical, dental, and vision, prescription drug coverage; Company-provided basic life insurance and Short- and Long-Term Disability; the option to participate in CSL’s 401(k) Savings Program; Paid Time Off (PTO) for use in connection with vacations, illness, and other personal business; and paid observed holidays as designated by the Company. For more information on CSL Plasma benefits visit https://cslbenefits.com/cslp.
CSL 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.
As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
