What are the responsibilities and job description for the Analyst, QC position at CSL?
QC Analyst (Immunology- Biochemistry)
Job Purpose
Primary responsibilities for this position include performing tasks associated with release testing and reviewing laboratory data. The analyst will be responsible for ensuring that CSL Seqirus samples are collected, tested, and reviewed according to quality requirements. This position will ensure results are valid, accurate and documented per applicable regulatory and corporate requirements.
If Upper Analyst position, the analyst will become a certified trainer to develop cross training with the group. The analyst will be required to perform and participate in tasks associated with method validation and transfers.
Days – Monday – Friday
Hours – (8am – 5pm)
Off shift coverage required for STAT testing
Responsibilities
Job Purpose
Primary responsibilities for this position include performing tasks associated with release testing and reviewing laboratory data. The analyst will be responsible for ensuring that CSL Seqirus samples are collected, tested, and reviewed according to quality requirements. This position will ensure results are valid, accurate and documented per applicable regulatory and corporate requirements.
If Upper Analyst position, the analyst will become a certified trainer to develop cross training with the group. The analyst will be required to perform and participate in tasks associated with method validation and transfers.
Days – Monday – Friday
Hours – (8am – 5pm)
Off shift coverage required for STAT testing
Responsibilities
- Performs testing and associated tasks without errors per applicable SOPs and protocols within Immunology/Biochemistry function.
- Properly documents test results in appropriates records and computer systems
- Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written.
- Participates in lean lab operation, 6S laboratory layout, preventive action & continuous improvement programs to reduce operating costs.
- Participates and performs in cross-training to support staff availability within QC department.
- May be required to perform additional shift work as required to support operations.
- Writes and/or revises applicable procedures as required
- Authors or may lead deviation and invalid assay assessments
- Performs peer review of data
- Develops expertise in assigned assays/techniques
- May provide informal guidance and support to other team members and leverages own knowledge to others
- Bachelor’s degree in Biochemistry or equivalent
- 5 years of laboratory experience
- 5 years of GMPs, safety regulations and data integrity
- Experience performing Biochemistry assays (ELISA, BCA, SRID, SDS-PAGE) required
- Knowledge of analytical methods and related instrumentation
- Knowledge of aseptic technique preferred
- GLIMS experience preferred
- Proficient in communication and multi-tasking
- Will be required to have a flu shot and maintain yearly