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You will be updated with latest job alerts via email$ 65520 - 114400
1 Vacancy
Preferred Laboratory Skillsets: Aseptic technique cell and tissue culture cell-based assays for characterizing cell and gene therapy products ELISA dPCR TCID50 assays NGS experience and flow cytometry. Strong scientific method writing and review skills preferred.
Preferred Experience: Familiarity with working in a cGMP environment. Quality Control Laboratory experience. Experience working in a regulated environment. Experience with GxP software systems. Experience with Microsoft Office applications. Experience with following and/or creating Standard Operating Procedures.
Job Responsibilities:
Independently execute quality/production processes with guidance to monitor and ensure compliance with all applicable regulatory requirements (e.g. FDA FACT USDA).
Collaborate across teams to support revision/continuous improvement of SOPs and/or process flows related to production/quality/TPQ/HAL.
Monitor production to ensure cGMP compliance by checking batch records for accuracy and equipment logs for completeness; address critical deviations.
Lead internal/external audits investigation of deviations and identification/implementation of corrective actions.
Monitor and document compliance with quality and regulatory requirements.
Guide/make recommendations for continuous improvement of production/quality/ compliance systems using documentation such as release specifications variances environmental monitoring reports and internal audits.
Regularly train and oversee the work of others in quality/production regulations systems and SOPs.
Perform other duties as assigned to meet the goals and objectives of the department and institution.
Maintains regular and predictable attendance.
Minimum Education and/or Training:
Bachelors degree in chemistry biology or a related field .
Masters degree preferred.
Minimum Experience:
Experience working with quality/production systems/processes and their maintenance/implementation as applicable to own area (e.g. cell processing cell culture vector production) preferred.
Experience working with quality/manufacturing regulations and guidelines (e.g. cGMP cGTP FACT) preferred.
Experience working with electronic systems commonly used in Quality Management Systems preferred as applicable.
Experience working with computerized databases preferred as applicable.
Proven performance in earlier role/ comparable role.
Compensation
In recognition of certain U.S. state and municipal pay transparency laws St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets experience and training licensure and certifications and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $65520 - $114400 per year for the role of Sr Quality Control Specialist- Childrens GMP.Explore our exceptional benefits!
No Search Firms
St. Jude Childrens Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.
Required Experience:
Director
Full-Time