St. Jude Children's Research Hospital

Senior Manufacturing Specialist

Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in chemistry, biology, or related field required.
  • Master's degree preferred.
  • 4+ years experience in production/quality in an industry setting required.
  • Preferred experience with quality/production systems and processes.
  • Experience with cGMP and other manufacturing regulations preferred.

Responsibilities

  • Independently execute quality and production processes while ensuring compliance with regulations.
  • Collaborate with teams to improve SOPs and process flows.
  • Monitor production to guarantee cGMP compliance by verifying batch records and equipment logs.
  • Lead audits and investigations into deviations, implementing corrective actions as necessary.
  • Document compliance with quality and regulatory standards.
  • Recommend improvements for production and quality compliance systems.
  • Train and oversee the work of others in quality and production standards.

Benefits

  • Commitment to a human-centered hiring experience.
  • Opportunities for professional growth and development within a prestigious organization.
Full Job Description

St. Jude’s is seeking a dedicated, reliable individual for the role of a Manufacturing Specialist or Senior Manufacturing Specialist to help with manufacturing activities in the GMP facility at St. Jude Children’s Research Hospital. Children’s GMP supports clinical trials on campus at St. Jude through the manufacture of biological drug products – these include viral vectors, monoclonal antibodies, and cellular therapy products.
 

The  Manufacturing Specialist independently works on the manufacturing of biological products and live viral vaccines for human clinical trials at St. Jude Children’s Research Hospital. Also, collaborates with the team to support continuous improvement and trains and guides the work of others in manufacturing.

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.

Minimum Education 

  • Bachelor's degree in chemistry, biology or a related field required.

  • Master's degree preferred.

Minimum Experience:

  • 4+ years experience in production/quality in industry setting required.

  • 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 $65,520 - $114,400 per year for the role of Senior Manufacturing Specialist.

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We are committed to a human-centered hiring experience. Technology may support portions of our process, but recruiting decisions involve human review and engagement. .



No Search Firms

St. Jude Children's 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.

About St. Jude Children's Research Hospital

St. Jude Children's Research Hospital is a pediatric treatment and research facility focused on children's catastrophic diseases, particularly leukemia and other cancers. The hospital was founded in 1962 by entertainer Danny Thomas and is located in Memphis, Tennessee. St. Jude is the first and only pediatric cancer center to be designated as a Comprehensive Cancer Center by the National Cancer Institute. The hospital has treated children from all 50 states and from around the world. St. Jude is known for its groundbreaking research and treatment of childhood cancer and other life-threatening diseases.
Learn more about St. Jude Children's Research Hospital
Size
4,500 employees
Industry
Founded
1962

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