Quality Control (QC) Microbiologist (experienced) - Continuous Learning Opportunities

Immediate opportunity for an expert Quality Control (QC) Microbiology with experience or specialty in endotoxin detection methods.  This is an exciting and unique role where the you will have the opportunity to implement novel technology into biological and pharmaceutical products and processes.

Schedule Shift: 1st shift, Mon.-Fri.

Position Type: Long term, contract role for 8 mos. (through 12/31/2024); most likely will be extended through Dec. 2026.

Essential Duties and Responsibilities:

• Drive implementation of new and rapid microbiology technologies that ensure data integrity, meet company quality standards, and support regulatory submissions and delivery of quality medicines for patients.
• Design and execute method development and GMP validation for recombinant factor C endotoxin testing.
• Contribute to method development and method qualification.
• Perform laboratory operations to support and implementation of compliant, state of art methodology and instrumentation.
• Provide scientific understanding and analytical support for development of new test method, validation, and specifications.
• Support for scientific report writing and document revision.
• Provide analytical troubleshooting support for investigations which require non routine/specialized service.
• Support microbiology technology validation and implementation for testing pharmaceutical products and manufacturing environment.
• Provide validation and testing data for these new methods and technologies for internal advocacy and external regulatory submission.
• Facilitate method transfer, validation, and implementation of new microbiology technologies at secondary commercial sites.
• Work to GMP standards as appropriate.
• Follow safe Laboratory Practices, regular safety training, and maintain accurate and complete safety records consistent with company policy and legal requirements.

Qualifications:

• Bachelor's degree (BS) in Microbiology, Biological Sciences, Biochemistry or related field.
• Three (3) years or more experience in working in research and/or analytical development and/or quality control functions.
• Demonstrated experience and good working knowledge of method development, method validation/qualification.
• Experience with GMP laboratory operations.
• Strong team working skills, able to perform collaborative work across interdisciplinary groups.
• Motivated, strong desire to learn/scientific curiosity, with cross functional learning agility.
• Good organizational skills, ability to multitask and adapt to fast changing priorities and deadlines.
• Excellent verbal and written communication skills.

Preferred Skills & Experience:

• An understanding of the theoretical and practical aspects of Pharmaceutical Microbiology (knowledge of rapid / alternative methodologies an advantage).
• Demonstrated hands-on and/or practical experience in endotoxin detection methods of pharmaceutical products and/or water.
• Capacity to think innovatively and flexibly for new microbiology methodology implementation, comfortable with complexity.
• Experience in microbiology method and equipment development and/or validation.
• Knowledge of biological and pharmaceutical product manufacturing and microbial control.
• Experience with FDA regulations.