Sr. Microbiologist/Microbiologist II

Job Description
How will you make an impact?
This microbiologist role will have a strong background in performing method development, method validation, method transfer activities as well as routine testing of raw materials, in-process testing and finished product. This exciting role will support microbiological activities for the Glaukos organization, which includes R&D as well as commercial manufacturing.
The candidate must have experience in cGMPs, regulatory body requirements and FDA compliance and must be proficient in microbiological testing per USP/EP/JP. The candidate must have an understanding of aseptic processes and manufacturing.
What You'll Do:

• Develop and implement microbiological strategies and procedures to ensure compliance with industry standards and regulations
• Perform method development, feasibility and validation of raw materials, in-process and final product.
• Conduct routine microbiological testing and analysis of samples, ensuring accuracy and reliability of results.
• Perform routine and stability testing of GLP and GMP suppliesWrite and revise SOP's, validation protocols/reports
• Perform testing as needed to generate data for validation and special projects.
• Make recommendations and validate new laboratory equipment (e.g., Installation Qualification, Operational Qualification (IQOQ), and Performance Qualification (PQ)Maintain accurate and up-to-date documentation of all microbiological activities, including test results, procedures, and reports
• Review and interpret test results, prepare reports, and communicate findings to relevant stakeholders
• Identify and implement improvements to existing microbiological processes, methods, and techniques to enhance efficiency and productivity
• Collaborate with cross-functional teams, such as quality assurance, research and development, and production, to support product development and continuous improvement initiatives
• Stay updated with the latest advancements and trends in the field of microbiology and recommend and implement new technologies and methodologies as appropriate
• Ensure compliance with relevant regulatory requirements and standards, such as Good Manufacturing Practices (GMP), Hazard Analysis and Critical Control Points (HACCP), and ISO standards

How will you get here?

• Bachelor's degree in Microbiology, Biology or related scientific field
• Minimum 8 years of related pharmaceutical experience in a cGMP environment
• Proficiency in microbiological techniques such as aseptic testing, microbial monitoring, gram staining, and plating
• Proficiency in testing according to AAMI/ISO/USP Standards
• Knowledge and control of laboratory equipment including calibration and maintenance
• Ability to understand and perform all required tasks by adhering to company Standard Operating Procedures and all current Good Manufacturing Practices
• Understanding of quality systems including change control, deviations and CAPAs; support investigations as needed
• Ability to handle multiple tasks concurrently and complete tasks in a timely manner
• Strong written and verbal language skills to effectively read and write SOP's and related labreports and effective communication skills to present data with personnel at all levels in the organization
• Excellent teamwork skills, organizational skills, and strong attention to detail
• Knowledgeable in regulatory requirements and industry standards related to microbiology
• Proficient in using microbiological testing equipment and software;
• Knowledge and proficiency in computer software (e.g. Microsoft Office programs)
• Attention to detail and high level of accuracy in performing microbiological tests and analysis and excellent analytical and problem-solving abilities to interpret test results, troubleshoot issues, and recommend solutions
• Ability to work collaboratively in cross-functional teams and adapt to changing priorities and deadlines
• Strong organizational and time management skills to prioritize tasks and meet project timelines
• Ability to lift 25 lbs.
• Ability to stand or sit 8 or more hours a day
• Work in a sterile environment wearing appropriate gowning and protective equipment

#GKOSUS
About Us
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.
Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.
Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.
Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.