Principal QC Microbiologist

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing

If you’re looking for a rewarding career, apply with us today

Job Description

Eurofins PSS is looking for a Subject Matter Expert (SME) in QC Microbiology for pharmaceuticals. The highly experienced employee will work at a client site as the only experienced staff member, and they must be able to be the point of contact for all questions related to quality control activities related to microbiology in the lab. Training of other employees, updating processes, performing required testing, and investigating non-conformances are all activities that may be required. This is not a leadership position but there is potential to eventually move into a leadership role.

The qualified individual MUST be an expert in:

• Sterility and Endotoxin Testing
• USP standards
• Growth promotion, Gram staining
• Environmental monitoring of pharmaceutical labs and manufacturing spaces
• Aseptic process media fills
• cGMPs

Responsibilities Include: 

• Perform sterility, endotoxin, pH, and osmolality testing on raw materials, drug substance, and drug product
• Perform gram stains, sub-culturing of isolates, growth promotion testing, and general cell culture
• Coordinate, schedule, and execute testing based on manufacturing schedules
• Direct performance in Aseptic Processing Media Fills and perform support testing, including visual inspection
• Maintain housekeeping and equipment maintenance, including organization, cleanliness, and logbooks
• Assist the Quality Control department in daily operations, as needed
• Author and revise QC SOPs and change controls as necessary to maintain compliance
• Author and execute qualification protocols and reports for microbiological assays
• Perform timely response to Out of Specification (OOS) results, including notification to area management. Perform and document laboratory investigations to ensure that potential problems and root causes are identified, impact assessed and actions to prevent recurrent are considered implemented. Execute associated CAPA.
• Ensure data integrity is maintained for all applications, programs, and executed work. Ability to document all work using Good Documentation Practices and ALCOA++ principles.
• Troubleshoot and analyze nonconforming data. Completion of thorough investigations to ensure that potential problems and root causes are identified, impact assessed and actions to prevent recurrence are considered and implemented.
• Perform internal audits and GEMBA walk-throughs of laboratory areas to maintain compliance
• Communicate with the individual Operations Departments (Manufacturing, Quality Assurance, Facilities) to ensure that Company objectives are met on schedule
• Perform viable and non-viable environmental monitoring in support of Manufacturing and Quality Control in the form of air testing, surface testing, personnel testing and particulate monitoring, inside the aseptic clean rooms, as necessary
• Oversight of critical processing steps performed by Manufacturing during aseptic product manufacture, ensuring accuracy of steps performed
• Training of other employees as necessary

Qualifications

BASIC MINIMUM REQUIREMENTS:

• BS in a related scientific discipline
• At least 4 years of micr