Join us! FDB is advancing tomorrow’s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community, and the world at large.  The QC Associate, Microbiology is responsible for partnering with management in supporting and maintaining QC microbiological functions for new and existing GMP manufacturing operations. This position will also support facility qualification operations for new GMP manufacturing areas including Environmental Monitoring Performance Qualification (EMPQ) and GMP utilities qualification.

Join us! FUJIFILM Diosynth Biotechnologies is advancing tomorrow’s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community, and the world at large. 

 QCM Associate, Microbiology

The QC Associate, Microbiology is responsible for partnering with management in supporting and maintaining QC microbiological functions for new and existing GMP manufacturing operations. This position will also support facility qualification operations for new GMP manufacturing areas including Environmental Monitoring Performance Qualification (EMPQ) and GMP utilities qualification.

Reports to: Supervisor, QC Microbiology

Location: Thousand Oaks, CA

Travel: Less than 10%

Shift: This role will support a 4 day/10-hour work schedule with Either Sunday – Wednesday, Wednesday – Saturday, Mon, Tue, Thu, Fri shifts.

Alternatively, this role can support a 5-day 8-hour shift from Mon-Fri.

Primary Responsibilities

• Collects and performs non-viable, viable air (active and passive) and surface monitoring and personnel monitoring to support routine environmental monitoring, in-process environmental monitoring, process simulation, aseptic operator qualification and gowning qualification
• Performs sampling and testing of GMP utilities such as compressed gases
• Documents Environmental Monitoring sampling using LIMS
• Executes microbiological assays such as bioburden, endotoxin, gram stain, mold identification, growth promotion and plate enumeration
• Reviews Environmental monitoring raw data generated by LIMS
• Supports EM data management including data entry, data verification, data download, generation of crystal reports from LIMS to support data trending
• Performs routine maintenance including support of calibration and sanitization of lab equipment and lab spaces
• Supports QC equipment qualification including implementation of new methods
• Revises procedures and forms with guidance from supervisors
• Supports internal and external inspections and audits.
• Generates Desigo reports for non-viable particulates testing during in-process environmental monitoring
• Tracks and support the calibration of EM equipment such as Climet and SAS.
• Generates Work Orders for equipment, data entries for material ingress
• Coordinates the shipping of isolates for microbial identification
• Performs special projects as assigned

Physical Requirements

• Subject to extended periods of sitting and/or standing in a laboratory and classified room environment.
• Ability to lift 50 lbs. and to work in controlled space laboratory required.
• Ability to use ladders to reach high sampling sites
• Ability to reach above the shoulder and bend to be able to gown.

Education and Professional Experience

• Requires a bachelor’s degree in Microbiology, Molecular and Cellular Biology, Biochemistry, or Biology or with at least one year of experience or an equivalent combination of education and experience.
• Quality Control experience in the pharmaceutical industry supporting cGMP manufacturing including site qualification and utility validation preferred.
• 0-2 or more years of directly relevant experience.

Position Requirements

• Direct experience is highly desirable in environmental monitoring, personnel monitoring, sterile gowning, and aseptic process control in accordance with ICH, USP and FDA guidelines.
• Direct experience is highly desirable in regulatory inspections.
• Must possess excellent verbal and written communication skills, good interpersonal skills.
• Experience in cGMP for cell therapy testing is a plus.
• Must be able to work in controlled environments requiring special gowning

 Salary and Benefits

• $30.50 to $36.50 per hour, depending on experience
• Medical, Dental and Vision
• Life Insurance
• 401k
• Paid Time Off

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBCHR@fujifilm.com).