QC Sample Receipt Analyst II

Fujifilm•College Station, TX

10d

About The Position

Position Overview The Sample Management Analyst II, under general direction, will be responsible for performing routine and non-routine support of samples submitted to the Quality Control (QC) Laboratory for evaluation. This position works as part of the Sample Management team to manage the receipt, organization and inventory of samples from manufacturing, clients, other Fujifilm facilities and third parties. The Sample Management Analyst II arranges sample shipments for outsource testing and shipments to Clients or other facilities and controls dispensing of samples for QC testing. Company Overview The work we do at FUJIFILM Biotechnologies Texas has never been more important—and we are looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions. If you’re ready to help transform the future of medicine, join FUJIFILM Biotechnologies. We offer a flexible work environment and we’re proud to cultivate a culture that will fuel your passion, energy, and drive—what we call Genki. Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it’s a dynamic location that blends convenience with innovation. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers Job Description

Requirements

Ability to build and foster relationships, cooperation, and collaboration across the organization
Aptitude to follow safety procedures outlined in the Chemical Hygiene Plan
Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated
Excellent attention to detail
Computer proficiency required
Ability to accurately complete required documentation
Excellent written and oral communication skills
Excellent organization and analytical skills
Experience prolonged standing, some bending, stooping, and stretching
Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required
Ability to sit for long periods to work on a computer
Lift up to 15 lbs regularly and up to 30 lbs on occasion
Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials
Ability to wear personal protective equipment including safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and shirt) and appropriate shoes required in most areas associated with this position
Attendance is mandatory
High School Diploma or GED, AND at least two (2) years of relevant GMP Experience OR;
Associate’s degree preferably in Biochemistry, Chemistry, Biology or related field AND at least one (1) years of relevant GMP Experience OR
Bachelor’s degree preferably in Biochemistry, Chemistry, Biology or related field.

Nice To Haves

Previous GMP Experience preferred.

Responsibilities

Follow Standard Operating Procedures (SOPs) and other related Good Laboratory Practices. (GLP)/Good Manufacturing Practices (GMP).
Manage test samples, critical reagents and reference materials.
Perform shipments to external testing facilities and clients.
Responsible for cleaning Sample Management laboratories and stocking with necessary supplies.
Maintaining inventory.
Fulfill QC Analyst sample requests.
Stability coordination.
Train new hires.
Host Bi-weekly Team Meetings.
Ability to work independently, along with ability to work well within a team.
Able to acknowledge DeltaV alarms for QC Sample Management Chambers.
Able to initiate deviations in Tackwise.
Perform other duties as assigned.