Quality Control Chemist Iii

The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy, and drive - what FDB call Genki.

College Station, Texas may be a small, university town, but the lively cultural scene and local amenities make it a great place for families as well as those who want the ease of small-town life and the convenience of living close to the vibrant pulse of big cities. Eighty-seven percent of Texas' population lives within a 180-mile radius, so we are in the center of it all in Texas. And our site is nestled in the hub of innovation, representing a source of pride for the area.

Summary: The Quality Control Chemist III, with limited supervision, will be responsible for participating in the Technology Transfer of established methods into the FUJIFILM Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. Following Tech-Transfer Activities, the candidate will be responsible for performing in-process, release and stability testing using the established analytical methods.

Essential Functions:

• Perform other duties as assigned.
• Assist with technical training of less experienced members of the team.
• Writes and revises Standard Operating Procedures (SOPs) and other Good Manufacturing Practices (GMP) documentation as appropriate.
• Assisting and initiating closure of deviations, CAPAs and Change Controls
• Creating manuals for processes/activities
• Qualification protocols
• Technical Writing to include:
• Transfer Protocols
• Sample plans (support & edit)
• Provides QC support for the sites Environmental Monitoring program and raw material analysis.
• Perform QC analytical testing for GMP in-process, release and stability testing as needed.
• Reviewing Methods for accuracy
• Facilitate the maintenance and repair of equipment
• Executes technical transfer, qualification and validation protocols as needed.

Required Skills & Abilities:

• Ability to work independently or in a team.
• Computer proficiency required.
• Ability to analyze raw data, assess assay and system suitability criteria, understand process from beginning to end, and explain process.
• Utilize MSDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.
• Excellent attention to detail.
• Excellent communication skills.
• Perform as a SME in the designated methods transferred into FDBT.
• Excellent written and oral communication skills.
• Ability to follow safety procedures outlined in the Chemical Hygiene Plan.
• Previous pipetting experience.
• Excellent organization and analytical skills.

Working Conditions & Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:

• Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.
• Ability to lift up to 30 pounds on occasion.
• Ability to sit for long periods to work on a computer.
• Experience prolonged standing, some bending, stooping, and stretching.
• Ability to wear personal protective equipment including safety glasses, lab coat, and gloves.
• Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.
• Attendance is mandatory.

Minimum Qualifications:

• Bachelor’s degree in Chemistry, Biochemistry, or related degree with three (3) years hands-on laboratory experience; OR
• Associates degree in Chemistry, Biochemistry, or related degree with five (5) years of hands-on laboratory experience;
• AND 2 years’ industry experience in a GMP / GxP or a comparable federally regulated environment.

Preferred Qualifications:

Familiar with monoclonal antibody testing methodology. Experience in assay troubleshooting and problem solving.

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.

We are an equal opportunity and affirmative action employer.  All qualified applicants will receive consideration without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, disability, protected veteran status or any other characteristic protected by applicable federal, state, or local law. If an accommodation to the application process is needed, please let us know.

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

Job Type: Full-time

Benefits:

• Health insurance
• Dental insurance
• Vision insurance
• Paid time off
• 401(k)

Schedule:

• Night shift
• 8 hour shift
• Day shift

Supplemental pay types:

• Signing bonus

Ability to commute/relocate:

• College Station, TX: Reliably commute or planning to relocate before starting work (Required)

Experience:

• HPLC/UPLC: 2 years (Required)
• CGMP: 1 year (Preferred)
• Empower: 1 year (Preferred)

Work Location: In person