Manufacturing Lead - Drug Product Operations
Company: FUJIFILM Holdings America Corporation
Location: College Station
Posted on: March 16, 2023
Job Description:
Overview Follow Your Genki to FUJIFILM Diosynth Biotechnologies
(FDB)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.Summary: The Manufacturing Lead - Drug Product
Operations will work directly with the processes associated with
the Vanrx SA25 Automated Filling machine. This includes but is not
limited to formulation, aseptic filling, vial inspection and vial
labeling following cGMP procedures. This individual will also lead
a team of employees directly or indirectly in the production of
Drug Product at FUJIFILM Diosynth. External US Essential
Functions:
- Responsible for the operation of Vanrx SA25 Vial Filling
Isolator.
- Responsible for overseeing the formulation of the bulk drug
product in accordance to procedures.
- Responsible for visual inspection and labeling of filled bulk
drug product vials in accordance to procedures.
- Responsible for writing, reviewing, and/or updating Standard
Operating Procedures (SOPs) and Batch Production Records
(BPRs).
- Document and maintain activity records according to cGMP
regulations and ensure team members are trained.
- Help implement project safety and quality assurance programs in
collaboration with senior staff and EH&S.
- Ensure proper documentation and execution of Batch Production
Records for assigned projects.
- Maintain confidentiality of proprietary company
information.
- Participate in incident investigations.
- Maintain an effective working relationship with others.
- Perform all other duties as assigned. Required Skills &
Abilities:
- Excellent oral and written communication skills as well as
excellent interpersonal and organizational skills.
- Demonstrated leadership, coaching and mentoring skills.
- Ability to train others to perform and maintain cGMP
standards
- Strong proficiency with Microsoft Office applications.
- Experience working in cleanroom environments.
- Must have flexible work hours, and be willing to work outside
of normal, scheduled hours, as necessary. Must be able to work
alternative hours and weekends as required.
- Self-discipline and good attention to detail.
- Excellent math and computer skills.
- Must have exceptional planning skills and be willing to
interface with colleagues in many different roles and functions
throughout the manufacturing facilities and lead projects. Working
Conditions & Physical Requirements:The physical demands described
here are representative of those that must be met by an employee,
in order to successfully perform the essential functions of this
job. Reasonable accommodations may be made to enable individuals
with disabilities to perform essential functions. While performing
the duties of this job, the employee is required on a regular basis
to:
- 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.
- Ability to lift up to 25 pounds; frequently, and up to 50
pounds; on occasion.
- Attendance is mandatory. Qualifications:
- Master's Degree preferably in Biology, Microbiology, Chemistry,
Biochemistry, Engineering or related field with 3 years relevant
experience of which 1 year must be in a GMP environment as a lead
or supervisor; OR
- Bachelor's Degree preferably in Biology, Microbiology,
Chemistry, Biochemistry, Engineering or related field with 5 years
relevant experience of which 1 year must be in a GMP environment as
a lead or supervisor; OR
- High School or Associates Degree preferably in Biology,
Microbiology, Chemistry, Biochemistry, Engineering, or related
field with 8 years relevant experience of which 5 year must be in a
GMP environment. Preferred Qualifications:
- Six Sigma Certification
- Cross training with downstream processes or other identified
functional areas.
- Biotechnology Certificate
- SAP experience
- Train the Trainer Certification
- Drug Product experience
- Handling of Live VirusWe 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 e-mail or call .
Keywords: FUJIFILM Holdings America Corporation, College Station , Manufacturing Lead - Drug Product Operations, Other , College Station, Texas
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