Scientist 2, QC Chemistry

Holly Springs, MS - USA

Monthly Salary: Not Disclosed

Posted on: 7 hours ago

Vacancies: 1 Vacancy

Department:

Quality Control

Job Summary

Position Overview

The Scientist 2 QC Chemistry is a technical subject matter expert (SME) responsible for QC analytical chemistry methods used in biological product manufacturing including chromatography (GC HPLC UPLC SEC) spectroscopy (MS GC/MS LC-MS/MS UV UV-Vis FTIR) electrophoresis (GE non-reducing and reducing CE-SDS imaged capillary isoelectric focusing (icIEF)) wet chemistry glycan analysis sub-visible particle analysis peptide mapping and physical appearance etc. The Scientist 2 QC Chemistry ensures GMP-compliant laboratory operations in accordance with regulatory guidelines. This role performs technical/compliance reviews and approves analytical results. The role approves laboratory exceptions invalid assays deviations change controls and corrective and preventative actions (CAPAs). The QC Chemistry Scientist II authors reviews and approves SOPs protocols and technical reports. The role serves as the subject matter expert (SME) for QC Chemistry in cross-functional projects and meetings.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs North Carolina. By end of 2025 well open North Americas largest end-to-end CDMO biopharmaceutical manufacturing facility offering drug substance production fill-finish and packaging under one roof.

Were looking for passionate mission-driven people to help us realize this exciting vision and deliver the next vaccine cure or therapy. We offer a dynamic work environment and were proud to cultivate a culture that will fuel your purpose energy and drivewhat we call Genki. Ready to shape the future of medicine Lets transform healthcare together!

Holly Springs North Carolina combines small-town warmth with proximity to Raleighs thriving tech scene making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70000 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: Description

What Youll Do

Performs physical and chemical analytical testing methods for biological products including chromatography (GC HPLC UPLC SEC) spectroscopy (MS GC/MS LC-MS/MS UV UV-Vis FTIR) electrophoresis (GE non-reducing and reducing CE-SDS imaged capillary isoelectric focusing (icIEF)) wet chemistry glycan analysis sub-visible particle analysis peptide mapping and physical appearance.
Ensures analytical testing of in-process drug substance (DS) drug product (DP) and stability samples is performed according to appropriate GMP regulations.
Performs laboratory work and peer reviews of analytical data in support of tech transfer and routine manufacturing.
Executes and reviews method qualification and validation activities and maintains lab equipment.
Monitors assay performance and implements improvements that ensure quality and efficiency within QC Chemistry.
Troubleshoots and investigates deviations and invalid assays performed in QC Chemistry.
Authors reviews and approves SOPs protocols reports change controls Trackwise deviations out-of-specification (OOS) and out-of-trend (OOT) investigations and CAPAs for the QC Chemistry team as needed.
Represents QC Chemistry in cross-functional collaborations with other QC Departments Manufacturing Process Science and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objective.
Manages and monitors lab activities as needed.
Provides training for QC Chemistry associates.
Provides technical support as the QC Chemistry SME during customer visits audits and regulatory inspections.
Participates in risk and gap assessments during project scoping as needed.
Authors technically-sound simple to moderately complex reports with limited guidance.
Collaborates with the LIMS team and IT department to build new method functionality that meets end-user and customer requirements.
Liaises with Contract Laboratory Organizations.

Minimum Qualifications

Bachelors Degree in Chemistry Biochemistry Biological Sciences Engineering or related science field with 8 years of relevant experience; OR
Masters Degree in Chemistry Biochemistry Biological Sciences Engineering or related science field with 6 years of relevant experience; OR
D. in Chemistry Biochemistry Biological Sciences Engineering or related science field with 4 years of relevant experience.
4 years of experience working in a regulated GMP environment.
In-depth technical knowledge and experience of physical and chemical analytical testing methods for biological products including chromatography (GC HPLC UPLC SEC) spectroscopy (MS GC/MS LC-MS/MS UV UV-Vis FTIR) electrophoresis (GE non-reducing and reducing CE-SDS imaged capillary isoelectric focusing (icIEF)) wet chemistry glycan analysis sub-visible particle analysis peptide mapping and physical appearance.
Advanced knowledge and experience of cGMPs ICH USP EP JP and FDA requirements as it relates to Chemistry analytical methods.
Familiarity with LIMS Software.
Ability to independently analyze raw data and assess assay and system suitability criteria.
Displays an advanced knowledge of GMP requirements for laboratory operations.
Demonstrated complex problem-solving skills.
Excellent organization and analytical skills.
Excellent technical writing presentation and communication skills.
Excellent interpersonal skills including the ability to work as part of a cross-functional team collaborate with external clients adapt to changing business needs communicate with confidence challenge others when necessary and display strong problem-solving capabilities.
Ability to plan prioritize and to complete own work and the work of others.
Excellent English oral and written communication skills as well as demonstrated expertise with Microsoft Excel Project Word and SmartSheet.

Preferred Qualifications

Experience with Customer Relationship Management.
Prior drug substance or manufacturing experience including process validation transfer commercialization and manufacturing support and troubleshooting.
Experience using quality systems (e.g. deviation management system change control corrective and preventive action (CAPA) document management system.

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 essential functions. While performing the duties of this job the employee is required on a regular basis to:

Will work in environment which may necessitate respiratory protection.
Ability to discern audible cues.
Ability to inspect or perform a task with 20/20 corrected vision visual acuity including distinguishing color.
Ability to stand for prolonged periods of time up to 120 minutes.
Ability to sit for prolonged periods of time up to 120 minutes.
Ability to conduct activities using repetitive motions that include wrist hands and/or fingers.
Ability to conduct work that includes moving objects up to 10 pounds.

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 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.

*LI-Onsite

EEO Information

Fujifilm is committedto 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.

ADA Information

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 ().

Required Experience:

Position OverviewThe Scientist 2 QC Chemistry is a technical subject matter expert (SME) responsible for QC analytical chemistry methods used in biological product manufacturing including chromatography (GC HPLC UPLC SEC) spectroscopy (MS GC/MS LC-MS/MS UV UV-Vis FTIR) electrophoresis (GE non-reduci...