FUJIFILM Biotechnologies
Sr. Analyst 1, QC Analytical Development Bioassay
FUJIFILM Biotechnologies, Holly Springs, North Carolina, United States, 27540
Sr. Analyst 1, QC Analytical Development Bioassay
Join to apply for the
Sr. Analyst 1, QC Analytical Development Bioassay
role at
FUJIFILM Biotechnologies
The Sr. Analyst 1, QC Analytical Development (QCAD) Bioassay supports the implementation of plate and cell‑based analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). This role supports the transfer and validation of methods such as residuals (HCP, DNA, Protein A), dot blot for product identity, ELISA ID/ Potency and various cell‑based assays. The Sr. Analyst 1, QC AD Bioassay ensures Good Manufacturing Practices (GMP) compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients and author and review procedures, SOPs, and technical reports.
What You'll Do
Executes analytical method transfers and validations for plate and cell‑based Bioassays for the QC Analytical Development team
Ensures compliance of analytical testing with appropriate GMP regulations
Participates in regular meetings for TT programs with cross‑functional teams and key stakeholders
Authors and reviews SOPs, protocols, and technical reports
Works cross‑functionally with Contract Laboratory Organizations (CLOs), QC testing teams, Quality Assurance (QA), and Process Science groups to ensure transfer of methods according to deadlines
Collaborates with the LIMS team and IT department to build new analytical method functionality that meets end‑user and customer requirements
Ensures compendial method oversight and scientific guidelines (e.g. ICH, EMA, FDA, etc.)
Supports regulatory requests and inspections
Supports the QCAD team to investigate any project challenges with necessary risk assessment tools and techniques, as needed
Supports best practices for TT and PPQ strategies globally, as required
Coordinates and supports QCAD Bioassay lab activities and provides training for QC Bioassay lab technicians
Performs other duties, as assigned
Minimum Requirements
B.S. in Microbiology, Virology, Biology, Biological Sciences, Engineering, or related science field with 2+ years of analytical laboratory experience preferably in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO) OR
M.S. in Virology, Microbiology, Biology, or related science field with 0+ years of previous experience
1+ years’ experience in a GMP environment
Experience with QC Bioassay testing methods including protein binding assays (e.g., ELISA, Dot Blot, etc.)
Experience with analytical method development, tech transfers and validation residual testing for DNA, Host Cell Protein (HCP), Protein A
Preferred Requirements
Master’s in Virology, Microbiology, Biology or related science field with 1+ years of related experience
Experience with LIMS software
Physical And Work Environment Requirements
Ability to discern audible cues.
Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
Ability to ascend or descend ladders, scaffolding, ramps, etc.
Ability to stand for prolonged periods of time up to 60 minutes.
Ability to sit for prolonged periods of time up to 60 minutes.
Ability to conduct activities using repetitive motions that include writes, hands and/or fingers.
Ability to conduct work that includes moving objects up to 10 pounds.
Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions.
Will work in small and/or enclosed spaces.
Will work in heights greater than 4 feet.
Seniority level Mid‑Senior level
Employment type Contract
Job function Quality Assurance
#J-18808-Ljbffr
Sr. Analyst 1, QC Analytical Development Bioassay
role at
FUJIFILM Biotechnologies
The Sr. Analyst 1, QC Analytical Development (QCAD) Bioassay supports the implementation of plate and cell‑based analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). This role supports the transfer and validation of methods such as residuals (HCP, DNA, Protein A), dot blot for product identity, ELISA ID/ Potency and various cell‑based assays. The Sr. Analyst 1, QC AD Bioassay ensures Good Manufacturing Practices (GMP) compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients and author and review procedures, SOPs, and technical reports.
What You'll Do
Executes analytical method transfers and validations for plate and cell‑based Bioassays for the QC Analytical Development team
Ensures compliance of analytical testing with appropriate GMP regulations
Participates in regular meetings for TT programs with cross‑functional teams and key stakeholders
Authors and reviews SOPs, protocols, and technical reports
Works cross‑functionally with Contract Laboratory Organizations (CLOs), QC testing teams, Quality Assurance (QA), and Process Science groups to ensure transfer of methods according to deadlines
Collaborates with the LIMS team and IT department to build new analytical method functionality that meets end‑user and customer requirements
Ensures compendial method oversight and scientific guidelines (e.g. ICH, EMA, FDA, etc.)
Supports regulatory requests and inspections
Supports the QCAD team to investigate any project challenges with necessary risk assessment tools and techniques, as needed
Supports best practices for TT and PPQ strategies globally, as required
Coordinates and supports QCAD Bioassay lab activities and provides training for QC Bioassay lab technicians
Performs other duties, as assigned
Minimum Requirements
B.S. in Microbiology, Virology, Biology, Biological Sciences, Engineering, or related science field with 2+ years of analytical laboratory experience preferably in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO) OR
M.S. in Virology, Microbiology, Biology, or related science field with 0+ years of previous experience
1+ years’ experience in a GMP environment
Experience with QC Bioassay testing methods including protein binding assays (e.g., ELISA, Dot Blot, etc.)
Experience with analytical method development, tech transfers and validation residual testing for DNA, Host Cell Protein (HCP), Protein A
Preferred Requirements
Master’s in Virology, Microbiology, Biology or related science field with 1+ years of related experience
Experience with LIMS software
Physical And Work Environment Requirements
Ability to discern audible cues.
Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
Ability to ascend or descend ladders, scaffolding, ramps, etc.
Ability to stand for prolonged periods of time up to 60 minutes.
Ability to sit for prolonged periods of time up to 60 minutes.
Ability to conduct activities using repetitive motions that include writes, hands and/or fingers.
Ability to conduct work that includes moving objects up to 10 pounds.
Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions.
Will work in small and/or enclosed spaces.
Will work in heights greater than 4 feet.
Seniority level Mid‑Senior level
Employment type Contract
Job function Quality Assurance
#J-18808-Ljbffr