Scientist II, Cell Line Development

AGC Biologics$66K — $106K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Life Sciences or related field, MS with 2+ years, or BS with 4+ years of relevant experience.
  • Hands-on experience in upstream cell culture development, particularly with bench scale bioreactors.
  • Familiarity with fed-batch operations is essential, and pilot scale experience is advantageous.
  • Strong oral and written communication skills are imperative.
  • Team-oriented with proven interpersonal effectiveness.
  • Previous experience in a cGMP environment is highly desirable.
  • Ability to manage multiple tasks effectively and progress in a dynamic setting.
  • Proficient in Microsoft tools, especially Excel, Word, and Outlook.

Responsibilities

  • Conducts bench scale cell culture process development and optimization studies.
  • Manages project workflow to ensure timely completion from planning to data evaluation.
  • Performs independent analysis and helps develop optimization strategies.
  • Authors study protocols and reports, ensuring clarity and accuracy of data reporting.
  • Supports tech transfer to GMP manufacturing and assists with investigational deviations.
  • Acts as a subject matter expert in cell culture during client interactions and meetings.
  • Maintains and authors operational procedures for lab equipment, ensuring functionality.

Benefits

  • Comprehensive training in essential job functions and safety procedures.
  • Opportunities for involvement in cross-departmental projects.
  • Participation in face-to-face client engagements to sharpen interpersonal skills.
Full Job Description
Job Title - Scientist ll, Cell Line Development

Work Location - Cranbury NJ

Job Summary

Designs, executes and authors upstream cell culture development, tech transfer, and optimization studies. Conducts pilot scale material generation runs. Partners with other internal PD teams during process tech transfer, and supports GMP manufacturing and related investigation studies. Participates in client calls and face to face meetings with minimum supervision.

Job Responsibilities
  • Works on bench scale cell culture process development, optimization and process transfer studies with minimum supervision. Conducts pilot-scale experiments for non-GMP material generation.
  • Manages project workflow to ensure on time delivery: from initial planning, experiment execution, to data evaluation.
  • Performs independent data analysis and interpretation and assists in strategies for optimization and troubleshooting.
  • Authors study protocols and reports, and ensures all data are reported clearly and accurately; Serves as trainer for inter and intradepartmental staff as needed.
  • Assists with tech transfer to GMP manufacturing, and supports deviations and investigations.
  • Serves as upstream cell culture SMEs to participates in client calls and face to face meetings. Provides project plans and updates to clients.
  • Authors Upstream lab equipment SOPs; maintains equipment functionality and coordinates repairs and preventative maintenance.
  • Performs job specific tasks in compliance with applicable Regulations, International Standards, and WuXi Biologics internal policies and guidelines.
  • Completes all required training (i.e. safety, equipment etc.).
  • Contributes to the overall operations and to the achievement of departmental goals.
  • May be required to assist in other departments or assigned other duties.


Qualifications
  • PhD in Life Sciences or related field, MS with 2+ years or BS with 4+ years of experience in a biopharmaceutical or biological contract testing/manufacturing organization.
  • Hands-on experience in upstream cell culture process development using bench scale bioreactors, experience with fed-batch operations.
  • Experience with pilot scale bioreactor operation is a plus.
  • Strong oral & written communication skills are required.
  • Ability to work effectively as part of a team and to exhibit effective interpersonal skills.
  • Experience in a cGMP environment is highly desirable.
  • Ability to take on multiple tasks simultaneously.
  • Proficient in Microsoft (Excel, Word, Outlook)


The anticipated salary range for this position is $66,000 - $ 106,000

The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertis and company business needs.

Similar Jobs

More Jobs at AGC Biologics

More Pharmaceuticals & Biotech Jobs

Find similar Scientist II, Cell Line Development jobs: