Scientist , Quality Control

Job Title

Scientist l, Quality Control (BIT Group)

Cranbury NJ

We are seeking a self‑motivated professional to fill the role of Scientist l in our QC department at the New Jersey site. The successful candidate will provide assay qualification, validation, routine sample testing under GMP environment for iCMC and standalone projects for a wide variety of biological modalities, including but not limited to vaccine, ADC, RNA, and antibodies. The position involves close collaboration with internal teams and clients to ensure timely project deliveries.

• Conduct assay transfer, qualification, validation, and routine testing for ELISA‑based assays, PCR‑based assays, and cell‑based assays.
• Generate, analyze, and document data with accuracy and compliance to GMP, GDP, and ALCOA+ standards.
• Perform second scientist review on worksheets and electronic data.
• Draft and review analytical method procedures, SOPs, protocols, and reports.
• Perform reagent qualification and cell banking activities.
• Participate in investigation of OOS, deviations, and atypical results; support root cause analysis and CAPA activities.
• Support method lifecycle activities, including transfer, qualification, validation, and maintenance.
• Collaborate with cross‑functional teams including Analytical Sciences, Manufacturing, and Quality Assurance to ensure timely project delivery.
• Utilize laboratory systems (e.g., LIMS and electronic systems) for data documentation and tracking.
• Support internal audits, client audits, and regulatory inspections as required.
• Support daily lab operation activities, including but not limited to lab equipment cleaning and maintenance.
• May be required to work on weekends or during off hours.

• Bachelor’s degree in Analytical Chemistry, Biochemistry, or related field with a minimum of 4 years of industry quality control experience.
• Or a Master’s degree in Analytical Chemistry, Biochemistry, or related field with a minimum of 2 years of industry quality control experience.
• Hands‑on experience with qPCR‑based, ELISA‑based assay is required.
• Hands‑on experience with cell‑based assay is required.
• Strong data analysis, organizational, and documentation skills.
• Strong communication and presentation skills.
• A minimum of two years of hands‑on experience in qPCR‑based, and ELISA‑based assay.
• A minimum of one year of hands‑on experience in cell‑based assay.
• Knowledge of PCR‑based, ELISA‑based assay principles.
• Knowledge of mammalian cell culture and cell‑based assay.
• Understanding of antibody and protein structural characteristics.
• Knowledge of large molecule drug development and life cycle management is preferred.
• Ability to adapt to fast‑paced working environment.
• Ability to adapt to frequent shift in responsibilities.
• Good communication and ability to work in a team‑oriented environment.
• Able to be organized and maintain a positive attitude in high‑stress working environment.

The anticipated pay range for this position is $60,000 - $96,000.

Job description does not intend to list all the duties and responsibilities assigned to this position. Employees holding this position would be required to perform other job‑related duties/responsibilities based on their expertise and company business needs.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.