Scientific Associate - Molecular Biology B7 II - USA

Title: Scientific Associate (Associate Expert Potency)

Location: East Hanover, Onsite

Introduction

As a key member of the Analytical Development team, this individual will support developmental activities to aid in delivering gene therapy to patients. The successful candidate will support technical and development projects designed to characterize gene therapy products through an assortment of analytical methods. This role will also contribute to cross-functional activities including monitoring and characterizing of processes and products to identify opportunities for continuous improvement. Growth mentality and passion to serve patients, their technical team, and development programs are a must.

Required Skills & Qualifications

• MS in Biology, Biochemistry, Bioengineering or related scientific discipline with 0-2 years of research experience in the area or BS with 4 years of equivalent education/experience may be accepted.
• Basic understanding of cell biology, protein biochemistry, and molecular biology.
• Experience with cell culture and aseptic technique is required.
• Quick learner, highly motivated, hard-working, and detail-oriented.
• Strong ability to work in a fast-paced team environment with highly goal-oriented approaches and to prioritize work from multiple projects with a can-do attitude is required.
• Prior work experience at the client or in the client's industry.

Applicants must be able to work directly for Artech on W2.

Preferred Skills & Qualifications

• Experience with bioassays/bioanalytical research using platforms such as ELISA, MSD, high-content imaging, and luminescence/fluorescence assays, qPCR/dPCR is desired, but not required.
• Previous experience in a GxP laboratory is desired, but not required.
• Excellent written and verbal communication skills.

Day-to-Day Responsibilities

• Participate in method development and qualification of cell-based potency assays suitable for both in-process and drug product (DP) lot release and quality attribute assessment for AAV and LVV viral vectors.
• Execute experiments under supervision to support development and optimizations for phase-appropriate bioassay and characterizations for drug regulatory filings.
• Be responsible for critical solution preparations under both research and GxP environment.
• Participate in cross-functional activities including critical reagent management, in-process sample handling, process development analytical supports, and assay method transfers to Quality Control/Clinical Research Organization laboratories.
• Perform sample testing and data analysis with developed analytical methods. Document experimental protocols, summaries, and reports. Maintain experiment records.
• Support critical laboratory activities including monitoring inventory levels for laboratory supplies.

Company Benefits & Culture

• Standard laboratory PPE is required, including safety glasses, a lab coat, and appropriate gloves.
• Access to and safe operation of laboratory analytical equipment is permitted only after completion of applicable training and in accordance with SOP requirements.
• Must comply with all HSE, data integrity, and quality requirements.

For immediate consideration please click APPLY to begin the screening process with Alex.