Associate Scientist, Late-Stage Process Development

ZipRecruiter; Philadelphia (Philadelphia County); On-site; USD 60,000 - 95,000; Full time

Job summary

An innovative firm is seeking an Associate Scientist to drive process development in a dynamic lab environment. This role involves leading experiments, supporting technology transfer, and ensuring compliance with safety and quality standards. Ideal candidates will possess a strong background in cell culture and process development, along with excellent communication and analytical skills. Join a team that values diversity and is committed to advancing cutting-edge biotechnological solutions. If you're ready to make a significant impact in the life sciences industry, this opportunity is perfect for you.

Qualifications

• PhD or Master's degree required with relevant industry experience.
• Proficiency in Microsoft Office and analytical software tools.

Responsibilities

• Lead process development experiments and analyze data.
• Support technology transfer to manufacturing partners.

Skills

Cell Culture

Process Development

Analytical Development

Communication Skills

Critical Thinking

Education

PhD in Chemical Engineering

Bachelor's Degree

Master's Degree

Tools

Microsoft Office

GraphPad

MiniTab

FACS DIVA

Job description

Overview

The Associate Scientist, Late-Stage Process Development will support process development projects related to automation and technology transfer. The ideal candidate will have cell culture experience, knowledge of process development or manufacturing support, and familiarity with cGLP/cGMPs.

Essential Functions and Responsibilities:

1. Lead or support process and analytical development experiments using various protocols and techniques.
2. Design studies for development and characterization independently; write protocols, execute experiments, analyze data, prepare reports, and present findings orally.
3. Support technology transfer of automation processes to internal or external manufacturing partners.
4. Evaluate new automation technologies to enhance process manufacturability within closed systems.
5. Assist in manufacturing investigations as needed.
6. Make detailed observations and document them promptly and accurately.
7. Support data and records management activities.
8. Stay current with training on new processes and analytical methods.
9. Maintain compliance with lab safety, environmental, and quality standards.
10. Adhere to Iovance Biotherapeutics core values, policies, procedures, and ethics.
11. Follow Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
12. Perform other duties as assigned.

Required Education, Skills, and Knowledge:

• PhD in chemical engineering, immunology, biology, microbiology, or related field with 0-2 years of industry experience; or a bachelor's degree with 8 years of industry experience; or a master's degree with 6 years of experience.
• Proficiency in Microsoft Office and spreadsheet software.
• Knowledge of GraphPad, MiniTab, and FACS DIVA software is desirable.
• Ability to interpret regulations and guidance documents; apply critical thinking; and communicate findings effectively both in writing and orally.
• Strong interpersonal, communication, and organizational skills; ability to multitask and work as part of a team.
• Willingness to travel up to 10-15% as needed.

Additional Experience:

• At least 2 years of experience in cell culture, cell therapy, biotechnology, or related life sciences industry.
• Experience with cell therapy process development, technology transfer, automation, and cell therapy manufacturing equipment (e.g., Miltenyi Prodigy, Lovo, G-Rex, Cytivas, Thermo).
• Skills in flow cytometry or qPCR are a plus.

Physical Demands and Activities:

• Ability to wear PPE and work with biohazards and chemicals.
• Stand/walk for 70% of the workday; sit for 30%.
• Perform activities like crouching, bending, reaching, and repetitive motions.
• Lift up to 45 pounds.
• Visual acuity for data analysis and computer work.

Mental Requirements:

Strong conceptual thinking, judgment, troubleshooting, problem-solving, and stress management skills. Ability to handle multiple priorities and meet deadlines.

Work Environment:

Combination of office and laboratory settings, with potential exposure to hazardous materials. Compliance with safety protocols is required.

Iovance values diversity and inclusion. We are an equal-opportunity employer. For accommodations, contact [e-mail].

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