LNP Production Intern (Full time) New Redmond, Washington, United States

Fresh Grads; Redmond (WA); On-site; USD 30,000 - 33,000; Full time

Benefits offered by this job

Lunch provided daily

Medical, dental, and vision insurance

Job summary

GenScript USA Inc/ProBio Inc. seeks a full-time LNP Production Intern to support manufacturing and quality control for mRNA-LNP formulations in Redmond, WA. The role involves formulation, purification, in-process testing, inventory, and documentation under SOPs in a fast-paced production setting.

The ideal candidate will be detail-oriented, organized, and capable of handling lab equipment, with 0–2 years of biotech experience and a willingness to work 40 hours weekly. Lunch is provided daily.

Qualifications

• Associate's or Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemical Engineering, Chemistry, or related field.
• 0-2 years of laboratory, manufacturing, or biotechnology experience.
• Strong attention to detail and documentation skills.
• Basic understanding of laboratory techniques and equipment.
• Ability to follow SOPs and work independently after training.
• Ability to lift up to 25 lbs and stand for extended periods.

Responsibilities

• Assist with preparation of buffers, reagents, lipids, and payload materials.
• Support mRNA-LNP formulation and downstream processing activities.
• Perform purification and concentration processes following approved SOPs.
• Operate laboratory equipment including centrifuges, filtration devices, TFF systems, and other production equipment.
• Assist in antibody‑decorated LNP preparation and purification processes following established procedures.
• Perform routine QC measurements including: Particle size, PDI, Zeta potential, Encapsulation efficiency and others.
• Accurately record and review production and QC data.
• Ensure all activities comply with GDP (Good Documentation Practices).
• Conduct sterile filtration, aliquoting, tube labeling, and packaging.
• Maintain sample traceability throughout production and shipping processes.

Skills

Attention to detail

Documentation

SOP adherence

Laboratory techniques

Sterile techniques

Education

Associate's degree

Bachelor's degree

Tools

Centrifuges

TFF systems

Pipettes

Job description

Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.

Role Description:

The LNP Production Intern supports the manufacturing and quality control activities associated with mRNA-LNP formulations and related nanoparticle products. This role is responsible for assisting with LNP formulation, purification, concentration, in-process quality testing, inventory management, documentation, and preparation of final products for shipment. The ideal candidate is detail-oriented, highly organized, and able to thrive in a fast-paced production environment while following established SOPs and quality standards. The responsibilities are aligned with existing LNP production workflows used by the team.

Key Responsibilities:

Production Operations:

• Assist with preparation of buffers, reagents, lipids, and payload materials.
• Support mRNA-LNP formulation and downstream processing activities.
• Perform purification and concentration processes following approved SOPs.
• Operate laboratory equipment including centrifuges, filtration devices, TFF systems, and other production equipment.
• Assist in antibody‑decorated LNP preparation and purification processes following established procedures.

In-Process Quality Control

• Perform routine QC measurements including: Particle size, PDI, Zeta potential, Encapsulation efficiency and others
• Accurately record and review production and QC data.
• Ensure all activities comply with GDP (Good Documentation Practices).
• Conduct sterile filtration, aliquoting, tube labeling, and packaging.
• Maintain sample traceability throughout production and shipping processes.

Inventory & Materials Management

• Follow all production SOPs, work instructions, and safety procedures.
• Complete batch records and laboratory documentation accurately.
• Maintain compliance with ISO and internal quality systems.
• Participate in training and continuous improvement initiatives.

Qualifications:

• Associate's degree or Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemical Engineering, Chemistry, or related field.
• 0-2 years of laboratory, manufacturing, or biotechnology experience.
• Strong attention to detail and documentation skills.
• Basic understanding of laboratory techniques and equipment.
• Ability to follow SOPs and work independently after training.
• Ability to lift up to 25 lbs and stand for extended periods
• Preferred having experience with mRNA production, LNP technology, sterile techniques, centrifugal filtration or TFF, DLS and experience in GMP, ISO regulated environment.

Please note that this is afull-time role based onsite in Redmond, WA with lunch provided daily. The hourly pay-rate is $22-$24 per hour.

Please note that we are not looking for candidates that are unable to commit to a full-time schedule of 40 hours per week.

Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well‑being initiatives, and peer‑to‑peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug‑free workplace.