Jobs Companies GenScript/ProBio Production Lead- LNP

About this Production Lead- LNP role at GenScript/ProBio

GenScript/ProBio · Onsite · Redmond, Washington, United States

About GenScript

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.

Work Location: Redmond, WA

Reports to: Sr. Production Manager, Product Development and Manufacturing, Life Science Group

 

Role Description:

We are seeking a highly motivated and experienced production lead on LNP to join our team. This position will be responsible for leading functions related to LNP production planning and delivery of customized LNP production jobs within the company. This position requires a high level of competence, strong leadership, and commitment to this role.

Key Responsibilities:

  • Work closely with department managers to develop and maintain production and QC schedules to deliver orders on time and efficiently with quality
  • Lead the team to develop and optimize the production workflow and upgrade the process to improve the delivery capabilities and customers’ satisfaction.
  • Coordinate with Supply Chain and QC teams to ensure material readiness and minimize production delays.
  • Lead production capacity planning and resource allocation activities to ensure efficient scheduling, optimal utilization of personnel and equipment, and on-time delivery of customer projects.
  • Proactively identifying and resolving common root causes of issues and addressing those to improve the overall quality of production stability.
  • Provide operational leadership to production team, including training, coaching, and team members’ leadership development.
  • Ensure accurate maintenance, reporting and forecasting of assigned production-related progress, problems and improvement plans on a biweekly basis.
  • Support cross functional team communications to develop LNP production platform capability.
  • Support tech transfer and process optimization to ensure quality of new product beta testing and launching.
  • Maintain proper training and performance documentation.

Qualifications:

  • Master or above in Biochemistry, Molecular Biology, Synthetic Biology, Microbiology, Biomedical Engineering, or related biomedical field with a minimum of 3-year experience in the pharmaceutical company, biotech or related industries
  • 1+ years of managerial experience in biotechnology production sector is required
  • Demonstrated initiative and pursuit of successful collaborative projects with interdisciplinary team
  • Excellent time management skills with commitment to ensure completion of tasks
  • Excellent written and oral communication skills.
  • Self-motivated and passionate. Comfortable to work in a fast-paced work environment

Benefit:

  • Medical Insurance/ Vision Insurance/ Dental Insurance
  • 401(k) & Retirement Savings Plan (RSP)
  • Short Term Disability Insurance
  • New Child Leave
  • Paid Time Off
  • Paid Company Holidays per year
  • Paid Sick Days (earned based on hours worked)
  • Compassionate Leave
  • Jury Duty Leave
  • Float day
  • Personal days

Perks: 

  • Free colleague meals during shift
  • Onsite massages Charis
  • Onsite gyms

Compensation:
Salary range: $70,000 – $85,000 total compensation, including bonus, depending on experience and qualifications.

Benefits:

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.

 

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform. 

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About GenScript/ProBio

About GenScript

GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.

GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

 

About ProBio

ProBio is a New Jersey-based fully integrated end-to-end contract development and manufacturing organization (CDMO) that focuses on enabling biotech and pharmaceutical companies to accelerate novel drug development and supply for clinical trials through to commercialization.

ProBio develops technology-driven proprietary platform processes to support the full lifecycle of biologics drug development and manufacturing of next generation medicine: biologics and advanced therapies. Our technical and operational expertise spans the discovery, development, and drug substance or drug product (DS/DP) manufacturing of antibody-based therapeutics, including monoclonal, bispecific, and multi-specific antibodies, recombinant proteins, plasmid DNA, viral vectors, mRNA, and vaccines. Additionally, we provide specialized integrated services in process development, bioanalytical development, formulation and in vitro/in vivo pharmacology.

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