GenScript/ProBio

Scientist, Analytical Development

Pennington, New Jersey, United States · Senior

Sponsorship not specified$80k-$110kDetected 28 days ago

StatisticsBusiness DevelopmentGMPMolecular BiologyNGSMass SpectrometryCommunicationProblem SolvingMicrosoft Office

About the role

The position reports to the Sr.
There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients.
QC Manager is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials and participating in the technology transfer.

Apply knowledge of bio separation techniques to support method development, troubleshooting, and process characterization
Support the establishment, development and optimization of Analytical Development (AD) and Quality Control (QC) laboratories to enable both Non-GMP and GMP testing
Design, develop, and execute analytical methods, including method development, method qualification/validation, technology transfer, and product testing.
Own method lifecycle management activities, including authoring and reviewing protocols, reports, and technical documentation.
Support procedure lifecycle activities, including authoring and reviewing Standard Operating Procedures (SOPs) and associated forms. Perform
Drive continuous improvement initiatives across AD and QC, identifying opportunities to enhance assay robustness, efficiency, and data quality.
Collaborate cross-functionally with Process Development, Manufacturing, and Quality teams to support product and process advancement.
Perform other duties as assigned based on business needs
Up to 15% traveling to support CDMO projects or business development activities.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Master's degree with 2+ years of relevant industry experience, or Bachelor's degree with 5+ years, or Ph.D. with relevant experience.
Experience executing assays in accordance with Standard Operating Procedures and protocols in a regulated or controlled environment.
Strong problem-solving skills with the ability to work independently and collaboratively in a fast-paced environment.
Familiar with principles of Good Documentation Practices, Data Integrity, and ALCOA+.
Strong interpersonal, verbal, and written communication skills.
Experience with Microsoft Office tools. Experience with statistics, coding, programming, troubleshooting, and/or data management software is a plus.
Pay range is estimated between $80k - $110k based on skill set and experience.
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

Degree in Chemistry, Biochemistry, Molecular Biology, or related scientific field
experience in gene and cell therapy is a plus.
Hands-on experience with analytical techniques such as UPLC/HPLC, CE-SDS and/or AUC
experience working with MALS and/or CAD detectors is a plus.
Experience with Next-Generation Sequencing (NGS) is a plus.
Experience with Microsoft Office tools.
Experience with statistics, coding, programming, troubleshooting, and/or data management software is a plus.

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.

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies.
We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services.
ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017.

equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce.

ity 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 protecte

This listing is sourced directly from GenScript/ProBio's careers page and normalized into a canonical job model.