Associate Scientist II, Process Development

@ LGC Group

Company Overview

LGC’s Diagnostics & Genomics Division develops and manufactures a comprehensive portfolio of diagnostic quality solutions and component materials, as well as integrated genomic products and services supporting the entire genomic workflow including nucleic acid sample preparation, oligos, probes, primers, sequencing cloning, protein expression, PCR instruments, reagents, and consumables. We serve IVD assay developers, pharmaceutical, CRO and academic institutions from early-stage research to routine clinical use.

Position Overview - Associate Scientist II, Process Development

As an Associate Scientist II in Process Development at LGC Group, based in Middleton, United States, you will assist in improving procedures in efficiency, quality, and robustness across various processes such as enzymes, competent cells, next-generation sequencing kits, and analytical testing. You will be involved with tech transfer, process development, and other duties as assigned by management.

Key Responsibilities

• Assist in cell line creation, upstream/downstream manufacturing, formulation and analytical development.
• Process, record, analyze, and report data using good documentation practices.
• Develop batch record and test method templates, SOPs for manufacturing and quality control.
• Prepare stability reports and aid in investigations of process deviations and non-conformances.
• Continuously improve control strategies following a Quality by Design framework.
• Communicate technical results to both technical and non-technical audiences.

Qualifications

• Bachelor’s degree in a relevant life-sciences field (or equivalent industry experience).
• Experience in manufacturing, quality control, or technical teams.
• Proficiency in biologics production processes and standard analytical techniques.
• Strong ability to follow SOPs and work instructions.
• Proficiency in Microsoft Office suite, especially Outlook, Word, and Excel.

Preferred Qualifications

• Experience with process and analytical equipment (e.g. Cytiva & Sartorius systems).
• Experience in drafting manufacturing production records and SOPs.
• Knowledge of GMP and ISO 13485 quality systems.

What We Offer

Competitive compensation with bonus programs, comprehensive medical/dental/vision benefits, FSA/HSA plans, insurance programs, 401(k) with matching, flexible work options, pet insurance, improved parental leave, immediate PTO, town hall meetings, social events and more.

Key skills/competency

• Process Development
• Analytical Skills
• Quality Systems
• Manufacturing
• Biologics
• Documentation
• Cell Culture
• NGS
• SOP Development
• Data Analysis