Eurofins Lancaster Laboratories

RNA-LNP Process Development - Lab Coordinator

Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S./MS degree in biological sciences, chemistry, or biomedical/chemical engineering with at least 3 years of relevant lab experience
  • Experience operating and maintaining Atka Avant and Agilent HPLC systems
  • Knowledge of inventory management systems and buffer preparation
  • Strong understanding of lab operations and safety protocols
  • Excellent organizational skills and attention to detail
  • Self-motivated problem solver able to manage multiple priorities
  • Proficiency in MS Office Suite
  • Ability to coordinate with various stakeholders including scientists and vendors

Responsibilities

  • Maintain a safe and high-performing laboratory environment
  • Support continuous improvement initiatives for lab operations
  • Build and manage inventory systems for raw materials and consumables
  • Prepare and document buffers, reagents, and stock solutions
  • Track and maintain laboratory equipment through an established maintenance program
  • Perform routine analytical tests to support RNA technology processes
  • Contribute to SOPs and track lab efficiency metrics
  • Collaborate with external vendors and cross-functional teams

Benefits

  • Comprehensive medical, dental, and vision coverage
  • Life and disability insurance
  • 401(k) plan with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonuses and merit-based increases
Full Job Description
We are seeking a Lab Manager to support a LNP and RNA Process Development team. The successful candidate will have a passion for driving efficient lab operations through excellence in la equipment maintenance, raw material inventory management, and execution of routine analytical assays. The successful candidate will have a desire to contribute to a team focused on establishing science-based manufacturing solutions for complex nucleic acid-based products. - Maintain a safe and high performing laboratory. - Support continuous improvement initiatives related to lab operations. - Build and maintain process development specific raw material and consumables inventory systems. - Prepare buffers, reagents, and stock solutions used for process development activities, following established recipes. - Maintain detailed preparation records in an electronic lab notebook (ELN). - Assist with routine maintenance tracking and upkeep of laboratory equipment used in process development. - Build and maintain equipment maintenance program. for Agilent HPLC, Akta Avant preparative liquid handling, and capillary gel electrophoresis (CGE) systems. - Opportunity to perform routine analytical tests to support understanding of RNA technology and processes; analytical assays include HPLC, CGE, and ELISA-based methods. - Opportunity to write lab maintenance protocols, SOPs, contribute to the weekly lab operations meeting, and track and analyze lab efficiency metrics. - Opportunity to collaborate with external vendors and cross-functional teams including analytical development, as well as the facilities and operations team. Qualifications Minimum Required Qualifications: - B.S./MS degree in biological sciences, chemistry, or biomedical/chemical engineering (or related field) with at least 3 years of relevant industry laboratory experience - Experience with the operation and maintenance of equipment commonly used in the process development of nucleic acids, including Atka Avant chromatography systems and Agilent HPLC systems. - Knowledge of inventory management systems and reagent/buffer preparation best practices. - Strong understanding of laboratory operations and safety protocols. - Proven ability to manage multiple priorities and work independently. - Excellent organizational skills and attention to detail. - Self-motivated with the ability to identify and solve problems proactively. - Ability to coordinate with scientists, vendors, and service providers. - Proficiency with MS Office Suite (Word, PowerPoint, Excel). - Strong work ethic and excitement for being part of an integrated operations team. - Must be able to work in an active lab environment. Preferred Qualifications: - Knowledge of nucleic acid (mRNA, gRNA), LNP, and/or biologics process development. - Knowledge of analytical methods used for nucleic acid and/or biologics process development, including HPLC, CGE, or ELISA experience. - Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information The position is full-time, Monday-Friday, 8am-5pm with overtime as needed. Candidates living within a commutable distance of Boston, MA are encouraged to apply. Excellent full-time benefits include: - Comprehensive medical coverage, dental, and vision options - Life and disability insurance - 401(k) with company match - Paid vacation and holidays - Eligibility for yearly goal-based bonus & merit-based increases - Compensation: $36.00-$42.00 per hour

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry

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