Eurofins Lancaster Laboratories

Pharmaceutical Manufacturing Support Engineer

Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BS in Biomedical Engineering or relevant field with 5 years of experience (co-ops/internships included); MS with 2 years preferred
  • Experience in GxP automation equipment lifecycle management
  • Knowledge in GxP Fill/Finish applications
  • Proficiency in sensors, circuit design, and automation control systems preferred
  • Demonstrated experience in biologics within the pharmaceutical sector

Responsibilities

  • Lead equipment qualification activities per industry standards for drug product manufacturing
  • Drive technical discussions to solve equipment and project-related issues
  • Design and implement automation for competitive manufacturing operations
  • Advance technical understanding of process impacts on drug products
  • Support Fill/Finish activities for stability batch production and continuous improvement efforts
  • Develop process engineering skills, including multiphysics software and statistical analysis

Benefits

  • Comprehensive medical, dental, and vision coverage
  • Life and disability insurance
  • 401(k) plan with company match
  • Paid vacation and holidays
Full Job Description
  • Lead equipment qualification activities according to industry standards to support drug product pharmaceutical manufacturing and R&D activities.
  • Lead, facilitate, and participate in technical discussions to successfully resolve problems with equipment suppliers, methods, project issues, and deviations.
  • Design, develop and deploy automation within manufacturing unit operations to ensure competitiveness and organizational excellence.
  • Progress the technical understanding of process impact on drug product, ensuring consistent scientific excellence and scientific quality standards are met.
  • Lead, support, and contribute to internal Fill/Finish activities in support of Lead Stability Development batch manufacturing. Responsible for ongoing production and continuous improvement initiatives.
  • Opportunity to develop process engineering skills including the use of multiphysics software for process modeling and the statistical analysis of data.


Qualifications

Education:
  • Minimum of a BS in Biomedical Engineering or relevant engineering concentration with 5 years of experience (including co-op, internships or industry experience) is required. MS with 2 years of work experience is preferred.

Qualifications:
  • Experience in GxP automation equipment commissioning, qualifications, and life-cycle management are required.
  • Experience and knowledge in GxP Fill/Finish applications is required
  • Proficiency in sensors and signal conditioning, circuit design/analysis and automation control systems are preferred.
  • Proven proficiency and experience in biologics (mAbs, gene therapies, cell therapies, etc.) within the pharmaceutical industry with a high level of technical understanding are preferred.
  • Effective communication skills by delivering information across multifunctional groups/sites and demonstrated leadership in providing integration of activities s are required.

Authorization to work in the United States indefinitely without restrictions or sponsorship

Additional Information

Position is full-time, Monday-Friday, generally 8 a.m. - 5 p.m., weekend work might be expected. Candidates currently living within a commutable distance of Malvern, PA 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

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

Similar Jobs

More Jobs at Eurofins Lancaster Laboratories

More Pharmaceuticals & Biotech Jobs

Find similar Pharmaceutical Manufacturing Support Engineer jobs: