W

Werfen

Global specialized diagnostics provider

Microbiologist / Program Coordinator

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeOrangeburg, NY, USA

About the Job

Requirements

  • A B.S. degree in microbiology or equivalent is required; an advanced degree is preferred.
  • Apply broad scientific principles, theories, and concepts in microbiology.
  • Demonstrated success developing similar programs in industrial settings such as food-processing plants, pharmaceuticals, or equivalent.
  • Experience in a regulated environment is a plus.
  • Ability to perform benchwork.
  • Knowledge of Microsoft Office.
  • SAP experience is preferred.
  • Strong communication and written skills.
  • Ability to travel when required to support microbial assessments of raw materials and product failure investigations.

Responsibilities

  • Develop and execute a comprehensive program to monitor and manage microbiological control across manufacturing processes, identifying and driving improvements to equipment, facilities, and procedures to ensure quality standards.
  • Develop a systematic microbial-control program for the facility, including a cleaning and sanitation program for the plant and equipment.
  • Develop and implement a testing regimen to tightly control microbial and fungal loads in the plant and equipment.
  • Develop a similar program with key suppliers where necessary.
  • Perform day-to-day microbiological testing.
  • Plan and conduct advanced scientific assignments requiring leadership and mastery of specialized techniques.
  • Apply the scientific method and experimental design to problem solving, using scientific expertise to solve problems requiring technical expertise.
  • Define mid-to-long-term objectives and implement plans to accomplish them.
  • May direct the work of other scientists.
  • Maintain accurate and precise documentation; write reports and technical summaries and may represent the company to outside organizations.
  • Maintain comprehensive knowledge of scientific literature and industry best practices concerning microorganism biology, sanitization from production processes and equipment, and preservatives applicable to IVD products.
  • Handle broad assignments and objectives under minimal direction to accomplish short-term goals.
  • Maintain work in a GMP environment.
  • Perform other related duties as directed by the manager.

Desired Qualifications

  • An advanced degree is preferred.
  • Experience in a regulated environment is a plus.
  • SAP experience is preferred.

About the Company

Werfen

Global specialized diagnostics provider

Werfen focuses on in vitro diagnostics, offering specialized diagnostic solutions for healthcare. It provides tests and instruments for areas like hemostasis (blood clotting), acute care diagnostics, and autoimmunity, used by clinical laboratories to detect and monitor diseases. The company's products combine diagnostic assays, reagents, and instrumentation that run in laboratory workflows to produce actionable patient results. Werfen differentiates itself through its long-standing family-owned heritage, strategic growth including the 1991 acquisition of Instrumentation Laboratory, and a global footprint that spans 30 countries with active presence in more than 100 territories. The goal is to improve patient care by expanding access to accurate, high-quality diagnostic tools and services while maintaining a strong commitment to quality and specialized solutions.

Company size
1,001-5,000
Company stage
Debt Financing
Total funding
$550M
Headquarters
Barcelona, Spain
Founded
1966

Recently Posted Jobs

Explore more opportunities at Werfen

See more jobs