QC Analyst I

Werfen; Orangeburg (NY); On-site; USD 30,000 - 33,000; Full time

Job summary

Werfen is a global diagnostics company seeking a laboratory analyst for the Orangeburg, NY area. The role involves performing automated and manual assays in Clinical Chemistry, Co-Oximeter, Coagulation and Microbiology contexts as per GMP requirements.

Responsibilities include interpreting results, maintaining strict documentation, and conducting stability and environmental testing. Occasional maintenance and calibration of lab equipment are expected in a fast-paced environment.

Qualifications

• Associates Degree in Science or Medical Technology or equivalent required.

Responsibilities

• Performs automated and manual assays as detailed in SOPs and QC Monographs, including raw material, in-process and finished product.
• Interprets test results against specifications and decides if assays pass or fail.
• Maintains documentation of all work performed in accordance with GMP requirements.
• Performs product stability, proficiency and environmental testing (Orangeburg).
• Responsible for routine preventive maintenance, general troubleshooting, general cleanliness and calibration of Lab equipment

Skills

Functional/technical skills

Education

Associates Degree in Science or Medical Technology or equivalent

Job description

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Overview

Position Summary

Performs analyses of Clinical Chemistry, Co-Oximeter, Coagulation and/or Microbiology controls and reagents using various automated and manual techniques in accordance with established Quality and GMP requirements.

Responsibilities

Key Accountabilities

Essential Functions

• Performs automated and manual assays as detailed in departmental/plant SOP's and QC Monographs, including raw material, in-process and finished product.
• Interprets test results against specifications and decides if assays pass or fail.
• Maintains documentation of all work performed in accordance with GMP requirements.
• Performs product stability, proficiency and environmental testing (Orangeburg).
• Responsible for routine preventive maintenance, general troubleshooting, general cleanliness and calibration of Lab equipment

Budget Managed (if Applicable)

• N/A

Internal Networking/Key Relationships

• To be determined based on department needs

Skills & Capabilities

• Functional/technical skills

Qualifications

Min Knowledge & Experience Required for the Position

• Associates Degree in Science or Medical Technology or equivalent required.

Physical Requirements

• This position requires the ability to lift and move materials per current OSHA standards.

International Mobility Required

• No

Travel Requirements

• No

The hourly wage range Werfen reasonably expects to pay for the position is $22 to $24. Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business.

Werfen is an Equal Opportunity employer and is committed to a diverse workplace.

Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact [e-mail] for assistance.

We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.

www.werfen.com