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. We operate directly in 30 countries and in more than 100 territories through distributors.
Our Headquarters are in Barcelona Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded 2.2 billion in 2024 and our workforce is more than 7000 strong.
JOB SUMMARY
The Scientist II in the Assay Development department is an IVD-experienced professional expected to contribute to development projects by applying technical expertise in assay design execution and problem-solving supporting activities from feasibility through validation.
Performs a broad range of laboratory work requiring application of professional judgment in the selection of specialized methods and techniques and their application to specific tasks. Provides project updates. Performs duties in research and development including the ability to perform specialized lab techniques and good laboratory documentation practices.
Key Accountabilities
Performs an expanded range of laboratory procedures and experiments.
Periodically communicates problems and progress to supervisor.
Occasionally communicates status updates and results across the organization.
Presents results to senior/other research staff.
Selects appropriate experimental and analytical methods and define protocols.
Schedules own and team tasks and activities in accordance with assignments and priorities.
Detects deviations in results and potential problems recommends modification in protocols or standard methodology to define the causes of deviations and overcome problems.
Under the supervision and approval of his/her supervisor writes specialized laboratory procedures and reviews existing Procedures and Methods.
Compiles and interprets experimental data performs calculations and prepares graphs to present and discuss them to his/her supervisor.
Writes research papers reports reviews and technical summaries.
Review electronic or paper laboratory notebook making sure that all data is accurately recorded in accordance with guidelines and procedures.
Must be capable of performing all duties required of a Scientist I.
Networking/Key relationships
To be determined based on department needs to include interactions such as:
Mainly with R&D Quality and Operations colleagues
Minimum Knowledge & Experience required for the position:
Educatoin
Required: Bachelors degree (Diplomatura) in the biological or related sciences.
Degree may be substituted by relevant skills and work experience
Valuable: Any additional degree higher than that required in the previous section
Experience:
Four (4) years previous scientific/in vitro diagnostic research experience required.
Valuable: experience in particle-based turbidimetric and/or chemiluminescent immunoassays.
Additional Skills/Knowledge:
Laboratory experience.
Basic knowledge of biological and chemical laboratory procedures. Ability to operate laboratory equipment.
Knowledge of basic software tools (Excel Word PowerPoint). Knowledge of SAP preferred.
Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading speaking and writing).
Skills & Capabilities:
Attention to detail and accuracy.
Able to apply general scientific methods and theoretical knowledge to tasks within one area of expertise.
Teamwork and interpersonal skills. Flexibility in order to work with and provide support for a number of people.
Oral and written communication skills.
Time management skills. Excellent organizational and multi-tasking skills.
Thorough knowledge of design control processes and familiarity with quality standards as required.
Excellent analytical skills.
Able to work independently on the project with moderate guidance.
Well organized able to handle large data sets and communicate results problems and progress to the supervisor and within the group as required.
Ability to adapt to R&D flexible and changing environment.
Certain troubleshooting ability required.
Reflects values of Werfen and OEM in the quality of work and working relationship.
Travel requirements:
Sporadic travel or short-term assignment to an external lab may be required
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. We operate directly in 30 countries and in more than 100 territories ...
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. We operate directly in 30 countries and in more than 100 territories through distributors.
Our Headquarters are in Barcelona Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded 2.2 billion in 2024 and our workforce is more than 7000 strong.
JOB SUMMARY
The Scientist II in the Assay Development department is an IVD-experienced professional expected to contribute to development projects by applying technical expertise in assay design execution and problem-solving supporting activities from feasibility through validation.
Performs a broad range of laboratory work requiring application of professional judgment in the selection of specialized methods and techniques and their application to specific tasks. Provides project updates. Performs duties in research and development including the ability to perform specialized lab techniques and good laboratory documentation practices.
Key Accountabilities
Performs an expanded range of laboratory procedures and experiments.
Periodically communicates problems and progress to supervisor.
Occasionally communicates status updates and results across the organization.
Presents results to senior/other research staff.
Selects appropriate experimental and analytical methods and define protocols.
Schedules own and team tasks and activities in accordance with assignments and priorities.
Detects deviations in results and potential problems recommends modification in protocols or standard methodology to define the causes of deviations and overcome problems.
Under the supervision and approval of his/her supervisor writes specialized laboratory procedures and reviews existing Procedures and Methods.
Compiles and interprets experimental data performs calculations and prepares graphs to present and discuss them to his/her supervisor.
Writes research papers reports reviews and technical summaries.
Review electronic or paper laboratory notebook making sure that all data is accurately recorded in accordance with guidelines and procedures.
Must be capable of performing all duties required of a Scientist I.
Networking/Key relationships
To be determined based on department needs to include interactions such as:
Mainly with R&D Quality and Operations colleagues
Minimum Knowledge & Experience required for the position:
Educatoin
Required: Bachelors degree (Diplomatura) in the biological or related sciences.
Degree may be substituted by relevant skills and work experience
Valuable: Any additional degree higher than that required in the previous section
Experience:
Four (4) years previous scientific/in vitro diagnostic research experience required.
Valuable: experience in particle-based turbidimetric and/or chemiluminescent immunoassays.
Additional Skills/Knowledge:
Laboratory experience.
Basic knowledge of biological and chemical laboratory procedures. Ability to operate laboratory equipment.
Knowledge of basic software tools (Excel Word PowerPoint). Knowledge of SAP preferred.
Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading speaking and writing).
Skills & Capabilities:
Attention to detail and accuracy.
Able to apply general scientific methods and theoretical knowledge to tasks within one area of expertise.
Teamwork and interpersonal skills. Flexibility in order to work with and provide support for a number of people.
Oral and written communication skills.
Time management skills. Excellent organizational and multi-tasking skills.
Thorough knowledge of design control processes and familiarity with quality standards as required.
Excellent analytical skills.
Able to work independently on the project with moderate guidance.
Well organized able to handle large data sets and communicate results problems and progress to the supervisor and within the group as required.
Ability to adapt to R&D flexible and changing environment.
Certain troubleshooting ability required.
Reflects values of Werfen and OEM in the quality of work and working relationship.
Travel requirements:
Sporadic travel or short-term assignment to an external lab may be required
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