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HomeCompaniesCareers Werfen Icims ComBiospecimen Specialist II

Biospecimen Specialist II

Careers Werfen Icims Com · Bedford, MA, US · Active · $70,000–$100,000 / day · iCIMS

Job facts

FieldValue
CompanyCareers Werfen Icims Com
TitleBiospecimen Specialist II
Normalized title-
Department / teamR&D
LocationBedford, MA, United States
Work model-
Employment typeFull Time
Salary$70,000–$100,000 / day
Statusactive
ATS provideriCIMS
Posted / first seen2024-06-20 / 2026-06-17
Changed / last seen2026-06-20 / 2026-06-20

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PageWhat it containsOpen
Company jobsActive postings from Careers Werfen Icims Com.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through iCIMS.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Bedford.Open
Department jobsActive postings in R&D.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyCareers Werfen Icims Com
Sourcead6dc023-8cbc-4355-a416-f4db8c71ddc9
ATS provideriCIMS

Description

Introduction 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 Job Summary Laboratory-focused role combining technical experience with project coordination skills. Coordinates collection, testing, and storage of biospecimens and their associated data for designated projects within the Biobanking group that support Biobanking operations, quality, and compliance. May support product development efforts of diagnostic instruments and reagents. Responsibilities Key Accountabilities Together with management, develops, implements, and monitors standard operating procedures (SOP) in the Biobanking Laboratory. Responsible for developing protocols for handling, testing, and creation of Biobank specimens in accordance with good laboratory practices (GLP) and proper scientific methods. Organizes and communicates with phlebotomists to collect, process and test human plasmas according to design specifications. Creates schedule for testing and characterization of blood samples in response to stakeholder needs in collaboration with biospecimen specialist(s) Responsible for regular review of sample and reagent quality and inventory; communicates inventory status and characterization to management. Provides recommended solutions where possible. May be responsible for long-term planning projects, requiring sample and reagent management design and execution. For assigned projects, responsible for maintaining specimen clinical and laboratory data in biobank database to facilitate proper categorization of samples with critical focus on data entry, data oversight, and data reconciliation. Collaborates with statisticians and scientists for data processing and data analysis activities to ensure quality standards are met. Delivers and communicates assigned project results in a succinct and timely manner to team members and cross-functionally, as needed; together with management, prepares technical documentation and reports as required. Coordinate with key vendors, internal supplier(s), to facilitate core lab functions / requirements (instrument maintenance). Other duties and/or projects as assigned. Networking/Key relationships R&D (Coagulation Analytical & Critical Care Teams). Biobanking and/or Phlebotomists at other Werfen Technology Centers. External Vendors – Commercial / Internal Suppliers. Qualifications Minimum Knowledge & Experience for the position: Bachelor’s degree in biology, biochemistry, chemistry or related scientific discipline or Medical Laboratory Science required. Minimum of 3 years’ experience in a clinical or research laboratory required; preferably in biospecimen handling and operational experience. Working knowledge in specimen handling and laboratory techniques required. Experience with Laboratory Information Management Systems (LIMS) and regulatory standards such as HIPAA required. Minimum of 3 years’ experience working with project management and database management tools, strongly preferred. Technical knowledge of automated clinical systems and assays preferred. Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement. Skills & Capabilities: Strong written and verbal communications skills Strong computer skills utilizing word processing, spreadsheets, databases, and email software. Proven experience providing excellent customer service to stakeholders and research collaborators. Ability to work independently, managing multiple priorities and/or project streams. Critical attention to detail. Strong organizational and time management skills; ability to handle complex procedures in tandem with project workload. Ability to apply critical thinking and problem-solving skills independently. Travel requirements: Up to 5% of the time. Occasional travel to other Werfen sites may be required. The annual salary range Werfen reasonably expects to pay for the position is $70,000 to $100,000. Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. 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 [email protected] 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

Full job record

Job IDd6d480e7c1792733bad678b9bde5bcc2de63d9bd
Org ID06122b82-5976-4a14-b66d-a0c2822cc06a
Source IDad6dc023-8cbc-4355-a416-f4db8c71ddc9
Board IDad6dc023-8cbc-4355-a416-f4db8c71ddc9
Providericims
Provider Job Key10469
TitleBiospecimen Specialist II
Normalized Title
Statusactive
Activeyes
Location TextBedford, MA, US
DepartmentR&D
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionMA
CityBedford
Salary RawIntroduction 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 Job Summary Laboratory-focused role combining technical experience with project coordination skills. Coordinates collection, testing, and storage of biospecimens and their associated data for designated projects within the Biobanking group that support Biobanking operations, quality, and compliance. May support product development efforts of diagnostic instruments and reagents. Responsibilities Key Accountabilities Together with management, develops, implements, and monitors standard operating procedures (SOP) in the Biobanking Laboratory. Responsible for developing protocols for handling, testing, and creation of Biobank specimens in accordance with good laboratory practices (GLP) and proper scientific methods. Organizes and communicates with phlebotomists to collect, process and test human plasmas according to design specifications. Creates schedule for testing and characterization of blood samples in response to stakeholder needs in collaboration with biospecimen specialist(s) Responsible for regular review of sample and reagent quality and inventory; communicates inventory status and characterization to management. Provides recommended solutions where possible. May be responsible for long-term planning projects, requiring sample and reagent management design and execution. For assigned projects, responsible for maintaining specimen clinical and laboratory data in biobank database to facilitate proper categorization of samples with critical focus on data entry, data oversight, and data reconciliation. Collaborates with statisticians and scientists for data processing and data analysis activities to ensure quality standards are met. Delivers and communicates assigned project results in a succinct and timely manner to team members and cross-functionally, as needed; together with management, prepares technical documentation and reports as required. Coordinate with key vendors, internal supplier(s), to facilitate core lab functions / requirements (instrument maintenance). Other duties and/or projects as assigned. Networking/Key relationships R&D (Coagulation Analytical & Critical Care Teams). Biobanking and/or Phlebotomists at other Werfen Technology Centers. External Vendors – Commercial / Internal Suppliers. Qualifications Minimum Knowledge & Experience for the position: Bachelor’s degree in biology, biochemistry, chemistry or related scientific discipline or Medical Laboratory Science required. Minimum of 3 years’ experience in a clinical or research laboratory required; preferably in biospecimen handling and operational experience. Working knowledge in specimen handling and laboratory techniques required. Experience with Laboratory Information Management Systems (LIMS) and regulatory standards such as HIPAA required. Minimum of 3 years’ experience working with project management and database management tools, strongly preferred. Technical knowledge of automated clinical systems and assays preferred. Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement. Skills & Capabilities: Strong written and verbal communications skills Strong computer skills utilizing word processing, spreadsheets, databases, and email software. Proven experience providing excellent customer service to stakeholders and research collaborators. Ability to work independently, managing multiple priorities and/or project streams. Critical attention to detail. Strong organizational and time management skills; ability to handle complex procedures in tandem with project workload. Ability to apply critical thinking and problem-solving skills independently. Travel requirements: Up to 5% of the time. Occasional travel to other Werfen sites may be required. The annual salary range Werfen reasonably expects to pay for the position is $70,000 to $100,000. Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. 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 [email protected] 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
Salary Min70,000
Salary Max100,000
Salary CurrencyUSD
Salary Periodday
Source URLhttps://careers-werfen.icims.com/jobs/10469/biospecimen-specialist-ii/job
Apply URLhttps://careers-werfen.icims.com/jobs/10469/biospecimen-specialist-ii/job
First Seen At2026-06-17 08:36:24Z
Last Seen At2026-06-20 08:36:28Z
Last Checked At2026-06-20 08:36:28Z
Last Changed At2026-06-20 08:36:28Z
Inactive At
Source Posted At2024-06-20 08:36:25Z
Source Updated At2026-06-16 16:12:04Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=careers-werfen.icims.com/date=2026-06-20/2026-06-20T08-36-24-710Z-15b2cb4c3d0e2c3df569356a53d26c80448860fe1e118bf056a7f77c65f6c1d6.json
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