Full-Time

Principal Mechanical Engineer

R&D

Updated on 8/1/2026

Deadline 8/1/27
Werfen

Werfen

1,001-5,000 employees

Global specialized diagnostics provider

Compensation Overview

$150k - $185k/yr

+ 401(k) employer match

Bedford, MA, USA

In Person

Some domestic and international travel may be required.

Category
Mechanical Engineering (2)
,
Required Skills
PTC Creo
GD&T
Data Analysis

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Requirements
  • A bachelor's degree in Engineering, Science, or a related field is required.
  • Twelve years of product development or relevant experience are required.
  • Eight or more years of product development or relevant experience are required for candidates with advanced degrees.
  • Internal candidates may substitute demonstrated proficiency in all current-level competencies and an acceptable performance history for the experience requirement.
  • Proficiency in English is required.
  • Some domestic and international travel may be required.
Responsibilities
  • Act as an individual contributor, core team member, or technical lead for a specific project or product line.
  • Complete assigned deliverables in accordance with approved schedules.
  • Author documentation and participate in activities supporting design control.
  • Independently plan, perform, and prioritize complex tasks in alignment with corporate goals.
  • Analyze and interpret data, identify trends, formulate next steps, and perform trade-off analysis when required.
  • Lead, design, or develop new test methods, specifications, technical apparatus, software, or processes for complex components and functions.
  • Evaluate complex designs or processes for acceptability, suitability, and cost, recommend preferred design options, and present trade-offs when required.
  • Identify product defects and outliers in results, and explain and document defects and their impact.
  • Communicate technical information to multidisciplinary teams through documentation, presentations, and technical summaries, and promote collaboration.
  • Maintain technical expertise in more than one area or serve as a subject-matter expert in at least one area.
  • Lead without authority, provide technical guidance to assigned engineers and technicians, and provide mentoring within or outside the department.
  • Provide technical support for or lead CAPA and complaint investigations.
  • Independently generate predictable schedules for functional activities while understanding cross-functional dependencies.
  • Review and provide input on deliverables from other functions when assigned.
  • Recommend and drive improvement initiatives and motivate others to implement them.
  • Assume CAPA ownership when assigned.
Desired Qualifications
  • In vitro medical device experience is highly desired.

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

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Simplify Jobs

Simplify's Take

What believers are saying

  • Oxford Nanopore collaboration strengthens transplant assay validation and faster matching workflows.
  • A 100-territory distributor network accelerates launch of new diagnostic products.
  • €2.2 billion 2024 sales and 7,000 employees support continued platform investment.

What critics are saying

  • Nanopore-enabled workflows can commoditize standalone transplant assays within 12 months.
  • Large-platform rivals like Roche and Abbott pressure pricing through bundled hospital contracts.
  • Regulatory validation demands under IVDR delay specialty assay launches and revenue recognition.

What makes Werfen unique

  • Family-owned since 1966, with direct operations in 30 countries.
  • Specialized diagnostics leader across hemostasis, acute care, transfusion, autoimmunity, and transplant.
  • Barcelona headquarters and U.S.-Europe technology centers support global product development.

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Benefits

Remote Work Options

Company News

TradingView
Mar 10th, 2026
AcouSort receives prepayment of royalties

AcouSort receives prepayment of royalties. AcouSort AB today announced the signing of an amendment to its license and distribution agreement with the leading blood-gas analyzer company, Werfen. Under the amendment, Werfen will prepay minimum royalties for 2027 and 2028. Together with Werfen's regular 2026 minimum royalty, the total sum payable to AcouSort in early 2026 amounts to approximately USD 1.3 million. "Based on our current cash position and this prepayment together with Werfen's regular 2026 minimum royalties alone will fund AcouSort into 2027," said AcouSort's CEO Dr. Torsten Freltoft. The original agreement was signed in spring 2018. Using AcouSort acoustofluidic background technology, the parties jointly developed the solution now implemented in Werfen's groundbreaking GEM Premier 7000 system for point-of-care blood gas analysis. The hemolysis detection in GEM Premier 7000 is based upon patented acoustofluidic technology for plasma separation, combined with photometric determination. In just 45 seconds, the GEM Premier 7000 detects hemolysis, while delivering a complete menu of blood-gas results (pH, pO2, pO2, sodium, potassium, ionized calcium, chloride, glucose, lactate, hematocrit, total hemoglobin, total bilirubin and CO-Oximetry). No other terms of the License and Distribution Agreement with Werfen have been changed. In terms of liquidity, the change takes effect within Q1, while revenue recognition occurs according to applicable accounting principles. This information is information that AcouSort is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact persons set out above, at 2026-03-10 17:30 CET. FOR FURTHER INFORMATION ABOUT ACOUSORT, PLEASE CONTACT: Torsten Freltoft, CEO Telephone: +45 2045 0854 E-mail:[email protected] ABOUT ACOUSORT AcouSort AB (corporate registration number 556824-1037) is an innovative technology company focusing on developing products and solutions for integrated preparation of biological samples. With the help of sound waves, the company's products can separate blood cells, concentrate, purify, and stain cells, exosomes, and bacteria from biological samples. The technology of the company's products is acoustofluidics, where sound waves and microfluidics enable automated handling of samples in a range of application areas, from research on new biomarkers to the development of new diagnostic systems for near-patient testing - so-called Point-of Care (POC) systems. The company's commercialization strategy is based on the already proven business model of providing separation modules to diagnostic system manufacturers for integrated sample preparation as well as to continue the commercialization of the company's research instruments. With the help of the company's products and development of point-of-care tests, new diagnostic systems and treatments are enabled, addressing some of the most challenging disease areas of our time: cancer, infectious diseases, and cardiovascular diseases. AcouSort is listed at Nasdaq First North Growth Market. The company's Certified Adviser is Tapper Partners AB. Attachments AcouSort receives prepayment of royalties

BioTecNika
Jan 5th, 2026
Biological Sciences Manufacturing Job at Werfen North America | Apply now

Biological sciences manufacturing job at Werfen North America | Apply now. Manufacturing Associate role at Werfen North America. Werfen North America is hiring for a Manufacturing Associate 1 position in San Diego, CA. This manufacturing job offers an opportunity to work in a regulated life sciences environment, supporting the production of advanced autoimmune diagnostic products used by clinicians worldwide. The Manufacturing Associate role is ideal for candidates seeking hands-on experience in diagnostic kit manufacturing while working with automated equipment and quality-driven processes. Job details: * Job Title: Manufacturing Associate 1 * Location: San Diego, California * Industry: Life Sciences / Diagnostics Manufacturing * Employment Type: Full-time * Department: Autoimmunity Manufacturing * Salary Range: $25/hr to $30/hr * Team: QUANTA Flash and Aptiva Manufacturing Team About Werfen North America: Werfen North America is a global leader in specialized diagnostics, focusing on autoimmune, hemostasis, acute care, and transfusion medicine. The company is committed to delivering high-quality diagnostic solutions that help healthcare professionals improve patient outcomes. Werfen North America operates under strict quality systems and regulatory standards, ensuring innovation, safety, and reliability across all manufacturing processes. Apply for more similar Manufacturing job offers in the USA. Educational requirements: * Bachelor's degree in biological or related sciences is required * Certificate program or Associate's degree with 3 - 4 years of relevant life sciences laboratory experience may be substituted * Relevant work experience may be considered in place of formal education at management's discretion Key responsibilities for Manufacturing Associate role: * Follow standard operating procedures and work instructions under supervision * Manufacture and test in-process components and diagnostic reagents * Participate in bulking and evaluation of reagents and components * Operate, clean, and maintain manufacturing equipment and instrumentation * Package and fill components according to manufacturing procedures * Maintain accurate Device History Records and related documentation * Assist with evaluation of raw materials when required * Ensure compliance with ISO, FDA, and Quality Management System regulations * Maintain a clean, safe, and organized lab and work environment * Reflect Werfen values in daily work and team interactions Skills required for Manufacturing Associate role: * Basic knowledge of laboratory practices and procedures * Understanding of Good Manufacturing Practices (GMP) * Strong attention to detail and quality standards * Ability to identify product defects or equipment issues * Problem-solving and troubleshooting skills * Effective time management skills * Ability to work collaboratively in a team environment * Willingness to learn and adapt in a regulated manufacturing setting Benefits of the Manufacturing Associate role: * Competitive hourly pay ranging from $25 to $30 per hour * Medical, dental, and vision insurance coverage * 401(k) retirement plan with employer match * Paid vacation and sick leave * Opportunity to work in a highly specialized diagnostic manufacturing environment * Career growth opportunities within Werfen North America

Citybuzz
Sep 9th, 2025
VolitionRx Partners with Werfen to Advance Diagnostic Testing for Antiphospholipid Syndrome

VolitionRx partners with Werfen to advance diagnostic testing for antiphospholipid syndrome.

The Bedford Citizen
Dec 11th, 2024
Werfen Opens New Building for Innovation at U.S. Technology Center on Hartwell Road

Werfen opens new building for innovation at U.S. Technology Center on Hartwell Road.

The Business Journals
Dec 3rd, 2024
Werfen to hire 'hundreds' in next few years as it expands in Bedford

Werfen to hire 'hundreds' in next few years as it expands in Bedford.