Senior Quality Engineer I
Company: Werfen
Location: Bedford
Posted on: May 26, 2025
Job Description:
Job InformationNumber ICIMS-2025-8746 Job function QA&RA Job
type Full-time Location Bedford - 180 Hartwell Road Bedford,
Massachusetts 01730 United States Country United States Shift 1st
About the PositionIntroduction Werfen 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:This position is responsible to ensure that
activities throughout the product lifecycle are in compliance with
procedures, standards and regulations applicable to our products.
The position independently develops, applies, and implements
methods, tools and practices to achieve product quality goals and
requirements in the areas of design, development, production,
distribution, maintenance and service. This is a technically
focused role requiring advanced skills in analyzing information,
reviewing technical reports, promoting process improvement,
requirements development, risk management, product development and
production controls. The position is expected to lead by example in
alignment with the company values to achieve objectives.
Responsibilities Key AccountabilitiesEssential Functions:
- Participates in the generation and review of quality documents
throughout the product lifecycle.
- Advises and directs teams regarding compliance to procedures,
standards and regulations. Implements changes to procedures in
alignment with evolving regulations.
- Ensures product quality meets requirements and documentation is
complete prior to approval.
- Participates on core teams supporting new product development
or design changes.
- Defends relevant quality topics in audits and corrective
actions to improve and maintain compliance of the QMS.
- On projects of significant scope, leads successful
implementation of Design Control and Product Realization
requirements for design, production and distribution of Werfen
products.
- On new product development and or product performance
investigations, provides guidance on most appropriate tools and
techniques available.
- Provides input on product requirements, acceptance criteria,
traceability, process monitoring, product evaluation, failure
investigation and complaint analysis.
- Ensures application of sound statistical methods and quality
tools in the evaluation and documentation of results related to
design control, purchased part qualifications, V&V, risk
analysis, production transfer, production, distribution and
marketing of Werfen products.
- Provides guidance on compliance of software to procedures and
standards including cyber security and privacy requirements
- Works with manufacturing, R&D, Service, Distribution, Sales
& Marketing, and others outside the company (as needed) to
recommend or prepare corrective/preventive actions (CAPA).
- Reviews and approves change orders for product performance,
process changes, labeling and marketing communications as
required.
- May manage and supervise the work of others.
- Leads cross-functional projects on technical and quality
issues.
- Other duties as assigned.Secondary Functions:
- Identifies compliance gaps and takes appropriate corrective
actions as needed
- Defends documents and procedures in internal and external
audits
- Participates in and may lead quality system improvement
projects as required. Budget Managed (if applicable):
- N/A Internal Networking/Key Relationships:To be determined
based on department needs, to include interactions such as:
- Works closely with other functions to generate compliant
documents by interpreting and explaining quality procedures,
applicable standards, regulations and best practices.
- Able to effectively communicate quality requirements to a broad
population of constituents.
- Ability to negotiate and influence others in establishing
direction toward improved quality and enhanced compliance. Skills &
Capabilities:The ideal candidate for this position will exhibit the
following skills and capabilities:
- Working knowledge of domestic and international
quality/regulatory standards related to our products
- Knowledge of quality management techniques (Lean, Six Sigma)
and statistical techniques required to measure and confirm
significant changes.
- Working knowledge of Werfen products, technology and
manufacturing processes including impact on customers and patient
requirements.
- Demonstrates judgement commensurate with experience regarding
application of regulatory requirements to data review, reports,
design changes, risk management, etc. to ensure compliance and
achieving business objectives. Demonstrated understanding of risk
based approach to processes and decisions. Competencies:
- Attention to Detail: Ability to pay close attention to detail
is required
- Accuracy: Work is accurate and complete
- Performance Standards: Demonstrated ability to meet department
goals
- Communication: Excellent written, verbal and presentation
skills
- Discretion: Acts with integrity in all situations and can
maintain appropriate confidentiality
- Multi-Tasking: Ability to manage multiple priorities, and
support changing business needs
- Collaboration: Ability to work within a multi-function team to
bring best solutions to the team or customer
- Independence: self-motivated-works under minimal
supervision
- Professionalism: Must demonstrate professionalism during all
interactions within company, customer and third parties
Qualifications Minimum Knowledge & Experience Required for the
Position: Education:
- Bachelor's degree or equivalent in engineering or
scienceExperience:
- A minimum of 8 years of experience in medical devices,
pharmaceuticals, diagnostic industry, or clinical laboratory or 5
years of experience with an advanced degreeAdditional
Skills/Knowledge:
- Duties necessitate broad and thorough knowledge of engineering
and science theory and principles, including R&D, quality
control, manufacturing and design engineering
- Understanding of the application of technical principles and
engineering problem solving to resolve complex issues.
- ASQ Quality Engineering Certification - Desirable
- LEAN/Six Sigma Certification - Desirable International
Mobility:
- Required: NoTravel Requirements:
- Approximately 10% of time 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 NAtalentacquisition@werfen.com 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 Required
Keywords: Werfen, Cambridge , Senior Quality Engineer I, Engineering , Bedford, Massachusetts
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