New · posted Oct 15
QuidelOrtho · Medical Devices
Quality Lead Design Transfer & Tech Transfer Strategy
- Rochester, NY
- On-site
- Full-time
- Senior & Principal
Open until filled
The role
QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic.
Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.
As we continue to grow as one QuidelOrtho we are seeking a Quality Lead, Design and Tech Transfer Strategy (Assay). The Design and Tech Transfer Strategy Quality Lead is a global individual contributor within QuidelOrtho' s Global Quality & Compliance (GQ&C) organization. This individual is responsible to ensure the design, implementation, and continuous improvement of Quality systems, processes, and programs that enable QuidelOrtho' s Right to Operate and support business agility, innovation, and growth.
The Quality Lead Engineer for Design & Technology Transfer Strategy (Assay) serves as a senior technical leader within the Quality organization, responsible for driving robust, compliant, and efficient design transfer and technology transfer strategies for invitro diagnostic (IVD) assays. This role partners closely with cross functional teams—including R&D, Tech Transfer, Design Quality, and Operations—to ensure that new products and process changes are transferred seamlessly into manufacturing with full adherence to global regulatory expectations. The Quality Lead provides authoritative interpretation of quality and regulatory requirements, deep product and process expertise, and proactive quality oversight to enable successful commercialization, lifecycle changes, and global inspection readiness.‑vitro diagnostic (IVD) assays. This role partners closely with cross‑functional teams—including R&D, Tech Transfer, Design Quality, and Operations—to ensure that new products and process changes are transferred seamlessly into manufacturing with full adherence to global regulatory expectations.
This individual is responsible for fostering a culture of engagement, collaboration, and performance. By integrating technical expertise and data-driven insights, the Principal Quality Partner ensures that Quality systems deliver sustainable business and compliance outcomes.
This position will be onsite in Rochester, NY or Raritan, NY.
The Individual
Required:
Bachelor’s degree in Life Sciences, Engineering, or a related technical discipline required.
10+ years of progressive experience in Quality, Compliance, or related fields within the Medical Device, IVD, or Biopharmaceutical industries
Strong understanding of Quality System regulations and standards, including ISO 13485, FDA 21 CFR 820, and IVDR.
Strong product and process knowledge relevant to assay development, verification/validation, and manufacturing workflows.
Demonstrated success driving Quality and Compliance initiatives that align with business strategy and regulatory expectations.
Excellent collaboration, influence, and communication skills across functional and organizational boundaries.
Strong analytical and problem-solving skills, with experience using data to drive decision-making and improvement.
Commitment to scientific integrity, compliance excellence, and continuous improvement.
Expert-level knowledge of Design Transfer and Technology Transfer for IVD assays, including process readiness, scale‑up, and transfer of product requirements into manufacturing.
Deep understanding of IVD regulatory and quality system requirements, such as ISO 13485, IVDR, FDA QSR, risk management (ISO 14971), and design control principles.
Strong product and process knowledge relevant to assay development, verification/validation, and manufacturing workflows.
Ability to interpret complex regulatory requirements and translate them into actionable design transfer and quality strategies.
Demonstrated experience evaluating process capability, process controls, and design outputs to ensure manufacturability and compliance.
Preferred:
Strong analytical and systems‑thinking skills to evaluate end‑to‑end product realization pathways.
Ability to anticipate risks in design transfer and proactively implement mitigation strategies.
Advanced degree (MS, PhD, MBA, or equivalent) in a relevant discipline.
Experience implementing or optimizing global Quality Management Systems (QMS) and digital tools.
Lean Six Sigma, PMP, or similar certification demonstrating process improvement expertise.
Experience supporting or leading Health Authority or Notified Body inspections.
Key Interactions
Internal: Tech Transfer, Operations, Supply Chain, R&D, Commercial, Regulatory Affairs, and other Quality & Compliance teams globally and regionally
External: Regulatory agencies, Notified Bodies, Contract manufacturers, Suppliers, and service providers.
How We Work
At QuidelOrtho, our culture is shaped by four core behaviors that guide how we collaborate, make decisions, and support each other and those we serve. The ideal candidate will exhibit these behaviors, as we believe they’re essential to how we thrive as a team and achieve meaningful impact:
Thrive Together – Collaborate intentionally, grow as a team
Make It Happen – Focus on priorities, embrace continuous improvement
Commit to Service – Cultivate a service mindset
Embrace Inclusion – Be open and authentic, welcome diverse perspectives
What you need
What you'll do
Serve as the primary Quality partner to the Technology Transfer team, providing strategic guidance and oversight throughout assay design transfer and tech transfer activities.
Lead development and execution of comprehensive design transfer and technology transfer quality strategies that ensure compliant, sustainable product realization.
Collaborate with Design Quality, Quality Operations, R&D, and Manufacturing teams to ensure alignment on design transfer deliverables, risk management, and process capability expectations.
Provide expert interpretation of applicable global regulatory and quality system requirements (e.g., ISO 13485, IVDR, FDA QSR) as they relate to design transfer, process transfer, verification/validation, and manufacturing readiness.
Apply deep product and process knowledge to assess transfer risks, guide process understanding, and ensure adequate controls are defined and implemented during scale‑up.
Support global audit and inspection activities as a subject matter expert and auditee for design transfer, tech transfer, and related quality system elements.
Proactively identify quality gaps, systemic risks, and continuous improvement opportunities within design transfer frameworks and lead cross-functional teams to implement solutions.‑improvement opportunities within design transfer frameworks and lead cross-functional teams to implement solutions.
Mentor engineers and contribute to development of organizational capability in design transfer strategy and regulatory compliance.
Perform other work-related duties as assigned.
Pay and benefits
$135,000 – $175,000 a year
Employer providedSalary Transparency
Salary range for this position takes into account a wide range of factors including: education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on that facts and circumstances of each case. Salary range for this position is $135,000 to $175,000 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time) and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.
Medical, dental, and vision insurance
Life and disability insurance
401(k) plan
Employee Stock Purchase Plan
Paid time off and paid holidays
Employee assistance program
Where you'll work
Rochester, NYOn-siteOpen in Maps (opens in a new tab)
More jobs in Rochester, NYWorking conditions
The work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment.
No strenuous physical activity required. May include occasional travel for site visits, leadership meetings, or regulatory support.
Equal opportunity, accessibility and legal noticesQuidelOrtho's statements, word for word
Equal Employment Opportunity
QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at [email protected].
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 26% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Senior & Principal roles in New York14 roles publishing pay
Senior & Principal roles in the US284 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $135,000 | — | $175,000 |
| New York (middle half) | $68,000 | $84,750 | $114,875 |
| All US (middle half) | $103,375 | $122,750 | $137,500 |
This role: QuidelOrtho's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not QuidelOrtho's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 43 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk13
- Collaboration and leadership13
- GMP and compliance12
- Lab testing and methods9
- Regulatory submissions4
- Validation and qualification3
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- European UnionEU IVDR (Regulation 2017/746)(official source, opens in a new tab)The EU In Vitro Diagnostic Medical Devices Regulation
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Risk management for medical devices
Company hiring pulse
QuidelOrtho on Regulatory Jobs
- 3
- Open roles
- 3
- Distinct roles
- 2
- Locations
By discipline
- Quality2 67%
- Regulatory1 33%
By level
- Senior & Principal2 67%
- Manager1 33%
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Quality Lead Design Transfer & Tech Transfer Strategy at QuidelOrtho
Open until filled. $135K–$175K a year, employer provided.