Medline

Makes and delivers medical supplies to hospitals

Principal Engineer Quality

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeShanghai, ChinaNo salary listed

About the Job

Requirements

A bachelor's degree or above in Biomedical Engineering, Chemical Engineering, Mechanical Engineering, Quality Management, Pharmaceutical Engineering, or a related major.
At least 7 years of work experience in the medical device industry, including solid IQ/OQ/PQ validation experience.
Familiarity with ISO 13485, medical device GMP, FDA 21 CFR 820, and EU MDR regulatory requirements.
Familiarity with statistical technology and its application, especially sampling methods.
Proficiency in independently writing, reviewing, and approving IQ/OQ/PQ protocols and validation reports.
Good understanding of medical device production processes, equipment validation, cleanrooms, and utility system qualification.
Strong English reading and writing ability, including the ability to understand and prepare English validation documents.
Rigorous, detail-oriented approach, communication, problem-solving, and cross-team coordination skills.
Availability to travel to Medline facilities and vendor sites approximately 30% of the time, potentially internationally.

Responsibilities

Act as the site Subject Matter Expert for validation of equipment, sterile packaging, mixing, water systems (PW/WFI and distribution loops), filling systems (aseptic and non-aseptic), cleaning processes (CIP/COP and manual cleaning validation), and injection molding processes.
Define critical process parameters (CPPs) and critical quality attributes (CQAs) for complex manufacturing processes using risk-based approaches.
Draft, review, approve, and finalize IQ, OQ, and PQ protocols and validation reports for medical device production equipment, testing equipment, and facility utilities.
Lead and oversee on-site validation execution and verify test data integrity, accuracy, and traceability.
Draft, review, and optimize validation standard operating procedures, validation master plans, and the related validation database.
Manage validation deviations, non-conformances, and change controls; drive corrective actions and closure.
Support internal and external audits, customer audits, and regulatory inspections with complete validation documentation.
Conduct technical communication and coordination with engineering, production, research and development, and cross-functional teams on validation matters.
Ensure all validation activities comply with ISO 13485, FDA QSR 21 CFR 820, MDR, and local medical device GMP requirements.

Job Summary

Job Description

Job Responsibilities

•

•Act as site Subject Matter Expert (SME) for validation of equipment, sterile packaging, mixing, water systems (PW/WFI, distribution loops), filling systems (aseptic and non-aseptic), cleaning processes (CIP/COP, manual cleaning validation), and injection molding processes.

•Define critical process parameters (CPPs) and critical quality attributes (CQAs) for complex manufacturing processes using risk-based approaches.

•Draft, review, approve and finalize IQ , OQ , PQ protocols and validation reports for medical device production equipment, testing equipment and facility utilities.

•Lead and oversee on-site validation execution, verify test data integrity, accuracy and traceability.

•Draft, review and optimize validation SOPs, validation master plans and related validation database.

•Manage validation deviations, non-conformances and change controls; drive corrective actions and closure.

•Support internal/external audit, customer audit and regulatory inspection with complete validation documentation.

•Conduct technical communication and coordination with engineering, production, R&D and cross-functional teams on validation matters.

•Ensure all validation activities comply with ISO 13485, FDA QSR 21 CFR 820, MDR and local medical device GMP requirements.

•

Job Requirements

•Bachelor degree or above in Biomedical Engineering, Chemical Engineering, Mechanical Engineering, Quality Management, Pharmaceutical Engineering or related majors.

•Minimum 7+ years working experience in medical device industry with solid IQ/OQ/PQ validation experience.

•Familiar with ISO 13485, medical device GMP, FDA 21 CFR 820 and EU MDR regulatory requirements; Familiar with Statistic technology and application, especially sampling method

•Proficient in writing, reviewing and approving IQ/OQ/PQ protocols and validation reports independently.

•Good understanding of medical device production process, equipment validation, cleanroom and utility system qualification.

•Strong English reading and writing ability, able to understand and prepare English validation documents.

•Rigorous, detail-oriented, good communication, problem-solving and cross-team coordination skills.

•Travel to both Medline facilities and vendor sites approximately 30%. (Potential international travel)

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging pagehere.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

About the Company

Medline

Makes and delivers medical supplies to hospitals

Medline makes and distributes medical and surgical supplies for hospitals, surgery centers, nursing homes, physician offices and other care sites. It runs its own factories alongside a large network of warehouses and delivery routes, so one company can produce exam gloves, gowns and surgical kits and then deliver them straight to the bedside. Many health systems sign multi-year prime vendor agreements that make Medline the source for most of their medical-surgical supplies. It earns money selling its own products and those of other manufacturers, together with supply chain services. Medline was founded in 1966 and is based in Northfield, Illinois.

Company size: 10,001+
Company stage: IPO
Headquarters: Northfield, IL
Founded: 1966

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