Supplier Quality Engineer II

Position Summary

The Supplier Quality Engineer II is responsible for planning and directing activities concerned with development, application and maintenance of quality standards for processes, materials and products in accordance with quality programs, plans, SOPs and policies of the company's Quality System. This position is also responsible for ensuring compliance with corporate policies and the company's active regulatory certifications. This role is focused on

supplier quality assurance and supply auditing.

Duties And Responsibilities

Participate in supplier quality related communication and feedback.
Support the Material Review Board by recommending or reviewing the disposition of Non-Conforming Material.
Participate in internal and supplier audits as needed. Ensure that audits are properly performed, documented, and completed in accordance with the annual audit procedure/schedule.
Conduct and assist during external/supplier audits associated with MSD's active regulatory certifications and requirement compliance.
Direct the need for Corrective and Preventive Actions (CAPA) and QMS continuous improvement projects. Ensure that corrective and preventive actions are issued as required, properly investigated, documented, effective, and completed on time.
Generate and analyze metrics needed to measure the effectiveness of the QMS.
Specific duties may vary depending upon departmental requirements

Experience And Qualifications

Bachelor's degree in a technical/scientific/engineering discipline is required.
Minimum 3 years of experience in biotechnology, medical devices, in vitro diagnostics, pharmaceuticals or related industry is required.
Working knowledge of and experience with ISO 9001 standard is required.
Experience with FDA's Quality System requirements (QSR) and ISO 13485 is preferred.
ASQ Certified (CQE, CRE, CQA) is beneficial.
A demonstrated level of consistency in performance and aptitude for managing additional responsibility and accountability are required for next level consideration.

Knowledge, Skills, and Abilities

Strong quality fundamentals and analytical background.
Logical problem solving through TQM, team building and quality systems tools and methods.
Demonstrated ability to organize and move project tasks forward in an orderly and structured fashion.
Working knowledge of cGMP, ISO and International regulations o Experience with developing, implementing and maintaining Quality System compliance.
Excellent oral and written communication and interpersonal skills. Effectively communicate issues/problems and results that impact timelines, accuracy and reliability of quality system data.
Proficiency in MS Office Suite o Capacity to learn additional software applications as the need arises.
A wide degree of creativity and latitude is expected including the ability to multi-task and work productively in demanding manufacturing and research environments with changing priorities

Physical Demands

This position requires the ability to communicate and exchange information, utilize equipment necessary to perform the job, and move about the office.

Work Environment

This position is performed in a standard office environment.

COMPENSATION SUMMARY

The annual base salary for this position ranges from $85,900 to $131,000. This salary range represents a general guideline as MSD considers other factors when presenting an offer of employment, such as scope and responsibilities of the position, external market factors, and the candidate's knowledge, skills, abilities, education and experience. Employees may qualify for a discretionary or non-discretionary bonus in addition to their base salary. These annual bonuses are intended to recognize individual performance and enable employees to benefit from the Company's overall success.

BENEFITS SUMMARY

At MSD, we offer a comprehensive benefits package to support our employees' well-being and financial security. In addition to competitive salaries, our benefits include medical, dental, and vision coverage, along with prescription benefits. We provide a 401(k) plan with company matching, flexible spending accounts, and company-paid short- and long-term disability insurance as well as group life and accidental death and dismemberment insurance. Our offerings also encompass paid vacation, paid sick leave, paid holidays, and paid parental leave, along with an employee assistance program. Additional voluntary perks include a fitness club membership contribution, pet insurance, identity theft protection, home and auto insurance discounts, and optional supplemental life insurance.

EEO/AA STATEMENT

MSD is an Equal Opportunity/Affirmative Action Employer. We are committed to fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. We welcome applications from all qualified candidates, making employment decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, genetic information, marital status, national origin, age, protected veteran status, pregnancy, disability status, or any other protected characteristic. For our full EEO/AA and Pay Transparency statement, please visit here. Meso Scale Diagnostics uses E-Verify to validate the work eligibility of candidates.