Job details Spherion is seeking a qualified and detail-oriented Validation Engineer to join a team in a dynamic and growing medical device environment.

Responsibilities:
Lead and execute equipment and process validation (IQ, OQ, PQ) including full documentation.
Develop and maintain engineering documents, work instructions (WIs), and validation protocols. ... Monitor, test, and analyze equipment and process performance.
Document and report test results according to regulatory standards.
Collaborate cross-functionally to transfer new products and processes into production.
Ensure continuous improvement and compliance with quality and safety standards.

Working hours: 8:00 AM - 5:00 PM

Skills:
Verbal and written communication skills; able to convey complex technical data to diverse audiences.
Excellent team player with a proactive and positive attitude.
Fast learner with a high level of attention to detail.
Fluent in English (both written and verbal).

Education:
Bachelors

Experience:
4-7 years

Qualifications:
BA in Mechanical Engineering or Biomedical Engineering (or related field).
Minimum 5 years of experience in R&D or Engineering roles within the medical device industry.
Solid understanding of medical device validation processes and related documentation.


Apply Now if you're ready to make a difference through quality engineering in a mission-driven company.

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Show lessShow more Spherion is seeking a qualified and detail-oriented Validation Engineer to join a team in a dynamic and growing medical device environment.

Responsibilities:
Lead and execute equipment and process validation (IQ, OQ, PQ) including full documentation.
Develop and maintain engineering documents, work instructions (WIs), and validation protocols.
Monitor, test, and analyze equipment and process performance.
Document and report test results according to regulatory standards.
Collaborate cross-functionally to transfer new products and processes into production.
Ensure continuous improvement and compliance with quality and safety standards.

Working hours: 8:00 AM - 5:00 PM

Skills:
Verbal and written communication skills; able to convey complex technical data to diverse audiences.
Excellent team player with a proactive and positive attitude.
Fast learner with a high level of attention to detail.
Fluent in English (both written and verbal).

Education:
Bachelors

Experience:
4-7 years

Qualifications:
BA in Mechanical Engineering or Biomedical Engineering (or related field). ... Minimum 5 years of experience in R&D or Engineering roles within the medical device industry.
Solid understanding of medical device validation processes and related documentation.


Apply Now if you're ready to make a difference through quality engineering in a mission-driven company.

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Show lessShow morekey responsibilities

Lead and execute equipment and process validation (IQ, OQ, PQ) including full documentation.Develop and maintain engineering documents, work instructions (WIs), and validation protocols.Monitor, test, and analyze equipment and process performance.Document and report test results according to regulatory standards.Collaborate cross-functionally to transfer new products and processes into production.Ensure continuous improvement and compliance with quality and safety standards.

experience

4-7 years

skills

Verbal and written communication skills; able to convey complex technical data to diverse audiences.Excellent team player with a proactive and positive attitude.Fast learner with a high level of attention to detail.Fluent in English (both written and verbal).

qualifications

BA in Mechanical Engineering or Biomedical Engineering (or related field).Minimum 5 years of experience in R&D or Engineering roles within the medical device industry.Solid understanding of medical device validation processes and related documentation.

education

Bachelors

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