Top 23453 Process validation engineer Jobs

Validation Engineer
Medline Industries —Hartland, WI
- $73,000 - $110,000 a year
- Full-time
- Bachelor of Science
- Writing skills
- Engineering
- Health insurance
- 401(k)
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Process Engineer
BCP Engineers & Consultants —Oak Ridge, TN
- $80 - $95 an hour
- Overtime
- Hybrid work
- Background check
- 7 years
- Analysis skills
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12d
Sr Chemical Process Design QA Engineer (Remote)
On-Board Companies —Portland, OR
- $72 - $85 an hour
- Email
- Remote
- Engineering
- Continuous improvement
- Mentoring
- 401(k)
- Life insurance
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4d
NPI Test Process Development Engineer
Insight Global —Agoura Hills, CA
- $70,000 - $125,000 a year
- Full-time
- Schematics
- Engineering
- Travel
- Health insurance
- Dental insurance
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10d
Validation Engineer
Validation & Engineering Group, Inc —New Albany, OH
- Full-time
- Engineering
- Mid-level
- Organizational skills
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Lead Validation Engineer
Zenith LifeScience —South Plainfield, NJ
- $136,000 a year
- Full-time
- 3 years
- Master's degree
- Databases
Validation Engineer
Katalyst Healthcares & Life Sciences —Bothell, WA
- Contract
- 5 years
- Engineering
- Senior level
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Validation Engineer
VERAZ INC —Boston, MA
- $30 - $45 an hour
- Full-time
- In-person
- 1 year
- Electrical Engineering
- Relocation assistance
- Health insurance
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5d
Process Validation Engineer
Katalyst Healthcares & Life Sciences —Bloomington, IN
- Contract
- Hybrid work
- Engineering
- Mid-level
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Process Validation Engineer
Agilent Technologies, Inc. —Frederick, CO
- $105,280 - $164,500 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
Process Validation & Cleaning Engineer
Amneal Pharmaceuticals —Piscataway, NJ
- $80,000 - $90,000 a year
- Full-time
- Microsoft Word
- Bachelor of Science
- Writing skills
- Health insurance
- 401(k) matching
Process Validation Associate / Engineer
Krystal Biotech —Pittsburgh, PA
- Full-time
- Bachelor's degree
- 1 year
- Communication skills
Quick Apply
Validation Engineer
Zenith LifeScience —South Plainfield, NJ
- $70,000 - $80,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Product management
Validation Engineer
CAI —Boston, MA
- $72,800 - $80,100 a year
- Full-time
- Customer service
- Mid-level
- Team management
Quick Apply
Senior CQV Engineer/Senior Validation Engineer Consultant
Katalyst Healthcares & Life Sciences —Devens, MA
- Weekends as needed
- Bachelor's degree
- Continuous improvement
- Senior level
Quick Apply
Validation Engineer - Upstream
Validation & Engineering Group, Inc —Punta Santiago, PR
- Extended hours
- Engineering
- Mid-level
- 3 years
Quick Apply
Process Engineer
Katalyst Healthcares & Life Sciences —Antioch, IL
- Contract
- 7 years
- Bachelor of Science
- English
Quick Apply
Validation Engineer
OPULENTSOFT —Northridge, CA
- Email
- Bachelor of Science
- Mid-level
- Communication skills
Senior Validation Engineer
Katalyst Healthcares & Life Sciences —Rock Hill, SC
- Weekends as needed
- Hybrid work
- Bachelor's degree
- Senior level
Quick Apply
Validation Engineer
EMD-Merck US —St. Louis, MO
- $72,700 - $118,700 a year
- Full-time
- Engineering
- Mid-level
- US work authorization
- Health insurance
- Paid time off
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Validation Engineer

Medline Industries -
Hartland, WI

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Job Details

Full-time
$73,000 - $110,000 a year

Benefits

Health insurance
401(k)
Paid time off
Employee assistance program

Qualifications

Project reporting
Biology
Statistics
Six Sigma Certification
Project engineering
Defect resolution root cause analysis
Master's degree in chemistry
Engineering development testing
Laboratory equipment performance testing and validation
ISO standards
Quality control statistical data analysis
Pharmaceutical regulatory compliance
Bachelor of Science
Writing skills
Engineering
Laboratory instrument validation
Equipment installation
Vendor coordination
Biomedical Engineering
Biotechnology
Mid-level
Master's degree in biology
Project management experience in manufacturing
Bachelor's degree in biology
Data summary reports
Quality reports
Minitab
Change management
Manufacturing standard operating procedures
Manufacturing facility experience

Full Job Description

Job SummaryResponsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing revalidation, engineering studies to evaluate new products or components, change control assessments, and coordination of computer and test method validations of applicable products.Job Description<ul><li>Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical device manufacturing.</li><li>Perform engineering studies to determine if projects are feasible.</li><li>Assist with measurement system analysis including Gage R&R.</li><li>Support product/design transfer activities including validations and creation of updates to documentation needed to manufacture OTC cosmetic and medical devices.</li><li>Support Change Assessment activities including assessment and qualification of changes to existing product components and implementation of products into manufacturing lines.</li><li>Support root cause investigations for non-conformances related to manufacturing validations.</li><li>Develop, prepare and install equipment and revise test validation procedures/protocols to ensure that a product is manufactured in accordance with appropriate regulatory agency validation requirement and current industry practices.</li><li>Responsible for IQ/OQ and PQ phases and implementation of validated SOPs.</li><li>Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.</li><li>Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.</li><li>Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve time lines for project completion.</li><li>Compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements.</li><li>Maintain all of the documentation pertaining to qualification and validation of assigned projects and equipment/systems.</li></ul>REQUIRED EXPERIENCEEducation <ul><li>Bachelor of Science Degree in Biology, Chemistry, or Engineering.</li></ul>Work Experience <ul><li>At least 2 years of validation experience in a cGMP Device or Drug environment.</li><li>Experience with validations of controlled environments or equipment validations in a regulated environment.</li><li>Experience with validation documentation and related change control.</li><li>Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.</li></ul>PREFERRED QUALIFICATIONS<ul><li>Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering.</li><li>Six Sigma certification.</li><li>3 years of validation experience in a cGMP Device or Drug environment.</li><li>Process validation experience in a pharmaceutical or Medical Device manufacturing environment.</li><li>Experience with validation of various product types such as liquid products, solid dosage products, and multi-component products.</li><li>Experience in FDA regulated environment.</li><li>Experience with ISO 13485 and ISO 11607 standards.</li><li>Experience with Measurement System Analysis.</li><li>Experience with Minitab statistical analysis software.</li><li>Experience with root cause analysis.</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.The anticipated salary range for this position:$73,000.00 - $110,000.00 AnnualThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click <a target="_blank" href="https://urldefense.com/v3/__https:/digital.alight.com/medline__;!!DjNdo6avjEs!o-bxZ6fy_WNH13q2FLYYmUMb1U4cic3ioox3ulm5dkpyivWM09cd64RN8rHuDH5AQKNiwEzHU2VbVJht5ginULSy5aJGsA$">here</a>.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 page <a target="_blank" href="https://www.medline.com/about-us/belonging/">here</a>.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.

Application Question(s):

Are you able to work on-site Monday through Friday?
Do you have prior experience with validation or similar in an FDA or cGMP regulated environment?

Experience:

validation, manufacturing, and/or process engineering: 3 years (Required)

Ability to Commute:

Hartland, WI (Required)

Ability to Relocate:

Hartland, WI: Relocate before starting work (Required)

Work Location: In person

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