Validation Engineer
DescriptionLooking for an exciting opportunity at a fast growing, employee-oriented company? Verista's 500
experts team up with the world's most recognizable brands in the life science industry to solve their business needs.
Whether it's compliance, quality management, verification, validation, automation, IT infrastructure, data analysis, manufacturing, or packaging, we deliver solutions that are right the first time.
Verista's experts include SMEs across the spectrum of pharma, medical devices and biotech industries.
As a result, we're uniquely capable of offering transformative, integrated solutions, new perspectives, and consistent results.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable our clients to improve the quality of patient healthcare worldwide.
Our talented and dedicated professionals are committed to making an impact every day.
We deliver solutions that are right the first time.
Typical Responsibilities of a Validation Engineer:
You generate, revise and execute Commissioning, Installation, Operational and Performance Qualification (IQ/OQ/PQ) Protocols for various life science lab, computer, manufacturing, packaging equipment and/or utilities systems.
You participate in issue identification, investigation and mitigation.
Generate test problem reports.
You participate in project teams executing various validation projects under the direction of a project manager or validation lead.
You provide routine progress and issue updates to the project team.
Temperature mapping execution RequirementsYou've earned your BS in chemical, biomedical, or biochemical engineering, biological sciences, or related field/experience.
You've gained 2-10 years relevant industry experience working in a cGMP environment.
You've got working knowledge of cGMP manufacturing as well as regulatory regulations and requirements for biotechnology, pharmaceuticals, and medical devices in your toolbox.
You've collected previous experience in writing and executing Validation protocols such as Installation, Operation and Performance Qualification documents.
Experience with start-up and qualification of cleanrooms, compressed gasses, RO/DI water, and IT infrastructure systems such as BAS and EMS.
Experience with start-up of manufacturing process equipment and various small benchtop equipment.
BenefitsBecause employees are the key to our success, Verista offers strong benefits and incentives including:
Health, Dental, and Vision Insurance401(k) Retirement Plan with a company matchPaid Time Off PayTuition Reimbursement9 Company Paid HolidaysPaid Long Term & Short Term Disability InsuranceTraining and DevelopmentPaid Maternity Leave and Parental LeaveTravel BonusEmployee Referral ProgramTuition ReimbursementMarriage LeaveBereavementVerista is an Equal Opportunity Employer.
Estimated Salary: $20 to $28 per hour based on qualifications.
experts team up with the world's most recognizable brands in the life science industry to solve their business needs.
Whether it's compliance, quality management, verification, validation, automation, IT infrastructure, data analysis, manufacturing, or packaging, we deliver solutions that are right the first time.
Verista's experts include SMEs across the spectrum of pharma, medical devices and biotech industries.
As a result, we're uniquely capable of offering transformative, integrated solutions, new perspectives, and consistent results.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable our clients to improve the quality of patient healthcare worldwide.
Our talented and dedicated professionals are committed to making an impact every day.
We deliver solutions that are right the first time.
Typical Responsibilities of a Validation Engineer:
You generate, revise and execute Commissioning, Installation, Operational and Performance Qualification (IQ/OQ/PQ) Protocols for various life science lab, computer, manufacturing, packaging equipment and/or utilities systems.
You participate in issue identification, investigation and mitigation.
Generate test problem reports.
You participate in project teams executing various validation projects under the direction of a project manager or validation lead.
You provide routine progress and issue updates to the project team.
Temperature mapping execution RequirementsYou've earned your BS in chemical, biomedical, or biochemical engineering, biological sciences, or related field/experience.
You've gained 2-10 years relevant industry experience working in a cGMP environment.
You've got working knowledge of cGMP manufacturing as well as regulatory regulations and requirements for biotechnology, pharmaceuticals, and medical devices in your toolbox.
You've collected previous experience in writing and executing Validation protocols such as Installation, Operation and Performance Qualification documents.
Experience with start-up and qualification of cleanrooms, compressed gasses, RO/DI water, and IT infrastructure systems such as BAS and EMS.
Experience with start-up of manufacturing process equipment and various small benchtop equipment.
BenefitsBecause employees are the key to our success, Verista offers strong benefits and incentives including:
Health, Dental, and Vision Insurance401(k) Retirement Plan with a company matchPaid Time Off PayTuition Reimbursement9 Company Paid HolidaysPaid Long Term & Short Term Disability InsuranceTraining and DevelopmentPaid Maternity Leave and Parental LeaveTravel BonusEmployee Referral ProgramTuition ReimbursementMarriage LeaveBereavementVerista is an Equal Opportunity Employer.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
