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Job Requirements of Validation Engineer IV:
-
Employment Type:
Full-Time
-
Location:
Des Plaines, IL (Onsite)
Do you meet the requirements for this job?
Validation Engineer IV
Generis Tek Inc.
Des Plaines, IL (Onsite)
Full-Time
Please Contact To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Monu Karwasara at email address can be reached on #
We have Contract Role QA Specialist II and III for our client at Des Plaines, IL. Please let me know if you or any of your friends would be interested in this position.
Position Details:
QA Specialist II and III - Des Plaines, IL
Location : Des Plaines, IL 60018
Project Duration : 6+ months of contract
Pay rate : $40/hr on W2
Job Description
Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success for assuring high product quality and meeting business needs. Main Responsibilities: Works with a cross functional team to review qualification and validation documents which meet Abbott and regulatory requirements. Supports the complete qualification and validation process to implement new manufacturing FUE and automation, process, test method validations in support of a manufacturing expansion. Especially in HPLC synthesis, purification and testing. Supports on-market change control projects.
Minimum Requirements: Bachelor’s degree in Life Science; Engineering; or closely related discipline is required OR relevant combination of education or experience. At least 5 years work experience in Quality or related field experience; Has a history of completing successful projects and driving positive compliance outcomes. Preferred: •Bachelor's or master’s degree in one of the following Engineering disciplines: Chemical, Electrical, Bio-medical, or Mechanical •5+ years of relative professional work experience in Medical Device Quality/Pharmaceutical or in a regulated industry.
Please Contact To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Monu Karwasara at email address can be reached on #
About Generis Tek: Generis Tek is a boutique it/professional staffing based in Chicago land. We offer both contingent labor & permanent placement services to several fortune 500 clients nationwide. Our philosophy is based on delivering long-term value and build lasting relationships with our clients, consultants and employees. Our fundamental success lies in understanding our clients’ specific needs and working very closely with our consultants to create a right fit for both sides. We aspire to be our client has most trusted business partner.
630-576-1932
.We have Contract Role QA Specialist II and III for our client at Des Plaines, IL. Please let me know if you or any of your friends would be interested in this position.
Position Details:
QA Specialist II and III - Des Plaines, IL
Location : Des Plaines, IL 60018
Project Duration : 6+ months of contract
Pay rate : $40/hr on W2
Job Description
Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success for assuring high product quality and meeting business needs. Main Responsibilities: Works with a cross functional team to review qualification and validation documents which meet Abbott and regulatory requirements. Supports the complete qualification and validation process to implement new manufacturing FUE and automation, process, test method validations in support of a manufacturing expansion. Especially in HPLC synthesis, purification and testing. Supports on-market change control projects.
Minimum Requirements: Bachelor’s degree in Life Science; Engineering; or closely related discipline is required OR relevant combination of education or experience. At least 5 years work experience in Quality or related field experience; Has a history of completing successful projects and driving positive compliance outcomes. Preferred: •Bachelor's or master’s degree in one of the following Engineering disciplines: Chemical, Electrical, Bio-medical, or Mechanical •5+ years of relative professional work experience in Medical Device Quality/Pharmaceutical or in a regulated industry.
- Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971
- Strong technical writing skills; Polished verbal and written communication skills
Please Contact To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Monu Karwasara at email address can be reached on #
630-576-1932
.About Generis Tek: Generis Tek is a boutique it/professional staffing based in Chicago land. We offer both contingent labor & permanent placement services to several fortune 500 clients nationwide. Our philosophy is based on delivering long-term value and build lasting relationships with our clients, consultants and employees. Our fundamental success lies in understanding our clients’ specific needs and working very closely with our consultants to create a right fit for both sides. We aspire to be our client has most trusted business partner.
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