Epicareer Might not Working Properly
Learn More
Please Turn on your JavaScript

Epicareer might not working properly because your browser javascript is turned off.

What is JavaScript?

JavaScript is like the magic behind making websites interactive. Basically, it makes Epicareer more enjoyable and engaging.
How do i turn this on?
Find tutorial for your browser below :
  1. Make sure the webpage is open.
  2. In the Safari app on your Mac, choose Safari > Preferences, then click Security.
  3. Make sure the Enable JavaScript checkbox is selected.
  4. Click Websites.
  5. On the left, click Content Blockers.
  6. Make sure Off is chosen in the pop-up menu next to the website.
  7. On the left, click Pop-up Windows.
  8. Make sure Allow is chosen in the pop-up menu next to the website.
Visit Site here
  1. Open Chrome on your computer.
  2. Click. then Settings.
  3. Click Privacy and Security.
  4. Click Site settings.
  5. Click JavaScript.
  6. Select Sites can use Javascript.
Visit Site here
  1. If you're running Windows OS, in the Firefox window, click Tools > Options.
  2. Tip: If you're running Mac OS, click the Firefox drop-down list > Preferences.
  3. On the Content tab, click the Enable JavaScript check box.
Visit Site here
  1. Click the "Settings and more" icon at the top right of the Edge browser window.
  2. Click Settings.
  3. From the Settings menu, click Cookies and site permissions.
  4. Scroll down and click on JavaScript.
  5. In the JavaScript window, toggle the slider to "on" or "allowed."
  6. Close the Settings tab.
  7. Refresh the page.
Visit Site here
  1. Go to Settings.
  2. Click Advanced in the left sidebar, and click Privacy & security.
  3. Under Privacy and security, click Site settings.
  4. Click JavaScript.
  5. At the top, turn on or off Allowed (recommended).
Visit Site here
Any Question? Contact us
logo
Jobs or company...

Mfg/Ops Quality Engineer 1

Salary undisclosed
Checking job availability...
Original
Simplified
What if the work you did every day could impact the lives of people you know? Or all of humanity?At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.Position Responsibilities
  • Provide quality assurance support for manufacturing operations, or field/ product quality.
  • Review and align manufacturing operational activities, such as Work instructions, Device History Records, Nonconformances, CAPA, RMA, and customer complaint investigations.
  • Ensure that facilities, equipment, materials, processes and product readiness comply with cGMP practices.
  • Review verification and engineering study reports and identify gaps for GMP compliance. Develop and execute strategies to close gaps in an efficient, technical, and compliant manner
  • Serve as Quality representative on project teams for reviewing the new product design transfers and/ or line transfers.
  • Identify and drive resolution of quality issues in Quality Management System and/ or manufacturing operations.
  • Work with cross-functional teams to resolve operational quality issues.
  • Trend, analyze and monitor key performance indicators, suggest improvements and escalate to supervisor/ management as necessary.
  • Participate in customer complaints and work closely with cross-functional teams to investigation issue and ensure timely response to corporate/ customer.
  • Work in accordance with procedures and integrated program plans to achieve and maintain the required level of product quality in preparation for FDA and ISO third party audits.
  • Support product risk management activities and ensure quality and completeness of project design history files, validation packages, and change orders
  • Coordinate issue resolution using a risk-based approach
Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.Position Requirements
  • Minimum of 1-2 years of related experience in manufacturing, quality assurance, and/ or process validation in a regulated environment. Fresh graduates can be considered.
  • Bachelor's Degree in Biology, Biochemistry, Chemistry or equivalent field is preferred.
  • Experience in the medical devices / IVD / biotech / pharmaceutical industry, or instrument hardware / software integration is an advantage.
  • Good interpersonal, verbal and written communication skills.
  • Familiar with 21 CFR 820 and ISO 13485 requirements.
  • Familiar with words processing, spreadsheets and presentation tools.
  • Familiar with failure investigation, technical report writing, data mining, trend analysis and statistical analysis.
  • Adaptable to fast-paced, dynamic work environment with shifting demands
  • Ability to operate with high level of independence to investigate and resolve compliance issues, lead projects, plan and implement improvements, and achieve goals.
All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.
What if the work you did every day could impact the lives of people you know? Or all of humanity?At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.Position Responsibilities
  • Provide quality assurance support for manufacturing operations, or field/ product quality.
  • Review and align manufacturing operational activities, such as Work instructions, Device History Records, Nonconformances, CAPA, RMA, and customer complaint investigations.
  • Ensure that facilities, equipment, materials, processes and product readiness comply with cGMP practices.
  • Review verification and engineering study reports and identify gaps for GMP compliance. Develop and execute strategies to close gaps in an efficient, technical, and compliant manner
  • Serve as Quality representative on project teams for reviewing the new product design transfers and/ or line transfers.
  • Identify and drive resolution of quality issues in Quality Management System and/ or manufacturing operations.
  • Work with cross-functional teams to resolve operational quality issues.
  • Trend, analyze and monitor key performance indicators, suggest improvements and escalate to supervisor/ management as necessary.
  • Participate in customer complaints and work closely with cross-functional teams to investigation issue and ensure timely response to corporate/ customer.
  • Work in accordance with procedures and integrated program plans to achieve and maintain the required level of product quality in preparation for FDA and ISO third party audits.
  • Support product risk management activities and ensure quality and completeness of project design history files, validation packages, and change orders
  • Coordinate issue resolution using a risk-based approach
Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.Position Requirements
  • Minimum of 1-2 years of related experience in manufacturing, quality assurance, and/ or process validation in a regulated environment. Fresh graduates can be considered.
  • Bachelor's Degree in Biology, Biochemistry, Chemistry or equivalent field is preferred.
  • Experience in the medical devices / IVD / biotech / pharmaceutical industry, or instrument hardware / software integration is an advantage.
  • Good interpersonal, verbal and written communication skills.
  • Familiar with 21 CFR 820 and ISO 13485 requirements.
  • Familiar with words processing, spreadsheets and presentation tools.
  • Familiar with failure investigation, technical report writing, data mining, trend analysis and statistical analysis.
  • Adaptable to fast-paced, dynamic work environment with shifting demands
  • Ability to operate with high level of independence to investigate and resolve compliance issues, lead projects, plan and implement improvements, and achieve goals.
All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.