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...

Quality Control Manager

Salary undisclosed
Checking job availability...
Original
Simplified

Type: full time/direct hire

Salary: $130k - $140k

Location: Pennington, NJ (100% onsite)

Position Overview

Quality Control Raw Material Manager will ensure that the raw materials and consumables used in production meet the required quality standards.

Key Responsibilities

  • Oversight: Oversee or execute the inspection, sampling and testing of incoming raw materials and consumables. Manage technology transfer of raw materials and consumables test methods.
  • Compliance: Design and implement Raw Materials Qualification program in compliance with FDA and EMA regulations. Ability to conduct risk assessments and implement risk mitigation strategies for raw materials.
  • Manage laboratory activities: Oversee or execute testing as needed on incoming raw materials and consumables, review the associated data, maintain accurate records of all inspections, test, vendor notifications and supplier evaluations.
  • Problem Solving: Resolve technical problems in the lab. Lead investigation for out of specification results and deviations. Implement continuous improvement initiatives to optimize raw material testing and release.
  • Team Leadership: Train laboratory personnel to ensure they are well versed in raw material and consumable test methods.
  • Documentation: Author procedures, specifications, risk assessments, protocols and summary reports. Manage all raw material QMS documents including change controls.
  • Data Management: Oversee the management and storage of raw material/consumable testing data, review to ensure it is accurate, securely stored and easily retrievable. Analyze data to identify trends and propose areas for improvement.
  • Client and Audit Management: Subject matter expert in raw material/consumables for regulatory and client audits for GMP compliance.

Qualifications

  • Education: This role requires strong work experience in analytical and sterility assurance testing technologies with a BSc or higher in chemistry, industrial engineering or related fields. Advanced degrees or additional certifications in relevant field preferred.
  • Experience: At least 7-10 years of experience in a leadership role within pharmaceutical or biotechnology industries and 3-5 years of leadership role in raw material testing and release. Significant experience working in a Good Manufacturing Practice (GMP) and Good Laboratory Practices (GLP) environment is crucial. Proficiency in quality control software including LIMS and data analysis tools.
  • Skills: Proficiency in analytical techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC) and mass Spectrometry (MS). Knowledge of Endotoxin and Sterility Assurance test methods.