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GE Healthcare Intern Quality Assurance, Online Application Process

GE Healthcare Intern Quality Assurance, Online Application Process

GE Healthcare Intern Quality Assurance, Online Application Process. GE (NYSE:GE) rises to the challenge of building a world that works. For more than 125 years, GE has invented the future of industry, and today the company’s dedicated team, leading technology, and global reach and capabilities help the world work more efficiently, reliably, and safely. GE’s people are diverse and dedicated, operating with the highest level of integrity and focus to fulfill GE’s mission and deliver for its customers.

Intern Quality Assurance

Posted of Company Website: Jul 23rd 2021

Job ID: R3585578

Relocation Assistance: No

Location: Amersham Place-Little Chalfont, Amersham, Buckinghamshire, HP7 9NA, United Kingdom

Job Description Summary

As an Intern within the Quality Assurance position in the GEHC PDx External Manufacturing Quality Assurance global team, you will support and oversee the manufacturing of various PET (Positron Emission Tomography) radiopharmaceutical products.

You will be exposed to the manufacturing process of PET products, oversight of a global contract manufacturing network of 40+ sites, product development, clinical trials and regulatory submissions.

The internship position is for 12 months from September 2021 to August 2022.

GE Healthcare is a leading global medical technology and digital solutions, innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

Job Description

Responsibilities:

  • CMO oversight – trending and data analysis of deviations and other key Key Performance Indicators (KPI) for inclusion in Quality Management Review (QMR) to monitor the performance of the CMO network.
  • Complaint investigation – coordination with third parties/CMO in the investigation of complaints. Trending of the root cause of investigations to identify trends and suitable CAPA
  • QMS/KPI – collection, entry and analysis of KPI into the database
  • Release of product – coordination/supply of release documentation to GEHC affiliates for local release activities
  • Technology Transfer – support in the technology transfer of PET agents to CMOS through the review and checking of data for inclusion in IMPD/MA regulatory submissions

Qualifications and experience

  • Undergoing Degree/Diploma in chemistry, biology, pharmacy or other relevant qualification to the pharmaceutical industry
  • Good interpersonal skills & written and oral proficiency in English
  • Computer literate

Eligibility requirements 

A good level of English and a valid work permit

APPLY ONLINE

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