Job Description Summary

Job Description

We offer you opportunity to

• Attain a life-long expertise in the field of pharmaceutical manufacturing.
• Learn from Qualified Persons with long experience.
• Learn how to manage deviations complaints corrective & preventative actions (CAPA) Product Quality Reviews (PQR) Equipment Qualification and Process Validation activities.
• Learn how to work with digital platforms like SAP LIMS Maximo Digital Batch Records Veeva and TrackWise Digital.
• Gain insight and experience in LEAN working principles.
• Gain insight and training in planning performing and reporting in-house audit inspections.
• Create modify review and complete Standard Operating Procedures (SOPs).
• Participate in audits executed by national & international regulatory bodies like the Norwegian Medicines Agency (NOMA) & FDA.
• Be a part of our sociable and highly competent working environment.
• Prepare yourself well for leadership and the position of Qualified Person.

Upon authorization by NOMA you will

• Become a member of our Qualified Persons team that currently certify the release of Active Pharmaceutical Ingredients (APIs) Aseptically prepared and Terminally sterilized pharmaceuticals Investigational Medicinal Pharmaceuticals for clinical phase trials or Positron Emission Tomography (PET) products for cancer diagnostics.
• Participate in Drug Product Development projects with the goal of releasing new drugs to the market.
• Authorize and endorse Standard Operating Procedures for department use.
• Plan participate and report audit inspections performed on international suppliers.
• Certify the release of GMP manufactured medicine batches to the global market.
• Train & teach GMP in our departments.
• Complaint handling

  Qualifications/Requirements

• Masters degree in Pharmacy (MSc. Pharm or ) approved by the Norwegian Department of Health
• Oral and written proficiency in the Norwegian language
• Practical experience in pharmaceutical manufacturing is valued but not essential.

• To be successful in this position you should

• Fulfill the criteria presented in the qualifications section above
• Enjoy systematic analytical critical and adaptive work processes.
• Enjoy working in an interdisciplinary team environment.
• Enjoy upholding quality standards that promote good pharmaceutical manufacturing and documentation practices.
• Be dependable reliable and willing to make holistic and pragmatic decisions in a timely manner.
• Enjoy managing several activities simultaneously and to deliver results within given time frames.
• Be legible for QP authorization within 2 years.

• Inclusion and Diversity

  GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race color religion national or ethnic origin sex sexual orientation gender identity or expression age disability protected veteran status or other characteristics protected by law.

  Behaviors

  We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus and drive ownership always with unyielding integrity.

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race color religion national or ethnic origin sex sexual orientation gender identity or expression age disability protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus and drive ownership always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything youd expect from an organization with global strength and scale and youll be surrounded by career opportunities in a culture that fosters care collaboration and support.

Additional Information