Vice President of Global Quality

Full Time
Fishers, IN
$290,000 - $310,000 a year
Posted
Job description
Global Pharmaceutical company with Equity and great compensation plan

This Jobot Job is hosted by: Garrett Mathison
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Salary: $290,000 - $310,000 per year

A bit about us:
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We are a global radiopharmaceutical company focused on revolutionizing the way cancer is treated. Our treatments focus on preserving healthy tissue while focusing our therapeutic isotopes on the cancerous cells. We have a team of both hybrid and remote employees across the globe supporting international roll-outs of cancer saving treatments and advancing late stage clinical products.

Why join us?
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We believe in supporting our employees both at home and in the workplace. We offer great compensation plans, annual bonuses, paid wellness days, and educational assistance. On top of this we offer full benefits and the option to work remote or hybrid.

Job Details
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Our company is seeking a highly skilled and experienced Vice President of Global Quality to join our team in the Radiopharmaceutical industry. The successful candidate will be responsible for ensuring that our company's products and services meet the highest quality standards across the globe. This is a permanent position that requires a minimum of 15 years of experience in the industry.

Responsibilities:
  • Develop and implement global quality strategies in alignment with the company's goals and objectives
  • Ensure compliance with GxP, cGMP, GCP, and other regulatory requirements
  • Oversee the quality system, including quality control, quality assurance, and quality improvement
  • Provide leadership and guidance to the quality team to ensure that quality standards are met
  • Collaborate with cross-functional teams to ensure that quality is integrated into all aspects of the business
  • Manage relationships with regulatory agencies and ensure that all regulatory requirements are met
  • Develop and maintain relationships with key stakeholders, including customers, suppliers, and partners
  • Provide input into the development of new products and services to ensure that quality is built in from the start
  • Lead the development and implementation of quality metrics to monitor and improve performance
  • Ensure that all radiopharmaceutical and biologics products meet the highest quality standards
  • Manage quality oversight of contract development and manufacturing organizations (CDMOs)
  • Provide quality oversight for clinical trials, including oncology trials

Qualifications:
  • Bachelor's degree in a scientific discipline, or equivalent experience
  • Minimum of 15 years of experience in the scientific industry, with a focus on quality
  • Strong knowledge of GxP, cGMP, GCP, and other regulatory requirements
  • Experience with radiopharmaceutical and biologics products
  • Experience with regulatory affairs and managing relationships with regulatory agencies
  • Experience managing quality oversight of CDMOs
  • Experience with oncology clinical trials
  • Strong leadership and communication skills
  • Ability to work collaboratively with cross-functional teams
  • Strong problem-solving skills and attention to detail
  • Ability to travel internationally as needed

If you are a highly skilled and experienced quality professional with a passion for ensuring that products and services meet the highest quality standards, we encourage you to apply for this exciting opportunity. Our company offers a competitive salary, comprehensive benefits, and opportunities for professional growth and development.

Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. #scientific #cgmp #radiopharmaceutical #gxp #gcp #oncology #biologics #cdmo #regulatory-affairs #quality-system #indtier1

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