General Manager/Site Head at Masis Professional Group in Wilmington, Massachusetts

Posted in Other about 2 hours ago.

Type: full-time





Job Description:

GENERAL MANAGER

JOB SUMMARY:

This position combines the responsibilities for a production site, including the oversight of different business units throughout the US, with the areas of sales management and business development. The General Manager oversees the daily production, storage and dispensing of radioactive products, equipment, and services along with site management responsibilities. Ensures business is in full regulatory and statutory compliance.

Performs and reviews sales and marketing activities. Negotiations with key customers and new business contacts. P&L responsibilities. Personnel responsibilities. Experience with GMP drug production.

ESSENTIAL DUTIES:
  • Site Management (including managing daily activities of US personnel)
  • Ensure radioactive products and drugs are manufactured and dispensed properly
  • Troubleshoot problematic orders
  • Ensure necessary validations and testing of the GMP manufacturing process and dispensing processes are carried out properly
  • Sales Management and Business Development activities (support of key customers and acquisition of new business opportunities especially for the GMP-Suite)
  • Perform and review of customer quotes and customer sales orders
  • Responsible for forecasting and meeting the company's budget
  • Attend relevant technical meetings and conferences
  • Oversees regulatory program
  • Takes care of day-to-day issues including personnel management, accounting, AP, AR management.

KNOWLEDGE, SKILLS AND ABILITIES: To perform this job successfully, an individual must be well rounded with GMP drug manufacture background. Radiopharmaceutical experience is preferred but will consider someone from regular pharmaceutical industry.

Education (or substitute experience) required:
  • BS degree Radiochemistry or Chemistry or similar.
  • An additional degree in Business Administration is an advantage

Minimum experience required: 8 years of related experience combining GMP Drug Production and direct managerial and supervisory experience.

Abilities and skills required: Knowledge of GMP-regulations, production and commercial operations. Ability to solve problems, to organize, plan and manage long term projects.
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