Industrialization Senior Specialist

Are you ready to join a growing, global drug development and manufacturing organization that puts people first?  Come to Adare!  We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world.  Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success.  With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare!

What can Adare offer you?

• Health Insurance
• Pension Plan
• Benefits
• Career growth and internal opportunities
• Production bonus
• Employee Recognition Programs

We are seeking to hire a  Industrialization Senior Specialist to join our Industrialization Team at Italian sites.

If any of the below describes you, we would love to meet you! 

Summary

Reporting directly to the Senior Manager, Industrialization - Italy, the Industrialization Senior Specialist supports industrialization department activities by providing her/his technical expertise and collaborating with relevant business units (e.g. R&D, Manufacturing, Quality, Regulatory, Business Development) during scale-up, process validation, technology transfer, implementation of manufacturing processes and life cycle management of existing products. This Senior Specialist works in an effective and cooperative manner under deadlines and in respects of Company policies, procedures and regulations.

Responsibilities:

• Carries out his/her work in compliance with company procedures and in accordance with the provisions of the Occupational Health and Safety Management System and Good Manufacturing Practices.
• Assesses technical feasibility, calculates cost of goods, prepares capital investments and capacity analyses of commercial products and Technology transfer opportunities.
• Collaborates with Business Support Team, Industrialization Manager and involved business units providing all the information needed to prepare commercial proposals.
• Works with Pharmaceutical Development (R&D) to scale-up and validate new products from lab to industrial scale and is accountable for industrial scale registration batches.
• Contributes to Life Cycle Management of existing commercial products, including recurrent manufacturing process validation activities, process improvement and optimization.
• Is accountable with Industrialization Team for the Manufacturing Process Validation Plan, writes protocols and reports, and provides technical assistance to Operations and Quality during the manufacturing process validation runs.
• Identifies quality improvement and cost reduction opportunities.
• Provides technical support and project management to add new sources of API, excipients, and packaging components.
• Provides technical support to Operational Excellence team, as needed.
• Works effectively under deadlines.
• Participates in the development and implementation of methods, procedures and regulations necessary for the smooth flow of business.
• Respects policies, procedures, and regulations in force in the company.
• Completes assigned tasks in a safe manner and in a constant state of alertness.
• Upholds Company policies, including the Ethics and Conduct Code.
• Works in a cooperative manner with managers, supervisors, coworkers, customers and the public.

Requirements:

• BS/BA degree in Health Science (e.g., Pharmaceutical Technology, Chemistry, Biology) from a five-year accredited university or college; plus 5 years of related experience required.
• Full Proficiency in Italian (main language) and in English 
• Strong know-how of technology transfer projects, especially for oral solid dosage forms
• Extensive knowledge of pharmaceutical technologies
• Excellent interpersonal written and oral communication skills
• Proficient in Microsoft Office including advanced skills in Excel.
• Ability to coordinate, contribute to and work within a cross-functional team.
• Ability to thrive in a dynamic and fast-paced environment.
• Ability to prioritize duties and manage multiple projects with minimal supervision.
• Exceptional attention to detail and excellent organizational skills
• Ability to accommodate up to 15% travel.

Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

Adare is an organization that works daily to break down any gender gap, in the awareness that the full valorization of female talent represents a fundamental element for a greater creation of economic and human value. In Adare both genders are equally represented even in the case of managerial roles. In Adare we have structured a management system useful for the certification of gender equality; therefore, we work daily to combat any form of non-inclusion in our management processes and in our internal and external communication. The selection process is no exception: our staff in charge of selection and recruitment are prohibited from asking questions that directly or indirectly relate to the topics of pregnancy, marriage or - in general - the responsibility of care. If you are a woman and you are reading this announcement, know that your gender will not represent an obstacle to the selection process.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES