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Job Purpose
We are looking for an Industrial BD & Integration Specialist to support the evaluation and execution of external growth opportunities, including M&A transactions and licensing deals, from a Technical Operations perspective.
The role contributes to the assessment of potential targets across the industrial value chain, focusing on COGS structure, supply chain robustness, quality and compliance track record, manufacturing capabilities, technology readiness and potential technology transfer requirements.
The Specialist will be involved in preliminary assessments and due diligence activities, working closely with cross functional Technical Operations teams (e.g. Supply Chain, Quality, MSAT, Manufacturing, …) to support a structured and timely industrial evaluation and to translate technical insights into business relevant inputs.
Following a successful due diligence, the role supports the industrial aspects of deal execution, including the preparation of transactional agreements (e.g. License Agreements, Commercial Supply Agreements) and the initial integration of acquired or in licensed assets, contributing to a smooth transition into the company’s operational framework.
Key Responsibilities
- Support in the analysis, compilation and consolidation of industrial and technical data related to Business Development initiatives, including M&A and licensing opportunities.
- Contribute to preliminary industrial assessments of potential targets, evaluating manufacturing feasibility, COGS structure, supply chain setup, quality and compliance history, and technology requirements.
- Coordinate cross‑functional Industrial Operations functions (e.g. Supply Chain, Quality, MSAT, Manufacturing, Engineering) during Due Diligence and post‑deal integration phases, ensuring alignment, completeness and timely delivery of assessments.
- Support the preparation of Due Diligence reports, consolidating inputs from multiple technical functions and translating scientific and technical findings into clear, business‑relevant conclusions for decision‑making
- Contribute to the identification, assessment and mitigation planning of technical, quality and supply chain risks, supporting fact‑based recommendations to management and Corporate Business Development.
- Actively support and coordinate, within the Industrial Operations Department, the drafting of transaction‑related documents (e.g. License Agreements, Commercial Supply Agreements, …) and contribute to negotiation activities, ensuring consistency between deal terms and industrial feasibility
- Assess feasibility and risks associated with timelines, costs, capacity and operational commitments embedded in deal terms, highlighting potential constraints and mitigation actions
- Support the initial integration phase following acquisition or deal closing, coordinating the execution of planned industrial and Technical Operations activities to ensure a smooth transition of the acquired or in‑licensed asset into the company’s portfolio
- Monitor and track progress against integration milestones, identifying technical, scientific or operational roadblocks and escalating issues as appropriate
Required Education
Bachelor's or Master's degree in Industrial Engineering, Economics, Business Administration, Management Engineering, or another quantitative discipline with a strong analytical focus.
Required Skills and Experience
- 2–4 years of experience in the pharmaceutical industry and/or consultancy sector
- Professional experience in Pharmaceutical Technical Operations, Manufacturing, Supply Chain, MSAT, Engineering, Quality, or related functions is considered an advantage.
- Exposure to consulting, transaction advisory, due diligence or private equity projects is considered a plus.
- Foundational understanding of GMP requirements, pharmaceutical manufacturing processes, technology transfer activities, and pharmaceutical supply chain operations.
- Strong analytical and problem-solving skills, with the ability to collect, structure and interpret data, identify key issues, and draw logical conclusions.
- Ability to assess operational considerations related to manufacturing, supply chain, quality, timelines, capacity, and costs.
- Good interpersonal and communication skills, with the ability to work effectively with limited guidance across cross-functional and multicultural teams.
- Ability to prepare and present information in a clear, structured and concise manner, both verbally and in writing.
- Strong organizational skills, with the ability to manage multiple priorities and perform effectively in fast-paced project environments with challenging deadlines.
- Advanced proficiency in Microsoft Excel and PowerPoint.
Required Languages
Fluent written and spoken English
Salary
Gross Annual Salary starting from: 45.000€
Please note: The salary indicated in this posting complies with local pay transparency regulations for Italian employment contracts. Final offers will be tailored to the successful candidate's experience, professional expertise, and interview journey, while ensuring internal equity. At Recordati, we are committed to a comprehensive, fair, and competitive remuneration system; a full overview of your total rewards package will be shared and discussed with you during the recruiting process.
1926
$2.4B
336
Recordati is a global pharmaceutical company based in Milan, Italy, with a history dating back to 1926. It operates in approximately 150 countries and employs around 4,580 people. The company focuses on developing, manufacturing, and commercializing medicines for both common diseases and rare conditions, emphasizing social and environmental responsibility. With fully integrated operations, Recordati covers research and development, manufacturing, and commercialization. It operates seven industrial plants and two chemical plants, supporting a diverse portfolio that includes prescription drugs for various medical conditions, over-the-counter pharmaceuticals, cosmetics, dietary supplements, and active pharmaceutical ingredients. Recordati markets over 190 drugs worldwide, including proprietary products like Zanidip®. The company serves a wide range of customers, including healthcare professionals, hospitals, and pharmacies. Recordati has expanded through acquisitions and licensing agreements, enhancing its presence in the rare diseases sector and strengthening its product offerings. Overall, Recordati is committed to innovation and improving health outcomes globally.
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