Sourcing Professional
About the job
- A bachelor's degree in pharmacy is required.
- Four to six years of experience in pharmaceutical sourcing or procurement, including at least two to three years in a managerial role.
- Proven experience in sourcing for regulated markets, including the EU, USA, and GCC, and accelerating development-to-launch timelines.
- In-depth knowledge of active pharmaceutical ingredients, excipients, and pharmaceutical development.
- Strong negotiation and supplier management skills focused on balancing speed, quality, and cost.
- Expertise in Good Manufacturing Practice, International Council for Harmonisation guidelines, and international compliance frameworks.
- Advanced proficiency in Oracle systems and analytical tools, including Excel and Power BI.
- Fluency in spoken and written English is required.
- Develop and implement sourcing strategies to ensure a qualified, compliant, and cost-effective supplier base.
- Lead sourcing activities for product development and commercial projects to ensure timely material availability and successful launches.
- Drive supplier performance, cost optimization, and operational excellence through strategic sourcing and continuous improvement.
- Lead the sourcing team and collaborate with cross-functional stakeholders to achieve business objectives and support organizational growth.
- A Master's degree or Master of Business Administration is preferred.
- Additional languages are an advantage.
About the company
EVA Pharma develops and manufactures affordable medicines for global markets, focusing on 12 therapeutic areas such as anti-infectives, metabolic health, oncology, and pediatrics. It operates four manufacturing facilities with a 5,000-strong team and produces over one million healthcare products daily. The company runs two regional research centers that use AI-driven prediction and mRNA R&D to develop biological products and first-of-its-kind capabilities in the Middle East and Africa. EVA Pharma distributes its products to more than 60 countries and seeks to expand access to high-quality medicines worldwide. Its differentiation comes from its scale, regional R&D capabilities, and commitment to sustainable access, aiming to meet pressing, unmet disease needs with reliable supply.
Company Size
1,001-5,000
Company Stage
N/A
Total Funding
N/A
Headquarters
Al Sharikat, Egypt
Founded
1997
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Simplify's Take
What believers are saying
- Egypt’s December 2024 insulin approval opens exportable manufacturing revenues and credibility with regulators.
- November 2025 EVA Pharma Oncology targets 22 million packs annually, with 11 more treatments planned.
- Access-heavy partnerships with Gilead, BeiGene, and Porton create multiple near-term revenue streams.
What critics are saying
- Gilead’s generic lenacapavir supply starts 2027, so execution delays destroy EVA Pharma’s moat.
- Oncology launches need Egypt market uptake; BRUKINSA, TEVIMBRA, and seven in-house products face entrenched competitors.
- Any FDA, EDA, or Gilead tech-transfer setback blocks EVA Pharma’s pivot into high-value biologics.
What makes Eva Pharma unique
- Egypt’s 2024 Lilly insulin approval proves EVA Pharma can localize complex biologics manufacturing.
- The 2024 Gilead lenacapavir license makes EVA Pharma Africa’s sole local generic producer.
- The 2025 BeiGene deal and 2025 Porton MOU extend EVA Pharma beyond generics into oncology and CAR-T.
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Company News
The collaboration will combine Porton Advanced's capabilities in manufacturing viral vectors and cell therapies with EVA Pharma's expanding presence in the high-tech biopharmaceutical sector.
This milestone stems from the companies' collaboration to expand access to affordable insulin to one million people living with diabetes in low- to middle-income countries annually by 2030INDIANAPOLIS and CAIRO, Dec. 17, 2024 /PRNewswire/ -- The Egyptian Drug Authority approved the insulin glargine injection manufactured by EVA Pharma through a collaboration with Eli Lilly and Company (NYSE: LLY). Launched in 2022, the collaboration aims to deliver a sustainable supply of high-quality, affordable human and analog insulin to at least one million people annually living with type 1 and type 2 diabetes in low- to middle-income countries (LMICs), most of which are in Africa. This marks the first regulatory approval of EVA Pharma's insulin drug products, following Lilly and EVA Pharma's collaboration announcement in December 2022. Under this agreement, Lilly has been supplying its active pharmaceutical ingredient (API) for insulin to EVA Pharma at a significantly reduced price and providing pro-bono technology transfer to enable EVA Pharma to formulate, fill and finish insulin vials and cartridges
In December 2022, Lilly announced an agreement with EVA Pharma to enhance sustainable access to affordable insulin in 56 low- and middle-income countries, mostly in Africa.
EVA Pharma is also developing its own COVID-19 vaccine and is pursuing further clinical research on next-generation vaccines.