
1 - 10 employees
💊 Pharmaceuticals
📋 Compliance
🤝 B2B
Pharmaceuticals • Compliance • B2B
Integraleaf is a regulatory consulting and outsourcing firm specializing in Qualified Person (QP) services and regulatory affairs for growth-oriented pharmaceutical companies, startups, SMEs, and cross-industry founders. They provide modular, practice-tested services including QP outsourcing (QP, responsible person for narcotics trade, wholesale, and manufacturing lead roles), GMP/GDP/GxP compliance, inspection and audit preparation (including mock audits and audits in non-EU countries), tailored SOP development, and cannabis regulatory support. Additional offerings include business development, strategic procurement and distribution support, financial advisory, and regulatory-compliant marketing and training to help clients scale safely and efficiently.
🕒 March 19
🗣️🇩🇪 German Required
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1 - 10 employees
💊 Pharmaceuticals
📋 Compliance
🤝 B2B
Pharmaceuticals • Compliance • B2B
Integraleaf is a regulatory consulting and outsourcing firm specializing in Qualified Person (QP) services and regulatory affairs for growth-oriented pharmaceutical companies, startups, SMEs, and cross-industry founders. They provide modular, practice-tested services including QP outsourcing (QP, responsible person for narcotics trade, wholesale, and manufacturing lead roles), GMP/GDP/GxP compliance, inspection and audit preparation (including mock audits and audits in non-EU countries), tailored SOP development, and cannabis regulatory support. Additional offerings include business development, strategic procurement and distribution support, financial advisory, and regulatory-compliant marketing and training to help clients scale safely and efficiently.
• Ensuring the proper manufacture and release of medical cannabis • Fulfilling duties as a Qualified Person in accordance with §15 of the German Medicines Act (AMG) • Acting as the Responsible Person under the Medicinal Cannabis Act (MedCanG) • Providing consultancy and training to cannabis companies within and outside Europe • Liaising and coordinating with the relevant authorities • Supporting and further developing quality standards and processes
• University degree in Pharmacy, Chemistry, or Biology • At least two years of practical professional experience in pharmaceutical quality assurance, production, or quality control • Thorough knowledge of Good Manufacturing Practice (GMP) and regulatory requirements in the pharmaceutical industry • Strong sense of responsibility, analytical skills, and decision-making ability • High level of initiative and the ability to work independently • Excellent communication skills • Business-fluent German and English, both written and spoken • Permanent residence in Germany • Willingness to undertake regular business travel within Germany • Willingness to travel occasionally worldwide (approx. 2–5 times per year) • Clean criminal record (does not need to be submitted with the application)
• Flexible working hours that can be adapted to your daily life • A fully remote position • A respectful and appreciative working environment • Trust-based, results-oriented leadership style • Flat hierarchies and short decision-making processes • A varied role in a fast-changing market • A dynamic and supportive team that will back you up • 30 days' vacation with flexible use • Possibility of profit-sharing based on performance
Apply Now🕒 March 19
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