Callisto Pharma Group
Jill Convery has a strong background in quality assurance and regulatory affairs within the pharmaceutical industry. With experience at companies like Callisto Pharma Group, 3M, and Boehringer Ingelheim Pharmaceuticals, Jill has worked in roles such as Quality Associate, Quality Engineer, QA Administrator, and Analytical Chemist. Jill is skilled in managing importation processes, batch documentation, liaising with stakeholders, updating SOPs, and performing internal audits. Jill holds a Certificate in GMP Pharmaceutical Quality Systems Auditor/Lead Auditor and has a background in Bioinformatics and Biotechnology.
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Callisto Pharma Group
PROVIDING SOLUTIONS, CREATING OPPORTUNITIES…. Callisto Pharma Group provide consultancy expertise across the complete pharmaceutical supply chain, from product development, licensing and pharmacovigilance, through to batch certification, import release and distribution. We provide our services internationally with Clients ranging from global manufacturers to single product licence holders. Our team have extensive experience of human, veterinary and herbal medicines, medical devices, borderline products, biocides and food supplements over most dosage forms. We work to your specific needs, providing tailored solutions and expertise to help enable your business to realise its potential. A PRACTICAL APPROACH…. Our approach is one of flexibility and adaptability; we listen to our clients’ needs and requirements, making a real difference to the assignments we are involved in. We believe our differentiator is how we use our experience and knowledge of what works in practice as well as in theory. Our expertise lies in our knowledge, operating in real world environments, recognising the fact that during any assignment we have an opportunity to positively impact our Clients business.