Lead the design and execution of reverse engineering studies, develop and validate analytical methods, and provide technical support to a pharmaceutical development team in a lab-based role. Key activities include:
1. Leading the design and execution of reverse engineering studies to support the development process for pharmaceutical equivalence projects
2. Developing and validating analytical methods, where required, to support reverse engineering studies in accordance with the relevant guidelines
3. Providing technical support to the pharmaceutical development team to aid in troubleshooting of analytical methods
4. Compiling and reviewing protocols and reports in line with both industry standard and company procedures
5. Maintaining an awareness of current guidelines in UK/Ireland, EU, US and ROW in relation to industry best practice for reverse engineering studies, dissolution studies, method development and validation, and where appropriate cascading training to the pharmaceutical development team for changing trends
The ideal candidate will have a Bachelor's degree in a chemistry, analytical or pharmacy related discipline, and at least 5 years of experience in a pharmaceutical development role. Essential skills include expertise in dissolution method development, experience in reverse engineering, and strong problem-solving and communication skills. The company offers a competitive salary, subsidised canteen, and development opportunities. The role is a technical manager position in a pharmaceutical company, responsible for leading a team of scientists developing a wide range of pharmaceutical dosage forms, including oral tablets, suspensions, sterile injectable suspensions and solutions, and intra-mammary preparations. The ideal candidate will have a passion for scientific discovery, a strong work ethic, and the ability to work effectively in a team environment.
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