We are seeking a knowledgeable and detail-oriented Pharmaceutical Consultant to join our team. This role is essential in providing expert guidance on pharmaceutical products and processes, ensuring compliance with industry regulations, and supporting product development initiatives. The ideal candidate will possess a strong background in biochemistry and quality control, along with hands-on laboratory experience.
Duties
Provide expert consultation on pharmaceutical product development and regulatory compliance.
Provide support & Strategic advice for regulatory submissions such investigational new drug submissions (IND), New drug applications (NDA), and Marketing Authorisation Applications (MAA)
Compliance Consulting: ensure clients adhere to UK and EU regulatory standards, including MHRA AND EMA AND ICH.
Assist in developing regulatory strategies for new and existing drugs.
Review and prepare regulatory documentation, ensuring compliance with relevant regulations and guidelines.
Conduct scientific research to support product innovation and improvement.
Oversee quality control processes to ensure adherence to CGMP (Current Good Manufacturing Practices) standards.
Collaborate with cross-functional teams to develop and implement laboratory information management systems.
Prepare detailed reports and presentations on findings and recommendations for stakeholders.
Qualifications
A degree in Biochemistry, Pharmaceutical Sciences, or a related field is essential.
Proven experience in scientific research and quality control within a pharmaceutical or biotechnology environment.
Familiarity with CGMP, MHRA, EMA and ICH regulations and their application in product development.
Previous experience is highly desirable.
Excellent analytical skills with a keen attention to detail.
Strong communication skills, both written and verbal, to effectively convey complex information. Join us as we strive to advance the pharmaceutical industry through innovative solutions and expert consultancy.
Job Type: Full-time