Radiochemist and Operations Specialist

vor 2 Wochen

Braunschweig, Deutschland Scitech Engineering Ltd Vollzeit

Job Advert

Scitech is a leading Pharmaceutical consultancy at the forefront of radiopharmaceutical innovation. With over 20 years of continuous experience, we specialise in providing comprehensive consulting services to clients in the radiopharma industry, offering expertise in regulatory compliance, quality assurance, and facility design. Our newly established Radiopharmaceutical Centre of Excellence in Germany is positioned to lead the way in traditional and new imaging diagnostics and targeted therapeutic radiopharmaceuticals.

**Role Overview**:
**Key Responsibilities**:

- Lead radiochemistry activities, including synthesis, purification, and analysis of radiopharmaceutical compounds, adhering to strict quality and regulatory standards.
- Oversee the day-to-day operations of radiopharmaceutical production facilities, ensuring compliance with GMP regulations and company policies.
- Develop and implement standard operating procedures (SOPs) for radiochemical processes, equipment operation, and quality control protocols.
- Collaborate with cross-functional teams to optimize production workflows, improve efficiency, and troubleshoot operational issues.
- Perform routine quality assurance checks and validation studies to ensure the integrity and purity of radiopharmaceutical products.
- Train and mentor junior staff members on radiochemical techniques, safety procedures, and operational best practices.
- Maintain accurate documentation and records of all radiochemistry activities, including batch records, analytical data, and regulatory submissions.
- Stay informed about advancements in radiochemistry technology and contribute to the continuous improvement of Scitech's operational processes.

**Qualifications**:

- Bachelor's or Master's degree in Chemistry, Radiochemistry, Pharmaceutical Sciences, or a related field.
- Proven experience in radiochemical synthesis, purification, and analysis, preferably in a pharmaceutical or radiopharmaceutical setting.
- Strong understanding of GMP regulations, quality control principles, and regulatory requirements for radiopharmaceutical manufacturing.
- Excellent organisational skills and attention to detail, with the ability to manage multiple projects simultaneously.
- Effective communication and interpersonal skills, with the ability to collaborate with internal teams and external stakeholders.
- Demonstrated leadership abilities and a proactive approach to problem-solving in a fast-paced environment.

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