Belgium Job Openings
Telix Pharmaceuticals (EMEA)
Manager, Radiochemistry
Seneffe
August 13, 2024
As the Manager, Radiochemistry, you will be reporting to the Production Director, you will play a pivotal role in our brand-new radiopharmaceutical production facilities. Your primary responsibilities will include orchestrating all strategic and operational activities related to the development and validation of radiopharmaceutical products. Additionally, you will be responsible for managing the Development & Validation team, including overseeing their work and professional development.
Key Accountabilities:
- Lead development, validation and technology transfer of radiopharmaceutical products within the facility.
- Drive process optimization and continuous improvement initiatives.
- Provide clear leadership and vision, inspire and motivate staff to achieve excellence, and mentor them as they develop new skills.
- Set team strategy and objectives, monitor ongoing progress and performance, and report on activities regularly to the Senior Management team.
- Be responsible for developing the appropriate team structure and resource plans, as well as policies and workflows to support the business objectives.
- Drive a collaborative work environment that focuses on facilitating the exchange of information and creating a strong culture of quality, compliance, and operational excellence within the team.
- Contribute to new business initiatives and projects.
- Remain current on industry and regulatory trends.
- Manage the budget, including forecasting and follow-up.
- Build long-term, trusting relationships with internal and external stakeholders, business partners, and authorities.
- Act as a company representative towards partners, visitors, and authorities. Execute public speaking and representational appearances in a professional manner.
- Ph D in Radiochemistry or nuclear medicine or equivalent relevant experience.
- Minimum of 10 years of combined experience in a radiochemistry/radiopharmacy laboratory or environment, and in the development, validation, and tech transfer of manufacturing processes within the pharmaceutical industry.
- Strong knowledge of radiometal chemistry.
- Technical understanding of large molecule peptides and antibodies, with a working knowledge of bioconjugation of antibodies.
- Hands-on experience in Alpha isotopes radiolabeling development would be considered as an asset.
- Prior experience in a management role is desirable.
- Good understanding and application of c GMP and regulatory requirements.
- Good understanding of drug development and associated regulation.
- Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
- Strong leadership, strategic and organizational abilities.
- Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
- Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
- Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
- Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
- Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
- Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
- Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
- Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills
- Language Skills: Fluent in English. French would be considered as an asset.
- Proficient in the use of Microsoft Office applications.
- Ability and willingness to work collaboratively with global team members across multiple time zones.
Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
VIEW OUR RECRUITMENT PRIVACY POLICY HERE
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