Job description
We are seeking an experienced scientist with excellent people skills and well-established project management credentials who is keen to learn more and join our dynamic and highly talented Analytical Research and Development group in Sandwich. Our offer:
Focus on work life balance and other benefits- Flexible workplace culture
- Full time and part time options
- Growth and Talent development
- Diverse and inclusive workforce
- Annual bonus
- Car allowance
Competitive compensation and flexible benefits package with a company car allowance, a good work-life balance and a fun, rewarding career with opportunities every day to work with other highly talented scientists on novel drug candidates. Myriad opportunities to learn new skills, develop existing strengths and coach and mentor other colleagues, while pursuing our purpose – to find breakthroughs that change patients’ lives.
The successful candidate will have a proven track record in pharmaceutical development from an analytical chemistry or formulation science background and will support Pfizer’s Pharmaceutical Sciences Small Molecule portfolio through direct management of analytical team(s). They will use their experience and broad knowledge of pharmaceutical R&D to guide teams in developing effective tools to characterise drug products and develop control strategies appropriate for clinical development and commercialisation of potential small molecule breakthrough medicines. They will work in cross-functional project teams and collaborate with chemists, engineers, analysts and formulators from across Pfizer’s global organisation.
Role
- Steer a team of analytical scientists in R&D drug product activities associated with novel, innovative, breakthrough medicines currently in clinical development, including treatments for Covid-19, rare infectious disease, cancer and other life-threatening conditions.
- Apply extensive knowledge and experience of pharmaceutical development to guide the development of robust analytical technologies and control strategies.
- Provide exemplary support to projects through all phases of clinical development through to commercial approval.
- Represent the ARD line on global, cross-functional project teams.
- Be accountable for relevant content of sections of CMC regulatory documentation, e.g. IND, IMPD, CTDs.
- Provide technical direction and coaching/mentoring to colleagues, the department and across Pharmaceutical Sciences.
- May provide presentations, training and advice to others to share learnings and promote increased scientific, technical and strategic comprehension around the area of pharmaceutical development.
- Be a positive advocate for new technology, process improvements and for the application of computational tools and digital design approaches.
Qualifications
Skills and Experience
- A team orientated person with significant, relevant experience in the pharmaceutical industry or a closely related industry.
- Excellent communication and project management skills for this highly interactive position.
- Very good knowledge of small molecule pharmaceutical development and global regulatory expectations, particularly with respect to analytical science, and an ability to apply scientific technical skills and knowledge to projects independently and proactively.
- Experience in contributing to the authoring of external publications and CMC regulatory submissions is highly desirable.
- A rational approach to problem solving with strong attention to detail and a desire to learn and grow their skills.
- Good laboratory safety understanding.
- Knowledgeable in the use of diverse computational, modelling and simulation tools would be beneficial.
- Experience in management is desirable.
Location: On Premise, Sandwich, Kent