Manager Analytical Development and Quality Control

12 -month contract, Full Time.

I am working with a leading pharmaceutical firm who are presenting a great opportunity for a Manager Analytical Development and Quality Control in Basel Switzerland

Background:
This position will be dedicated to one project - a late phase project. Hence, the ideal candidate must have experience in late-stage projects, regulatory submission and writing of the dossier.
From a technical point of view experience in dissolution is required.
Expertise in vaccines, large molecules or antibody drug conjugate.
Responsible for a project portfolio of up to 4 small projects (typically up to phase 2) or 1-2 highly complex or late-stage projects (typically phase 3 and commercial).
There will be no direct reports.
Full-time onsite presence (no home office)
This contract will be based in Basel. Our client is offering an hourly rate between CHF 78 CHF 86 depending on experience.

Must Haves:
In addition to knowledge of the GMP/regulatory requirements, a strong background in analytical chemistry is required
Broad knowledge in analytical chemistry. Basic knowledge in synthetic chemistry, drug substance processing and/or formulation development, pharmaceutical processing with a deep understanding of pharmaceutical sciences related to drug substance or product development
Experience in the development and performance of analytical tests for a variety of drug substances and products
Personality and disposition to manage professionals effectively in a matrix system
Diligent attention to details. Willingness to limited travel. Mature stable person with a positive and dynamic demeanour
High flexibility, superior communication, time-management and team-working skills
Ability to work independently and to take initiative
Proficient in English. Life-long learning mindset and a strong sense of accountability

If interested, please feel free to contact myself Ibrahim Bokolo via email: (url removed) or (phone number removed).