Process Manager

Bruxelles (BE)
vendredi 2 juin 2017
Date limite
lundi 17 juillet 2017
Niveau d'expérience
> 10 ans d'expérience
Type de contrat
Temps de travail
Temps plein

ASIT biotech s.a. (formerly Biotech Tools) is a clinical stage biopharmaceutical company focused on the development and future commercialization of a range of breakthrough immunotherapy products for the treatment of allergies, based on its ASIT+TM technology platform.

ASIT biotech is looking for a

Process Manager


Job Description


The ideal candidate has an in-depth knowledge of protein purification and characterisation in the manufacturing department inside of biopharma or pharma industry.


The  job requires at least  10  years of experience  including 5  years in industrial production supervision.


We need a change agent who is passionate, has high energy, and is results-oriented. This role needs to have experience with state-of-the-art project management tools, and processes. You should have the ability to manage critical situations.




In the context of the management of externalized GMP compliant manufacturing operations:


•    Coach, support and coordinate the purification operations in an industrial scale.


•    Supervise the technology and knowhow transfer, establish the GMP production documentation, set data and trends analyses and the follow up of investigations no compliances.


•    Overview, manage and facilitate manufacturing operations conducted at and by independent third party contract manufacturing organizations.


•   Maintain technology, regulatory surveys.


•    Plan, schedule, and control project activities to fulfil objectives and satisfy project requirements.


•    Lead, coordinate, facilitate, and motivate all internal and external manufacturing teams to reach alignment on project goals and deliverables.


•   Manage projects within established scope, schedule, and budget.


•    Develop and document high-level strategies for accomplishing specific project objectives.


•    Facilitate and lead effective project meetings, manage change and conflict, and develop resource planning estimates to manage project workload and productivity.


•    Support, inform and align with cross functional project management team members to ensure success of projects, including development operations, quality control, quality assurance and regulatory affairs departments.


•    Manage a young, enthusiastic and talented team of researchers



Skills & expertise


•   Master’s degree in Engineering, Chemistry or Biochemistry


•    More than 10 years of industry experience in research, tech transfer and production of purification of proteins (scientific and technical) in an industrial environment (pharmaceutical, biotechnology, and/or medical device industries).


•    Interpersonal and leadership skills to effectively communicate and build relationships with a broad spectrum of audiences at all organizational levels as well as with third party contract manufacturing organizations.


•    Sound technical aptitude and proven ability to grasp general knowledge of multiple disciplines and technologies.


•    Strong competencies in organization and rigor with the ability to lead multiple activities and resources while maintaining a focus on quality.


•   Results oriented.


•   Work ethic, integrity, and professional conduct and appearance.


•    Ability to produce and present clear, concise, and professionally written communications and presentations.


•   Positive attitude, plenty of energy, and excellent interpersonal skills.


•   Commitment to the company objectives and its success.


•   Able to manage rapid change. Agility.






  • A full time position, permanent contract
  • A remuneration that will be in line with the industry standards + additional benefits.
  • An innovative leading company, which could enable you to explore interesting career opportunities.
  • A multicultural work environment in which competence and quality play an important role



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