Technical Project Manager - Visp, Schweiz - ProClinical

ProClinical
ProClinical
Geprüftes Unternehmen
Visp, Schweiz

vor 2 Wochen

Lena Schneider

Geschrieben von:

Lena Schneider

beBee Recruiter


Beschreibung

Salary:

Highly Competitive


Job type:

ContractDiscipline:

Project Management
Location:

Switzerland- Visp, Schweiz

  • Posting date: 22 Feb 2024

Reference:
59072

Proclinical are recruiting for a Technical Project Manager to join a pharmaceutical organisation. This role is on a contract basis.


Responsibilities:


  • Accountable for the management of the design engineering business from idea to BOD approval.
  • Guide the technical project team to accomplish project objectives and milestones as well as be accountable for the development of the basis of design and potentially implement it until end of OQ.
  • Collaborate with shareholders to develop and own the development of the project scope outline.
  • Assist the selection of design engineering method and partner selection which involves the development of a design deliverables list.
  • Guarantee that the client's technical standards are efficiently discussed and comprehended through the development of a project technical standard.
  • Other duties may be assigned.

Key Skills and Requirements:


  • Educated to a degree/advanced degree level in an engineering field such as process, pharmaceutical, biochemical or similar.
  • Demonstrable experience in project engineering and project management for a chemical, biochemical, pharmaceutical organisation with global experience.
  • A taskfocused individual who is comfortable working towards set goals and a background in accomplishing outcomes.
  • Familiarity within cost control and timetabling linked to investment projects.
  • Acquaintance within engineering aspects of facility design to build a compliant but costefficient plant.
  • Expertise on modern CQV approaches to minimise the time from construction accomplishment to routine production while maintaining compliance.
  • Computer literacy.
  • Comprehension of how the CDMO industry/business works.
  • Works well both in a team as well as independently.
  • Influential and communication skills both verbally and in writing.
  • Fluency in the English language.
  • Leadership abilities.
  • An organised individual with the ability to work on various tasks and priorities concurrently.
  • Capable of resolving issues.
  • Project management skills.
  • Prior involvement in engineering and cGMP manufacturing of chemical and biological APIs.


Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

Engineering

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