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Senior Technical Program Lead

vor 2 Monaten

Visp, Schweiz Proclinical Group Vollzeit

Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry
Have a look below and apply or send me your CV directly.

Proclinical is seeking an experienced Technical Program Lead for a temporary contract position of 12 months which is based in Visp, Switzerland.

Join the team and be part of an innovative company that values inclusion, growth, and impact. Our dynamic work environment offers brilliant opportunities for advancement. We're seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Manage a program which focuses on aligning technical specifications and standards to meet our requirements, aiming to derive cost benefits from OPEX and CAPEX projects, and/or redefining best practices to sustain or improve quality as primary targets.
  • Coordinate and track the technical specification and standards creation and updates associated with the targeted areas for improvement, including guidance documents, procedures, and policies where necessary.
  • Collaborate with internal SMEs and standard owners to progress the technical specification and standard review, ensuring alignment with the site's requirements and industry best practices.
  • Support project teams in resolving technical or specification-related issues by facilitating technical competence across multiple disciplines, in addition to coordinating and communicating.
  • Provide regular 'Time, Cost, Quality' updates for the program to SteerCo and C-level as requested.
  • Assist in the development of the turnover process including roles and responsibilities, workflows, and interfaces.
  • Support in the coordination of the turnover scope with Engineering, Construction, and CQV.
  • Prepare and support system boundaries for process and non-process systems.
  • Manage and direct Mechanical Completions Walkdowns, including capture of punch items.
  • Punchlist Management.
  • Prepare Construction Turnover Packages (CTOP).
  • Process and prepare mechanical completion certificates.
  • Receipt and process construction dossiers from contractors.

Key Skills and Requirements:

  • Master's degree in a relevant field (e.g., Engineering, Project Management) or equivalent work experience.
  • Proven relevant work experience (engineering senior level individual with multi-discipline experience in large investment projects, i.e., Pharma/Biotech industry delivery, from concept to commercialization).
  • Strong history in project management, in LEAN management or a related role, with a focus on technical specifications and standards review.
  • Strong understanding of industry best practices and standards applicable to CAPEX projects.
  • Excellent analytical and problem-solving skills, with the ability to identify areas of improvement and ensure technical specifications meet desired outcomes.
  • Effective communication and collaboration skills, with the ability to work with cross-functional teams and stakeholders, including experience in Change management and C-level communication.
  • Detail-oriented with strong organizational skills, capable of tracking and monitoring technical specifications throughout the project lifecycle.
  • Familiarity with project management tools and software is preferred.
  • Fluency in English is a must; fluency in German is advantageous.
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