Jobs / Switzerland / Tech'Firm Industrie AG

Tech'Firm Industrie AG

Process Engineering Expert – Pharma / Biotech (m/w/d)

Switzerland Posted yesterday

Apply on company site ↗ Source: EURES (European Commission) Tailor my CV

Free account: one tailored CV and cover letter included. You always apply on the employer’s own page.

Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal: ask the recruiter.

  • No government sponsor record hereThis employer posted directly and does not match a government sponsor register.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →

About the role

Shape the Future of Biopharmaceutical Manufacturing with Techfirm Engineering! 🇨🇭 Techfirm Engineering is looking for an experienced Process Engineering Expert – Pharma / Biotech (m/w/d) to join our Industrial Services team in Switzerland. The selected consultant will play a key role in investment projects within a biopharmaceutical manufacturing environment, providing technical leadership across process technologies from concept development and design to procurement, commissioning, start-up, and qualification. Working closely with Quality Assurance (QA), Operations, Plant Engineering, Procurement, and CQV teams, you will ensure that process systems are designed, implemented, and qualified in accordance with applicable regulatory requirements, technical standards, and project objectives. **RESPONSIBILITIES** -Provide technical leadership and expertise across process technologies and systems. -Support investment projects throughout the concept, design, procurement, start-up, commissioning, and qualification phases. -Develop process concepts, design solutions, and process philosophies in collaboration with QA, Operations, and Engineering. -Define, develop, and roll out process standards and engineering philosophies aligned with global and local requirements. -Coordinate technical activities involving multiple stakeholders and ensure clear alignment across project teams. -Provide construction support and lead the development of commissioning philosophies and field commissioning activities. -Support qualification activities in close collaboration with Commissioning, Qualification, and Validation (CQV) teams. -Organize and lead technical review meetings to ensure cross-functional alignment and approvals. -Collaborate closely with QA, Operations, Plant Engineering, and Procurement to address all technical, operational, and quality requirements. -Ensure that process solutions comply with applicable regulations, internal standards, and established solutions across the company's global network. **WHAT WE ARE LOOKING FOR** **EDUCATION & EXPERIENCE** -Master’s degree in Process Engineering, Chemical Engineering, Biotechnology, Bioprocess Engineering, or a related technical field is required. -Extensive experience in Process Engineering within the pharmaceutical or biopharmaceutical industry. -Proven expertise in process system design, engineering, and implementation within investment projects. -Strong experience across the project lifecycle, from concept development and design through procurement, commissioning, start-up, and qualification. -Knowledge of biopharmaceutical manufacturing processes and associated process equipment. -Experience collaborating with CQV, QA, Operations, Plant Engineering, and Procurement teams. -Strong understanding of GMP requirements, regulatory standards, and engineering best practices. -Experience leading technical reviews, coordinating multidisciplinary stakeholders, and providing expert-level technical guidance. **PERSONAL SKILLS** -Strong technical leadership and decision-making capabilities. -Excellent project coordination and stakeholder management skills. -Structured, proactive, and solution-oriented working style. -Ability to align multiple stakeholders and drive cross-functional decisions. -Strong communication skills and the ability to provide clear technical direction. -Collaborative mindset with a strong focus on quality, compliance, and technical excellence. **LANGUAGES** -Fluent German is mandatory (written and spoken). -Good command of English, both written and spoken, is required. **WHY TECHFIRM?** At Techfirm Engineering, you will: 🇨🇭 Join a Swiss-established company with more than 25 years of experience in the Swiss industrial market. 🧬 Contribute to complex and meaningful proj

Apply on company site ↗