Retrofit Automation Engineer (Freelance)
We are looking for an Automation Engineer specialising in retrofit, machine integration, and PLC programming for complex machinery like glass processing and similar. This project offers very high flexibility in terms of working days, working hours and also workload. So this could be ideal as a side project or similar, working next to existing projects and clients. 
Responsibilities: Execution of retrofit projects for existing machines Modification and expansion of PLC programs (manufacturer flexible, e.g., Siemens, Pilz) Implementation of safety controllers (e.g., Pilz) Integration of machines into existing systems Creation and updating of circuit diagrams and parts lists Work with pneumatics, hydraulics, and electrical components Close collaboration with mechanical engineers to define requirements Support in optimising the machine park Requirements: Experience in retrofit projects Solid knowledge of PLC programming  Knowledge of pneumatics, hydraulics, and safety controllers preferred Hands-on mentality and enthusiasm for working with older machines Technical understanding of mechanics and handling systems
  **Please apply directly online with your CV, if you are eligible to work in Switzerland **
headcount AG

Elektriker / Electrician (w/m/d)
Für unseren Kunden in Bern suchen wir derzeit eine/n Elektriker für das Engineering-Team, um Installationen, Wartungen und Reparaturen an den Anlagen auszuführen.
Aufgaben:
Durchführung von Installationen, Instandhaltungs- und Reparaturarbeiten an elektrischen Anlagen und Systemen Sicherstellung der Einhaltung aller geltenden Normen und Vorgaben Fehleranalyse sowie rasche und nachhaltige Behebung elektrischer Störungen an Produktions- und Infrastrukturkomponenten Pflege und Erstellung technischer Dokumentationen (z.?B. Stromlaufpläne, Prüf- und Wartungsberichte) gemäss den regulatorischen Anforderungen (GMP) Profil: Abgeschlossene Berufsausbildung als Elektroinstallateur EFZ oder Elektromonteur EFZ Berufserfahrung, idealerweise in einem GMP-regulierten Umfeld (z.?B. Pharma-, Biotech-, Chemie- oder Lebensmittelbranche)  Deutschkenntnisse in Wort und Schrift, Englischkenntnisse von Vorteil Sicherer Umgang mit Steuerungs- und Überwachungssoftware sowie fundierte MS-Office-Kenntnisse und Erfahrung mit Instandhaltungssoftware
**Please apply directly online with your CV, if you are eligible to work in Switzerland **
headcount AG

Formulation & Process Development (Project) Manager

Description
Our client is a leading pharmaceutical company seeking an experienced Senior Project Manager to drive the development and manufacturing of innovative softgel formulations.
Responsibilities Lead the development of pharmaceutical dosage forms and softgel manufacturing processes. Manage project planning, budgeting, and coordination with internal and external stakeholders. Optimize formulation and manufacturing processes, including encapsulation and drying. Ensure regulatory compliance with GMP, FDA, and ICH guidelines. Oversee technology transfer from R&D to production. Troubleshoot formulation and process issues, ensuring quality and efficiency. Prepare technical and regulatory documentation.
Requirements Master’s or Ph.D. in Pharmaceutical Sciences, Chemistry, or related field. Significant experience in softgel formulation development. Strong expertise in encapsulation processes, gelatin composition, and lipid-based formulations. Knowledge of analytical methods, stability studies, and regulatory requirements. Fluent in German and English.

Gebietsleiter Augenoptik (m/w/d) Zentral- & Ostschweiz 
Unser Kunde, ein führendes Unternehmen im Bereich der Augenoptik, sucht eine/n engagierte/n und kundenorientierte/n Gebietsleiter (m/w/d) für den Vertrieb hochwertiger Kontaktlinsen und Pflegemittel. In dieser Rolle bringen Sie innovative Produkte auf den Markt, betreuen bestehende Kunden und bauen nachhaltige Geschäftsbeziehungen auf.
Ihre Aufgaben:
Vertrieb eines vielseitigen und innovativen Produktportfolios im Bereich Kontaktlinsen und Pflegemittel
Aufbau und Pflege langfristiger Kundenbeziehungen mit Kontaktlinsenspezialisten, Augenoptikern und Fachgeschäften
Entwicklung und Umsetzung massgeschneiderter Vertriebskonzepte gemeinsam mit den Kunden
Planung und Organisation von Produktschulungen, Veranstaltungen und Messen
Effiziente Terminplanung und Berichtswesen zur kontinuierlichen Optimierung der Vertriebsaktivitäten
Ihr Profil:
Erfahrung in der Augenoptik und/oder im Vertriebsmanagement
Kontaktfreudige, souveräne Persönlichkeit mit starkem Kundenfokus
Analytisches Denkvermögen und Offenheit für neue Ideen in einem dynamischen Umfeld
Selbstständige, strukturierte Arbeitsweise und hohe Eigenmotivation
Führerschein der Klasse B sowie sichere PC-Kenntnisse, insbesondere in Microsoft Office
Unser Angebot:
Unbefristete Festanstellung in einem innovativen Unternehmen mit motivierendem Betriebsklima
Eigenverantwortliches Arbeiten in einem dynamischen Team mit kurzen Entscheidungswegen
Umfangreiche Einarbeitung sowie kontinuierliche Schulungen und Weiterbildungen
Flexible Arbeitszeiten, mobiles Arbeiten und 30 Tage Urlaub
Attraktive Vergütung mit Bonusregelung sowie ein Dienstwagen zur privaten Nutzung
Bereit für den nächsten Karriereschritt?
Wir freuen uns auf Ihre Bewerbung!

Clinical Trial Liaison Manager
Location: Basel
Contract: 12-month contract
Start Date: ASAP
Workload: Full-time

Overview:
Our client, a global pharmaceutical company, is looking for a Clinical Trial Liaison Manager (CTLM). This role is focused on trial delivery and oversight, ensuring high-quality data and timely patient recruitment.

Key Responsibilities:
Acting as the sponsor’s main point of contact for site staff and investigators Supporting Principal Investigators in developing and executing enrolment strategies Collaborating with CRAs and site coordinators to improve recruitment and site performance Overseeing and tracking patient recruitment across assigned sites and countries Conducting Sponsor Oversight Monitoring Visits (SOVs) to ensure CRO monitoring quality Supporting site teams in maintaining protocol adherence and resolving operational issues Monitoring data quality through remote and on-site review Maintaining strong relationships with key sites and providing operational insights Escalating risks and challenges to internal trial teams or the CRO in a timely manner Ensuring compliance with GCP, local regulations, SOPs, and internal policies
Required Qualifications:
Bachelor’s degree in pharmaceutical sciences, biology, healthcare, or related field Experience working with CROs and managing trial site performance Strong knowledge of the clinical trial landscape, including patient pathways and recruitment dynamics Skilled in stakeholder communication (internal teams, sites, KOLs, networks, CROs, etc.) Demonstrated leadership with the ability to influence without authority Proactive problem-solver with strong analytical and organizational skills
Fluent in English and French (written and spoken) – additional languages are a plus Familiar with tools and systems used to manage clinical studies Willing to travel up to 60%

Please apply directly online with your CV.

**Please only apply if you are eligible to work in Switzerland and the EU *
headcount AG

Ever dreamt of being an Astronaut or a Pro Athlete? How about being the best at something, just for the ride?
Great - this might be of interest to you!
We're expanding our  team and seeking experienced Recruitment Professionals ready to elevate their game. Say goodbye to unrealistic KPIs, micromanagement and 24/7 office presence, and embrace a role where you can truly focus on creating a world class service by growing both - as a consultant and as an individual. 
This 360 role focuses on delivering top-tier technical and scientific talent to our European client base. Partnering with leading Life Science companies, you'll be part of a highly capable team in an environment that encourages your personal growth by commitment, curiosity and authenticity.
If you're a big-game player who loves people, thrives in a team, and is fueled by the idea of delivering the best-in-class service to an industry that sustains human life, you might want to say hello.


KEY RESPONSIBILITIES

European Talent Sourcing: Search, identify, and deliver high-quality talent to the Life Science industry across Europe.  Full Life Cycle Ownership : Own the recruitment process from job intake all the way to sourcing, presentation and contract negotiations. Key Account Management: Actively participate in client interactions with our strong existing client base, understanding their unique needs and provide tailored recruitment solutions.  Client Development: Proactively identify and pursue new business opportunities, contributing to the expansion of our client base within the Pharma/Biotech & Devices sectors. Network Building: Participate in networking events to meet prospects to maintain and develop long-term relationships. Collaborative Team Player: Be on eye-level with your colleagues and our leadership, share your ideas, support your team. 
REQUIREMENTS

First experience in agency recruitment (1-3 years), preferably in Life Science or related industries. Demonstrated ability to source and deliver talent across Europe. First experience in Sales or BD. Genuine drive to create an outstanding experience for other people. Professional fluency in German and English (both are must haves due to our client base) EU or Swiss work permit. Be a nice person.
BENEFITS

Human-centric culture, experienced leadership, minimal KPIs, genuine support for your development. Immerse yourself in a highly international environment. Work from a beautiful office in the heart of Zurich, just 5 minutes from the lake. Benefit from high flexibility in work hours, including the option for home office or work from abroad. Constant training and a career success plan to fuel your professional growth. People who sing when they are winning.

ABOUT HEADCOUNT
headcount AG is a Zurich-based consultancy serving clients in the pharmaceutical, biotechnology, medical device and digital healthcare space. At headcount, we are thriving to create the best recruitment experience possible - for our candidates and clients alike. Based on our core values of authenticity, curiosity and commitment, we aim to deliver top-tier staffing solutions, so our clients and candidates can focus on doing what they do best: advancing human healthcare.
Get in touch!

Clinical Development Director
Location: Basel
Contract: 6-month 
Start Date: ASAP
Workload: Full-time
We are seeking a Director of Clinical Development to lead the medical and strategic efforts behind ongoing evidence generation. This role is key to supporting market expansion and long-term product positioning.
Your Tasks: 
Drive the development and execution of evidence generation strategies to support commercialization and market access. Provide medical and scientific leadership ensuring seamless progression from late-stage development to post-marketing activities. Guide protocol development, study design, and clinical data interpretation. Collaborate cross-functionally with regulatory, commercial, and market access teams to align clinical deliverables with business goals. Act as a senior expert and coach for the clinical development team, ensuring knowledge transfer and operational continuity from day one. Support internal decision-making with clinical insights and risk mitigation strategies. Represent Clinical Development in cross-functional leadership discussions. Directly oversee and contribute to trial execution, ensuring seamless progression from late-stage development to post-marketing activities.
Your Profile:
Medical Doctor (MD). Extensive experience in clinical development, particularly in post-approval or late-phase (II/III) activities . Background in rare diseases , neurology , neuromuscular , or pediatric indications is a plus. Proven ability to translate clinical data into strategic evidence generation plans. Skilled in cross-functional collaboration with regulatory, market access, and commercial teams.

Please apply directly online with your CV.
**Please only apply if you are eligible to work in Switzerland and the EU *
headcount AG

Clinical Operations Lead
Location: Basel
Contract: 6-month 
Start Date: ASAP
Workload: Full-time
Our client, a Swiss biopharmaceutical company, is seeking a Clinical Operations Lead to oversee ongoing clinical activities and lead a small team through a period of change and growth. This is a hands-on leadership role, ideal for someone who thrives in dynamic environments and can bring clarity, structure, and motivation to a fast-evolving team.
Your Tasks: 
Lead and support a clinical team (CTLs and CRAs), providing day-to-day guidance and long-term vision. Oversee clinical trial execution, ensuring adherence to timelines, budgets, and quality standards . Ensure strong collaboration with CROs, regulatory, and market access teams to align clinical operations with global submissions and commercial strategies. Take ownership of clinical trial planning and forecasting , with a focus on accountability and proactive risk mitigation. Act as a key interface with internal stakeholders, including finance and executive teams, to report progress and secure alignment on timelines and resources.
Drive motivation and engagement within the clinical operations team through structured leadership and transparent communication. Contribute to submission readiness activities and ensure operational excellence across the board.
Your Profile:
Medical Doctor (MD). Solid experience in clinical trial management , with prior oversight of both CTLs and CRAs. Proven ability to bring structure and clarity to growing or transitioning teams. Strong track record working with CROs , regulatory, and commercial access functions. Experienced in managing clinical timelines, budgets, and vendor performance .
Please apply directly online with your CV.
**Please only apply if you are eligible to work in Switzerland and the EU *
headcount AG

Wir bieten Dir: Aufstiegsmöglichkeiten eine interessante Herausforderung in einem erfolgreichen und stetig wachsenden Unternehmen angenehmes Arbeitsklima im jungen Team abwechslungsreiche Aufgaben gute und faire Entlöhnung Dein Aufgabenbereich: Neu- und Umbauten Unterhaltsarbeiten Wege und Plätze erstellen Pflegearbeiten
Wir erwarten: Ausbildung zum Landschaftsgärtner EFZ rasche Auffassungsgabe Teamfähigkeit speditive und exakte Arbeitsweise Haben wir dein Interesse geweckt? Dann freuen wir uns auf die Zustellung deine Bewerbungsunterlagen.

Für unsere Kundin suchen wir für den Shop in Wetzikon einen oder eine talentierte Sales Consultant Telekommunikation / Consum Electronis / Multimedia. Wir bieten Dir: Fixer Stundenlohn von 33.06 CHF Brutto bei einer 40 Stundenwoche und Provision Umfassende Einarbeitung in die Produkte und das Unternehmen Professionelle Betreuung vor und während der Anstellung Festanstellung in Aussicht Spannende Entwicklungsmöglichkeiten innerhalb des Unternehmens Das erwartet Dich: Beratung und Verkauf von Dienstleistungen im gesamten Portfolio Mithilfe bei der Ladengestaltung und der Produktepräsentation Begeisterung der Kunden und für beste Kundenzufriedenheit sorgen Erledigung von Spezialaufträgen nach Anweisung des Shopleiters Führung der Kasse Das fordern wir: Abgeschlossene Lehre als Verkäufer / Verkäuferin / Detailhandelsfachmann / Detailhandelsfachfrau / Detailhandelsassistent / Detailhandelsassistentin / Fähigkeitszeugnis / EFZ /EBA Erfahrung in der Kundenbetreuung und Freude am Kundenkontakt Deutschkenntnisse Selbstsicheres Auftreten Technische Affinität flexibel, auch an Wochenenden verfügbar Bei Einstellung muss ein Strafregisterauszug vorgelegt werden, welcher nicht älter als 3 Monate ist und ohne Einträge Haben wir Dein Interesse geweckt? Dann freuen wir uns auf die Zustellung Deiner Bewerbungsunterlagen.