Celgene International SaRL Posted October 13, 2026

Technician Manufacturing, Launch Operations

Boudry, Switzerland Full time
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Celgene International SaRL is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”, a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Mission principale:

Le Technician Manufacturing, Launch Operations aura pour mission d’assurer les activités de fabrication des produits essentiellement sous forme de

comprimés, dans le respect de la réglementation BPF / GMPs, des règles d’hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.

Responsabilités:

Réaliser des opérations de production tel que la pesée des matières, la préparation des mélanges de poudre ainsi que la conduite de ligne automatisée dans les activités de fabrication de comprimés suivant son curriculum de formation et selon les procédures en vigueur du système qualité.

Supporter techniquement les opérateurs dans les activités de production. Participer et supporter de manière active aux transferts de nouveaux produits, à la validation des procédés industriels, à la fabrication des lots de validation et à la qualification des équipements.

Maitriser l’outil MES (Manufacturing Execution System) dans la gestion des dossiers de lot et des consommations associées.

Maîtriser et effectuer le nettoyage des équipements du matériel et des salles liées aux différentes étapes de production.

Effectuer les changements de format et le vide de ligne production.

Mettre à jour et créer des documents techniques nécessaires au fonctionnement des équipements et de la ligne (instructions d’utilisation, de nettoyage).

Se conformer aux directives et instructions définies dans le système qualité de notre site pharmaceutique.

Assurer la réalisation des opérations de production des lots techniques, commerciaux et cliniques en environnement GMP et travailler de façon autonome et efficace selon les consignes de son responsable.

Contrôler, enregistrer et compléter les documents de travail préétablis pour assurer un suivi des opérations réalisées (dossiers de lots remplis selon les BPF / GMP).

Effectuer les contrôles physiques élémentaire des produits fabriqués.

Se conformer aux objectifs de production notamment au respect du planning établi.

Assurer le suivi jusqu’à la reprise de la production lors d’intervention demaintenance sur un équipement.• Analyser les pannes d’équipements et être support à la maintenance encas d’intervention.

Réaliser les changements de formats et réglages de base définis dans les procédures.

Être référent technique pour les opérateurs.

Former les nouveaux collaborateurs et les opérateurs sur les différentes lignes de production et être le réfèrent de la formation (On the Job Qualified Trainer).

Participer à l’amélioration continue en proposant des idées d’améliorations sur les lignes.

Se conformer aux règles de sécurité et de sureté du sitepharmaceutique.

Annoncer les situations dangereuses, les presqu’accidents/incidents etles accidents qui pourraient survenir sur le site auprès de sonresponsable direct et auprès du département EHS (Environment, Health& Safety).

Cette description de poste n’est pas exhaustive ; d’autres tâches et responsabilités peuvent être confiées en fonction des besoins de l’entreprise.

Profil requis:

Avoir une formation initiale de niveau CFC et une expérience de 5 ans dans la production pharmaceutique ou idéalement 3 ans comme technicien dans l’industrie Pharmaceutique.

Connaître parfaitement l’environnement BPF / GMP, et avoir une bonne connaissance de l’industrie pharmaceutique, notamment dans les différents process de fabrication de forme solide tel que la compression de poudres, la granulation humide / sèche, le pelliculage.

Avoir une parfaite maîtrise du français et des notions d’anglais (A2).

Etre organisé et rigoureux, et avoir de grandes qualités relationnelles pour un travail d’équipe.

Communiquer de façon claire avec les services support ainsi que les personnes responsables du développement des nouveaux produits.

Avoir un esprit critique et est force de proposition dans un but d’amélioration continue (certification yellow belt).

Savoir utiliser les outils informatiques (Word, Excel, Power point, Outlook) et de maitriser le fonctionnement d’un MES.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to  adastaffingsupport@bms.com . Visit  careers.bms.com/eeo-accessibility  to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:  https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at  https://careers.bms.com/fraud-protection .

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at  TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1607223 : Technician Manufacturing, Launch Operations

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Boudry, Switzerland
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.

3753Comparable roles tracked
3372Currently active
173Companies hiring similar roles
64Countries represented

Salary context

921 of 3753 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Biologics Support Operator I (3rd Shift) · AbbVie $14/hr – $26/hr (≈ $29,099–$54,122/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $41,610 – $381,150 (median $125,550)

Where these roles are based

Top locations among the 3753 comparable roles

United States1739
Germany251
India166
France146
Ireland137
China123

+ 58 more countries

Seniority mix

1670 of 3753 peers have a known seniority level

Senior431
Manager381
Intern/Fellow/Postdoc259
Associate162
Principal138
Associate Director119
Director115
Senior Director57
Executive/VP8

Therapeutic area mix

24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Roche Basel, Basel-City, Switzerland
Same function Same country
40%similar
Novartis Basel (City), Switzerland
Same function Same country
40%similar
Novartis Basel (City), Switzerland
Same function Same country
40%similar
Novartis Muttenz (with Canteen), Switzerland
Same function Same country
40%similar
UCB Bulle, Gruyere, Switzerland
Same function Same country
40%similar
Roche Rotkreuz, Zug, Switzerland
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in Switzerland, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
CMC Expert Analytical Development focus Parenterals&Devices
Roche · Basel, Basel-City, Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Lernende/r Logistiker/in EFZ
Novartis · Basel (City), Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Biotech Manufacturing Technician USP
UCB · Bulle, Gruyere, Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Lehrstelle als Chemie- und Pharmatechnolog:in EFZ (ab August 2027)
Roche · Basel, Basel-City, Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.