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Senior ms&t engineer

Neuenburg
BioTalent
EUR 100’000 - EUR 125’000 pro Jahr
Inserat online seit: 5 Juni
Beschreibung

2 days ago Be among the first 25 applicants

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Senior Consultant - Key Account Management at BioTalent, part of The IN Group | R&D within Life Sciences - UK/EU/US

Permanent - full-time

Are you a seasoned professional in the pharmaceutical industry looking to take your expertise to the next level?

BioTalent have teamed up with a global leader in pharmaceutical manufacturing services, and we are seeking an MS&T Engineer to join their state-of-the-art facility in Neuchâtel, Switzerland. This is your chance to work on cutting-edge projects, collaborate with cross-functional teams, and play a vital role in the development of life-changing treatments.

Key Highlights of the Role

1. Lead the introduction of new oral solid dosage forms, including capsules and tablets, ensuring seamless tech transfer and compliance.
2. Conduct risk assessments, gap analyses, and provide technical leadership for manufacturing projects.
3. Act as the key liaison for cross-functional teams, driving alignment between QA, packaging, and production operations.
4. Support the definition and implementation of Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs).
5. Champion continuous improvement initiatives, proactively identifying and resolving manufacturing challenges.
6. Manage CAPA implementation and ensure compliance with international regulatory frameworks like EU-GMP, Annex 11, and 21 CFR.
7. Provide mentorship to less experienced colleagues, fostering a culture of collaboration and learning.
8. Collaborate with clients to deliver high-quality results within tight deadlines.
9. Utilize bilingual fluency (English and French) to support diverse, multinational teams.
10. Join a site poised for growth, with plans to double capacity and expand into injectable manufacturing and lipid nanoparticle capabilities.

What We’re Looking For

1. Education: BS/MS in Engineering or a related technical discipline.
2. Experience: 10–15 years in the pharmaceutical industry, with a proven track record in new product introductions and validation of solid dosage forms.
3. Skills: Strong project management, problem-solving abilities, and familiarity with electronic documentation systems.
4. Language: Fluent in English and French, with excellent communication and interpersonal skills.

This position offers a unique opportunity to contribute to a rapidly growing site, be part of an innovative global team, and make a real difference in patients' lives.


Seniority level

Mid-Senior level


Employment type

Full-time


Job function

Quality Assurance


Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Engineering Services

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