Manager Msit Mfg Science Drug Substance

vor 2 Wochen

Bern, Schweiz Johnson & Johnson Vollzeit

Key Responsibilities:

- Lead, coach, and develop Process Engineers, conducting regular 1:1 conversations and team meetings.
- Provide manufacturing technical support, troubleshooting, and data management assistance.
- Define resource needs (capital, expense, and headcount) to meet current and future development requirements.
- Recruit, hire, retain, train, and motivate a scientifically and technically competent team.
- Provide opportunities for staff career development and growth.
- Support or lead site initiatives and projects.
- Actively maintain and enhance quality standards on-site.
- Collaborate with the team on technology transfers to GMP Operations and create associated documentation.
- Support the evaluation and implementation of new technologies concerning GxP Operations in collaboration with relevant stakeholders.
- Identify and implement cGMP and compliance improvements.
- Act as the change owner/initiator, accountable for initiating and following up on changes in alignment with cGMP, EHS, Production schedules, and user requirements.
- Provide support during audits and inspections

**Qualifications**:
Qualifications:

- Master degree in Biotechnology, Life Sciences, or a related field
- Advanced knowledge in Upstream (mammalian cells and bacteria fermentation) and Downstream technologies
- Proven experience of several years in a manufacturing or process engineering environment, preferably within the pharmaceutical industry.
- Strong leadership and team development skills.
- In-depth knowledge of cGMP regulations and quality standards.
- Excellent problem-solving and data management skills.
- Strong communication and interpersonal abilities.
- Experience with technology transfer and project management.
- Fluent in english and preferable also in german

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