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J&J Family of Companies Manager MSIT Mfg Science Drug Substance in Bern, Switzerland

We are seeking a motivated and experienced Manager to lead, coach, and develop a team of Process Engineers within the MSIT Manufacturing Science Drug Substance group. This role requires a proactive approach to provide technical support, ensure compliance, and promote a culture of continuous improvement. The successful candidate will oversee a team of 12 professionals while working collaboratively across various departments to drive operational excellence in drug substance manufacturing.

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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