Job Description - Manager MSIT Mfg Science Drug Substance (2506232072W)
Manager MSIT Mfg Science Drug Substance - 2506232072W
Description
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:
* Master's 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 preferably also in German.
Primary Location
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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