The Head Oligonucleotide Manufacturing
vor 2 Wochen
Bachem is a leading CDMO for TIDES, peptides and oligonucleotides. Together with our colleagues and customers we transform lives with innovative medicines. We are seeking a highly motivated leader to join us as Head Oligonucleotide Manufacturing. This individual will lead all oligonucleotide manufacturing units at Bachem, Switzerland. The oligonucleotide manufacturing organization is fast-growing and currently consists of three departments (pilot scale, production scale, and large scale) and is involved in a new greenfield project for a new site including one of the world’s largest oligonucleotide production facilities.
**The Head Oligonucleotide Manufacturing**
- Manages and controls the activities of the oligonucleotide manufacturing organization through direct reports (i.e., directors, department heads, senior group leaders)
- Responsible for planning, budgeting, output, profitability, and attracting and developing talents.
- Decides on critical production matters and ensures that best in class synthetic oligonucleotide-related services and products are delivered by the oligonucleotide manufacturing organization to customers and stakeholders.
- Full financial accountability for functional area, owns and implements strategies for long-range capacity planning, as well as upgrading of capital investments into existing or new sites in line with strategic planning for the oligonucleotide business unit.
- Drives continous improvement and efficiency.
- Responsible for digitalization and automation efforts in the oligonucleotide manufacturing organization
- Represents the function internally and towards external Stakeholders.
**Key Responsibilities**
- Provides senior leadership for fast-growing oligonucleotide manufacturing organization in Switzerland
- Shapes the future of the oligonucleotide business as part of the management team.
- Build and grow the newly established large-scale production team, and prepare the oligonucleotide organization for further growth including ramp up of a new site
- Together with Head Oligonucleotides, MSAT and Engineering, implement a technology roadmap to increase levels of automation and digitalization
- Ensure the implementation of strategic capacity adjustments and innovation projects to enable future growth, in line with HSE and sustainability targets.
- Ensure continuous world leading CDMO services and products for our customers: cost-efficient, fast, and reliable delivery in line with regulatory requirements (i.e., cGMP) for synthetic oligonucleotides and related services
- Optimize financial performance, increase revenue per head, increase gross profit, increase asset and resource utilization
- Proven track record to build and grow high-performing teams
- Drives a culture of growth, development, diversity, and performance
- Implements changes through role modelling, and coaching.
- Fosters continuous improvement and innovation
- Ability to inspire an organization
- Passion for people development and people management
**Experience & Expertise Minimum qualifications**:
- Master in Life Sciences or related field
- Minimum of 8 years experience in manufacturing (Biotech/Life Science CDMO or pharma/biotech) industry
- Minimum of 3 years experience at a senior level leading a big size life science, organization GMP/FDA regulated industry such as pharmaceutical and biopharmaceutical or CDMO
- Language skills: English, excellent skills (oral, written) and German basic skills required
Preferred qualifications:
- PhD in Life Science or related field
- Experience with regulated products or services, excellent working knowledge of GMP regulations, and direct experience in communicating with quality auditors and inspectors
- Experience with common continuous improvement tools (e.g., lean/six sigma) - Leadership skills in managing change, influencing others in matrix organizations, attracting/developing talent
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