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Manager Manufacturing Operation (USP/DSP, CDMO)
Pharmaceutical Product Development (PPD)
Lengnau, Switzerland
Job Description
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
We're looking for a
Manager Manufacturing Operation (USP/DSP, CDLocation: Lengnau onsite
As a Manager Manufacturing Operation you lead a manufacturing area (upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products. You support the project teams in the design, commissioning, qualification and validation of new production lines for recombinant products.
Your Responsibilities:Responsible for the daily operations of Upstream processes in manufacturing suites, including schedule, shift rotations
Lead and develop Manufacturing Team in order to run areas robustly and efficiently, ensuring appropriate succession planning
Participates in defining robust process parameters during routine manufacturing campaigns
Build multi-functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Technology, Engineering, Validation, and other relevant functional areas
Works closely with the PMO, Engineering, Quality and Business Technology to support the design, procurement and commissioning of production equipment and automation systems in accordance with process requirements and compliance.
Participates in Technology Transfer and operational readiness activities to implement new production processes and new lines.
Supports CVQ, PQ, Process Validation execution.
Maintains dedication to Thermo Fisher Scientific values and alignment to ethics and legal compliance standards.
Takes personal accountability for their presence, performance, and efficiency for the achievement of defined objectives.
Thinks and acts with a customer-centric approach.
Is intellectually curious and accepts Practical Process Improvement (continuous improvement).
Relentlessly attracts and develops talent to deliver outstanding performance and achieve their full potential.
Removes barriers to success and enables a work environment where colleagues can be their best self and motivated to excel.
Enables strategic focus by setting the right objectives prioritizing work and resources across the team and organization to improve impact.
Your QualificationsBachelor/Master in Chemistry / Biochemistry / Biology / Food Science
>10 years successful experience in pharmaceuticals operations in a GMP relevant environment
the function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
- Fluently in German and English (speak and written)
- Good knowledge and competence in the field of automated processes
- Experience in leading teams
Occasional weekend work according to need of production planning
On-call support
Responsible for the daily operations of Upstream processes in manufacturing suites, including schedule, shift rotations
Lead and develop Manufacturing Team in order to run areas robustly and efficiently, ensuring appropriate succession planning
Participates in defining robust process parameters during routine manufacturing campaigns
Build multi-functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Technology, Engineering, Validation, and other relevant functional areas
Works closely with the PMO, Engineering, Quality and Business Technology to support the design, procurement and commissioning of production equipment and automation systems in accordance with process requirements and compliance.
Participates in Technology Transfer and operational readiness activities to implement new production processes and new lines.
Supports CVQ, PQ, Process Validation execution.
Maintains dedication to Thermo Fisher Scientific values and alignment to ethics and legal compliance standards.
Takes personal accountability for their presence, performance, and efficiency for the achievement of defined objectives.
Thinks and acts with a customer-centric approach.
Is intellectually curious and accepts Practical Process Improvement (continuous improvement).
Relentlessly attracts and develops talent to deliver outstanding performance and achieve their full potential.
Removes barriers to success and enables a work environment where colleagues can be their best self and motivated to excel.
Enables strategic focus by setting the right objectives prioritizing work and resources across the team and organization to improve impact.
Your QualificationsBachelor/Master in Chemistry / Biochemistry / Biology / Food Science
>10 years successful experience in pharmaceuticals operations in a GMP relevant environment
the function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
- Fluently in German and English (speak and written)
- Good knowledge and competence in the field of automated processes
- Experience in leading teams
Occasional weekend work according to need of production planning
On-call support
Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
>10 years successful experience in pharmaceuticals operations in a GMP relevant environment
the function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
- Fluently in German and English (speak and written)
- Good knowledge and competence in the field of automated processes
- Experience in leading teams
Occasional weekend work according to need of production planning
On-call support
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. You will work in an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve sophisticated scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Job posted: 2024-04-04
