DSP Bioprocess Expert at Visp

DSP Bioprocess Expert

Location: Valais

Contract Type: Temporary Contract (6 months, renewable)

Start Date: ASAP

Experience Required: Minimum 10 years

About the Position

We are looking for a highly experienced DSP Bioprocess Engineer to join a leading biopharmaceutical manufacturing environment. This role is ideal for a senior professional with extensive expertise in downstream processing (DSP), GMP manufacturing operations, and process optimization.

As a key technical expert, you will be responsible for supporting commercial and clinical manufacturing activities, ensuring operational excellence, regulatory compliance, and process robustness. You will work closely with Manufacturing, Quality, Engineering, Validation, Automation, and Project teams to drive efficient and reliable production performance while contributing to continuous improvement initiatives across the facility.

Key Responsibilities

Manufacturing Operations

• Plan, coordinate, and oversee DSP manufacturing campaigns from preparation through execution and completion.
• Monitor production performance and ensure timely and compliant execution of manufacturing activities.
• Analyze process data, evaluate results, and provide technical support during manufacturing operations.
• Troubleshoot process and equipment-related issues to minimize downtime and improve operational efficiency.
• Support production teams in delivering manufacturing objectives while maintaining high standards of quality and compliance.

Technical Leadership & Process Ownership

• Serve as the manufacturing Subject Matter Expert (SME) for assigned products and DSP processes.
• Provide technical guidance and leadership to cross-functional teams.
• Ensure manufacturing processes remain aligned with industry best practices and regulatory expectations.
• Drive process understanding and contribute to the continuous development of manufacturing expertise within the organization.

Quality, Compliance & Risk Management

• Lead and support risk assessments related to manufacturing operations, cleaning processes, environmental monitoring, and product-specific activities.
• Participate in investigations, deviation management, CAPA implementation, and change control activities.
• Ensure adherence to cGMP standards, quality requirements, and EHS regulations.
• Support inspection readiness and participate in customer, regulatory, and internal audits.

Documentation & GMP Systems

• Prepare, review, and maintain manufacturing documentation in accordance with GMP requirements.
• Ensure the accuracy and compliance of batch records, SOPs, manufacturing instructions, and risk assessments.
• Contribute to the continuous improvement of documentation practices and GMP systems.

Training & Operational Support

• Develop and deliver technical training for manufacturing personnel.
• Support production leadership in workforce development and capability-building activities.
• Promote a culture of quality, safety, compliance, and operational excellence.

Projects & Technology Transfer

• Provide manufacturing expertise for capital investment projects and facility improvement initiatives.
• Support equipment selection, commissioning, qualification, and operational readiness activities.
• Participate in technology transfers and implementation of new products and manufacturing processes.
• Collaborate with Engineering, Validation, Automation, and Quality departments to ensure successful project delivery.

Continuous Improvement

• Identify opportunities to improve process efficiency, product quality, safety, and productivity.
• Lead optimization initiatives within downstream processing operations.
• Contribute to the standardization of manufacturing processes, equipment utilization, and operational practices.

Candidate Profile

Education

• Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related scientific discipline.
• Fluent English, is mandatory.
• German is considered a major advantage and will be highly valued.