Technician Qc Physico-chemistry jobs at Incyte in Switzerland

Job Summary (Primary function)

Essential Functions of the Job (Key responsibilities)

Performs the QC analysis to support raw materials, production release and stability plan of drug substance (HPLC, UPLC, CGE, pH, FTIR, Osmolality, Protein Concentration or ELISA tests, appearance).

Perform the sampling and the testing of Raw Materials

Performs the review of analytical data.

Act as a a key user for QC equipment software and method setup.

Performs basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs etc.).

Proactively propose problem resolutions

Efficiently contribute to method tech transfer.

Author, review and maintain Standard Operating Procedures, Work Instructions, and other quality control documents.

Supports selection, purchase and commissioning of new equipment.

Supports management supply of QC consumables, reagents and standards.

Supports maintenance/calibration of equipment and keeps relationship with suppliers.

Contribute to the efficient management of samples.

Proactively propose problem resolutions.

Raise, investigate and close events, deviations and non-conformances.

Contribute positively to a strong culture of business integrity and ethics.

Act within compliance and legal requirements as well as within company guidelines.

Qualifications (Minimal acceptable level of education, work experience, and competency)

CFC or higher degree in analytical chemistry/biochemistry

At least 5 years’ experience in the biotech, pharmaceutical or chemical environment

Hands-on experience in a GMP environment and a Quality Control environment.

Good knowledge of analytical method transfer and analytical method validation.

Solid knowledge in spectroscopic, HPLC, CE and ELISA techniques.

Solid knowledge of Empower or Soft Max PRO.

Good writing skills.

Excellent team spirit.

Autonomy

French: Native or Fluent

English: Good knowledge

Knowledge of most common office software.

Work the weekend may be required

ENERGIES, ENVIRONMENT, HEALTH & SAFETY

We ensure the efficient use of our resources and systems, with the aim of optimizing and increasing our energy performance.

We are committed to identifying, record (via EEHS tool), preventing and actively reducing all risks to the health and safety of our employees, through continuous improvement of our processes.

Respecting, promoting and implementing the EEHS policy is an integral part of every function.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Learn more at:

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .

Job Summary (Primary function)

Essential Functions of the Job (Key responsibilities)

·Performs the sampling and the testing of Raw Materials

·Performs analytical raw data review related to the sampling and testing of Raw Materials

·Actively contributes to method implementation and equipment implementation.

·Act as a key user for QC equipment software and method setup.

·Performs basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs etc.).

·Proactively propose problem resolutions

·Efficiently contribute to method tech transfer.

·Author, review and maintain Standard Operating Procedures, Work Instructions, and other quality control documents.

·Supports selection, purchase and commissioning of new equipment.

·Supports management supply of QC consumables, reagents and standards.

·Supports maintenance/calibration of equipment and keeps relationship with suppliers.

·Contribute to the efficient management of samples.

·Proactively propose problem resolutions.

·Raise, investigate and close events, deviations and non-conformances.

·Contribute positively to a strong culture of business integrity and ethics.

·Act within compliance and legal requirements as well as within company guidelines.

Qualifications (Minimal acceptable level of education, work experience, and competency)

·CFC or higher degree in analytical chemistry/biochemistry

·At least 5 years’ experience in the biotech, pharmaceutical or chemical environment

·Hands-on experience in a GMP environment and a Quality Control environment.

·Good knowledge of analytical method transfer and analytical method validation.

·Solid knowledge in spectroscopic techniques.

·Good writing skills.

·Excellent team spirit.

·Autonomy

·French: Native or Fluent

·English: Basic knowledge

·Knowledge of most common office software.

·Work the weekend may be required.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Learn more at:

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .

Job Summary (Primary function)

This includes (but is not limited to) the planification of testing, the definition of the analyses to be carried out, the management of sampling (plan and execute), the management of internal & external results/data review and their approval within the defined lead time.

The QC Lab Supervisor owns the deviations, CAPA and change controls for the QC activities under his/her responsibilities.

Essential Functions of the Job (Key responsibilities)

Leadership & Management

·Supervise, mentor, and develop QC analysts in the physico-chemistry laboratory.

·Plan and allocate daily laboratory activities to meet testing schedules and manufacturing timelines.

Laboratory Operations

·Accountable for the routine and non-routine QC Physico-Chemistry testing of in-process samples, drug substances with a variety of physico-chemical methods (e.g., HPLC, UPLC, CE, SoloVPE, ELISA.).

·Ensure adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and all relevant regulatory standards (FDA, EMA, ICH).

·Ensures that all QC equipment are appropriately qualified and fit for purpose for cGMPs activities

·Troubleshoots analytical instruments, assays, and technical issues to maintain laboratory efficiency.

Quality & Compliance

·Review and approve laboratory data, test results, and associated documentation.

·Conducts investigations of out-of-specification (OOS), deviations, and non-conformances.

·Maintain up-to-date SOPs, protocols, and training records to ensure regulatory compliance.

·Participate in audits and inspections

Continuous Improvement & Projects

·Drive laboratory process improvements, automation, and digitalization initiatives.

·Participate in method validation, transfer, and lifecycle management projects.

·Collaborate with cross-functional teams (Manufacturing, QA, Regulatory Affairs, Development) to support product lifecycle and inspections.

·Provide inputs for establishing the QC laboratory budget and operating in the defined approved budget

Qualifications (Minimal acceptable level of education, work experience, and competence)

·Bachelor (in Physico-chemistry, Biotechnology) with 10 years or higher degree (in Physico-chemistry, Biotechnology) with at least 10 years of experience in a laboratory environment.

·Strong experience in a GMP environment, in a biotechnology or pharmaceutical company.

·QC Laboratory supervision experience required demonstrated ability to set vision and direction for a team including setting expectations and motivating results Experience with Quality systems such as Deviation, CAPA, Change Control systems required

·Deep knowledge of Analytical testing and Pharmacopoeias

·Ability to work in a highly regulated and fast-changing environment

·Highly developed team spirit

·Proactivity and pragmatism

·Rigorous and organized

·Be able to make proposals

·Have a spirit of synthesis

·Language: French (fluent) and English (advanced; C1)

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Learn more at:

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .

Job Summary (Primary function)

The Senior Cybersecurity Architect is responsible for developing security architecture across all technology stacks, including on-premises, cloud (AWS / Azure / SaaS) environments. This role requires hands-on technical skills needed for evaluating, selecting, implementing and managing cybersecurity tools and technologies. It also needs working closely with business, infrastructure, and other IT teams to assure security for a variety of technology solutions. s. Additionally, the Senior Cybersecurity Architect will manage consulting resources and lead projects to ensure the organization’s security posture aligns with industry best practices and organizational goals.

***This is a 4-day on-site position***

Essential Functions of the Job (Key responsibilities)

·Develop cybersecurity architecture, ensuring alignment with organizational goals and industry best practices across all technology stacks, including on-premises, cloud, to manage current and merging security risks.

·Lead the evaluation and selection, implementation and management of comprehensive security solutions, ensuring robust protection for the organization’s assets.

·Conduct vulnerability assessments, penetration testing, and security reviews, collaborating with various teams on remediation efforts.

·Provide expert guidance on security controls and best practices for both on-premises and cloud-based solutions to IT and business teams.

·Perform detailed security investigations, document findings and recommendations for complex incidents, and resolve issues while preserving forensic evidence.

·Identify and implement continuous improvements in security-related processes and technologies.

·Mentor other cybersecurity professionals in the team, to upskill them to meet the organizational requirements

·Lead and manage cybersecurity projects, ensuring timely delivery and alignment with organizational objectives.

·Collaborate with the Security Operations Center (SOC) and other teams to enhance detection and response capabilities.

Qualifications (Minimal acceptable level of education, work experience, and competency)

·7 - 10 years of experience in IT with a focus on Cybersecurity and Cloud security services.

·4+ years of Cloud Security architecture experience.

·Relevant certifications (e.g., CISSP, CCSP, AWS/Azure Certified Security Solutions architect) preferred.

·Proven experience in managing and leading cybersecurity teams and projects.

·Extensive knowledge of networking protocols and technologies, network security architecture, and engineering.

·Expertise in cloud (AWS andAzure) and on-premises security and related technologies.

·In-depth knowledge and experience with various security tools and technologies, including End-Point Security, SIEM, DLP, IRM, vulnerability assessment, and patch management.

·Comprehensive understanding of risk and vulnerability mitigation.

·Knowledge of security standards and guidelines from NIST and SANS.

·Extensive hands-on administrative experience with infrastructure and/or automation tools including but not limited to Windows/Linux and other OS and/or modern cloud service plans.

·Basic knowledge of ITIL.

·Strong project management skills, including experience with project planning, execution, and monitoring.

·Excellent relationship-building skills with both internal and external stakeholders.

·Strong organizational and communication skills.

·Must be a self-starter and work well independently, as well as within a team environment.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Learn more at:

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .

is responsible for Microbiological Quality Control (QC) activities to support product testing (IPC, DS, DP), environmental and utilities monitoring, aseptic processes, and coordination of outsourced potency assay, microbial and viral safety testing, including cell-based assays and microscopy-based methods. This role ensures activities are conducted in compliance with cGMPs, regulatory expectations, and internal quality standards.

Key Responsibilities

• Act within compliance and legal requirements, as well as within company policies and procedures.
• Lead all microbiological QC activities including: Environmental Monitoring (EM) and Clean Utilities Sampling/Testing (UTY), In-process Control (IPC) and Drug Substance/Drug Product (DS/DP) microbiological testing, Aseptic process monitoring and support to sterility assurance
• Responsible for Aseptic Process Simulation (APS) testing activities, ensuring compliance with sterility assurance and regulatory expectations.
• Manage incoming control testing of media and plates for APS.
• Responsible for the sampling and monitoring of clean utilities and controlled environments.
• Oversee and coordinate outsourced testing for: Sterility, Mycoplasma, Viral safety, and Cell-based assays
• Oversee and coordinate microbiological method verifications and tech transfer and ensure laboratory readiness for new products/processes.
• Ensure timely and accurate review/approval of microbiology-related protocols, reports, SOPs and work instructions.
• Actively participate in inspections by Health Authorities and ensure readiness of the microbiology team.
• Support purchase requisitions and follow-up of purchase orders to ensure business needs are met in a timely manner.
• Create a positive, collaborative, and high-performance team environment aligned with Incyte values.
• Lead the microbiology QC team, ensuring proper resource allocation, clear team plans, and effective execution of lab activities.
• Manage performance, provide coaching, technical guidance and career development support to team members.
• Assign training requirements and monitor training status for the team to ensure compliance and continuous learning.
• Lead microbiology deviation management, investigations, CAPAs, and participate in cross-functional root cause analyses.
• Ensure appropriate qualification and maintenance of microbiological QC equipment.
• Act as Quality Champion for the microbiology QC group, ensuring a high level of compliance, ownership, and inspection readiness.
• Lead implementation of 5S and Lean practices in the microbiology laboratory.
• Monitor and report microbiology-related quality indicators and contribute to department budget planning.
• Ensure all QC activities comply with cGMPs and HSE policies, and foster a safety-first culture.

Requirements

• Significant experience in microbiology QC within a GMP biotech environment, including substantial leadership experience (typically demonstrated by 10+ years in the field and 5+ years in a leadership role, or equivalent combination of education, training, and experience).
• Strong knowledge of GMP microbiology, aseptic practices, and environmental monitoring.
• Proven experience managing teams and fostering development and collaboration.
• Experience in adventitious agent testing and coordination of external labs.
• Ability to interact effectively with Health Authorities and lead teams through inspections.
• Strong project management, organizational, and cross-functional communication skills.
• Proficiency in quality systems (deviation, CAPA, change control).
• Fluent in French and English.
• MSc or equivalent degree in microbiology, biotechnology, or related scientific discipline.

Energies, Envionment, Health & Safety

• We promote working conditions that respect sustainable development and Incyte's ethical values, with an emphasis on health, well-being and reducing our environmental impact.
• We ensure the efficient use of our resources and systems, with the aim of optimizing and increasing our energy performance.
• We are committed to identifying, recording, preventing and actively reducing all risks to the health and safety of our employees, through continuous improvement of our processes.
• Respecting, promoting and implementing the EEHS policy is an integral part of every function.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Learn more at:

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .