דרושים ב-Incyte ב-Switzerland

Job Summary (Primary function)
The Oncology/Hematology Specialist acts as primary customer contact for demand creation by executing the marketing strategy and promoting products.

Essential Functions of the Job (Key responsibilities)

• The willingness and ability to travel as required, with accommodations available for individuals with disabilities.
• Engage with customers through various channels, including in-person at their offices, virtually, or as requested, ensuring accessibility and inclusivity for all individuals.
• Execute on marketing strategies, deliver branded sales messages and disease state education, execute planned promotional programs.
• Represent in a professional, compliant, and ethical manner.
• Provide feedback on marketing tools and tactics and effectiveness reviews of sales activities.
• Utilize team members to address customer needs and ensure access to Incyte products for patients who need them.
• Provide exceptional customer service through total account management, which includes ensuring product access and triaging all medical or reimbursement issues.
• Execute on marketing strategies, deliver branded and disease state sales messages, execute planned promotional programs.
• Demonstrate and communicate to external stakeholders in depth knowledge of the clinical benefits of Incyte's products.
• Develop and maintain strong disease state knowledge and exemplary selling skills.
• Create and maintain a strategically developed business plan that reflects in depth local market and account specific knowledge.
• Consistently achieve or exceed revenue targets.

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

• Local Oncology market knowledge.
• Customer centric selling approach.
• Possession of a valid driver's license and a satisfactory driving record, or the ability to obtain one if required for the role.
• Demonstrate ability to work effectively in matrix teams.
• Demonstrate ability to gain consistent access and develop strong professional relationships with health care providers in community and academic settings.
• History of successful sales performance documented in annual reviews and sales reports. Demonstrate strong business analytics and account management skills.
• Minimum of relevant experience in the Hematology/Oncology market, with a preference for experience in hematology.
• Minimum of several years of successful biotech/pharmaceutical sales experience, or equivalent relevant experience.
• A bachelor's degree or equivalent experience is preferred.
• The ability to travel is required using various modes of transportation (car, air, train, etc.). The level and frequency of travel, including overnights, will depend on the specific territory and/or business purpose or need. We encourage applications from individuals with disabilities and will provide reasonable accommodations to support travel requirements.
• Demonstrated leadership capabilities, welcoming diverse perspectives and fostering an inclusive team environment.
• Product 'access' knowledge.
• Strong communication skills, including the ability to engage with diverse audiences.
• Strong business planning acumen.

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 .

The duration of the internship is expected to cover a period of 12 months.The position is based in Morges, Switzerland and reports to the Senior Manager, External Manufacturing and Partnerships

• Conduct forecast accuracy analysis for all products and partners supplied by the International Supply Chain team, investigate root causes of variability with the affected markets, propose action plans to improve key performance indicators (KPIs) and report periodically these metrics.
• Support team members for selected contract manufacturing organizations (CMOs) or partners in the follow-up of new product launches and participation in partners meetings.
• Review adherence of selected alliance customers to the established contractual terms such as respect of lead-times and volumes.
• Support the International Supply Chain team in Demand Planning activities such as maintenance and review of master data, and to ensure accurate forecast is always maintained in the IBP system.
• Participate and provide inputs to selected intra or inter-departments projects such as improvement of Demand Planning Processes and forecast updates from the partners, attendance and preparation for S&OP meetings.
• Support other general and periodic activities of the department such as review of business contingency plans (BCP) or review/update of department procedures (SOPs) to adapt to evolving activities.
• Provide general support to the supply chain operations in Europe and RELAM and APAC regions.
• Contribute positively to a strong culture of business integrity and ethics.
• Act within compliance and legal requirements as well as within company guidelines.
  

• Master or Bachelor’s degree in business school, supply chain, or equivalent.
• English fluency written and spoken (the company language).
• Basic understanding and strong interest in supply chain management.
• Good analytical, organizational and execution skills.
• Ability and willingness to work on several activities and projects in parallel.
• Good interpersonal skills to interact with colleagues as well as external partners from different levels and cultures.
• Ability to work independently and as part of a team at the same time.
• Proficiency in usual Microsoft applications and IT savvy.
• Strong commitment to business ethics.
• Knowledge or understanding of ERP system functionalities and purpose is a plus.
• Interest or basic knowledge/understanding of the life science industry is a plus.

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 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 .

The manager will ensure QA deliverables related to classified rooms and utilities qualification, filling line validation, and overall operational GMP readiness in accordance with cGMP regulations, company policies, and regulatory requirements, including Eudralex GMP Annex 1.

DUTIES AND RESPONSIBILITIES

Project phase – Design, Qualification & Commissioning

·Act as the QA lead in engineering projects involving aseptic filling line, isolator and cleanroom infrastructure.

·Ensure early QA involvement in design and risk assessments, embedding GMP, Annex 1 and data integrity principles into system architecture and process flow.

·Oversee and approve qualification activities (FAT/SAT, IOPQ), ensuring quality requirements are met prior to operational release.

·Lead the QA assessments of change controls and ensure traceability from design to execution.

·Drive quality risk management throughout the project lifecycle supporting a right first-time approach in commissioning and validation

·Support the development and approval of GMP documentation, including SOPs, master batch records and protocol required for the new process or equipment.

·Ensure Annex 1 alignment by integrating contamination control principles, Contamination Control Strategy elements and aseptic process simulation requirements into project deliverables.

·Represent the QA function in project meetings to ensure alignment with technical and regulatory expectations.

Operational phase – Aseptic Manufacturing Operations

·Lead the QA activities related to aseptic filling ensuring compliance with Annex 1 and GMP requirements.

·Ensure timely review and approval of SOPs, deviations, CAPAs, change controls and batch records, maintaining product release timelines and quality standards.

·Be the primary QA contact during regulatory inspections and internal audits, demonstrating mastery of aseptic quality systems and facility knowledge.

·Lead by example in the cleanroom environment and foster an aseptic mindset, supporting all team members in maintaining the highest standards of sterility assurance

·Analyze Quality KPIs, lead continuous improvement initiatives and escalate quality trends to management

·Support Inspection readiness activities and represent QA function for engineering and manufacturing related matters in Health Authorities inspections

·Collaborate with cross-functional teams, including production, engineering, and manufacturing sciences, to drive quality and operational excellence.

·Promote a culture of compliance and continuous improvement throughout the project lifecycle.

·Ensure all activities comply with safety requirements, company policies, and applicable regulations.

REQUIREMENTS

·Demonstrated experience in qualification, validation and GMP operations.

·Significant experience in aseptic process activities (experience in isolator technology is an asset). Candidates with equivalent relevant experience are encouraged to apply

·Extensive experience in Quality Assurance oversight of pharmaceutical manufacturing projects. Candidates with equivalent relevant experience are encouraged to apply.

·Academic degree in natural or applied sciences (Pharmacy, Chemistry, Biotechnology, Engineering, or related field).

·Strong knowledge of cGMP and international regulatory requirements for facility qualification and process validation.

·Strong knowledge of Eudralex GMP Annex 1 and Sterility Assurance concepts.

·Strong analytical and problem-solving skills.

·Excellent verbal and written communication skills with a structured approach.

·Fluent in French (written and spoken); proficiency in English is an asset.

·Ability to work independently and collaborate with multidisciplinary teams.

The aforementioned activities can be delegated to the QA Manager Tech. Transfer, to the QA Manager Operations and Engineering and to the QA Associate Directors.

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 .