44 jobs voor Research And Development Manager gevonden in Antwerpen (Provincie)

For the research context and a full decsription: please visit our website https://www.itg.be/en/jobs and research opportunities.Role.

As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Clinical Research business to maximize organization growth.

Concretely this means:

• that with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Clinical research Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business;
• that you will network actively to identify new opportunities in the (bio)pharmaceutical industry and establish key relationships;
• that you will negotiate and close business deals;
• that you will build strong relationships with the internal functional departments and maintain in depth knowledge of their services in order to support lateral business opportunities;
• that you will represent customer needs to internal functional departments and follow up on the proposal and contract development process;
• that you will further develop and maintain the CRM database.

Data Engineer / Data Scientist As a global Research Organization to the biopharmaceutical industry, CellCarta provides access to a broad offering of biomarker platforms and services.

The Business Development Manager develops sales-concepts, by identifying potential products, conducting market research, generating product requirements and determining specifications.Next to this, he/she helps build the pricing-strategy, and sets time-integrated plans for product introduction.As the Business Developer is working in close cooperation with the sales and product management teams, he/she is also developing distribution-channels and ensures commercial co-existence with clients.In this job, you will spend most of your time in the field.

Key areas of responsibilities and accountability

• Prospecting and determining clients' needs and desires by specifying the clients' product and production process
• Recommends the nature and scope of present and future product lines by reviewing product specifications and requirements; appraising product packaging changes.
• Assesses market competition by comparing the company's product to competitors' products.
• Obtains product market share by working with sales director to develop product sales strategies.
• Provides information for management by preparing short-term and long-term product sales forecasts and special reports and analyses; answering questions and requests.
• Introduces and markets new products by developing time-integrated plans with sales and marketing.
• Completes market operational requirements by scheduling technical trainings of employees and third party salespeople of new products; following up on work results.
• Maintains product management results by counselling and disciplining employees; planning, monitoring, and appraising sales results.
• Contributes to team effort by accomplishing related results as needed.
• Prospects, initiates and follows up new sales projects in the market in a progressive, consistent and structural way

Our solutions are a key part of most industries electronics, medical research, renewable energy, food production, infrastructure and many more.Working with us means working with the latest technologies and groundbreaking, sustainable innovations..

We are looking for an experienced Clinical Pharmacology Manager to expand our DMPK team.The role will involve leading the strategic and management of Clinical Pharmacology and DMPK activities supporting the drug development of our small and large molecule pipelines..

VITO is a Flemish independent research organization in the field of cleantech and sustainable development.Our goal?To accelerate the transition to a sustainable world..The Remote Sensing unit processes petabytes of Earth observation data.

Your main responsibilities:

• Manage and/or perform the implementation, validation and follow-up of all computer system projects within a Gx.P environment.
• Ensure that computer systems used in clinical research are in compliance with the current applicable regulatory requirements and guidelines, including but not limited to 21 CFR Part 11, Annex 11, and GAMP 5.
• Work closely with IT, the Quality Assurance department and other business departments to ensure the successful implementation of computer system validation activities.
• Write high-quality validation documents, including validation plans, protocols, and reports.
• Perform Periodic Reviews and manage system changes to ensure that all systems remain in a validated state during their entire System Development Life Cycle.
• Participate in sponsor and vendor audits.
• Collaborate with the related business departments to ensure that validation activities are completed on time and within budget.

Are You Ready to Make It Happen at Mondelēz International?.Join our Mission to Lead the Future of Snacking.

At Mind.Gap, we are currently looking for a.Market Researcher that speaks French to reinforce the project team.As a Market expert, you will play a very important role in the success of the project. .Mind.

The Agfa Gevaert Group develops, produces and distributes an extensive range of analog and digital imaging systems and IT solutions, mainly for the printing industry and the healthcare sector, as well as for specific industrial applications.Are you ready to join the forefront of innovation in wide format printing technology?Agfa is seeking a dynamic Global Field Service Engineer to take our global install base to new heights.As a Global Field Service Engineer, you'll be the go to expert for resolving technical escalations from our worldwide install base.

You will be responsible for conducting research directed to developing creative solutions toanalytical chemistry problems across a portfolio of projects.In the Process AnalyticalResearch (PAR) team, we focus on the analytical aspects during the development of newsynthetic organic transformations.As part of the DPDS small molecule Process Analytical Research unit, the successfulcandidate will be embedded in one of our active chemical route development projects whereshe/he will participate in the development of suitable analytical methods for thecharacterization of small chemical intermediates or novel modalities and support withintroduction of novel and innovative analytical techniques.

As a Lead Generator at Eagle.Burgmann, you will play a pivotal role in driving our marketing and lead management initiatives.Your primary responsibilities include rolling out Eagle.

We, at Sanofi, are there beside people in need, as a health journey partner..+100,000 employees, representing 142 nationalities.90 countries where Sanofi is present, providing healthcare solutions in 170 countries.

As Business Development Specialist you report to the Business Development Manager and are responsible for, among other things:

• Research and analysis into the strategic markets segments to better understand market specifics, trends and to detect potential commercial opportunities for Green Planet.
• Anticipate market needs, define action plans and follow up their implementation.
• Develop an extensive network in the industry by frequent contacts, visits and follow ups.
• Set-up price strategy and negotiate at key accounts.
• Create new business opportunities.
• Spend significant time in the field at relevant trade shows, conferences and exhibitions.
• Build-up technical know-how on Green Planet and their related variety of applications.
• Report to all the internal stakeholders (sales, technical service, R&D) to reach the defined strategic business goals.

As a Contractor in Small Molecule Method Development, you'll harness your expertise to ensure the highest quality standards in drug development while contributing to our mission of creating a world without disease.

Job description

As a Contractor in the Small Molecule Method Development group, you will collaborate with expert professionals in Gas Chromatography, Good Manufacturing Practices, and analytical development.Your role will involve the development and validation of robust and reliable test methods for purity determination in Raw Materials, Starting Materials, Intermediates, Active Pharmaceutical Ingredients, and Drug Products.Your work directly contributes to ensuring the safety and efficacy of our products, ultimately benefiting patients worldwide.

Responsibilities

• Coordinate and execute analytical gas chromatographic work, including method development, validation, and transfer, to ensure the necessary quality attributes for the projects in scope.
• Contribute to the expansion of the team's analytical expertise towards new modalities.
• Actively participate in assessing and implementing newly marketed GC methodologies and equipment.
• Independently manage assigned projects in line with project and team deliverables.
• Apply state-of-the-art knowledge to ensure the quality of results during investigations and troubleshooting efforts.
• Ensure compliance with regulatory requirements, GMP, and safety standards.
• Guarantee accurate GMP documentation and review of generated data, along with protocol and report writing.

Summary.We are seeking a driven, high energy, early in career sales professional who is motivated to drive new business and uncover opportunities with our rapidly growing team..

KANEKA Biodegradable Polymer Green Planet™ is the first ever 100% bio based polymer produced via a revolutionary bio fermentation process using renewable vegetable oils as feedstock.

Are you looking for an exciting new opportunity?Cell.Carta, a renowned Contract Research Organization, is actively seeking a highly skilled and motivated.Technical Expert to join our dynamic team.

We, at Sanofi, are there beside people in need, as a health journey partner..+100,000 employees, representing 142 nationalities.90 countries where Sanofi is present, providing healthcare solutions in 170 countries.

Key Responsibilities:..The QA Engineer acts as the day to day liaison with internal and external customers for quality related activities..Ensure GMP compliance of Sanofi products manufactured and/or tested at a contract facility..

Are you looking for an exciting new opportunity?Cell.Carta, a renowned Contract Research Organization, is actively seeking a highly skilled and motivated.Medical Writer to join our dynamic team.

• Streamline and implement the MINERVA supply chain process within SCK CEN context Ensure implementation of existing SCK CEN procedures in the MINERVA program; Cooperate with business partners (Purchasing, Legal) and stakeholders within the MINERVA program to optimize this process, focusing on quality and efficiency; If needed, provide additional work instructions specific to MINERVA and coach/ train Minerva program members in the execution of their role.

MissionAs a ‘.Customer Value Proposition Product Manager' you will be part of the.

As a Business Analyst, you create value by building the bridge between IT and the business.You work to improve and streamline processes that help your organisation meet its goals and objectives.

Back End Developers are in charge of the architecture and (business) logic in the background of an application.They usually manage the database and the underlying conceptual business model, fitting in new requirements when necessary.

Eagle.Burgmann is one of the internationally leading companies for industrial sealing technology.

The Cloud Developer is responsible for developing cloud based applications and solutions.This can go from small server applications to big microservices that talk to each other.