Modelling & PAT Scientist

Posted 9 Days Ago
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Lisbon, PRT
In-Office
Mid level
Pharmaceutical
The Role
Develops and implements process analytical technology, mechanistic modelling, simulation, and statistical tools for pharmaceutical development and manufacturing. Provides technical support for drug substance, intermediate, and drug product projects; supports technology transfer, scale-up, batch and continuous manufacturing, GMP production, and PAT qualification. The role also prepares technical reports, promotes innovation and knowledge sharing, supports customers, and contributes to publications, patents, and process improvements.
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About Hovione

 

At Hovione, we help partners turn scientific innovation into medicines that reach patients around the world. For more than 65 years, we have connected science, technology, and manufacturing to scale complex ideas into high-quality and innovative solutions that truly make a difference.


As an international Contract Development and Manufacturing Organization (CDMO), we support the development and manufacture of drug substances, intermediates, and drug products across the full life cycle. We are globally recognized for our leadership in specialized technologies such as Spray Drying and Continuous Tableting. But what truly sets us apart is not just what we do — it is how we do it: with purpose, care, collaboration, and a deep commitment to doing the right things right.


Our people are the reason for our success. We are a global and diverse team of more than 2,600 team members across Europe, the USA, and Asia, bringing together different experiences and perspectives to help our partners to overcome complex challenges. We believe that an inclusive environment — where everyone, regardless of background, identity or ability, is respected, heard and empowered to contribute — is essential to drive innovation, ensure quality, and secure long‑term sustainable success.


And as we grow, so do the opportunities for our people to develop, broaden their perspectives, and build meaningful careers. Because at Hovione, better starts with those who choose to make a difference every day. Will you be one of them?

You will be responsible to:

Suggests, develops and implements process analytical tools to boost the company efficiency in the areas of Drug Substance, Drug Product Intermediate and Drug Product. Oversees and qualifies the implementation of these tools in the manufacturing assets in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Assures modelling practices and methodologies are aligned with the state of the art. Promotes the scientific excellence and innovation in the area of Modelling and PAT and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.


- Provide technical support (process analytical and statistical) in projects, ensuring perfect execution, customer satisfaction and the achievement of the established objectives

- Increase process knowledge of unit operation by resorting to mechanistic modelling during process development and provide mechanistic modelling support of unit operations during development projects

- Implement successfully PAT tools and practices

- Participate in the Technology Transfer and scale-up of projects to Pilot Plant and Manufacturing Areas

- Participate in the design and development of batch and continuous manufacturing processes

- Write reports from RD development campaigns and GMP manufacturing

- Promote, continuously, best practices, innovation and knowledge sharing within the company

- Promote the company through presentations at conferences and to customers, an identify patents and publication opportunities

- Ensure all assigned tasks are planned and delivered on time, safely, efficiently, reliably and in a cost-effective manner

- Propose improvements to the area as appropriate and solve problems

- Make quality and timely decisions within the Modelling & PAT tasks under her / his responsibility

- Gather relevant data to inform the decision makers regarding complex issues

- Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others)

- Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice.

We are looking to recruit a Candidate:

- University, or equivalent, qualification in Engineering or scientific field (mandatory), preferably with a PhD

- Typically requires 3-5 years of relevant experience in a production environment, preferable within the Pharmaceutical Industry or a Ph.D. degree in a relevant scientific field

- Strong understanding and knowledge process modelling, simulation principles, PAT and statistical tools (including chemometrics)

- Fluency in English is a requirement

- Computer literate with good working knowledge of the MS Office package and relevant modeling software (Python, Matlab, Simca, JMP)

- Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down 


Hovione is a proud Equal Opportunity Employer


Inclusion and diversity are key to us. We are committed to creating an inclusive recruitment experience and welcome applications from all qualified candidates. If you require any reasonable accommodation or support during the application or interview process, please contact us, and we will be happy to assist.


Notice to Agencies and Search Firms Representatives


Hovione does not accept unsolicited resumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral.

Skills Required

  • University or equivalent qualification in Engineering or a scientific field
  • Three to five years of relevant experience in a production environment, or a PhD in a relevant scientific field
  • Experience in the pharmaceutical industry or production environment
  • Strong knowledge of process modelling and simulation principles
  • Strong knowledge of process analytical technology and statistical tools, including chemometrics
  • Fluency in English
  • Computer literacy and working knowledge of Microsoft Office
  • Working knowledge of relevant modelling software, including Python, MATLAB, SIMCA, and JMP
  • PhD qualification
  • Ability to perform tasks according to company rules and procedures, including GMP and HSE requirements
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The Company
HQ: Lisbon
2,090 Employees
Year Founded: 1959

What We Do

Hovione is an international company with over 60 years of experience in pharmaceutical development and manufacturing operations. As a Contract Development and Manufacturing Organization (CDMO) with a fully integrated offering of services for drug substances, drug product intermediates and drug products. The company has four FDA inspected sites in the USA, Portugal, Ireland and China and development laboratories in Lisbon, Portugal and New Jersey, USA. Hovione provides pharmaceutical customers services for the development and compliant manufacture of innovative drugs, including highly potent compounds, and customized product solutions across the entire drug life cycle. In the inhalation area, Hovione offers a complete range of services, from API, formulation development and devices. Hovione´s culture is based on innovation, quality and dependability. Hovione was the first Chemical/ Pharmaceutical Company to become a Certified B Corp, is a member of Rx-360, EFCG and participates actively in industry quality improvement initiatives to lead new global industry standards.

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