Analytical Scientist

Posted 4 Days Ago
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Lisbon, PRT
In-Office
Mid level
Pharmaceutical
The Role
Performs qualitative and quantitative analysis of pharmaceutical compounds and products, develops and validates analytical methods, prepares reports and protocols, investigates issues, and recommends CAPAs. Coordinates analytical project timelines, reviews team data, supports customers and client visits, provides training, and ensures compliance with GMP, HSE, regulatory, and quality standards. Contributes scientific expertise, process improvements, innovation, and intellectual property development.
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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:

Performs qualitative and quantitative analyses of compounds, including drug substances, drug product intermediates and drug product. Recommends the analytical characterization package (Chemical, physical, performance) and controls the quality and accuracy of the data in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Promotes the scientific excellence and innovation in the Analytical area and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.


- Perform and provide support to the development of analytical methods and the implementation of innovative and new analytical methodologies

- Coordinate priorities with Area responsible and Project manager to ensure that the timelines of the analytical work (such as method development, validation protocols, validation execution, and validation reports) of the project are met

- Prepare and revise analytical reports and protocols

- Actively participate in investigations and propose corrective and preventive actions (CAPA)

- Discuss actively with customers technical and scientific issues of projects under own scope

- Support client visits

- Discuss and review analytical data generated by the team

- Provide training internally and to other areas as required

- 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 Analytical 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 Chemistry, Chemical Engineering, Pharmaceutical Sciences or in similar Chemistry/ Biochemistry/ Health Sciences fields (mandatory)

- PhD qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or in similar Chemistry/ Biochemistry/ Health Sciences fields (desired)

- Typically requires 3-5 years of relevant experience in Analytical Chemistry and /or Scientific background in relevant field (PhD considered as relevant experience) preferably in the Pharmaceutical Industry

- Strong understanding and knowledge of scientific domains relevant to the pharma industry

- Fluency in English is a requirement

- Computer literate with good working knowledge of the MS Office package

- 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 Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related Chemistry, Biochemistry, or Health Sciences field
  • PhD in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related Chemistry, Biochemistry, or Health Sciences field
  • Typically 3–5 years of relevant experience in Analytical Chemistry or a relevant scientific field
  • Strong understanding and knowledge of scientific domains relevant to the pharmaceutical industry
  • Fluency in English
  • Good working knowledge of Microsoft Office
  • Knowledge, experience, and skills to perform tasks according to established rules and procedures
  • Ability to work in compliance with GMP, HSE, regulatory, quality, and internal procedural 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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