2,049,876open jobs
122,877companies
238,391added this week
Browse all
Salary
≈ $33k – $69k per year (Estimated)
Location
In office (Lisbon)
Seniority
Staff

Confirmed on the employer's own hiring board on Nov 2, 2026. First seen by Alion on Sep 29, 2026. Hovione scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Hovione is a specialist integrated contract development and manufacturing organisation (CDMO) based in Loures, near Lisbon, that develops and manufactures drug substances, intermediates and drug products and offers particle engineering for pharmaceutical partners. Founded in 1959 by Ivan and Diane Villax and still an independent family-owned group, it operates manufacturing sites in Portugal, Ireland, the United States and Macau. It hires process, automation and maintenance engineers, quality assurance and quality control staff, HSE specialists, operators and warehouse staff, modelling and PAT scientists, finance technicians and graduate trainees.

Join a Market Leader

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.

- Ensure the information flow between the laboratory and the several internal and external customers

- Review and approve the analytical data generated by the team

- Prepare reports and other type of official documentation rendered by the analytical data

- Support project teams on solving and troubleshooting technical and analytical challenges on their specific area of expertise

- Establish and maintain a continuous improvement plan

- Participate in investigations and propose corrective and preventive actions

- To ensure the proper equipment verification and calibration as per procedures in place

- To ensure the team only generate data on equipment “in service” and properly verified and/or calibrated as per procedures in place

- Supervise the TMs assigned to his/her area of responsibility and distribute work tasks. Provide input to ensure HR processes run smoothly, namely in terms of recruitment, integration, training needs and performance management in accordance with the company's HR policies. Ensure all TMs are aligned and motivated towards achieving Hovione's goals, values and culture by promoting their personal and professional development whilst maximizing productivity

- Ensure area goals are properly cascaded to the team

- Ensure 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) within his/ her TMs

- 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:

- Degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or in similar Chemistry/ Biochemistry/ Health Sciences fields, or equivalent job experience

- Requires relevant experience in Analytical Development or other relevant areas within the Pharmaceutical industry

- Knowledge and Experience in cGMP (desirable) and HSEE practices (mandatory)

- Experience in coordinating others in the field (desired)

- Possess solid knowledge of Analytical Chemistry / Analytical Development and associated laboratory practices, and is able to share them with others

- Good communication skills (verbal and written)

- Skilled at running work processes and its related tools

- Fluency in English is highly desirable

- 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.

Free account
Stop reading job ads. Get the ones that fit.
One free account turns this page into a shortlist built around your stack, your level and your pay.
Match on every job. Stack, seniority, pay and location, scored against your profile.
2,049,876 open roles. Read straight off company career pages, refreshed every day.
Unlimited applications. Every one you send is tracked in one place, on-site or on a company board.
3 tailored CVs a month. Rewritten for the exact job you are applying to. Included free.
Create a free account Continue with Google
Free forever. No card. Under a minute.

Your match

How well do you fit this role?
Two answers are enough for a real match. No account needed.
Check my fit
Answers stay in this browser until you create an account.

Recommended for you based on this role

Management
Similar stack
Same company
Lisbon
In office · Full-Time · 5+ years exp · Bachelor's Degree · Lisbon
Apply
In office · 4+ years exp · Bengaluru
Analytics
Microsoft Excel
Management
Asana
Trello
ClickUp
Jira
Agile
Scrum
Apply
푸드CX팀장 9 min ago
In office · 7+ years exp · Seoul
Apply
Chef de secteur H/F 2 hours ago
$73k – $78k per year · In office · Full-Time · 5+ years exp · Saint-Jean-de-la-Ruelle
Apply
In office · Full-Time · Grand Junction
Apply
In office · 5+ years exp · Bachelor's Degree
MedTech
CAPA
Apply
In office · 2+ years exp · Bachelor's Degree
Analytics
Power BI
Microsoft Excel
MedTech
CAPA
Apply
Hybrid · Contractor · 2+ years exp · Lima
JavaScript
Java
TypeScript
SQL
Java
Spring Boot
DevOps
Git
GitLab
Management
Scrum
QA
Swagger
MedTech
CAPA
Apply
$165k – $210k per year · Remote (likely United States) · Full-Time · 8+ years exp
DevOps
GCP
Life Sciences
Good Clinical Practice
ICH Guidelines
MedTech
21 CFR Part 11
CAPA
Apply
≈ $78k – $166k per year (Estimated) · In office · Full-Time · PhD · Bubendorf
Life Sciences
GMP
MedTech
CAPA
Apply
≈ $32k – $67k per year (Estimated) · In office · Portugal
Life Sciences
GMP
LIMS
Apply
≈ $32k – $67k per year (Estimated) · In office · Bachelor's Degree · Loures
MedTech
CAPA
Apply
Senior Project Manager 2 months ago
≈ $37k – $83k per year (Estimated) · In office · 5+ years exp · Master's Degree · Loures
Apply
In office · Bachelor's Degree · Portugal
Design
AutoCAD
Life Sciences
GMP
Apply
In office · Portugal
Life Sciences
GMP
MedTech
CAPA
Apply
Remote (Portugal) · Full-Time · Lisbon
Analytics
Microsoft Excel
Marketing
Salesforce
Apply
In office · Full-Time · Lisbon
Apply
≈ $49k – $116k per year (Estimated) · In office · Full-Time · Lisbon
Apply
≈ $46k – $111k per year (Estimated) · Hybrid · 3+ years exp · Lisbon
DevOps
Terraform
Ansible
VMWare
DNS
DHCP
VLAN
Apply
In office · Part-Time · Master's Degree · Lisbon
Apply
See all jobs
This is one of many
2,049,876 more open roles from verified company boards, updated every day.