Hiring.Camp

Analytical Team Lead

En Hovione

·

Yesterday

Location
Lisbon, PT
Department
Education
Seniority
Lead
Closing date
Today
Source
iCIMS

Description

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.

Skills

GMPCompliance

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