Analyst

Posted 9 Days Ago
Be an Early Applicant
Cork, IRL
In-Office
Mid level
Pharmaceutical
The Role
Performs finished-product and stability testing in a GMP-regulated QC laboratory using wet chemistry, HPLC, GC, and other analytical techniques. Reviews data, troubleshoots instruments, maintains laboratory records and equipment, manages consumables, investigates OOS/OOT results, supports audits, and ensures compliance with GMP, safety, and environmental standards.
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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:
  • Test finished product and stability samples in line with the laboratory testing schedule.
  • Perform wet chemistry and instrumental analysis, including HPLC and GC, and troubleshoot issues with these techniques.
  • Review analytical data.
  • Maintain all checklists, laboratory records and notebooks you are involved in to GMP standards and in accordance with Hovione internal procedures.
  • Maintain good hygiene and housekeeping in the laboratory.
  • Carry out routine calibration and maintenance of laboratory instruments, and manage the necessary consumables.
  • Identify and report discrepancies, deviations and non-conformances in testing or laboratory practices.
  • Raise and support investigations into OOS, OOT and atypical results, and other QC incidents.
  • Collaborate with internal departments using established communication platforms and processes.
  • Support audits and contribute to continuous improvement initiatives.
  • Take on additional tasks to support laboratory activities as required.
  • Comply with all safety, environmental and GMP regulations and standards.
We are looking to recruit a Candidate:
  • Qualification in chemistry, analytical chemistry, chemical engineering, a pharmaceutical-related field or another relevant science.
  • Minimum of 3 years' practical experience in a GMP-regulated QC laboratory in the pharmaceutical or a related industry.
  • Extensive hands-on testing experience, including wet chemistry and instrumental techniques such as HPLC and GC using Empower software, with the ability to troubleshoot these techniques.
  • Experience in performing review of data.
  • Technical understanding of GMP, analytical theory and analytical techniques.
  • Clear and open communication skills, both written and verbal.
  • Computer literate, with working knowledge of Microsoft Office.
  • The knowledge, experience and skills to carry out tasks in line with established rules and procedures.

Desirable

  • Experience with additional techniques such as Karl Fischer (KF), particle size analysis, capillary electrophoresis or ion chromatography.
  • Knowledge of HSE standards.

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

  • Qualification in chemistry, analytical chemistry, chemical engineering, pharmaceutical science, or another relevant science
  • At least 3 years of practical experience in a GMP-regulated QC laboratory in the pharmaceutical or related industry
  • Hands-on testing experience with wet chemistry and instrumental techniques including HPLC and GC
  • Experience using Empower software
  • Ability to troubleshoot HPLC, GC, and other analytical techniques
  • Experience reviewing analytical data
  • Technical understanding of GMP, analytical theory, and analytical techniques
  • Clear written and verbal communication skills
  • Computer literacy and working knowledge of Microsoft Office
  • Experience with Karl Fischer, particle size analysis, capillary electrophoresis, or ion chromatography
  • Knowledge of HSE standards
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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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