Analyst

UNAVAILABLE; Cork; On-site; EUR 42,000 - 64,000; Full time

Job summary

Hovione in Cork, Ireland, is seeking a Quality Control Analyst to organize daily sample analysis, support laboratory plans and KPIs, and ensure GMP-compliant testing.

The role includes analysis of materials and products, maintenance of records, contribution to audits, and ongoing improvements, with a 12-hour rotating shift pattern.

A BSc in a relevant science and GMP experience are required; strong English communication and laboratory instrumentation skills are essential.

Qualifications

• Knowledge of GMP regulations and laboratory practices in a QC setting.
• Experience with analytical instrumentation and supporting equipment maintenance.
• Proficient with Microsoft Office and data recording.
• Excellent written and verbal English communication.

Responsibilities

• Organize and prioritize daily activities to ensure timely and accurate sample analysis and support laboratory plans and KPIs.
• Adhere to testing schedules to maintain an efficient QC system.
• Perform analysis of raw materials, intermediates, finished products, and other analytical services in compliance with regulatory and customer requirements.
• Maintain laboratory records, notebooks, and checklists in accordance with GMP requirements and internal procedures.
• Identify, document, and raise discrepancies, deviations and non-conformances; support investigations as needed.

Skills

GMP knowledge

Analytical techniques

Laboratory instrumentation

Microsoft Office

English communication

Education

BSc in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Leaving Certificate

Tools

HPLC

GC

Instrument maintenance

Job 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:

• Organize and prioritize daily activities to ensure timely and accurate sample analysis, supporting laboratory plans and KPIs.
• Adhere to laboratory testing schedules to maintain an efficient Quality Control (QC) system.
• Perform analysis of raw materials, intermediates, finished products, and other analytical services in compliance with regulatory and customer requirements.
• Take ownership of generated analytical data, ensuring compliance with GMP, HSE, operating procedures, and industry standards.
• Maintain laboratory records, notebooks, and checklists in accordance with GMP requirements and internal procedures.
• Ensure high standards of laboratory housekeeping, hygiene, and compliance.
• Perform routine calibration, preventive maintenance, and corrective maintenance of laboratory equipment.
• Request and manage laboratory consumables and spare parts as required.
• Identify, document, and raise discrepancies, deviations, and non-conformances.
• Raise and support investigations related to OOS, OOT, atypical results, deviations, and QC incidents.
• Communicate effectively with internal stakeholders using established processes and systems.
• Support internal and external audits as required.
• Contribute to continuous improvement initiatives, projects, and other laboratory activities.
• Proactively seek clarification and information when requirements or data are unclear.
• Complete annual performance management activities, including self-assessments.
• Perform all activities safely and in compliance with Environmental, Health & Safety (EHS) requirements.
• Ensure QC activities are conducted in accordance with GMP, regulatory requirements, customer specifications, company procedures, and quality standards.
• Support the management and control of Quality Control activities to ensure compliance with applicable regulations and contractual obligations.

We are looking to recruit a Candidate:

Education

• BSc degree in Chemistry, Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or another relevant scientific discipline (required).
• Leaving Certificate or equivalent secondary education.

Experience

• Previous experience in a Quality Control laboratory or a similar analytical role.
• Experience working within a GMP-regulated pharmaceutical or related industry environment (required).
• Knowledge of GMP regulations and HSE requirements (preferred).

Technical Skills

• Good understanding of analytical techniques, laboratory practices, and GMP requirements.
• Experience using laboratory instrumentation and supporting equipment maintenance activities.
• Computer literacy, including proficiency with Microsoft Office applications.
• Ability to follow procedures, regulations, and quality standards accurately.

Communication & Languages

• Strong written and verbal communication skills.
• Good command of English, both written and spoken.

Other Requirements

• Availability to work a 12-hour rotating shift pattern:
  • 2 Day Shifts (07:00-19:00)
  • 2 Night Shifts (19:00-07:00)
  • 4 Days Off
  • Cycle repeats
• Demonstrated ability to perform duties safely, effectively, and in compliance with company policies and regulatory requirements.

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.