Technical Quality Placement Student

Almac Group; Craigavon; Presencial; GBP 21 000 - 29 000; Tempo integral

Resumo da oferta

Almac Group in Craigavon is offering a 12‑month placement in the Technical Quality team from July 2027 to July 2028. 37.5 hours per week in a highly regulated pharma environment, supporting equipment, facilities, utilities and software validation activities.

You will prepare design documents, validation plans and reports, assess systems against regulatory standards and help with remediation actions. Strong MS Word/Excel/Outlook skills and academic study in science/engineering are required.

Qualificações

• Organised and accurate with ability to manage several tasks
• Excellent written and verbal communication skills
• Experience in fast-paced environments (part-time work or work experience)
• Proficiency with MS Word, Excel and Outlook

Responsabilidades

• Assist in preparing project design documents, validation plans, risk assessments, protocols and reports
• Support validation activities for equipment, facilities, utilities and software systems
• Collate and analyse process validation data and assist with testing
• Maintain project schedules and coordinate with project teams to keep validation on track
• Liaise with internal teams, suppliers, manufacturers, clients and external validation resources

Conhecimentos

Organised

Accurate

Strong communication

Teamwork

Time management

Formação académica

GCSE Maths & English A-C

A Levels or equivalent

Undergraduate or postgraduate science/technical degree (engineering or IT)

Ferramentas

Microsoft Word

Microsoft Excel

Outlook

Descrição da oferta de emprego

Description

Hours: 37.5 hours per week

Duration: 12 Month Placement from July 2027 – July 2028

Business Unit: Pharma Services

Location: Craigavon

Open To: Students studying a Science or Technical related degree that requires a year in industry.

The Opportunity

Join the Technical Quality team at Almac Pharma Services and gain hands‑on experience supporting business and continuous improvement projects in a highly regulated pharmaceutical environment. You will contribute to the qualification of equipment, facilities, utilities and software systems, as well as the validation of manufacturing and packaging processes.

• Support the preparation of project design documents, validation plans, risk assessments, protocols and reports.
• Help assess systems against regulatory standards and contribute to practical remediation actions.
• Collate and analyse process validation data and assist with validation testing activities.
• Maintain project schedules and work with colleagues across project teams to keep validation activities on track.
• Liaise with internal teams, suppliers, manufacturers, clients and external validation resources.

Joining Almac means becoming part of a fast‑paced, growing organisation within a highly regulated industry. We offer a supportive and collaborative working environment, with excellent opportunities for learning, development and long‑term career progression across the Almac Group.

Our approach is simple: we support, develop and reward our people, build fulfilling careers and together we advance human health. Find out more: Life at Almac

What you need to be successful

This opportunity would suit a student who is organised, accurate and keen to build practical experience in technical quality and validation.

• GCSE Mathematics and English, or equivalent, at Grade A-C, plus A Levels or equivalent.
• Currently studying at undergraduate or postgraduate level in a science or technical discipline, such as engineering or IT.
• Experience of working in a fast‑paced environment, for example through part‑time work or work experience.
• Confidence using Microsoft Word, Excel and Outlook.
• Strong written and verbal communication skills, with the ability to manage several tasks and work effectively both independently and within a team.

Additional science or technical qualifications, experience within a regulated quality system, or knowledge of validation requirements in the pharmaceutical industry would be advantageous.

Applicants must have eligibility to work in the UK with no restrictions or possess a valid work permit that will allow you to take up full‑time employment in the UK.

Further information

For further information on the job specific responsibilities, essential and desirable criteria, please review the job description attached to the online job posting.

This role may require regular coverage beyond normal working hours. Applicants must be able to fulfil this requirement.

Closing Date

We will no longer be accepting applications after 5pm on Sunday 1st November 2026.