Production Co-ordinator (Packaging)

TN United Kingdom; Armagh; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking a Production Co-ordinator to join their dynamic team. This role involves supporting the production packaging department, ensuring compliance with GMP standards, and managing quality documentation. The ideal candidate will possess strong communication skills and attention to detail, with a background in quality systems or manufacturing environments. Join a forward-thinking company that values diversity and offers a supportive environment for personal and professional growth. If you're ready to make an impact in the pharmaceutical sector, this opportunity is for you!

Benefits

34 days holiday per annum

Qualifications

• GCSEs in English and Maths at Grade C or above required.
• Experience in a quality system or manufacturing environment is essential.

Responsibilities

• Support production packaging department ensuring GMP compliance.
• Generate and manage GMP documentation for packaging operations.

Skills

Effective communication skills

Attention to detail

Ability to work independently

IT applications proficiency (Word, Excel, Outlook)

Education

GCSEs in English and Maths

A-Level Qualification

Level 5 Qualification

Tools

WOLF

Job description

Social network you want to login/join with:

Client:

Cpl

Location:

Armagh, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

1e35e6fab4c4

Job Views:

3

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

Production Co-ordinator (Packaging) - Almac Pharma Services

CPL has partnered with the ALMAC Group to recruit a Production Co-ordinator for their team on a temporary, ongoing contract.

Location:

ALMAC Global Headquarters, Craigavon

Benefits:

34 days holiday per annum

Hours:

37.5 hours per week, Monday to Friday

Overall Role Objective:

The post holder will support the production packaging department at Almac Pharma Services by ensuring GMP compliance and quality activities for pharmaceutical packaging.

Job Responsibilities:

1. Quality Management System (QMS):
   • Implement actions from QMS plans as directed by the Senior Production Support Officer.
   • Maintain all quality system indexes and electronic tracking systems (e.g., WOLF).
2. Process Documentation:
   • Generate GMP documentation in approved formats for packaging operations.
   • Manage and distribute controlled documents, maintaining current versions in hard copy and electronically.
   • Ensure document control storage/archive areas are tidy and organized.
   • Archive, retrieve, and track GMP documentation.
   • Approve new and updated Bills of Materials.

Minimum Requirements:

• GCSEs (or equivalent) at Grade C or above in English and Maths
• A-Level Qualification
• Experience in a quality system or manufacturing environment
• Ability to work independently and as part of a team
• Effective communication skills (written and verbal)
• Proficiency in IT applications (Word, Excel, Outlook)
• Attention to detail
• Ability to plan and prioritize workload

Preferred Qualifications and Experience:

• Level 5 Qualification
• ECDL Qualification
• Experience in pharmaceutical or regulated environments
• Knowledge of cGMP
• Ability to assess and comment on new processes and documentation
• Technical process understanding and explanation skills

Additional Information:

For further details, apply directly below or contact Luke Bush. Successful candidates will need to complete a criminal record check through Access NI. Cpl is an equal opportunities employer and values diversity. Be You, Be Kind, Be Proud.