Manufacturing Technicians

Team Horizon; Connacht; On-site; EUR 40,000 - 60,000; Full time

Job summary

A prominent manufacturing company in Ireland is looking for Manufacturing Technicians to support clinical manufacturing processes. You will ensure compliance with GMP and manage various manufacturing activities, including batch preparation and environmental monitoring. Ideal candidates should have a 3rd level qualification and relevant industry experience. Join a team that values a defined career path and work-life balance.

Benefits

Great benefits

Defined career path

Work-life balance

Qualifications

• 18-24 months minimum experience in the pharmaceutical or medical device industry.
• Strong knowledge of GMP regulatory guidelines and quality systems.
• Experience working in project and team-based environments.

Responsibilities

• Responsible for all manufacturing activities to support tech transfer.
• Ensure drug product manufacturing meets compliance with GMP.
• Prepare components and equipment for processing in Grade A environments.

Skills

Aseptic practices

Communication skills

Problem-solving skills

Technical writing

Education

3rd level qualification in relevant discipline

Tools

Single use technologies

Autoclave sterilization

Job description

Team Horizon is seeking Manufacturing Technicians for our Clients operations team in Mayo. In this role you will be responsible for all manufacturing activities necessary to support a tech transfer of a NPI to accommodate clinical manufacture of small and large molecule products

Why you should apply:

• Great benefits, a defined career path, and work-life balance!

As part of a team, you will be responsible for ensuring that drug product manufacturing is performed in compliance with site and GMP procedures, and that scheduling and manufacturing meets global request timelines.

What you will be doing:

• Your new duties will involve Manufacturing, Process Development, Biologic Drug Product commercial support, and New Product Introduction/Project Management.
• Manufacturing of pharmaceutical products at different stages of lifecycle including clinical, non-clinical and pre-clinical material.
• Batch preparation activities (vial washing, load sterilization, area preparation).
• Work aseptically or as required by the classification of the production area(s)
• Perform compounding, sterile filtration and sterile filling activities
• Work with various vendors on the development/improvement of new and existing systems regarding single use technologies.
• Prepare components and equipment for processing into Grade A environments
• Aid in running a multi-product suite, changing between different product campaigns without issue.
• Perform environmental monitoring
• Comply with Good Manufacturing Practices (GMP) and with Standard Operating Procedures (SOPs)
• Review and contribute to technical documents, including protocols, reports and batch manufacturing documents
• Participate in cross-functional teams with other functions, including R&D, Engineering, Quality, Supply Chain, Operations and Validation
• Adhere and support all EHS standard procedures and policies

What you need to apply:

• 3rd level qualification in relevant discipline and/or
• 18-24 months minimum experience in the pharmaceutical or medical device industry
• Prior knowledge of aseptic practices in clean room environments is essential.
• Strong knowledge of GMP regulatory guidelines, quality systems, drug product manufacturing and validation is desirable
• Understanding of autoclave sterilization, depryogenation, and filter integrity testing is desirable.
• Knowledge of lyophilization and freeze dryer operations is desirable.
• Experience with single use technologies is desirable.
• Well-developed technical writing, organisational, and communication skills are essential.
• Experience working in project and team-based environments is essential.
• Pro-active approach with proven problem-solving skills is desirable