GMP Production Operative (Pharmaceutical) Dunboyne, €17.91 per hour

Job Type: Full-time

Pay: €17.91 per hour plus 33% shift premium

Expected hours: 40 per week

Location: Dunboyne, Co. Meath

Experience: GMP: 1 year (preferred)

Position Overview:

• This role will be part of the Manufacturing Self Directed work team/Hub in our new state of the art single use multi-product biotech facility in Dunboyne, County Meath, Ireland.
• The organisational structure at the site will be based on self-directed work teams (SDWT) where decisions will be made at the level where the data exists.
• The Production Operator is responsible for all procedures and processes associated with the manufacture of Drug Substance at Dunboyne manufacturing facility, at the highest standards of Safety, Quality and Compliance.
• The Production Operator will be responsible for undertaking manufacturing operations involved in the production of biologic drug substances on their designated shift.
• There are some different levels for the Operators.
• This role is a site-based role.
• This role will involve working shifts. This is a 4 Cycle 24/7 Shift role with 33.33% shift premium.
• All the candidates are required to complete and pass an aptitude test before the interview.

Key Responsibilities:

Primary responsibilities include but not limited to:

• Support operations team to consistently deliver on specific Key Performance Indicators (KPIs), e.g. Environmental Health and Safety (EHS) metrics, Production Plan, Overall Equipment Effectiveness (OEE), compliance and team training.
• Complete COMMIT cards to highlight ways of working within our SDWT’s and Hubs and across our site that support our COMMIT culture.
• Provide immediate feedback to others at any time to reinforce good safety and improvement behaviours and acts.
• Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures (SOPs).
• Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
• Routinely talk about any safety issues you are concerned about.
• Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
• Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
• Adhere to Right First-Time principles.
• Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
• Escalate issues as appropriate to manager/designee.
• Maintain a high level of personal expertise and working knowledge of all aspects of the manufacturing process and process equipment through continuous training and development.
• Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan and site schedule.
• Challenge and identify improvements to the safety and environmental programmes on site.
• Celebrate with use of proactive recognition tools that inspire teams and individuals you collaborate with.
• Take part in shift handovers and tier 1 meetings, raising concerns or issues promptly and providing options for resolutions.
• Act as an ERT during emergency situation if trained.

Benefits:

• Benefit from our ethical principles.
• Pre-interview preparation before attending the interview and help to use STAR technology to answer the questions.
• While placed on client sites you will be an integral part of our team, gaining support and access to the knowledge and experience of our cross-functional Life Science team.
• We offer attractive rates – competitive margins compared to our competitors.
• Payment on time and in full.
• We are recognised as approved suppliers to leading key pharmaceutical and medical device companies.

You must have the right to work in Ireland for this role.