Job Type: Contract
Job ID: JO-2104-25828
Consultant: Karen McHugh
Are you a Project Process Engineer / Project Manager with 8+ years recent relevant experience in a process engineering/projects role in the Pharma/Biotech/Chemical industry?
Do you have Pharmaceutical Manufacturing Process understanding and experience e.g. dry blending, compression, compaction, coating, granulation (wet and dry), containment, material handling etc.?
If interested in this role, call Karen on +353 1 7978720 to discuss or forward your CV to email@example.com for review
Project Process Engineer / Project Manager - Pharma Projects - Dublin
Our Client is one of Ireland's leading EPCm consultancies and a global player in the Semiconductor, Pharma and Biotech sectors with offices in Cork and Dublin.
They have a large number of Biotech projects in the pipeline and will be looking for process engineers to get involved in these projects.
The Process Projects Engineer is a crucial role within the Engineering department to ensure the introduction of new equipment and processes and to perform technical development of existing processes.
Working in a highly regulated and cGMP environment within the pharmaceutical industry the Process Engineer will report directly to the Programme Manager on all aspects of the role including but not limited to; introduction of new projects, troubleshooting issues, equipment upgrade and procurement
in the manufacturing/packaging and process validation activities.
This is a projects based role.
The successful candidate must have strong leadership and planning qualities, be adaptable to change and be comfortable leading cross functional teams delivering to strict deadlines and budgets.
Pharmaceutical process knowledge and equipment procurement and validation experience is required.
Leading and Managing projects for the introduction of new Solid Oral Dose products, equipment and processes to meet all safety, quality, regulatory and operational requirements.
Process mapping, gap analysis/identification for new and existing pharmaceutical manufacturing processes.
Process development (as part of technical transfer), troubleshooting and optimisation.
Project management and co-ordination including planning, scheduling, task management and delegation, milestone planning, communication and reporting.
Delivering projects on time and on budget.
Managing and executing process and equipment trials and validation.
Leading cross functional teams as part of project planning and deployment including collaboration with supporting departments such as Production/Operations, Quality, Safety, Regulatory Affairs, Facilities and Engineering, Supply Chain and Finance, Project scoping and gap analysis.
Equipment specification/design/procurement/installation and validation.
Optimisation of existing processes to achieve product output targets.
Co-ordinating changes using the Client approved change control procedure to ensure that cGMP is adhered to.
Generation, review and approval of project documentation (Scope, User Requirement Specifications etc), trial reports and Standard Operating Procedures.
Support validation activities for project activities including review of validation documentation and attendance at validation activities (FAT, IQ, OQ etc).
To ensure that all new equipment is bought in accordance with appropriate site procedures & regulations.
Directing of more junior process team members.
To provide technical support to system end users of new and existing equipment including but not limited to troubleshooting technical issues and assisting with process investigations.
Involvement in Continuous Improvement activities.
To facilitate and participate in meetings and workshops as part of Project and Continuous Improvement activities.
To develop user materials (e.g. SOPs + training aids) and provide training on new equipment/process functionality.
Perform technical review of updates to Standard Operating Procedures (SOPs) related to the equipment/process.
To approve plant SOPs and other documents as required, ensuring the acceptability of content and format.
To adhere fully to all safety policies, procedures and regulations.
To participate in all training and assessment activities related to the role.
To perform all activities in accordance with current Good Manufacturing Practice.
To record any deviations relating to the role out of projects, that you are responsible for, through the plant Process Deviation System.
B.Eng in Chemical and Processing Engineering or appropriate science or engineering discipline.
A minimum of 8+ years’ recent relevant experience in a process engineering/projects role in the Pharma/Biotech/Chemical industry.
Pharmaceutical Manufacturing Process understanding and experience e.g. dry blending, compression, compaction, coating, granulation (wet and dry), containment, material handling etc.
A proven track record in process development, support and improvement is required.
The ability to organise, plan and execute multiple tasks to tight schedules
Experience with leading cross functional teams is desirable.
Flexibility and ability to adapt to changing priorities is required.
Proven track record of project based activities in the pharmaceutical industry.
Experience with process technologies.
Experience with process equipment procurement.
Good communication skills combined with an imaginative and creative approach to problem solving.
Strong leadership skills and the ability to work in cross-functional team environments, as well as independently.
Contract rates of €60 - €70 per hour, depending on role
18 month contract minimum
Karen McHugh is the consultant managing this position.
If you are a Process Design Engineer interested in roles based in Dublin, you can contact Karen by e-mail at firstname.lastname@example.org or phone +353-1-7978720 for a confidential chat.
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