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Supports the Process Sciences Department through small scale laboratory experiments, as well as analysis, troubleshooting, and validation of manufacturing bioprocesses. Develops and writes protocols for small-scale process validation studies. Carries out small-scale purification process validation studies.
Reporting to the Engineering Manager the Process Discipline Manager has technical, quality, managerial and administrative responsibility for the Process department. The Process Discipline Manager participates directly in projects and directs a team in supporting all discipline aspects of client projects.
This candidate will be responsible for the development and validation of downstream processes. Support the scale up, optimization and validation of the downstream processes Technical transfer of biopharmaceutical manufacturing process to site
Job – Senior Process Engineer - Immediate long term job opportunity exists for a Lead Process Engineer with 5+ year’s experience in pharmaceutical industry. Immediate long term job opportunity exists for a Senior Process Engineer with 8+ year’s experience in pharmaceutical industry.
Our client, a progressive and innovative pharmaceutical company in Waterford, has an opportunity for a Process Validation Engineer to join their team. The primary function of the role is to ensure process validation activities are completed in line with internal and regulatory procedures and guidelines.
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An exciting job opportunity for a Senior Process Engineer to focus on all aspects of process improvement and delivering innovative engineering solutions with a well known comppany in Co. Clare. Job title: Senior Process Engineer
We are currently recruiting for a NPD Process Technologist who will report to the New Product Development Manager based in Tipperary. The NPD Process Technologist will report to the New Product Development Manager and works in conjunction with the New Product Development team, to ensure the effective and efficient operation of the department
Our Waterford based Pharma client is now seeking a R&D Sterile Process Team Lead to support the R&D department by providing significant fill-finish technical expertise to support all aspects of the manufacturing of sterile products - Support all aspects of the manufacturing process from formulation and filling to visual inspection
The successful candidate will ensure the introduction of new equipment and processes and perform technical development of the blending and blistering/capsule processes System owner of the blending and blistering processes and lead and manage the development and introduction of products, equipment and processes these systems
The successful candidate will take a lead role within the Process Development group where they will be responsible for the development, optimisation, transfer and validation of cell culture processes within a GMP facility. Build, lead and develop an Upstream Process Development team - Develop, optimise and validate the upstream process
Working with counterparts in Production, QA, and Engineering departments and as a team, you will be responsible for all manufacturing IT systems/processes in use. To administer and support all IT Processes in Pharmaceutical Manufacturing environment. Identify, evaluate and implement opportunities for continuous IT process improvement.
Use Six Sigma and Lean tools & techniques to analyze business processes and identify project opportunities - Complete process reviews to identify process bottlenecks and capacity constraints, identify and implement ways to eliminate. Act as change lead and key member of team implementing Process excellence strategy for the site.
Responsible for understanding complex business processes, eliciting and documenting requirements and coordinating communication among various business groups and IT. Will work closely with IT management and the clients to identify and specify business requirements and processes in diverse development platforms, computing environments
To provide ongoing quality support to product and process improvement in operations and to drive timely resolution of all customer reported issues. The person in this position will ensure process quality improvement through ongoing process and product auditing and ensure ongoing compliance & conformance to applicable regulations and standards.
Improve the CI process across teams - Proficient in testing techniques, utilizing test automation frameworks and processes, and have a strong knowledge on all phases of testing. Ability to use initiative and willing to generate ideas to continuously refine testing processes to improve quality.
Improve the CI process across teams - Proficient in testing techniques, utilizing test automation frameworks and processes, and have a strong knowledge on all phases of testing. Ability to use initiative and willing to generate ideas to continuously refine testing processes to improve quality. Competitive salary & benefits package available. The Role
In this role, you will be primary software application support for Laboratory and QA Systems, secondary support for manufacturing operation systems, supporting your internal customers by addressing user business process inquiries/requests, creating/modifying user accounts and modifying system activity.
Support the development of new processes and provide technical assistance to current processes on site. Process Introduction of New Automation and Manufacturing Solutions to support new and existing projects. Perform DOE’s, FMEA’s to enhance design processes as well as improve yields and utilization through reduced cycle and efficient set-ups.
Supervises the manufacturing team in relation to process execution for Upstream/Midstream and Downstream processes. Interfaces with other departments, such as Facilities, Process Development, Process Analytical - Our client, a large pharmaceutical company based in Limerick is currently looking to hire a Biotech Production Supervisor to join their team.
Troubleshoot production processes to address product issues and improve process control. Constantly evaluate existing processes and establish teams to continuously improve these processes. Sound know-how and experience in of manufacturing, process automation, business and shop floor systems to effectively manage operations.
Assess manufacturing requirements and capabilities prior to the transfer of new processes into the manufacturing facilities. Provide process transfer support to external facilities, including generation of process descriptions and facility fit comparisons. Project Manage required for a Leading Pharmaceutical Company in Limerick
The Supply Chain Planning Specialist will be required to support/drive process and system improvement projects in line with business needs and in turn employ change management skills as part of any project roll outs.
Communicate and co-operate with Maintenance Management, Process Engineering, Production Management, Machine Operators and other Technicians - Escalate ongoing issues to Maintenance Management, Process Engineering and Production Management - Bausch + Lomb are happy to announce that we are currently recruiting a Maintenance Technician on a permanent basis
Summary: Provide technical support for internal and external technology transfer of biopharmaceutical drug substance manufacturing processes for monoclonal antibodies/therapeutic proteins and provide post transfer support.