Careers in Ireland

Zenith Technologies is one of Europe's leading Automation Engineering companies, providing innovative, reliable and technically-advanced process measurement, automation and MES solutions to a large range of industries, including Pharmaceutical, Bulk Chemical, Biologics and Brewing. ZT is a progressive company with offices located in Ireland, England, North America and Singapore.

Technical Recruitment Specialists

As part of the Secondment team, the Technical Recruitment Specialists will be responsible for sourcing and recruiting talented Technical / Engineering staff to join our teams both in house and on customer sites. We currently have several positions across different regions (Ireland, UK, Continental Europe).

The job responsibilities will involve:

Assist in developing and administering a strategy for identifying and recruiting potential hires
Provide resourcing support to agreed functional areas, including candidate sourcing, CV screening, database management, candidate management, interviewing and selection.
Facilitate the recruitment process including scheduling interviews, carrying out reference checks, producing contracts, etc.
Provide guidance and advice to hiring managers and ensure that they are briefed and compliant with current employment legislation.
Participate and assist in the co-ordination of various tactical staffing initiatives when required
Continually improve the company's staffing and recruiting policies, guidelines and systems

Education & Experience:

Minimum of 2 years Technical Recruitment (preferably Engineering) experience is essential
Self-motivating, with high levels of enthusiasm, energy and drive
Strong multi-tasking and organisational skills
Ability to work as part of a team is essential
The person will have a Degree/qualification relevant to HR/Business or Technical/Engineering.
The person should be results-focused with excellent communication, interpersonal and team-playing skills.

800xA Engineers

We are currently seeking a number of 800xA Engineers, both Senior and Junior level Engineers are required. Suitable candidates will be Degree qualified with at least 2 years+ experience in the Pharma / Biopharma sectors.

Lead Systems Engineer

We are currently seeking a Lead Systems Engineer for a Client site in Connaught. This role is initially a 6 month contract which may be extended thereafter depending on project requirements.

The ideal candidate will have at least 5-7 years Systems experience in the Pharmaceutical sector. Strong Delta V experience is essential for this role. You must be Degree qualified with an excellent knowledge of GMP, GAMP, safety and environmental regulatory requirements.
You must also be a team player with the ability to work to meet client deadlines efficiently.

Validation Engineer

We are currently seeking a Validation Engineer for a contract role.

Responsibilities:

Thorough knowledge of Computer Systems Validation in a Pharmaceutical environment
Writing Validation Protocols
Reviewing and advising on software lifecycle documentation requirements.
Reviewing and advising on SOP's
Good understanding of control and cGMP software systems and networks
High level of Computer Literacy
Ability to work to client's site standards
Compliance with quality standards for CSV and 21 CFR Part 11

Key Requirements:

Suitable candidates will have at least 3 - 5 years Validation Engineering experience in a regulated pharmaceutical / biopharmaceutical environment. As a team player you will possess strong organisational skills and will have experience of working to tight deadlines.

MES Engineers

We are currently recruiting for a number of MES Engineers. Vacancies include a Werum MES Engineer, a MES Validation Engineer and a MES Project Manager. The ideal candidates will be Degree Qualified and will have 3years+ experience in the pharmaceutical sector.

PCS7 Software Engineer

We are currently seeking a PCS7 Software Engineer who has at least 5 years of PCS7 programming experience in the Pharma industry.

Must have used the S88 approach to programming for a fully recipe controlled batch Pharma plant.
Previous Lead experience of PCS7 programming would be advantageous
Proficient in generating design and testing documentation.

You will need:

Excellent understanding of Automation systems
Minimum of 5 years relevant experience
Preferably Degree Qualified
Familiar with the ISA S.88 model for Batch Control Systems
Knowledge of GMP, GAMP, safety and environmental regulatory requirements
Team player with the ability to work to meet client deadlines efficiently

Project / Process Engineer

We are currently seeking experienced Project / Process Engineers. Interested applicants should be flexible with regard to travel.

Responsibilities:

Provide process and project engineering support through completion of projects as required.
Understand the core fundamental issues and develop mitigation plans for all issues identified.
Develop User Requirements for systems by engaging with the site operations, site EHS, maintenance, utilities, technical and quality teams ensuring that the proposed solutions are acceptable.
Maintain project records, calculations, assumptions in line with site procedures.
Understand the Global Engineering Standards and ensure that all proposals developed are aligned to standards.
Plans, executes and tracks the progress of the project through the design phases and ensures that the key deliverables are adhered to.
Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g. FMEA, Fishbone diagrams, 5 why's etc.
Responsible for delivery of training, while focusing on continuous process improvement using Lean Principles.
Troubleshoots equipment problems, identifies need for new equipment and/or modifications to existing equipment to optimize throughput and reduce process cycle times; Drive change through Change control
Serves as the point-of-contact for new equipment and/or modifications to existing equipment
Facilitates focus on continuous improvement activities utilizing six sigma and lean methology
Provides input review and approval for atypical , observation, and process capability investigations
Participates in internal and external audits and inspections
Recognizes and investigates opportunities for financial savings and supports opportunities for financial savings by providing resources, expertise and project work
Participates in development of profit plan and budgets

Requirements:

Degree Qualified (Engineering or other technical field preferred) or Associate Degree with 5-10 years related technical industry experience required
Five years experience in the biotech / pharmaceutical GMP industry.
Experience in high speed manufacturing environment an advantage.
Experience with HVAC, Autoclaves, SIP/CIP, Formulation an advantage.
Applicant should have previously demonstrated strong team and communication skills, flexibility, motivation, ability to project manage, with a strong emphasis around safety and compliance practices.
Applicants should actively support, participate and embrace an empowered team culture and have excellent communication skills

DeltaV Engineer

We are currently seeking experienced Delta-V Engineers of varying levels with a minimum of 2 years experience for a number of roles we currently have available. Interested applicants should be flexible with regard to travel.

Responsibilities:

Generate Functional Design Specifications for the Delta-V DCS system
Generate Delta-V Batch code (FBD & SFC's)
Generate and execute test documentation & protocols as part of a cross discipline team
Red-line design documentation (FDS) and drawings
Trouble shoot DCS software problems
Raise and process change requests for hardware / software changes

Requirements:

Good understanding of Automation systems
Minimum of 2 years Delta-V DCS batch configuration experience
Preferably Degree Qualified
Familiar with the ISA S.88 model for Batch Control Systems
Experience within the pharmaceutical industry
Knowledge of GMP, GAMP, safety and environmental regulatory requirements
Team player with the ability to work to meet client deadlines efficiently

Commissioning & Qualification Engineers

We are currently seeking experienced C&Q Engineers. Interested applicants should be flexible with regard to travel.

Responsibilities:

C&Q experience on systems including Clean Utilities, Filling Lines, Transfer Panels and Vessels experience preferred.
Document Preparation and Execution Skills required
Knowledge of GMP, GDP requirements
Experience of working with Construction Contractors and Vendors
Can work on own initiative and within a team
Ensure a high standard of cGMP documentation which is compliant with regulations
Knowledge of GAMP, safety and environmental regulatory requirements

Requirements:

Degree in Engineering or related discipline
Min 5 years pharmaceutical / biotech experience
Team player with the ability to work to meet client deadlines efficiently.

The above job descriptions are not an exhaustive list of the job holders responsibilities.

Zenith Technologies is an equal opportunities employer and all applications will be kept in the strictest of confidence.

To apply, please send an updated CV to jobs@zenithtechnologies.com quoting the Job Title in the subject line or call +353 21 4370200 for further information.