Search Results: 50 vacancies
...Adherence to spare part management system and accompanying documentation
• Attends internal meetings to help establish priorities and assigned tasks
• Promoting a teamwork culture within the facility
• Ensure all relevant documentation is filled out as per company...
...) if they have relevant project site experience.
* Proven track record in delivering Capital Projects - new equipment, utilities, facilities, etc.
* Good knowledge of change control and C&Q processes/execution.
Must have demonstrated relevant site experience of one or more...
...to visit existing and potential customers from time to time) and attending trade shows.
• Researching and identifying potential customers... ...(NDA’s).
• Delivering product demonstrations and providing a facility tour to existing and prospective customers and providing post-sales...
...over 6,000 people across ten sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and... ...co-ordination to direct reports.
Manage your team’s time and attendance, including absenteeism/overtime review and occupational health...
...Integrity policies and regulatory requirements.
* Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA,
* European cGMP and GAMP standards.
* Generation/...
...combination of education and experience.
~1-2 years’ experience working in Quality or a related field in commercial cGMP health care facility. Less experience may be appropriate with advanced degree.
~ Experience with Microsoft Word and Excel and having an eye for detail...
Team Horizon is seeking a Validation Engineer on a permanent basis for our client’s manufacturing facility in the Northwest.
Why you should apply:
* You will get the opportunity to coordinate, implement and actively participate in the site Validation Program and general Technical...
...Manufacturing Manager and will have circa. 7 direct reports.
This is an exciting opportunity to join a state-of-the-art start up facility where will lead and contribute to the safe operations of the API manufacturing team in line with all safety, regulatory and operational...
...Integrity policies and regulatory requirements.
Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies.
Generation/maintenance of the Validation Master Plans....
...procedures and process in accordance to site safety requirements.
Provide backup support and escort services for the Utilities and Facilities system:
UPS, Electrical switchgear, and distribution network.
Fire protection, detection, and alarm system.
Building...
...commissioning and validation in a cGMP pharmaceutical industry.
~ Experience of start-ups and/or new product introductions to pharmaceutical facilities is desirable.
~ Detailed Knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry preferred.
~...
...and contribution of psychology by providing professional consultation, education, guidance, and support to others, as appropriate.
Attend meetings, committees and / or conferences as required.
Work in an ethical and professional manner at all times.
Promote a culture...
...organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements.
Are you intrigued? Do you want to learn more?
A snapshot of your...
...Process improvement / cost reduction projects.
* Lead your regular weekly / bi-weekly Project review meetings with your Project team.
* Attend the weekly Tier 1 meeting with your manager.
* Liaise with Senior Engineering Manager, Equipment Vendor, Quality Leads, Validation...
...visitors.
Develop and modify procedures as needed to support the manufacturing
operation.
Participate in process, equipment, and facilities validations efforts and
projects implementations.
Liasing with operations, quality and S&T to ensure equipment and process...
...process for new product.
Providing operational technical support for process related issue resolution.
Performing gap analysis, facility fit studies, process safety and risk analysis for NPI.
Monitoring and analysis of process data during manufacturing....
...The QA Specialist ensures product manufacturing complies with GMP and Regulatory standards. Responsibilities include validating facility, equipment, and utilities, as well as reviewing and approving validation documentation . This individual contributor role requires...
€15.49 per hour
...An innovative approach to problem solving
A quality focused approach to production
Please note this is a 24/7 Manufacturing facility. Applicants need to be flexible to work shifts including weekends.
Monday - Friday shifts:
Evening Shift 4pm – 12pm – Monday to...
...well understood, robust, fit-for-purpose process control strategy for each new product introduction (NPI).
Author gap assessments, facility fit studies, process safety and risk assessments for NPI.
Design, onboarding, and testing of single use assemblies for use in...
...record within the last five years is permitted.
Additional Information
Regardless of your socio-economic background, university attended, subject studied and degree attained, Enterprise will always look at how you perform against our competencies and will judge you on...