Job Description
A fantastic opportunity has arisen for a Technical Specialist. You will be responsible for assisting in the effective and efficient running of analytical projects and will be active members within the wider Technology team to provide Technical support, guidance and expertise to ensure the success of the team.
Our site in Brinny, Co. Cork has been a vibrant part of the pharmaceutical sector in the South-East region for over 35 years. With a successful legacy of developing and commercially supplying biotech products including some of our most successful treatments for Oncology, Hepatitis C, and Rheumatoid Arthritis, Brinny is now specialising in the development and manufacture of innovative novel vaccines and testing of immuno-oncology medicines.
Bring energy, knowledge, innovation to carry out the following:
* Knowledgeable in protein chemistry and analytical techniques such as ELISA/Bioassay methods, Method validations, method transfers and Equipment qualifications in a GMP environment.
* Perform laboratory experiments required to deliver on project timelines.
* Participate in continuous improvement initiatives, including method optimisation and troubleshooting.
* Preparation of documentation associated with the projects in accordance with GDP (good documentation practice) and site procedures.
* Lead and participate in cross-functional projects, problem solving teams for troubleshooting, and investigations across site.
* Prepare, review and approval of technical documents, procedures, CAPAs, change control, deviations, metrics, etc.
* Adhere to highest quality standards.
* The Analytical Sciences (AS) group require a Technical Specialist with strong analytical experience to provide multidisciplinary expertise and technical support to the Analytical Sciences team.
What skills you will need:
In order to excel in this role, you will more than likely have:
* MSc/BSc. qualification (Science).
* At least 3 years’ industry experience working with ELISA/Bioassay in a QC/Analytical role group.
* High level written and verbal communications with advanced PC skills.
* Self-motivated and ability to work as part of a team with good project management skills.
* Demonstrated ability to fully realize improvement initiatives.
* Demonstrated successes in a team environment, such as project teams, problem solving teams etc.
* Stakeholder management of multiple decision makers, corporate colleagues, cross functional teams.
* Desired Qualifications/Experience: Minitab, Softmax Pro, JMP, Trackwise.
* Project management qualification such as, Project Management Professional (PMP).
As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.
As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.
We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.
So, if you are ready to:
Invent solutions to meet unmet healthcare needs, please apply today.
Employee Status: Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements: Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date: 02/3/2025
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID: R332290
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