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| Advertiser Name | Sanofi EU | | Advertiser Type: | Company |
| Classification: | 6227 | | Subclassification: | |
| Country: | Ireland | | Location: | Ireland |
| Language: | English - United Kingdom (en-GB) | | Contact Name: | |
| Employment Type: | Permanent | | Workhours: | Not Specified |
Description:
About Waterford
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
About the job
Our Team:
We are a highly motivated and committed Team of Quality Assurance specialists conducting a wide portfolio of highly specialised activities to support 24/7 Lyophilisation Operations in Sanofi Waterford. Our team works in a fast-paced organisation delivering solutions for our patients and customer needs.
Main responsibilities:
Indicate here the main job responsibilities with bullets points, avoiding Sanofi corporate jargon, acronyms, and gender-coded words (you can check if your language is neutral on this site )
Acts as Quality support for systems/processes providing guidance/feedback on quality issues
QA Specialist to focus on Batch release execution
Assist in achieving timely and compliant final product disposition.
Review, approve, and support procedures and production/testing records as required.
Ensure compliance with aseptic techniques and sterile manufacturing regulations
Perform timely review of documentation / investigations / reports highlighting and assisting in the resolution of concerns commensurate with risk
Collaborate with cross-functional teams to support quality initiatives and continuous improvement efforts.
Work with relevant departments to ensure timely closure of quality actions / findings
Conduct duties in a safe manner and report all safety issues or concerns
Maintain work area to good housekeeping standards
Support team in achieving team goals/targets
Attend team meetings as required
Measure and report RFT / trend data and work with departments to resolve recurring issues
Participate in internal supplier and regulatory audits and key quality initiatives as appropriate
Perform critical/ constructive review of procedures and practices
Support deviation investigations ensuring deviations are closed prior to product release
Ensure compliance to Good Manufacturing Practices (cGMP) at all times
Experience:
Minimum of 5 years of experience working in a pharmaceutical or biotechnological organization
Minimum of 2 years leader experience working in a cGMP in a regulated environment
Strong knowledge of QA methodologies, tools, and processes.
Experience with quality oversight in manufacturing operations.
Excellent analytical, problem-solving, and decision-making skills.
Strong attention to detail and ability to work in a fast-paced environment.
Experience with regulatory inspections and audits is a plus.
Soft skills:
Excellent interpersonal skills
Excellent influencing skills
Excellent presentation skills
Flexible approach - comfortable with on-going change
Takes personable responsibility for their actions
Good communicator who is comfortable to work as part of a team
Focused on achieving results
Self-starter and able to work under minimum supervision
Technical skills:
Education:
Languages:
Fluent English
Pursue Progress, discover Extraordinary.
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at
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