QA Specialist
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| Job Type | Contractor |
| Area | Westmeath, Ireland |
| Sector | QualityOperations & Manufacturing |
| Start Date | |
| Advertiser | Ashling Guthrie |
| Job Ref | #2133 |
| Job Views | 471 |
- Description
- We are seeking applications for an experienced QA Specialist our Clients Bulk Drug Substance (BDS) facility.
Why you should apply:
This is an opportunity to join a fast moving, rapidly growing entrepreneurial organisation that pursues its mission to transform patients' lives with persistence, dedication and perseverance. We are driven because we know their lives depend on it.
If you are Patient focused, like to challenge conventional thinking and enjoy collaborating to solve complex problems – then this is the company for you.
What you will be doing:
The Specialist for Drug Substance Manufacturing will be responsible, with management support, for providing oversight of quality activities associated with drug substance manufacturing processes.
The Specialist contributes and guides completion of milestones associated with specific projects and supports ongoing quality assurance responsibilities in support of: Manufacturing oversight and new product introduction including equipment validation, automation changes, SOP and master batch record approval, Change Control, Deviations, CAPAs and Supplier Management.
Performs all responsibilities in accordance with company policies, procedures, and federal regulations.
Will be responsible for supporting drug substance manufacturing and assessing the compliance of this program against best industry practice and current regulatory expectations.
What you need to apply:
Academic degree in natural or applied sciences (Pharmacy, biology, biotechnology, engineering)
3 years in international pharmaceutical and/or biotech industry
Sound awareness and understanding of pharmaceutical business
