QAV Specialist

Offering an exciting opportunity to work with a global bio pharmaceutical company based in Athlone. A long term 12 month contract with potential for extension.

The Quality Assurance Specialist executes the site QA activities in order to protect the safety, quality and efficacy of the products, thereby ensuring the availability of correct, safe product and assuring the security of the company’s business and global markets.  


This key role must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases.


In particular, this will involve partnering with major stakeholders such as Manufacturing, Validation, Engineering to optimize patient supply.

 
Skills:   

• Strong knowledge of cGMP requirements for bio pharmaceutical and/or sterile manufacturing
• Experience performing review and approval of validation studies in cGMP bio pharmaceutical is an advantage
• Planning and organizing skills are required to plan and to adjust to changing priorities.
• High level technical skills including analytical, auditing, pharmaceutical manufacturing and regulatory inspection management.
• Excellent interpersonal skills are required, as is the ability to communicate well, both verbally and written.
• Management experience is an advantage

 

Education:         

Third level qualification e.g. B.Sc. in science/pharmacy with a minimum of 3 years’ experience in cGMP Quality environment; or equivalent combination of education and experience.



The candidate must have the rights to work in the location stated in the job advert.

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