Quality Opportunities
Almac Group
Date: 1 week ago
City: Craigavon
Contract type: Full time
Hours: 37.5 hours per week - flexible and hybrid working options available (terms & conditions apply).
Salary: Competitive plus excellent benefits package
Business Unit: Pharma Services
Location: Based at our Craigavon headquarters
The Quality Assurance (QA) department plays a crucial role in ensuring that medicines produced are safe and effective, and that APS adheres to all regulations and guidelines set by health authorities, such as the MHRA. QA supports the entire production process, from compilation of batch records and procedures that govern the operations, to assessing the impact when things don’t go as planned.
Our Teams include:
Levels of experience: Graduates with no previous industry experience are welcome and will be supported through a bespoke training and development program.
If you are interested in applying for one of these exciting roles, please upload a copy of your CV to the online portal, ensuring you detail how you meet the requirements for the role. Please upload your CV in PDF format where possible.
**All applicants must be eligible to work in the UK, or hold a valid visa/work permit that allows you to work in the UK on a full time permanent basis with no restrictions**
Further information on the essential and desirable criteria required for this role can be found in the Job Description attached to this advert.
Salary: Competitive plus excellent benefits package
Business Unit: Pharma Services
Location: Based at our Craigavon headquarters
The Quality Assurance (QA) department plays a crucial role in ensuring that medicines produced are safe and effective, and that APS adheres to all regulations and guidelines set by health authorities, such as the MHRA. QA supports the entire production process, from compilation of batch records and procedures that govern the operations, to assessing the impact when things don’t go as planned.
Our Teams include:
- Quality Operations: Responsible for ensuring the manufacturing, Packaging and distribution of our Pharmaceutical Products comply with regulatory standards and our internal Quality Processes through understanding of the principles of GMP & GDP.
- Quality Compliance: Responsible for ensuring the Pharmaceutical Quality System, including procedures and processes, adhere to regulatory requirements.
- Product Quality: Responsible for ensuring each batch of product manufactured meets the required quality standards before it is certified for use.
- Technical Quality: Responsible for ensuring that our systems and processes meet the required quality standards. It is a GMP requirement that manufacturers control the critical aspects of their operations through qualification and validation over the life cycle of the product and process. This ensures systems and processes are fit for purpose and ultimately ensures the safety of our patients.
Levels of experience: Graduates with no previous industry experience are welcome and will be supported through a bespoke training and development program.
If you are interested in applying for one of these exciting roles, please upload a copy of your CV to the online portal, ensuring you detail how you meet the requirements for the role. Please upload your CV in PDF format where possible.
**All applicants must be eligible to work in the UK, or hold a valid visa/work permit that allows you to work in the UK on a full time permanent basis with no restrictions**
Further information on the essential and desirable criteria required for this role can be found in the Job Description attached to this advert.
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