Qp, Little Island

Last update 2023-12-02
Expires 2024-01-02
ID #1813057839
Qp, Little Island
Ireland, Cork, Little Island,
Modified August 23, 2023


The Role & What You Will Be DoingEvery day, we rise to the challenge to make a difference and here’s how the QP role will make an impact:Ensure that product batches and their manufacture comply with the requirements of the marketing authorisation and the manufacturer's licence.Certify that the product was manufactured in accordance with the principles and guidelines of Good Manufacturing Practice.Validation of primary manufacturing and testing processes.Recording of relevant manufacturing information and that all necessary checks and tests have been performed.Any deviations or planned changes have been documented and approved in accordance with a defined procedure.Ensure that any changes requiring a variation to the marketing or manufacturing authorisations have been approved by the regulatory authority.Confirm that any additional sampling, testing or inspection necessary as a result of a deviation has been completed or initiated.All Production and QC documentation has been completed and approved by relevant personnel.Audits, self-inspections and spot checks have been carried out and documented by experienced personnel, as required.Ensure that all necessary checks have been completed as part of the batch release process, in accordance with the established procedure.All relevant factors directly or indirectly associated with the product or batch under review must also be taken into consideration.Participate in the Change Control procedure in accordance with the relevant SOPs.About Your Skills & ExperienceFor this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:Must have a third level qualification in a scientific disciplineRelevant experience in the pharmaceutical industry.The person must have fulfilled the education requirements for the role of the Qualified Person (Pharmacist with the relevant experience or a Diploma in Pharmaceutical Manufacturing Technology).Experience in Oral Solid Dosage pharmaceutical manufacturing would be beneficial.Strong organizational skills with the ability to multitask and prioritise workload.Proficiency in speaking, comprehending, reading and writing English is required.At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.Benefits at ViatrisAt Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary:Excellent career progression opportunitiesWork-life balance initiativesBonus schemeHealth insurancePensionDiversity & Inclusion at ViatrisAt Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at ViatrisCorporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit At Viatris, we offercompetitivesalaries, benefitsandan inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Job details:

Job type: Full time
Contract type: Permanent
Salary type: Monthly
Occupation: Qp

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