Site Name: Italy - ParmaPosted Date: Oct 2 2024Are you looking for an opportunity to support a Quality Management team in the day to day operations in a manufacturing environment?
If so, this is the role for you.As Operational Quality Specialist staff you will be responsible for supporting in implementing and maintaining an effective and robust quality management system.
You will also perform day to day quality operations to ensure lean and efficient ways of working to meet compliance standards.This role will provide YOU the opportunity to lead key activities to progress YOUR career.
These responsibilities include some of the following:Lead process deviations, ensuring that all investigations are thorough and completeDevelop local processes to conduct root cause analysis; identify where corrective/preventative actions plans are required and ensure they are effectively implemented, monitored, and closed outElaborate product quality impact assessments for batches involved in product incidentsMonitor quality performance and key performance indicators assigned to third parties to ensure quality and compliance issues are identified, communicated, and resolvedSupport the Quality Manager to ensure that an effective local product incident process is in place and manage any product quality related issues and train staff as appropriatePerform activities to support the risk management process to ensure effective management, timely reporting, review and escalation of quality risksEnsure all product specifications and related documents are maintained and compliant to current registered detailsSupport the local change control process to ensure all planned major changes are effectively and compliantly managedEnsure as appropriate documentation of batch records and retention of samplesBasic Qualifications SkillsWe are looking for professionals with these required skills to achieve our goals:Bachelor's degree in a science-related fieldExperience in pharmaceutical quality assurance systems, particularly in the area of process deviations coordination (RCA, quality impact assessment, CAPA definition)Experience with regulatory requirements pertaining to good manufacturing practicesExperience working with effective quality documentation systemsPreferred Qualifications SkillsPlease note the following skills are not necessary, just preferred, if you do not have them, please still apply:Excellent written and verbal communication skillsAnalytical thinker with good attention to detail and problem-solving skills in a structured processTeam player with the ability to work in cross-functional teamsAbility to work under pressureAble to identify areas of continuous improvement and innovative ways of workingAbility to demonstrate flexible thinkingClosing Date for Applications – October 13th, 2024Please take a copy of the Job Description, as this will not be available post closure of the advert.When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above.Why GSK?
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive.Our success absolutely depends on our people.
While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive.
We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be.
A place where they can be themselves – feeling welcome, valued, and included.
Where they can keep growing and look after their wellbeing.
So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).GSK is an Equal Opportunity/Affirmative Action Employer.
All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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