OPERATIONAL QUALITY OVERSIGHT SPECIALIST

Description.
Site Name.
Italy - Parma Posted Date.
Mar Are 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.
We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included.
We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.
Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK This role will provide YOU the opportunity to lead key activities to progress YOUR career.
These responsibilities include some of the following.
Perform quality oversight directly on the shop floor, guaranteeing that all the GMP standards are met during operations Execute and deliver quality objectives, quality improvement plan, and trends against the quality key performance indicators to drive continuous improvement Monitor quality performance and key performance indicators assigned to third parties to ensure quality and compliance issues are identified, communicated, and resolved Support 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 appropriate Develop local processes to conduct root cause analysis; identify where corrective/preventative actions plans are required and ensure they are effectively implemented, monitored, and closed out Perform activities to support the risk management process to ensure effective management, timely reporting, review and escalation of quality risks Ensure all product specifications and related documents are maintained and compliant to current registered details Support the local change control process to ensure all planned major changes are effectively and compliantly managed Support the complaints management process to ensure potential issues are determine quickly, linked to the adverse events, reported, and follow up on product complaints Support Quality Manager in ensuring product storage and distribution performed by third party warehousing and distribution service providers complies with GSK standards Ensure as appropriate documentation of batch records and retention of samples Why you? Basic Qualifications & Skills We are looking for professionals with these required skills to achieve our goals.
Bachelor’s degree in a science-related field Experience within the Pharmaceutical/Consumer Healthcare industries Experience in quality assurance systems particularly in the areas of batch manufacturing and release, product incidents and performing self-inspection Experience with regulatory requirements pertaining to good manufacturing practices and good documentation practices Experience working with effective quality documentation systems Preferred Qualifications & Skills Please note the following skills are not necessary, just preferred, if you do not have them, please still apply.
Previous role as a quality associate or specialist for sterile manufacturing Excellent written and verbal communication skills Analytical thinker with good attention to detail and problem-solving skills in a structured process Team player with the ability to work in cross-functional teams Ability to work under pressure Identify areas of continuous improvement and innovative ways of working Ability to demonstrate flexible thinking Strong general computer literacy with Intermediate skills in Microsoft Word, Excel, Power Point and Outlook Closing Date for Applications – April Please 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.
The information that you have provided in your cover letter and CV will be used to assess your application.
Why Us? 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 organization where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.
billion people by the end of .
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 workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.
We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at (US Toll Free) or + (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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For more information, please visit GSK’s Transparency Reporting For the Record site.
Qualifications.
UNAVAILABLE Responsabilities.
UNAVAILABLE Skills.
UNAVAILABLE