Haleon Dungarvan, County Waterford, Ireland
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Join to apply for the QC Analyst **Register your Interest** role at Haleon
Haleon Dungarvan, County Waterford, Ireland
Join to apply for the QC Analyst **Register your Interest** role at Haleon
With our ongoing transformation we hire a number of QC Analysts each year and we are keen to learn the interest of professionals in this space before roles comes available.
Please see the below job description and apply to register your interest.
The role of the QC Analyst this Analysis of Raw Material, Intermediate, Stability samples and/or Finished Products, Peer Data Review and other micro duties / training including: Completion of Micro environmental testing, micro analysis of Raw Material & finished Products, may be assigned as required.
Responsibilities:
* Permit and promote only expected Haleon behaviours and activities,
* Sampling and testing activities carried out in line with GLP and business targets,
* Achieves Lead-time targets (and proactively addresses barriers to achievement),
* Adheres to full EHS compliance in QC and site activities,
* Adheres to full GLP compliance in QC and site activities,
* Adheres to DI expectations,
* Ensures QC documentation is completed in accordance to cGLP or cGDP practices, including records in site electronic systems e.g. M-ERP / VQMS / LIMS etc.
* On time completion of CAPAs and other site metrics.
* Completes On-The-Job Training process & maintains own training record through the span of employment in the company.
* Supports PPR (Medicinal only) and other site processes,
* Ownership of Laboratory CI Processes, support of site CI / HAPs projects.
* Excellent communication/interpersonal skills with a strong affiliation with customer support.
* Accountable for all aspect of one’s work and must have a can-do attitude.
Impact of role on business objectives:
* Ensure QC team work in a safe manner and in accordance with GxP,
* Training of QC team for specific tasks in accordance with GxP,
* Decision-making and liaison with internal departments in order to gather information in order to disposition product in accordance with GMP,
* Liaison with corporate colleagues as required to resolve issues,
* Highlighting issues to the Quality Control Manager / Quality Control Team Lead (or designee), OQ Manager and Quality Director as appropriate.
* Reviewing completed analytical reports prior to OQ approval,
* Preparation and review of in-house procedures (SOPs),
* Troubleshooting analytical problems,
* Scheduling in-house functions to ensure that the QC team operates as efficiently as possible and that product lead times are maintained,
* Support site CI / HAPs projects.
* Assist the QC function in preparation for, and during external agency audits and internal Haleon audits.
Required Skills Sets & Experience:
* Educated to a primary or higher degree level-Chemistry or associated science.
* 2-3 years' experience in a pharmaceutical / healthcare industry.
* Understanding of appropriate Directives, Standards, Quality Management Systems related to the manufacture of
* Medical Device and Medicinal for required markets.
* Ability to provide key input into management team decisions
Preferred Skill sets and Experience:
* Third level science-based degree (preferably post graduate).
Care to join us. Find out what life at Haleon is really like www.haleon.com/careers/
At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.
Haleon is an Equal Opportunity 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.
Accommodation Requests
If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific accommodations you are requesting. We’ll provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Consumer Services
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