With our ongoing transformation, we hire a number of QC Analysts each year and are keen to learn the interest of professionals in this space before roles become available.
Please see the below job description and apply to register your interest.
The role of the QC Analyst involves 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, which 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 with 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 aspects 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 to gather information 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 the QC team operates efficiently and maintains product lead times,
* 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).
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.
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.
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