Senior QC Scientist

Posted 2 Days Ago
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Limerick
Senior level
Biotech • Pharmaceutical
The Role
The Senior QC Scientist will conduct assay validation and provide technical guidance for QC testing and assay development. Responsibilities include reviewing test procedures, participating in regulatory inspections, and contributing to cross-functional improvement initiatives. A strong background in microbiology, chemistry, or biology, along with experience in the pharmaceutical or biotechnology industries, is required.
Summary Generated by Built In

Within this role you will perform assay transfers, validation and investigation activities for QC. Provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.

As a Senior QC Specialist a typical day might include, but is not limited to, the following:

  • Performing assay validation for QC
  • Reviewing new test procedures and assays
  • Evaluating and bring in new methodologies, techniques, and equipment as needed
  • Generating and/or supporting the completion of compliance records, CAPAs, change controls and deviation notifications as needed
  • Evaluating assay performance through yearly method performance reports
  • Facilitating assay transfers from R&D and to business partners
  • Organising analytical assay transfer internally and externally
  • Performing additional studies supporting regulatory filing eg. Bridging/comparability studies
  • Participating in technical troubleshooting and problem investigation
  • Reviewing analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance
  • Participating in training programs for analysts
  • Supporting and participate in regulatory inspections
  • Participating in cross-functional improvement initiatives/kaizens

This role might be for you if:

  • You enjoy working in a fast-paced environment and you have the innate ability to balance multiple projects, prioritise them and complete them independently, while excelling at keeping all impacted parties well advised
  • You are able to work in a team environment but can also take ownership of large technical reports and projects
  • You can develop and drive scientific and/or business-related improvement ideas

To be considered for this opportunity, candidates should hold a PhD in Microbiology, Chemistry, Biology, or a related field with 2+ years of experience, preferably in the pharmaceutical or biotechnology industries; an MSc with 7+ years of proven experience; or a BSc, which will be considered based on the candidate's years of experience and technical background, particularly within the pharmaceutical or biotechnology sectors

#LI-Onsite #IRELIM #JOBSIEST 

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions.  For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.  Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Top Skills

Analytical Development
Assay Validation
Capas
Method Performance Reports
Regulatory Compliance
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The Company
HQ: New York, New York
15,000 Employees
Hybrid Workplace
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.

Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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