QC Micro Analyst

Regeneron Pharmaceuticals, Inc.; Limerick; Sur place; EUR 22 000 - 34 000; Plein temps

Résumé du poste

Regeneron Pharmaceuticals, Inc. in Limerick is seeking an Associate QC Micro Analyst to join the Quality Control Microbiology team in Raheen. The role involves performing microbiological testing to support cGMP manufacturing and product quality.

You will conduct environmental monitoring, log and analyze samples for bioburdn and endotoxin testing, review data, and ensure compliance with GMP standards. Requires a BS/BA in Microbiology or Life Sciences and 0-2 years' experience; on-site with

Qualifications

• Bachelor’s degree in Microbiology, Biotechnology, Life Sciences or related field (or equivalent).
• 0–2 years of relevant laboratory experience for Associate level.
• Experience in GMP/pharmaceutical/regulated environment is advantageous.
• Strong understanding of microbiological lab techniques and good documentation practices.

Responsabilités

• Perform microbiological testing to support cGMP manufacturing operations and product quality.
• Conduct environmental monitoring: air, surface and settling plate sampling.
• Collect, log and analyze samples for bioburden, endotoxin and microbial identification testing.
• Review laboratory data, document conclusions and support investigations.
• Ensure compliance with GMP requirements, SOPs and regulatory standards.

Connaissances

Microbiology

Documentation

Formation

BS/BA in Microbiology or Life Sciences

Description du poste

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently seeking an Associate QC Micro Analyst to join our Quality Control Microbiology team in Raheen, Limerick.

When & Where

• Location: Raheen, Limerick, Ireland
• Shift work may be required based on business needs

What You'll Do

• Perform microbiological testing to support cGMP manufacturing operations and product quality
• Conduct environmental monitoring activities, including viable and non-viable air, surface and settling plate monitoring
• Collect, log and analyze samples for bioburden, endotoxin and microbial identification testing
• Review laboratory data, complete documentation and support laboratory investigations as required
• Ensure all activities are performed in compliance with GMP requirements, SOPs and regulatory standards
• Collaborate with cross-functional teams to support manufacturing operations and continuous improvement initiatives

The Environment And Physical Rhythms Of This Role

• Work within laboratory, manufacturing and cleanroom environments
• Follow aseptic and gowning procedures in controlled GMP areas
• Maintain a high level of accuracy, attention to detail and data integrity
• Balance multiple priorities while meeting timelines and compliance requirements
• Work independently while also collaborating with cross-functional teams
• Participate in a culture of continuous improvement and operational excellence

Let's Find Out If We're a Fit

• Requires a BS/BA in Microbiology, Biotechnology, Life Sciences or a related field, or an equivalent combination of education and experience
• For Associate QC Micro Analyst: 0-2 years of relevant laboratory experience
• Experience in a GMP, pharmaceutical, biotechnology or regulated environment is advantageous
• Strong understanding of microbiological laboratory techniques and good documentation practices

Does this sound like you? We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (hourly)

€16.42 - €25.59