Temp - QC Microbiology Scientist

Regeneron; Ireland; On-site; EUR 40,000 - 60,000; Full time

Job summary

A leading biotechnology company in Ireland seeks a candidate to perform development, optimization, and validation in the QC Microbiology group. The ideal candidate will have a BS/BA in Microbiology and 2+ years of relevant experience. Responsibilities include method validation, technical documentation, and coaching junior staff. Join a diverse team that values inclusivity and offers comprehensive benefits.

Benefits

Health and wellness programs

Fitness centers

Equity awards

Annual bonuses

Paid time off

Qualifications

• 2+ years of validated experience in microbiology.
• Strong background in pharmaceutical microbiology and GMP.
• Experience in QC labs and aseptic techniques.

Responsibilities

• Validate methods and equipment related to microbiological testing.
• Write technical documentation including validation reports.
• Lead technical troubleshooting and investigations.
• Coach junior team members on microbiology lab practices.

Skills

Independent work

Trouble-shooting skills

Attention to detail

Written and oral communication

Education

BS/BA in Microbiology or related field

Job description

Overview

Within this role you will perform testing method development, optimization and validation for the QC Microbiology group. Provide technical support and guidance for release testing, in-process testing, and microbiological investigations. Provide technical expertise in regards to Environmental Monitoring.

This role might be for you if:

• You have a proven record to work independently or as part of a team
• You possess strong trouble-shooting and problem solving skills
• You have strong attention to detail & excellent written and oral skills

To be considered for this opportunity you should have a BS/BA or equivalent experience in Microbiology or related field and 2+ years of validated experience, or equivalent combination of education and experience.

Responsibilities

• Validating methods and equipment related to sterility, bioburden, endotoxin testing, and microbial identifications.
• Writing technical documentation, including position papers, validation reports, and microbiological investigations.
• Culturing organisms, conducting research, and characterizing them for use in investigations and cleaning development.
• Reviewing new test procedures and assays for accuracy and compliance.
• Evaluating and acquiring new methodologies, techniques, and equipment as needed.
• Overseeing contract laboratory testing to ensure quality and compliance.
• Setting product specifications and alert/action levels for microbiological standards.
• Leading technical troubleshooting and problem investigations.
• Reviewing assay, process, and equipment validation reports, as well as other technical documents for correctness and regulatory compliance.
• Coaching junior team members on good microbiology lab practices and modern aseptic techniques.
• Leading audits of vendors, external laboratories, business partners, and contracted manufacturers as needed.
• Supporting and participating in regulatory inspections to ensure compliance.
• Possessing a strong background in pharmaceutical microbiology, GMP working experience in QC labs, and aseptic techniques.
• Demonstrating investigational skills and working knowledge of microbiology assay development and validation.
• Requiring advanced knowledge of aseptic manufacturing operations.

Qualifications

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!

Equal Opportunity Employer Statement

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.

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.