Careers Integrated Resources Inc
Senior Quality Microbiologist
Careers Integrated Resources Inc, North Haven, Connecticut, United States
Title : Sr Quality Microbiologist
Location :North Haven, CT- Onsite
Duration: 12 Months+
Shift: 1st Shift
Pay Range: $50-$57/hr. on w2
Requires a Baccalaureate degree.
Must Have 5+ years of experience in the medical device industry with a strong background in microbiology laboratory processes and relevant ISO, USP, and industry standards Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, EU-MDR, and other relevant medical device regulations Outstanding communication and interpersonal skills with the ability to work effectively with cross-functional teams and external stakeholders. Proficiency in Microsoft Office Suite and quality management systems (QMS) Strong technical writing capability 5+ years of experience with Bioburden, Sterility, Bacterial Endotoxin testing, and cleanroom environmental monitoring Nice To Have Solid understanding of ISO 17025 and laboratory compliance
HM's Top Needs: Experience with Bioburden, Sterility, Endotoxin and Environmental monitoring tests Proficiency with Microsoft office suite and strong technical writing skills Experience in a quality control focused Microbiology lab environment We are looking for a Microbiologist with experience in supporting medical device manufacturing. Experience with bioburden, sterility, bacterial endotoxin, and environmental monitoring methods is strongly preferred. Strong technical writing skills and experience using document control systems is required. Education Required: Bachelors Years’ Experience Required: At least 5 years of relevant laboratory experience along with a Bachelor’s degree. Will the contractor be working 40 hours a week? If not, weekly estimate? Yes Work Location: Do they need to be local to any office and if so where? North Haven, CT Does this person need to be on site? If so, full time or part time? Full time, On-Site
Requires a Baccalaureate degree.
Must Have 5+ years of experience in the medical device industry with a strong background in microbiology laboratory processes and relevant ISO, USP, and industry standards Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, EU-MDR, and other relevant medical device regulations Outstanding communication and interpersonal skills with the ability to work effectively with cross-functional teams and external stakeholders. Proficiency in Microsoft Office Suite and quality management systems (QMS) Strong technical writing capability 5+ years of experience with Bioburden, Sterility, Bacterial Endotoxin testing, and cleanroom environmental monitoring Nice To Have Solid understanding of ISO 17025 and laboratory compliance
HM's Top Needs: Experience with Bioburden, Sterility, Endotoxin and Environmental monitoring tests Proficiency with Microsoft office suite and strong technical writing skills Experience in a quality control focused Microbiology lab environment We are looking for a Microbiologist with experience in supporting medical device manufacturing. Experience with bioburden, sterility, bacterial endotoxin, and environmental monitoring methods is strongly preferred. Strong technical writing skills and experience using document control systems is required. Education Required: Bachelors Years’ Experience Required: At least 5 years of relevant laboratory experience along with a Bachelor’s degree. Will the contractor be working 40 hours a week? If not, weekly estimate? Yes Work Location: Do they need to be local to any office and if so where? North Haven, CT Does this person need to be on site? If so, full time or part time? Full time, On-Site