Quality Control Analyst I
Ridgefield, New Jersey Permanent Date posted Nov. 15, 2024Job Title: Quality Control Analyst I
Location: Ridgefield, NJ
About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The Micro QC Analyst I is dedicated to the Microbiology Laboratory and EM Monitoring Program.The role of the Micro QC Analyst I will be that of various Microbial testing, EM monitoring of the aseptic production areas, ordering and stocking supplies, creating/reviewing SOPs, investigation writing, data entry.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities
The Micro QC Analyst I is part of the Quality Assurance Department at Ridgefield, NJ. This role is responsible for providing the day-to-day operation, testing and EM monitoring for the Micro team.
The candidate must have previous quality control microbiology experience. Experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon or endotoxin assays is preferred
Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas.
SOP review, creation and approval is preferred
OOS investigations writing is preferred
Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs.
Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data.
Interact with Project Teams and cross-functional groups related to site operations
Cohesive Micro player in the Micro department who is willing to assist or help a fellow analyst.
The Micro QC Analyst I is expected to act on and demonstrate the Sanofi LEAD competencies:
Act for Change: Embrace change and innovation and initiate new and improved ways of working.
Cooperate transversally: Collaborate effectively with peers, stakeholders and partners across the organization to positively impact business results.
Develop People: Take responsibility for developing one’s self and mentor other Micro Personnel in anticipation of future business needs or to assist the micro department.
About You
HSE
It is required that individuals care for their own safety and wellbeing. Individuals must promote a safe working environment for employees and contractors working in their area of responsibility.
The individual must support all Sanofi and site HSE policies as well as ensure that work performed is compliant with local HSE regulations.
Individuals must complete all required HSE trainings. Everyone is required to report all accidents and incidents and support investigations in their areas of responsibility. Individuals must ensure timely closure of HSE actions owned by their departments.
Education / Experience
Physical Requirements include the capacity to lift and carry up to 20 pounds, kneel, reach and stretch, and to stand for at least 4 hours.
BA/BS in Microbiology/Biology with at least 1 year of experience in CGMP, pharma or lab environment is required.
Practical experience in general microbiology laboratory techniques working with bacteria, yeast and mold.
Prior experience with data review, authoring SOPS, Change Controls, out of specification investigations and report writing is recommended.
Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing
Excellent technical writing skills
Ability to collaborate effectively with personnel and between departments
Problem-solving skills
Strong communicator
Works independently
Working knowledge of Word, Excel and PowerPoint
Working Hours
Consist of two possible shifts
Monday - Friday from 7:00 am to 3:30 pm, or Monday - Friday form 10:00 am to 6:30 pm
Some flex in the start and end times may be allowed; weekend work and overtime as required.
Why Choose Us
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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