QC Analyst - Microbiology

**Job Title:** QC Analyst - Microbiology**Location:** Framingham, MA**Shift:****Sun-Wed 12:00 pm - 10:30 pm****Wed - Sat 12:00 pm - 10:30 pm****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 Quality Control team is dedicated to the development and validation ofmethodologies using state-of-the-art technology and responsible for ensuring that all production lots and materials meet the required quality standards, supporting regulatory compliance, and operational excellence of the organization.**Main Responsibilities:*** Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans* Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks* Recording all expected raw data, calculations, information related to his/her tasks, to comply with cGMP and data integrity requirements* Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified* Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans* Informing his/her manager of any quality or HSE event (deviations, OOS,) in a timely manner to ensure investigation and impact assessment are performed appropriately* Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately* Executing assigned CAPAs related to remediation plans, continuous improvements* Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately**Additional Accountabilities:**Ability to perform tasks in a Quality Control Laboratory environment and capable of lifting at least 10 pounds. May be required to pass vision exam to perform specific responsibilities. May be required to enter into controlled environments following proper gowning protocols**About You****Basic Qualifications:*** High School Diploma with a minimum of 4 Years of relevant industry experience.* Associate Degree with 2-4 Years of relevant industry experience.* Bachelor’s Degree with 0-2 Years of relevant industry experience.* Proficient with Microsoft Office tools such as Word, Excel & PowerPoint.**Preferred Qualifications:*** 1 Year of Experience in a GMP lab environment.* Proficiency in Microsoft Office tools such as: Word, Excel & PowerPoint.* Experience with lab-based data management systems.* Experience in a Quality Control Laboratory.* Experience with Environmental Monitoring, including Water Testing.**Special Working Conditions:*** Work in a laboratory with minimal use of chemicals.* Ability to lift 10 lbs.* 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.#GD-SG #LI-GZ#LI-Onsite #vhd# Pursue *progress*, discover *extraordinary*Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !*US and Puerto Rico Residents Only*Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.*North America Applicants Only*The salary range for this position is:$27.24 - $36.32All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . #J-18808-Ljbffr Sanofi