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Site Quality Operations Senior Auditor


This is a Contract position in Framingham, MA posted June 12, 2019.

Site Quality Operations Senior AuditorThis position will report to the Associate Director of Quality and will assist in maintaining the quality systems and GMP compliance in support of gene therapy products at Sanofi.Perform review of Batch records and associated documents in support of release of intermediates.Participate or lead in investigation of all lot-associated deviations, change controls, Environmental Management System (BMS) investigations, action notices and environmental excursions as required.Perform QA presence on the floor/person in plantPerform various QMS trending/reporting functions.Ensure compliance to the relevant SOP and corporate standards.Lead/Participate in investigation of non-lot associated deviations, change controls (CCR/LCR), BuildingParticipate in walkthrough program.Manage assigned site QA projects.Ensure that documentation and operations meet established requirements of cGMPs, Internal SOPs and company policies.

Draft and revise procedures (DCR) as required.Serve as an internal auditor for the site.Actively participate in the preparation, execution and follow-up for audits from Global Quality Auditors.Participate or facilitate FMEA/Risk as appropriate.May serve as team leader for continuous improvement teams or investigative teams.Investigate quality critical alarms.Assist in the development of Quality Technical Agreements (QTA).Performs work that requires decision making and the consistent exercise of independent judgment and discretion.Perform Quality Assurance review for deviations, investigations, DCRs and complaints and manage associated files.Review and approve Validation protocols and technical reports as appropriate.Assist in the oversight of the sterility assurance program.Perform, External auditsMaster’s Degree & 3 years of experience OR Bachelor’s Degree & 5 years of experience in cGMP.Preferred Qualifications:Excellent communications skills both written and verbal.Strong critical thinking ability.

Strong leadership ability.Effective time management and organizational skills.Strong attention to detail and ability to lead others in a team setting.Special Working ConditionsExperience with CDMOs Ability to gown and enter clean roomsAbility to perform visual inspection for final productMay require up to 15% of travel (Domestic and international)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-SGLI-GZAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.

We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.

We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.Sanofi is dedicated to supporting people through their health challenges.

We are a global biopharmaceutical company focused on human health.

We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering.

We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.Sanofi, Empowering Life