Job Title: US Product Quality Complaints Sample Room Technician
Location: Framingham, MA
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.
This position is responsible for activities related to management of complaint samples related to Product Technical Complaints for medical devices, pharmaceutical products, biologics and combination products. Knowledge of regulatory requirements, GMP, GDP, quality & compliance and complaint handling is preferred.
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?
Training will be conducted on site in Bridgewater, NJ in Jan/Feb 2025.
Main Responsibilities:
Responsible for E2E operations conducted in PQC Sample Room
On site support 5 days/week, ability to work wearing PPE
Responsible for handling used complaint samples received from patients/pharmacies/clinics, etc.
Process returned complaint samples as per PQC Sample Room Manual
Identifies and handles lot discrepancies correctly with returned complaint samples.
Updates the complaint records in the systems.
Prepares products for shipments to the manufacturing sites
Prepare shipping labels using FedEx equipment.
Assemble shipping containers to the sites
Deliver assembled mailers to main Sanofi mail room or arrange for daily pick up
Responsible for resolving all discrepancies directly with the reporters
Create new complaints in local and global systems
Identify complaints for FAR/BPDR (Field Alert and Biological Product Deviation Report) reporting as necessary
Use various Excel reports for daily operations.
Act as a SME on PQC Sample Room operations and provide support during audits and inspections
Act as a trainer for new associates
Manage revisions to PQC Sample Room Manual
Complete all required trainings (i.e. DOT, IATA, blood borne pathogens)
Manage all supplies and maintain inventory required for daily operation of a PQC Sample Room
Order supplies and work directly with the vendors for customized PO
Responsible for maintaining all equipment and tools in PQC Sample Room
Proficient with use of all databases within the department
Knowledge of GxP
Knowledge of all Sanofi products marketed in the US
Understands PQC process flow
Understands the FDA complaints regulations for the drug, combinations products and medical devices.
Maintains PQC reports as needed
Understands export shipping requirements for shipment of waste pharmaceuticals to overseas manufacturing sites.
Prepare international shipping manifests, commercial invoices and customs forms
Provides complaint support to other company departments including Customer Service, Medical Information, Pharmacovigilance, Sales Associates, Regulatory, Commercial, Operations, Legal, and Risk Management.
Performs other duties as assigned.
Ability to lift/move 20lb and work standing 50%
Maintains use of Universal Precautions while working
About You
Knowledge, Skills and Experience
Associate degree in science or related field of study
2 years of pharmaceutical industry experience. Will consider an advanced degree in lieu of years of experience.
Strong Verbal and Written Communication skills.
Excellent interpersonal skills.
Strong organizational and prioritization skills.
Ability to multi-task in a fast-paced environment
Strong understanding of Good Documentation Practices
Ability to lift/move 20lb and work standing 50% while wearing personal protective equipment
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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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 ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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.