Posted : Tuesday, August 27, 2024 05:52 PM
Overview
From Research and Development to Sales and Marketing, Sanofi offers a wide range of possibilities.
Discover our open positions and become a health journey partner.
Success Profile Do you have what it takes for a successful career with Sanofi? Courageous Results-driven Proactive Problem-Solver Leadership Team player Culture: Play to Win Growth Innovation Efficiency Collaboration Benefits Health & Wellness Comprehensive coverage including medical, dental, vision, and health and wellness programs.
Financial Sanofi wants to ensure employees are equipped for financial health, Sanofi provides a competitive 401K Match program and Financial Wel-Being Tools and Programs.
Culture At Sanofi, we demonstrate our commitment to inclusion and diversity through Culture groups and programs.
There are many ways to make a difference and connect with other Sanofi employees: including ERG groups and 2 PAID days off to Volunteer.
Work/Life Balance Sanofi provides significant Work/Life benefits to help you excel beyond the workday.
Including Workplace Flexibility through part‑time, remote work, flex‑time and job share options.
Quote "At Sanofi, We are guided by a deep appreciation and understanding of what it means to live with a rare blood disorder, and we learn by listening to the community – patients, caregivers physicians, and other healthcare professionals.
" Shannon Resetich US Head Rare Diseases & Blood Disorders Responsibilities Production Technician – Vaccine 3rd Shift Inspection ABOUT THE ROLE: Must be able to work weekends and holidays as needed.
Performs production in accordance with volume fluctuation, business need and effective procedures.
Responsible for Manufacturing activities in assigned area.
Identifies all production issues and relays them to the leadership team.
Works to prepare assigned areas for the oncoming shifts.
Completes tasks and corresponding documentation as required by cGMP.
Position includes responsibilities to hand pack, operate machinery, change over duties, and clean-up functions, to assure a smooth transition between product lines.
Works with Senior Technicians and Managers to ensure a smooth operation.
Works to become trained in all assigned training modules.
Trains and orients new team members (at any level) as assigned.
Follows all procedures put into effect to ensure your safety as well as the safety of others.
Participates in monthly safety meetings.
Report all safety issues, concerns, incidents and near misses to the team leadership.
Actively participates in safety walk throughs coordinated by the department’s safety team.
Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.
Follows effective procedures to ensure the production of a safe and efficacious product.
Works to understand cGMP’s.
Identifies areas of deficiency to the leadership team and offers potential suggestions for improvements.
Participates in both deviation investigations when appropriate and implementation plans to ensure a quality product.
Works with the leadership team to complete deviation investigations and root cause analysis.
Works to complete quality documentation (PDR’s, logbooks, etc.
) accurately in a timely manner.
CFR (code of federal regulations) / PAI inspection readiness.
FDA audit understanding and awareness.
Participates in team meetings.
Actively communicates improvement ideas, issues, concerns, etc.
to team members.
Participates in cross functional teams where necessary to complete projects in an effective and timely manner.
Ensures proper process area operation by pre and post run set up and maintenance of equipment.
Recommends changes to PDR's, SOPS and SWIs when warranted.
Write and edit documents under supervision.
Seeks out cross training in other areas whenever possible.
Responsible for assisting in writing and assisting incident investigations, CAPA's, change controls, along with assisting the higher tech levels and Principle Investigators with projects.
All other duties as assigned.
BASIC QUALIFICATIONS: HS diploma or equiv and 2+ years in cGMP or Pharmaceutical experience Associates with 1 + yrs in cGMP or Pharmaceutical experience Bachelor’s with 0 + yrs in cGMP or Pharmaceutical experience Prior or related cGMP or Pharmaceutical experience recommended Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity.
THE FINE PRINT For influenza production roles (excluding FFIP roles): candidate must be able to be receive influenza vaccine which is required for building access For aseptic area production roles (excluding Flu production tech roles): candidate must be able to obtain and maintain current aseptic gowning qualification This position may be required to be moved or temporarily flexed to another department or building within the FFIP operation due to business needs.
Additionally, candidates should expect to work in multiple buildings.
Some over-time/off-shift work hours may be required based on business needs.
We will attempt to provide as much advance notice as possible, two weeks where applicable if any such change is needed.
Must be able to lift up to 25 lbs.
, and bend/lift/move objects as part of the job.
Able to stand for up to 8 hours a day (with occasional breaks) 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-SP #LI-SP At 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.
Discover our open positions and become a health journey partner.
Success Profile Do you have what it takes for a successful career with Sanofi? Courageous Results-driven Proactive Problem-Solver Leadership Team player Culture: Play to Win Growth Innovation Efficiency Collaboration Benefits Health & Wellness Comprehensive coverage including medical, dental, vision, and health and wellness programs.
Financial Sanofi wants to ensure employees are equipped for financial health, Sanofi provides a competitive 401K Match program and Financial Wel-Being Tools and Programs.
Culture At Sanofi, we demonstrate our commitment to inclusion and diversity through Culture groups and programs.
There are many ways to make a difference and connect with other Sanofi employees: including ERG groups and 2 PAID days off to Volunteer.
Work/Life Balance Sanofi provides significant Work/Life benefits to help you excel beyond the workday.
Including Workplace Flexibility through part‑time, remote work, flex‑time and job share options.
Quote "At Sanofi, We are guided by a deep appreciation and understanding of what it means to live with a rare blood disorder, and we learn by listening to the community – patients, caregivers physicians, and other healthcare professionals.
" Shannon Resetich US Head Rare Diseases & Blood Disorders Responsibilities Production Technician – Vaccine 3rd Shift Inspection ABOUT THE ROLE: Must be able to work weekends and holidays as needed.
Performs production in accordance with volume fluctuation, business need and effective procedures.
Responsible for Manufacturing activities in assigned area.
Identifies all production issues and relays them to the leadership team.
Works to prepare assigned areas for the oncoming shifts.
Completes tasks and corresponding documentation as required by cGMP.
Position includes responsibilities to hand pack, operate machinery, change over duties, and clean-up functions, to assure a smooth transition between product lines.
Works with Senior Technicians and Managers to ensure a smooth operation.
Works to become trained in all assigned training modules.
Trains and orients new team members (at any level) as assigned.
Follows all procedures put into effect to ensure your safety as well as the safety of others.
Participates in monthly safety meetings.
Report all safety issues, concerns, incidents and near misses to the team leadership.
Actively participates in safety walk throughs coordinated by the department’s safety team.
Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.
Follows effective procedures to ensure the production of a safe and efficacious product.
Works to understand cGMP’s.
Identifies areas of deficiency to the leadership team and offers potential suggestions for improvements.
Participates in both deviation investigations when appropriate and implementation plans to ensure a quality product.
Works with the leadership team to complete deviation investigations and root cause analysis.
Works to complete quality documentation (PDR’s, logbooks, etc.
) accurately in a timely manner.
CFR (code of federal regulations) / PAI inspection readiness.
FDA audit understanding and awareness.
Participates in team meetings.
Actively communicates improvement ideas, issues, concerns, etc.
to team members.
Participates in cross functional teams where necessary to complete projects in an effective and timely manner.
Ensures proper process area operation by pre and post run set up and maintenance of equipment.
Recommends changes to PDR's, SOPS and SWIs when warranted.
Write and edit documents under supervision.
Seeks out cross training in other areas whenever possible.
Responsible for assisting in writing and assisting incident investigations, CAPA's, change controls, along with assisting the higher tech levels and Principle Investigators with projects.
All other duties as assigned.
BASIC QUALIFICATIONS: HS diploma or equiv and 2+ years in cGMP or Pharmaceutical experience Associates with 1 + yrs in cGMP or Pharmaceutical experience Bachelor’s with 0 + yrs in cGMP or Pharmaceutical experience Prior or related cGMP or Pharmaceutical experience recommended Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity.
THE FINE PRINT For influenza production roles (excluding FFIP roles): candidate must be able to be receive influenza vaccine which is required for building access For aseptic area production roles (excluding Flu production tech roles): candidate must be able to obtain and maintain current aseptic gowning qualification This position may be required to be moved or temporarily flexed to another department or building within the FFIP operation due to business needs.
Additionally, candidates should expect to work in multiple buildings.
Some over-time/off-shift work hours may be required based on business needs.
We will attempt to provide as much advance notice as possible, two weeks where applicable if any such change is needed.
Must be able to lift up to 25 lbs.
, and bend/lift/move objects as part of the job.
Able to stand for up to 8 hours a day (with occasional breaks) 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-SP #LI-SP At 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.
• Phone : NA
• Location : 1 Discovery Drive, Swiftwater, PA
• Post ID: 9095816727