跳至主要内容
两名身穿白色实验室外套的女性一起看着电脑屏幕

Production Technician - Vaccine

Swiftwater, 宾夕法尼亚州 Permanent 发布日期 18/06/2024
立即申请

Job Title: Production Technician - Vaccine

Location: Swiftwater, PA

About the Job

This will be a 2nd shift position.

This is a B77 Filling.

Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs. Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals.  Must attend shift change daily to ensure preparedness for workday. Completes Real Time SAP transactions on all aspects of Inventory Management. Obtains and Maintains access to necessary systems as needed (SAP, RT Reports, Gibralter, HMI, SCADA access, Virtual Standards, etc.). Reports production issues and observations and relays to leadership team. Understands science behind process steps and technology including aseptic processing.  Works to prepare area for oncoming shifts. Works with Senior technicians, Lead technicians and Managers to ensure continuous operation. Maintains aseptic work environment. Must be able to train and work in multiple production areas in the Filling umbrella including material movement, LYO and Isolator. Must be able to complete training in all areas as required. This role is for a nonexempt employee working in the Filling Department. Their Bi-weekly pay is based on previous experience and education time.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Key Accountabilities:

  • Performs production in accordance with volume fluctuation, business need, and effective procedures.

  • Must be flexible to ensure staffing for changing business volume and needs.

  • Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals.  

  • Must attend shift change daily to ensure preparedness for workday.

  • Completes Real Time SAP transactions on all aspects of Inventory Management.

  • Obtains and Maintains access to necessary systems as needed (SAP, RT Reports, Gibralter, HMI, SCADA access, Virtual Standards, etc.).

  • Reports production issues and observations and relays to leadership team.

  • Understands science behind process steps and technology including aseptic processing.  

  • Works to prepare area for oncoming shifts.

  • Works with Senior technicians, Lead technicians and Managers to ensure continuous operation.

  • Maintains aseptic work environment.

  • Must be able to train and work in multiple production areas in the Filling umbrella including material movement, LYO and Isolator.

  • Must be able to complete training in all areas as required.

  • This role is for a nonexempt employee working in the Filling Department. Their Bi-weekly pay is based on previous experience and education time. 

Their responsibilities are, but are not limited to:

Safety:

  • Follows all procedures put into effect to ensure your safety as well as the safety of others.  Participates in monthly safety meetings.

  • Reports all safety issues, concerns, incidents and near misses to the team leadership.

  • Actively participates in safety walkthroughs 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.

  • Utilizes +QDCI boards for Safety issues

  • Attends Safety Meetings.

Quality:

  • FDA audit understanding and awareness.  Ensures areas are following proper procedures at all times

  • Identifies possible deviation occurrences and prevents or aids in investigations and root cause analysis. 

  • Ensures completion of quality documentation (BFR’s, logbooks, etc) accurately in a timely manner.

  • Understands the function of the quality group and works with them to maintain a positive rapport.

  • Maintains acceptable execution with no emerging negative trends in procedural deviations

Delivery:

  • Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs

  • Completes tasks and corresponding documentation as required by cGMP to ensure document completion.

  • Works to prepare assigned areas for the oncoming shifts to ensure continuous operation.

  • Must ensure maintenance of gowning and Physical dexterity to complete proper set up of machines so not to impact the safety, quality, and integrity of the product.

  • All other duties as assigned. Adheres to all other company time keeping and attendance policies.

  • Ensures all Final Container materials required for production are available prior to need. These materials must be ready for aseptic filling operations to ensure the safety, quality, purity, and integrity of the product is maintained.

  • Ensures the completion of Real Time SAP transactions in an accurate and timely manner to ensure accurate inventory.

Cost:

  • Executes procedure as documented to avoid deviations.

  • Responsibly uses material in an efficient manner to reduce waste.

  • Utilizes Filling Standards to capture and record real time filling data and Change Over Activities.

  • Actively communicates improvement ideas, issues, concerns, etc. to team members along with providing solutions.

Involvement:

  • Follows proper documentation as required by cGMP.

  • Has a thorough working knowledge of cGMP’s and works to help others understand. 

  • In on time and attends and participates in Shift Change.

  • Maintains acceptable training as described in key requirements.

All other duties as assigned.

About you

Basic Qualifications

  • High School diploma or GED with 1+ years prior manufacturing work experience

  • Associate degree with less than 1-year prior manufacturing work experience

Preferred Qualifications

  • BS degree and any prior manufacturing work experience

  • Prior experience in the Swiftwater Biologics and/or FFIP departments or other good manufacturing practices (GMP) facilities

  • Experiences with Lyophilization and Isolators is preferred.  

  • Knowledge and access to SAP, Trackwise, Master, EMS, PMS, SCADA, RT Reports, and Labware is preferred

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.

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
#LI-Onsite​

立即申请
  • 您还没有查看任何职位。

  • 您还没有保存任何职位。

实验室里的女人通过放大镜观察小瓶

在美国的职位

加入我们的美国团队。我们将为您提供专家指导和培训平台,从而帮助我们营造良好的企业文化。我们鼓励您以饱满的热情和充沛的精力投入到工作中,然后发挥自身能力推进药物和疫苗的研发,同时将研发到临床治疗的时间减半。

体验可能性

  • Ama

    Ama puts her project management techniques and ServiceNow knowledge to use to help advance Sanofi’s Digital Data operating model. Learn how our team connects data and AI to do what’s never been done before.

    了解更多
  • Cambridge Crossing

    We're bringing together 2,500 people from across our organization — R&D, Medical, Commercial and Global colleagues all working to realize the power of collaboration.

    了解更多
  • Innovation in Action

    Our flexible lab of the future will transform how we conduct research, while our innovation center will be fully integrated with existing R&D locations.

    了解更多
  • Sanofi’s AI Centre of Excellence in Toronto

    The Centre is focused on using leading technologies to develop world-class data and artificial intelligence (AI) products to create value for the health sector.

    了解更多
  • Sanofi Canada's Philanthropic Efforts

    By chasing the miracles of science to improve people’s lives, we surprise ourselves with what we can achieve. Our team is humbled by the impact our efforts make.

    了解更多
  • Sustainable and Green

    Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.

    了解更多
  • 您保存的职位

    了解更多
  • 我们的办公地点

    我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。

    了解更多
  • 勇敢追梦,奔赴美好未来

    想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。

    了解更多
  • 您和我们相互依存,共同成长

    我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。

    了解更多
  • 心怀梦想,成就一番事业

    我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。

    了解更多
  • 我们的人与文化

    我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。

    了解更多
  • 我们的故事

    我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。

    了解更多
  • 为什么选择我们?

    我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。

    了解更多