自动化工程师负责人,MES与数字系统 - 项目Farma
Lead Automation Engineer, MES & Digital Systems - Project Farma
加入PerkinElmer,您将选择一位在科学解决方案领域经验丰富、值得信赖的领导者,依托全球服务网络和分销中心,提供适时的解决方案,满足关键客户的需求。拥有80多年推动科学进步的传承,以及为更健康的世界创新的使命,我们的专业团队与商业、政府、学术和医疗保健客户紧密合作,交付我们广泛的分析解决方案和OneSource服务。
职位名称
Lead Automation Engineer, MES & Digital Systems - Project Farma
工作地点
美国远程办公 - AL,美国远程办公 - CA,美国远程办公 - CO,美国远程办公 - DC,美国远程办公 - IL,美国远程办公 - IN,美国远程办公 - MA,美国远程办公 - MD,美国远程办公 - MO,美国远程办公 - NC,美国远程办公 - NJ,美国远程办公 - NY,美国远程办公 - OH,美国远程办公 - OR,美国远程办公 - PA,美国远程办公 - TX,美国远程办公 - VA
职位描述
Project Farma将考虑具有4至16年以上相关经验的候选人。成功人选需居住在Project Farma的主要市场之一,并愿意在国内出差以满足客户项目需求。
· 市场地点包括但不限于:波士顿、费城、DMV、北新泽西、芝加哥、印第安纳波利斯、哥伦布、圣路易斯、堪萨斯城、罗利-达勒姆、休斯顿、达拉斯、博尔德、波特兰、旧金山、圣地亚哥和洛杉矶。
Lead Automation Engineer, MES & Digital Systems负责在生物制药、药品和新型疗法制造设施中,提供数字系统设计、实施和生命周期管理的专业知识。这是一个可计费的全职岗位,需要具备多种MES平台、数据仓库、序列化及与制造应用(ERP、LIMS、CMMS等)集成的经验,并能够编写、解读和主导文档,如用户需求规范(URS)、功能需求规范(FRS)、功能叙述和详细系统架构设计。
除了技术经验,Lead Automation Engineer, MES & Digital Systems在Project Farma服务项目交付期间担任客户联络人。他们通过项目交付确保客户满意度,并维护和拓展客户关系。
主要职责
自动化设计与架构
- 为生物制药、药品和先进疗法制造(DCS、PLC/SCADA、MES、历史记录器、网络层)开发系统架构和数据流。
- 开发产品
查看英文原文
When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.
Job Title
Lead Automation Engineer, MES & Digital Systems - Project Farma
Location(s)
US Remote - AL, US Remote - CA, US Remote - CO, US Remote - DC, US Remote - IL, US Remote - IN, US Remote - MA, US Remote - MD, US Remote - MO, US Remote - NC, US Remote - NJ, US Remote - NY, US Remote - OH, US Remote - OR, US Remote - PA, US Remote - TX, US Remote - VAJob Description
Project Farma will consider candidates' ranging from 4 - 16+ years' relevant experience. The successful candidate will reside in one of Project Farma's primary markets and be willing to travel domestically, to meet client project requests.
· Market locations include but are not limited to: Boston, Philadelphia, DMV, Northern New Jersey, Chicago, Indianapolis, Columbus, St Louis, Kansas City, Raleigh-Durham, Houston, Dallas, Boulder, Portland, San Francisco, San Diego, and Los Angeles.
The Lead Automation Engineer, MES & Digital Systems provides subject matter expertise in the design, implementation, and lifecycle management of digital systems across biologics, pharmaceutical, and novel therapy manufacturing facilities. This is a fully billable role, requiring experience with various MES platforms, Data Repositories, Serialization and integration to manufacturing applications (ERP, LIMS, CMMS, etc) and the ability to author, interpret, and lead documentation such as URS, FRS, Functional Narratives, and detailed system architecture designs.
In addition to technical experience, the Lead Automation Engineer, MES & Digital Systems acts as client liaison during delivery of Project Farma service engagements. They are strategically responsible for client satisfaction through project delivery while maintaining and growing client relationships. Key
Responsibilities
Automation Design & Architecture
- Develop system architectures and data flows for biologics, pharmaceutical, and advanced therapy manufacturing (DCS, PLC/SCADA, MES, historians, network layers).
- Develop product recipe strategies across the full application layer of ERP, MES and DCS Batch.
- Detailed knowledge of Master data and how to define and control Master Data.
- Create ISA-88/ISA-95-aligned architecture diagrams, inc Application and Data Flow diagrams.
- Ensure architecture supports scalability, cybersecurity, data integrity, and multi-product flexibility.
URS / FRS / Design Documentation
- Lead the creation, review, and approval of: URS (User Requirements Specifications), FRS (Functional Requirements Specifications), DS / DDS (Design Specifications), Functional & Control Narratives, Recipe Design Documentation (ISA-88 compliant), Automation Standards & Engineering Guidelines
- Work cross functionally to translate process requirements into robust digital system design documents.
Digital System Implementation
- Configure, program, and deploy Digital System within the manufacturing environment.
- Develop, modify, and test MES (eBR, RbE, eLogbooks, Equipment Tracking, Weigh & Dispense), LIMS, Serialization and CMMS application functionality.
- Support integration of OEM skids: bioreactors, chromatography systems, filtration skids, CIP/SIP, and fill finish equipment.
Commissioning, Validation & GMP Compliance
- Detailed knowledge of FAT, SAT, IQ/OQ, and PQ protocols in alignment with GAMP 5 and 21 CFR Part 11.
- 2/2
- Ensure all changes meet data integrity requirements, change control processes, and validation lifecycle rules.
- Lead deviation investigations, CAPAs, and risk assessments related to Digital systems.
Manufacturing & Operations Support
- Serve as SME for troubleshooting, system optimization, batch failure analysis, and performance enhancements.
- Support 24/7 operations through structured root cause analysis and resolution of Digital System issues.
- Develop long-term lifecycle plans for upgrades, patches, and system expansions.
Cross Functional Leadership
- Collaborate with IT/OT, process engineering, MSAT, quality, and capital project teams to deliver integrated system solutions.
- Manage vendors, system integrators, and OEMs; review design packages and ensure alignment with internal standards.
- Mentor junior engineers and act as technical SME during audits and regulatory inspections.
Experience Required
- Bachelor’s degree in Engineering (Automation, Electrical, Chemical, Mechanical, or related).
- Minimum 4-16+ years in automation engineering within GMP life sciences (biotech, pharma, ATMP).
- Expert-level experience with various MES platforms, Data Repositories, Serialization and integration to manufacturing applications (ERP, LIMS, CMMS, etc).
- Proven ability to author, interpret, and own URS/FRS/DS documentation.
- Experience designing system applications and data flows across the full spectrum of manufacturing applications.
- Strong understanding of ISA-88 batch control, ISA-95 manufacturing hierarchy, and GAMP 5.
- Hands-on experience supporting biologics and sterile/aseptic manufacturing environments.
- Understanding multisite standards for global manufacturers
Other Preferred
- Strong communicator and influencer across engineering, quality, IT/OT, and manufacturing.
- Structured thinker with advanced troubleshooting and problem solving skills.
- Skilled at managing multiple priorities in a high pressure, regulated environment.
- Demonstrated leadership and mentorship abilities.
Project Farmais committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce.
Applicants mustbe authorized towork in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.
The annual compensation range for this full-time position is $80,000 - $198,000. The final base pay offered to the successful candidate will bedeterminedby factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training.
PerkinElmer is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce.Originally posted on Himalayas