Title:  Senior Automation Engineer

Job Title: Senior Automation Engineer 

Reporting to: Director Engineering & Facilities. 

Department: Engineering & Facilities. 

About Syngene 

Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. 

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. 

Job Summary 

Responsible for designing, developing, managing, and/or maintaining equipment which is used to monitor and control engineering systems, machinery, and processes. Also responsible for the interface between the hardware and software development for the automation system. Provide professional assistance and technical advice to support ongoing operations/manufacturing investigations through data analysis and team-based problem-solving methodologies.   

Primary Responsibilities: 

• Responsible for requirements gathering, design, configuration, integration and implementation of process control solutions for the manufacturing industry including batch software, PLC / DCS systems, HMI packages, SCADA systems, Visual Basic and PC networking technology 

• Possesses strong knowledge of computer system validation and related practices, including governmental regulations. Developing broader skills and applies this knowledge and skills to perform a variety of standard activities 

• Preparation of design packages and specification, functional specifications related to software and hardware RFPs, design review, vendor/contractor selection, constructability reviews, approval of submittals, and preparation and oversight of validation and regulatory submissions 

• Preparation of engineering standards, approval of submittals, and authoring PMs, SOPs, Commissioning Protocols, and conducting training for new equipment installations. 

• Author, review, and approve automation system lifecycle design documentation (user requirements, functional and design specifications, commissioning, and qualification protocols)  

• Act as a coach and mentor to other members of the Project Engineering and SMEs on project teams to drive continuous improvement, knowledge transfer, and professional growth of both you and your colleagues 

• Identify areas to drive down project costs through lessons learned and develop specific improvement strategies to realize these savings.    

• Has wide-ranging experience, using professional concepts and company objectives to resolve complex issues in more efficient ways than lower levels. 

• Work on complex issues where analysis of situations/data require in-depth evaluation of variable, identified factors. 

• Exercises judgment normally in selecting methods, techniques, and evaluation criteria in resolving issues. 

• Determines own instructions and procedures on day-to-day tasks and new assignments. 

• Drive the complete execution of assigned projects in manner that drives high engagement from project team members.   
  
  

Education & Qualifications: 

• A minimum of 8 years of experience in a biopharmaceutical or related environment in a project or construction management related role 

• BS in Engineering, Science, Project/Program Management, or equivalent experience 

• EE or Computer Science preferred 

• Technology/Equipment (DP/DS/Clinical/Commercial/SS/SU) emphasis will vary by site, candidate is expected to be able to guide site to top quartile operational safety, efficiency, and reliability for these technologies.  

• Ability to think and act both strategically and tactically 

• Highly effective verbal and written communicator at all levels of the organization 

• Demonstrated ability to effectively prioritize and coordinate activities  

• Proficiency in Microsoft Office applications 

• Strong knowledge of engineering and related practices, including governmental regulations – ISPE GAMP, EU Annex 11, CFR 210, 211, Part 11 

• Proven programming experience with either of the following industrial automation systems: Allen-Bradley PLCs or Emerson DeltaV DCS 

• Must have knowledge of process manufacturing field instrumentation, technology, and batch process manufacturing expertise 

• Experience in all phases of the automation life cycle: Requirements documentation, detailed design generation, implementation, system integration, testing, on-site startup and ongoing system maintenance 

Equal Opportunity Employer: 

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, colour, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.