Siemens healthcare diagnostics Jobs

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Automation Expert – Product Development (Healthcare & Medical Device)

CellBios Healthcare And Lifesciences
Chennai, Tamil Nadu

Apply Now

Job details

Qualifications

LabView
MATLAB
Doctoral degree
Engineering
Java
Master's degree
C++
Programmable logic controllers
Quality assurance
C
Bachelor's degree
Product development
Distributed control systems
Robotics
Communication skills
Sensors
Python
FDA regulations

Full job description

Location: Chennai

Department: Product Development

Job Summary:

We are seeking an Automation Expert to join our Product Development team, focusing on leveraging automation to drive innovation in healthcare and pharmaceutical products. This role will design and implement automated systems to enhance the development process from concept through testing ensuring efficiency, precision, and compliance with industry standards. The ideal candidate brings technical expertise in automation and a strong preference for experience in biotechnological or medical environments, where they can accelerate the creation of impactful solutions.

Key Responsibilities:

Automation Systems: Proficiency in designing and implementing automation solutions, including programmable logic controllers (PLCs), distributed control systems (DCS), and supervisory control and data acquisition (SCADA) systems.
Control Systems: Knowledge of process control principles, including PID (Proportional-Integral-Derivative) controllers, feedback loops, and real-time monitoring.
Robotics and Instrumentation: Experience with robotic systems, sensors, actuators, and other instrumentation used in bioprocess automation (e.g., bioreactors, fermenters).
Bioprocess knowledge: Understanding of bioprocessing techniques such as fermentation, cell culture, downstream processing (e.g., purification, filtration), and scale-up from lab to production.Familiarity with biological systems, including microbial and mammalian cell cultures, and their integration with automated workflows.
Knowledge of Good Manufacturing Practices (GMP) and regulatory standards (e.g., FDA, EMA) relevant to bioprocess environments
Technology Selection: Research and recommend automation technologies tailored to biotechnology and medical product development needs.
Cross-Functional Collaboration: Partner with R&D, quality assurance, and regulatory teams to align automation efforts with project timelines, quality standards, and compliance needs.
Regulatory Compliance: Ensure automated systems adhere to healthcare and pharmaceutical standards (e.g., GMP, FDA 21 CFR Part 11), supporting validation and documentation efforts.
Training & Support: Train team members on automation tools and foster their adoption to enhance productivity across the product development lifecycle.

Qualifications:

Education: Bachelor’s degree in engineering (biomedical, mechanical, electrical, mechatronics, embedded systems), computer science, or a related field; advanced degree (MS, PhD) is a plus.

Experience: 4+ years of experience in automation engineering or a related role, with a focus on product development; preferred experience in healthcare and medical devices.

Technical Knowledge:

Proficiency in programming languages such as Python, C++, or Java for developing automation scripts and control algorithms.
Experience with software platforms like LabVIEW, MATLAB, or similar tools for simulation, data analysis, and system modeling.
Experience with automation software (e.g., Siemens PCS 7, Rockwell Automation, DeltaV, etc.)
Understanding of product development cycles in regulated environments, such as medical devices, diagnostics, or drug formulation.

Skills:

Strong problem-solving skills with an emphasis on process improvement.
Hands-on experience designing and maintaining automated systems.
Ability to work effectively in multidisciplinary teams with scientific and regulatory stakeholders.
Excellent communication and documentation skills.

Preferred:

Experience with biotechnology/medical-specific automation, such as bioreactor control unit design.
Familiarity with regulatory standards (e.g., FDA, EMA) and quality systems (e.g., ISO 13485, GxP).

Key Competencies:

Innovative thinking with a practical focus
Precision and attention to regulatory detail
Adaptability in a fast-evolving industry

Collaborative and proactive approach

Send your resume to: [email protected]

Apply Now

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