Associate Automation Specialist

Job Description

The Automation Engineering (Auto Eng) Team within the Pharmaceutical Operations Engineering (POE) Department is seeking a highly motivated and detail-oriented individual to work in a fast-paced job that provides both technical and project management responsibility. The Associate Specialist - Engineering Auto Eng position will report to the Director, Engineering, Automation Lead position and will be a member of the Auto Eng Team at the Rahway NJ facility. The Auto Eng Team is responsible for development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation systems spanning various clinical manufacturing facilities. In this role, you will be responsible for optimizing and maintaining our manufacturing processes using process control systems and automation and operational technologies.

Responsibilities:

• Assist in the design, implementation, and optimization of process control systems to improve production efficiency and product quality.

• Collaborate with cross-functional teams, including operations, maintenance, and quality assurance, to identify areas for improvement and implement solutions.

• Conduct data analysis and interpretation to identify trends, anomalies, and opportunities for process optimization.

• Participate in troubleshooting and resolving technical issues related to process control systems, instrumentation, and equipment.

• Support commissioning and startup activities for new processes or equipment.

• Develop and maintain documentation, including standard operating procedures, control system configuration, and equipment specifications.

• Stay updated on industry trends and advancements in process control technologies, automation/operation technology, and pharmaceutics/drug development/design.

• Apply knowledge of automation/operation technology, such as PLC – Ladder Logic/Structured Text, Ethernet/Networking, and Analog/Metrology, to enhance process control systems.

• Utilize data science and data processing tools to analyze and interpret data for process improvement, including database querying and data programming.

• Ensure compliance with data integrity, CFR, GMP/regulations, and system life cycle documentation methodology specific to the pharmaceutical industry.

Education Requirements:

• Bachelor's degree in: Engineering, Science, Information Technology, or related field (with expected graduation by August 2024).

• Advanced degree preferred.

Requirements:

• Strong analytical and problem-solving skills with attention to detail.

• Knowledge of process control principles, instrumentation, and control systems.

• Proficiency in programming languages such as Python or C.

• Familiarity with automation/operation technology, including PLCs, Industrial Networking, and Analog/Metrology.

• Understanding of pharmaceutics and drug development and/or sterile fill finish principles.

• Knowledge of data integrity, CFR, GMP/regulations, and system life cycle documentation methodology.

• Ability to work effectively both independently and as part of a team.

• Excellent communication skills with the ability to convey technical information to diverse audiences.

• Applies general knowledge of company business developed through education …