DeltaV DCS Engineer – GMP Pharma Manufacturing

CAC Staffing; Indianapolis (IN); On-site; USD 85,000 - 120,000; Full time

Job summary

CAC Staffing is seeking a skilled Automation Engineer for a contract position in Indianapolis, IN. This role involves participating in a groundbreaking facility expansion project in the pharmaceutical sector. Applicants must have a strong background in Delta V DCS implementation and coding, alongside significant experience in automation projects.

The ideal candidate should hold an Associates or Bachelors degree and possess 7-10 years of relevant experience. This position is expected to last for 12+ months, ensuring adherence to rigorous GMP standards throughout.

Qualifications

• Experience in Delta V DCS implementation, including control strategies and batch processes.
• Strong Delta V coding and programming skills required.
• Experience with automation projects, product delivery, and pharmaceutical industry.

Responsibilities

• Join a groundbreaking facility expansion project in manufacturing.
• Implement cutting-edge manufacturing processes following GMP standards.
• Ensure operational excellence and successful delivery of projects.

Skills

Delta V DCS implementation experience

Delta V Coding and Programming experience

Automation Project Experience

Delta V recipe Authoring and configuration

Configuration and Coding

Product Delivery

Pharmaceutical experience

Biosynthetic purification

7-10 years prior experience

Education

Associates or Bachelors degree

Job description

CAC Staffing is seeking a skilled Automation Engineer for a contract position in Indianapolis, IN. This role involves participating in a groundbreaking facility expansion project in the pharmaceutical sector. Applicants must have a strong background in Delta V DCS implementation and coding, alongside significant experience in automation projects.

The ideal candidate should hold an Associates or Bachelors degree and possess 7-10 years of relevant experience. This position is expected to last for 12+ months, ensuring adherence to rigorous GMP standards throughout.