Senior Controls/System Engineer - CDMO - Providence

Providence, Rhode Island Permanent USD100,000 - USD140,000 per year
  • Ensure precision, compliance, and innovation in drug substance API manufacturing
  • Global CDMO with several US sites supporting full lifecycle of drug development

About Our Client

This client is a growing international full-service CDMO within the biotechnology space looking to aggressively expand its footprint in the US. The company has a strong base of API/Small Molecule, Biologics, Clinical Research, Bioanalytical Sciences, DMPK, Cell and Gene Therapy and other capability centers across the US. This business has developed a fantastic brand in the US through exceptional service which drives repeat business. This specific role is at their Providence location, specializing in late stage large scale API development and manufacturing.

Job Description

My client is looking for an experienced Senior Control/Systems Engineer with a passion for instrument automation and process control in the pharmaceutical industry. As a Senior Control/Systems Engineer, you will be at the forefront of ensuring precision, compliance, and innovation in drug substance API manufacturing and development at their esteemed Global CDMO. If you have a strong background in instrument automation, cGMP, API production, and experience with FDA, OSHA, and EPA regulations, this coudl be the right fit for you.

  • Instrument Automation: Lead the design, implementation, and maintenance of instrument automation systems to optimize API manufacturing processes.

  • Process Control: Oversee process control maintenance activities, ensuring seamless operation and rapid issue resolution.

  • Regulatory Compliance: Apply your in-depth knowledge of cGMP, FDA, OSHA, and EPA regulations to maintain strict compliance throughout the manufacturing process.

  • Collaboration: Collaborate effectively with cross-functional teams to drive innovation and continuous improvement in instrument automation and process control.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

  • Educational Background: Bachelor's or Master's degree in Control/Systems Engineering or a related field.

  • Experience: A minimum of 5 years of experience in Control/Systems Engineering within the pharmaceutical or biotechnology industry.

  • Instrument Automation: Proficiency in instrument automation design, implementation, and maintenance.

  • Process Control: Strong expertise in process control systems and the ability to troubleshoot and resolve control-related issues.

  • Regulatory Knowledge: A deep understanding of cGMP, FDA, OSHA, and EPA regulations and their application in API manufacturing.

  • Collaboration: Excellent communication and teamwork skills to work effectively with multidisciplinary teams.

What's on Offer

  • Competitive base salary
  • Excellent benefits package
  • Relocation package
  • Standard PTO Policy
  • Work on site in state of the art large scale cGMP Manufacturing space
  • Pivotal role for company's aggressive expansion
  • Company has multiple US sites and is investing in new infrastructures
Connor Colombo
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Job summary

Life Sciences
Sub Sector
Healthcare / Pharmaceutical
Contract Type
Consultant name
Connor Colombo
Job Reference