DeltaV Automation Engineer

Trinity Consultants - Aztec Technologies, Inc.

Boston (MA)

On-site

USD 90,000 - 115,000

Full time

14 days+

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Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A leading engineering and consulting firm is seeking a Life Sciences Talent Acquisition Specialist in the Greater Boston area. The successful candidate will design and implement process control solutions, requiring strong automation engineering skills and knowledge of compliance regulations in the biotech field. This full-time position offers a competitive salary range of $90,000 to $115,000 along with benefits such as medical and vision insurance.

Qualifications

Experience in the biotech/pharma industry is essential.
Specific knowledge of cGMPs and batch process control is required.
Knowledge of regulatory compliance including FDA regulations.

Responsibilities

Design, configuration, integration and implementation of process control solutions.
Train operators and engineers on control systems.
Manage automation projects as assigned.

Skills

Automation engineering skills

Technical writing

Understanding of P&IDs drawings

Knowledge of cGMPs

Commissioning and startup of control systems

Education

Bachelor’s or master’s degree in mechanical engineering or related discipline

Tools

Emerson Delta V DCS

PLC

HMI

SCADA systems

Job description

Life Sciences Talent Acquisition Specialist

Seeking various levels of experience:

3 - 7 years
7 - 14 years
14+ years

Trinity Consultants, Inc., a leading international EHS, life sciences and environment consulting services with 1500+ engineers worldwide.

Aztec Technologies is an engineering and consulting firm providing expertise in the pharmaceutical and biotechnology industries. Aztec Technologies and Aztec Process Automation are part of Trinity Consultants Company.

Aztec Technologies provides solutions for Manufacturing Applications:

Process and Facility Automation

With offices across 3 continents, consulting firm with over 20 years of experience within the biopharmaceutical and pharmaceuticals industries.

The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems, and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set. This is an outstanding opportunity to join our growing team and to work in the Life Sciences space that will enhance professional opportunities!

Candidates need to be local or willing to relocate to the areas of operation where we have open opportunities for immediate hire in the Greater Boston area:

Responsibilities

Design, configuration, integration and implementation of process control solutions for the Life Sciences industry.
Design, program, implement, test and document Emerson Delta V DCSs.
Develop User Requirement Specifications.
Develop Software and Hardware Design Specifications.
Develop control system validation/testing protocols.
Develop electrical panel schematics.
Develop scope of supply documents.
Manage automation projects as assigned.
Monitor progress of projects.
Install, test, and start-up control systems on-site.
Work with plant engineers and operators to implement control strategies.
Train operators and engineers on control systems.

Qualifications

Requires a bachelor’s or master’s degree in mechanical engineering, Chemical Engineering, or related discipline degree is required.
Must have experience in the biotech/pharma industry.
Strong knowledge of the S88 Batch structure is required.
Strong knowledge on review and understanding of P&IDs drawings.
Strong knowledge of automation narratives and architecture of DeltaV experience is a must.
Experience in commissioning and startup of control systems is required.
Experience with PLC, HMI, and SCADA systems is a plus.
Experience with control system networking technologies and PC networking technologies is a plus.
SCADA Platforms: Rockwell, Siemens, Wonderware, GE knowledge is a plus.
Specific knowledge of cGMPs and batch process control in the life science industry.
Knowledge of regulatory compliance inclusive of cGMP, 21 CFR Part 11 requirements, FDA regulations.