Senior Automation Engineer (cGMP - DeltaV - Pharmaceutical) - Massachusetts, Boston

The announced job offer is made public by the firm: AM Technical Solutions, Inc and it was included in jobs list the date of: 2022-10-22 in the website greenenergyjobsonline.com.

It is announced that they have a job offer at the category of Engineering and the jobs location is in the state of Massachusetts at the city Boston, in the country US - at this current ZipCode: 02298

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Senior Automation Engineer (cGMP - DeltaV - Pharmaceutical)

Boston, MA area

Summary:

AM Technical Solutions is seeking a knowledgeable Automation professional to work with a pharmaceutical client in the Boston, MA area. The ideal candidate should have previous pharmaceutical or biotech knowledge and be adept with DeltaV systems.

AMTS has opportunities throughout the country and overseas supporting multiple locations in MA, NH, RI, NC, Europe, and other locations.

Responsibilities:

Support the configuration, administration, and maintenance activities of the site manufacturing automation systems.

Lead projects in the design, development, and qualification of automated processes, equipment, and systems; including managing the work of internal engineers and outside vendors.

Identify opportunities to improve existing processes, equipment, systems, and infrastructure.

Directly support operations with troubleshooting and issue resolution with respect to automation systems.

Develop automation User Requirements Specifications (URS) based on customer need.

Develop the design and specifications for DCS, PLC and SCADA-based process control systems for projects.

Develop the design of process control and automation systems in compliance with cGMP, GAMP, related industry standards and customer requirements.

Assist process engineering development of P&IDs and process control requirements as well as Functional Requirement Specifications (FRS).

Able to work effectively with senior-level contacts through strong interpersonal skills and acumen.

Maintaining life cycle management of control system and documentation within applicable procedural documents.

Designing, building and system administration of DeltaV systems.

Qualifications and Experience:

Bachelor's degree in Engineering, Computer Science or related technological field.

3+ years of relevant work experience with automation systems with pharmaceutical industry.

Effective written and verbal communications skills.

Previous experience in a GMP manufacturing or operations environment.

Experience with computer systems validation practices (GAMP).

Experience authoring and reviewing standard operating procedures, on-the-job-trainings, and other controlled documents.

Experience in managing small to medium-sized projects and outside vendors.