Automation Engineer - Plainville, United States - Insight Global

Insight Global Plainville, United States

3 weeks ago

Description

Day-to-Day

Insight Global is seeking a junior Automation Engineer to join one of our top pharmaceutical clients in Plainville, MA.

This individual will be responsible for supporting the facility with a scope encompassing automation systems for GMP Manufacturing, Quality Control, Process Development, and their Warehouse Operations.

Responsibilities will also include supporting functions for all clinical and commercial drug manufacturing of gene therapy products, leading automation activates during tech transfers of new products and provide support throughout the company's manufacturing campaigns.

This individual should have at least 2 years of experience within the biotech engineering/ manufacturing space, specifically in a GMP environment.

The role will be collaborating with Manufacturing, Manufacturing Sciences, Quality Assurance, Quality Control, Information Systems, and other Engineering teams to complete all responsibilities as well as supporting manufacturing equipment and analytical equipment including implementing modifications to improve operational performance and product quality.

This is a great opportunity for an entry level engineer to take on more responsibility at a renowned company

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.

We are an equal opportunity/affirmative action employer that believes everyone matters.

Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances.

If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to .

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Required Skills & Experience

Must-Haves

* 2+ years of engineering experience in a GMP environment

Go-getter attitude who is eager to learn and grow
Experience reviewing and supporting the execution of Commissioning, Qualification and Validation (CQV) Activities
Bachelor of Science degree in Computer Sciences OR Engineering (Automation, Electrical, Chemical or Mechanical).
Previous experience with DeltaV, DCS and/or PLC coding and automation hardware

Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching.

Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

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