This is a full time onsite role at our Bethlehem facility.
NOTE: A Bachelor’s Degree in Electrical Engineering or related discipline or equivalent automation related job experience is required for this position.
Company Overview:
ABEC is a leading supplier to the biopharmaceutical manufacturing industry. ABEC's unique value is based on combining long experience with the ability to engineer, design, manufacture, commission, qualify, and service the entire bioprocess to reduce overall cost, shorten time to market, and maximize productivity. ABEC's products include process and equipment engineering/consulting services, comprehensive site services, bioreactors and fermenters, filtration and chromatography systems, prep and hold systems, and cleaning/sterilization systems.
Benefits include:
DAY 1 Benefits - Medical, Dental and Vision insurance 3 Weeks Paid Vacation & 10 Paid HolidaysCompany paid life insuranceIndustry leading 401K plan (40% match!)Air-conditioned facilitiesCollege tuition benefit programEmployee Referral Program
The Automation Engineer utilizes independent judgment to perform the day-to-day project duties of designing, developing and releasing deliverables used in the fabrication of equipment for pilot and commercial scale biopharmaceutical manufacturing (primarily piping assemblies for fluid & gas handling and motorized agitation systems). Primary responsibility involves generating design plans. This position requires a high level of attention to detail along with the ability to develop a strong understanding of Bioprocessing Equipment design standards.
Responsibilities:
Requirements:
Bachelor’s degree in electrical engineering or related discipline or equivalent automation related job experience.5+ years with current automation systems experience.Proficient with one or more of the following hardware/software platforms: Allen-Bradley, Delta V, or Siemens.Current automation and control systems design, development, and programming from scope and P&ID framework.English language proficiency, both written and oral speaking skills.cGMP and GAMP 5 experience in Bio-Pharm or Pharmaceutical industry experience preferred.Detail oriented with a solid understanding of current programming standards, industry design fundamentals, and related simulation/de-bugging processes.Excellent written and verbal communication skills.Good organizational skills with the ability to multi-task across functional groups.Must work well both independently and in a team-oriented, collaborative environment.Limited travel will be required (not expected to exceed 20%). International travel possible.Awareness of and prior experience with implementing Continuous Improvement (CI) a plus.Prior Lean/Six Sigma experience a plus.