What are the responsibilities and job description for the Process Engineer position at Sonitalent LLC?
Job Title – Process Engineer (2pm-2am)
Job Location : Dallas area, TX, 100% onsite - Need to be local
Duration – 6 Months
Visa - Any Visa except H1B,CPT
Mode Of Interview – Phone/Skype
Note – Need LinkedIn
Duration: 6-7 months (2pm-2am shifts) - alternating 2 days on, 2 days off, 3 days on, 2 days off (potential extensions)
Description: Our client is looking for a process engineer to help out with API manufacturing and special projects around the site. Special projects include driving yield improvements, optimization of cycle times, supporting investigations, and execute functional tests and IQ/OQ for rockwell factorytalk automation 2.0. This person would need some familiarity with automation and validating HMI’s preferably factorytalk automation 2.0. Day to day tasks will consist of being on the manufacturing floor, problem solving, continued process verification and more.
They really just need someone that can be on the floor during manufacturing and troubleshoot equipment etc., not design the facility layout or validate the equipment, but in real time help with any manufacturing issues
Focus more heavily on candidates with deeper hands-on pharmaceutical manufacturing experience. People with stronger operational manufacturing/process ownership and more direct plant-floor engineering experience within pharmaceutical environments. Specifically looking for Process Engineers who have operated directly within manufacturing environments and supported day-to-day plant operations, ideally in API or batch pharma manufacturing settings.
Must-Have Requirements
- On-site presence in Coppell, Texas (DFW). This is an onsite position; remote work is not available.
- Texas-based candidates are strongly preferred. Non-local candidates must be willing to relocate for the duration of the contract.
- Ability to work the 2:00 PM – 2:00 AM floor support shift.
- Comfortable working a 12-hour rotating schedule (2 days on/2 days off, 3 days on/2 days off) and every other weekend.
- Willingness to occasionally support alternate shifts and provide backfill coverage as needed.
- Familiarity with pharmaceutical batch manufacturing processes.
- Self-starter with the ability to work independently in a fast-paced manufacturing environment.
- Strong technical writing and analytical skills, including trend analysis and impact assessments related to quality, safety, and production KPIs.
- Comfortable learning and working with new technologies across IT, MES, PCS, Safety, and Quality systems.
- Experience with FactoryTalk Rockwell Automation Platform and AVEVA/Wonderware SCADA.
- Familiarity with OSIsoft PI Data Historian and PI ProcessBook.
- Experience supporting or executing qualification and validation activities, including IQ, OQ, PQ, and PPQ for new systems and equipment.
Skills Needed: API manufacturing, executing validation protocols on automation systems
Plus: Factorytalk automation 2.0, Yield improvements, optimization of cycle times