Catalent · 22 hours ago
Process Engineer I
Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. The Process Engineer I supports day-to-day development and commercial manufacturing operations for oral solid dose (OSD) products, focusing on equipment readiness, process execution support, data analysis, and documentation under cGMP.
BiotechnologyHealth CareManufacturingPharmaceutical
Responsibilities
Provide floor support for manufacturing/packaging activities; monitor processes, perform basic troubleshooting, and escalate issues appropriately
Assist with commissioning, qualification, and validation (FAT/SAT/IQ/OQ/PQ) of process equipment with guidance from senior engineers and Validation
Collect, trend, and analyze process data; summarize findings and recommend routine corrective actions
Participate in investigations (deviations, OOS/OOT, complaints) and execute corrective/preventive actions (CAPAs)
Draft and maintain cGMP documentation (SOPs, work instructions, batch records, standard test procedures) and support change controls
Support creation of User Requirements (URS) and equipment specifications as assigned; interface with vendors for routine technical information
Contribute to continuous improvement projects (5S, SMED, Lean, Six Sigma) to increase safety, quality, delivery, and cost performance
Adhere to EHS requirements; identify hazards and support implementation of countermeasures
Provide basic training to operators on procedures and equipment operation under supervision
Qualification
Required
Bachelor's in Engineering or related discipline
Ability to stand and walk in production areas; lift/push/pull up to 25 lbs. occasionally; work around moving/mechanical equipment
This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent
Preferred
Experience with oral solid dosage (OSD) products in a pharmaceutical manufacturing environment
Familiarity with validation protocols and change control
Work in a fast-paced, performance-driven, customer-focused environment
Benefits
152 hours of PTO + 8 paid holidays
Company
Catalent
Catalent - Blow-Fill-Seal Sterile CDMO Business is focusing on complex clinical to commercial stage formulation and manufacturing. It is a sub-organization of Catalent Pharma Solutions.
H1B Sponsorship
Catalent has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2022 (1)
Funding
Current Stage
Late StageTotal Funding
unknown2021-01-06Acquired
Leadership Team
Recent News
Maryland Daily Record
2025-11-23
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