Process Engineer I jobs in United States
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Catalent · 1 day 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 products, focusing on equipment readiness, process execution support, data analysis, and documentation under cGMP.

BiotechnologyHealth CareManufacturingPharmaceutical
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H1B Sponsor Likelynote

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

Oral Solid Dosage (OSD)CGMP DocumentationValidation ProtocolsContinuous ImprovementData AnalysisBasic TroubleshootingTeam CollaborationTechnical Communication

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

Preferred

Experience with oral solid dosage (OSD) products in a pharmaceutical manufacturing environment
Familiarity with validation protocols and change control

Benefits

152 hours of PTO + 8 paid holidays

Company

Catalent

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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 Stage
Total Funding
unknown
2021-01-06Acquired

Leadership Team

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Alessandro Maselli
President & Chief Executive Officer
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Charles Lickfold
Senior Vice President, Chief Information Officer
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Company data provided by crunchbase