Note: The job is a remote job and is open to candidates in USA. Virtue America is seeking an entry-level Manufacturing Engineer to support pharmaceutical and life sciences manufacturing operations. The role assists with manufacturing processes, equipment support, process improvement, validation, troubleshooting, technical documentation, data analysis, and regulatory compliance.
Responsibilities
- Manufacturing Support: Assist with day-to-day manufacturing engineering activities and production processes
- Process Improvement: Support process optimization and continuous improvement initiatives to improve efficiency, quality, safety, and productivity
- Equipment Support: Assist with equipment installation, setup, troubleshooting, qualification, and performance improvement activities
- Validation Support: Assist with IQ, OQ, PQ , equipment qualification, and process validation activities
- Production Support: Work with manufacturing teams to identify and resolve process and equipment-related issues
- Documentation Management: Prepare and maintain SOPs, work instructions, batch records, technical reports, equipment documentation, and engineering records
- Deviation & CAPA Support: Assist with deviation investigations, root-cause analysis, risk assessments, corrective actions, and CAPA activities
- Data Analysis: Collect and analyze manufacturing and process data to identify trends and opportunities for improvement
- Regulatory Compliance: Ensure manufacturing engineering activities comply with cGMP, FDA, GDP , safety, and company quality requirements
- Cross-Functional Collaboration: Work closely with QA, QC, Production, Validation, Engineering, Maintenance, and Supply Chain teams
- Continuous Improvement: Participate in Lean Manufacturing, Six Sigma , and operational excellence initiatives
Skills
- • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, Pharmaceutical Engineering, Biotechnology, Life Sciences , or a related field
- • Basic understanding of pharmaceutical and life sciences manufacturing processes
- • Familiarity with cGMP, SOPs, process validation, equipment qualification , and manufacturing documentation
- • Basic knowledge of troubleshooting, root-cause analysis, risk assessment, and CAPA
- • Understanding of manufacturing processes, process flow, equipment, and basic data analysis
- • Strong analytical, problem-solving, and organizational skills
- • Excellent written and verbal communication skills with strong attention to detail
- • Ability to work effectively in a regulated manufacturing environment
- • Fresh graduates and candidates with 0–2 years of relevant experience are encouraged to apply
- • Familiarity with Lean Manufacturing or Six Sigma concepts is preferred
Benefits
- Remote work
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