Remote Pharma Manufacturing Specialist - Process Compliance

Pharmavise Corporation; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

PharmaviseConsulting Corp. is seeking a Pharmaceutical Manufacturing Specialist for a remote role in the United States.

You will apply engineering principles to optimize manufacturing processes, collaborate with cross-functional teams, and lead process improvement initiatives to ensure quality and regulatory compliance. Ideal candidates have 5+ years in pharma manufacturing, solid dosage, liquids, or sterile product experience, and familiarity with cGMP and regulatory inspections.

Qualifications

• Bachelor's degree in engineering required; advanced degree preferred.
• Minimum 5 years in pharmaceutical manufacturing with engineering focus.
• Knowledge of cGMP, FDA/EMA regulatory guidelines.

Responsibilities

• Support pharmaceutical manufacturing operations by applying engineering principles to optimize processes, equipment, and facilities.
• Collaborate with cross-functional teams to ensure efficient and compliant operations.
• Lead or participate in process improvement initiatives and new technologies implementation.
• Conduct risk assessments and develop mitigation strategies for manufacturing processes and equipment.
• Provide technical support for troubleshooting deviations and CAPAs.
• Assist design, installation, qualification, and validation of manufacturing equipment and facilities.

Skills

Engineering background

Regulatory compliance

Process optimization

Cross-functional collaboration

CAPA

SOPs

Education

Bachelor's degree in engineering (chemical/ mechanical/ electrical)

Advanced degree preferred

Tools

Process simulation software

Data analysis tools

Job description

PharmaviseConsulting Corp. is seeking a Pharmaceutical Manufacturing Specialist for a remote role in the United States.

You will apply engineering principles to optimize manufacturing processes, collaborate with cross-functional teams, and lead process improvement initiatives to ensure quality and regulatory compliance. Ideal candidates have 5+ years in pharma manufacturing, solid dosage, liquids, or sterile product experience, and familiarity with cGMP and regulatory inspections.