Principal Software Test Engineer - Automation

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About the role

The Manager, Pharmacovigilance Safety Operations is responsible for overseeing pharmacovigilance safety operations in a remote, Washington location. The position is a contract role.

Responsibilities

• Oversee pharmacovigilance safety operations
• Ensure compliance with regulatory standards
• Manage adverse event reporting processes
• Collaborate with cross-functional teams to improve safety outcomes

Requirements

• Bachelor's degree in a relevant field
• Minimum 5 years of experience in pharmacovigilance or related field
• Strong understanding of regulatory requirements
• Excellent communication and leadership skills

Qualifications

• Proven ability to manage complex projects
• Experience with pharmacovigilance software systems
• Knowledge of Good Clinical Practice (GCP)

Skills

• Pharmacovigilance expertise
• Project management skills
• Regulatory compliance knowledge

Benefits

• Flexible work schedule
• Professional development opportunities
• Competitive compensation package

Pay

• $70,000 - $90,000 annually

Schedule

• Full-time

Technical Transfer Specialist – Manufacturing Operations

The Technical Transfer Specialist is based in Tucson, Arizona and works on-site. This is a contract role.

About the role

The Technical Transfer Specialist is responsible for transferring manufacturing processes from one facility to another, ensuring seamless operation and quality control.

Responsibilities

• Develop and implement technical transfer plans
• Coordinate with cross-functional teams to ensure process transfer success
• Monitor and report on process performance
• Provide technical support during process transfers

Requirements

• Bachelor's degree in a relevant field
• Minimum 3 years of experience in manufacturing operations or related field
• Strong understanding of manufacturing processes and quality control
• Excellent organizational and problem-solving skills

Qualifications

• Experience with process validation and verification
• Knowledge of cGMP guidelines
• Ability to work independently and as part of a team

Skills

• Manufacturing expertise
• Process validation and verification skills
• Quality control knowledge

Benefits

• Competitive compensation package
• Professional development opportunities
• Flexible work schedule

Pay

• $60,000 - $80,000 annually

Schedule

• Full-time