Migration Lead - Veeva QualityDocs

Cpl Life Sciences; United States; Remote; USD 48,000 - 66,000; Full time

Job summary

A leading life sciences company seeks a Subject Matter Expert (SME) for Veeva QualityDocs. The role involves providing expert guidance, developing best practices in quality management systems, and ensuring regulatory compliance. The ideal candidate will have extensive experience in the life sciences sector, focusing on implementing innovative solutions successfully.

Benefits

Flexible work environment with the option to work remotely

Opportunities for professional growth and development

Qualifications

• Minimum of 5 years of experience in the life sciences industry.
• Proficiency in using Veeva QualityDocs or similar document management systems.
• Excellent verbal and written communication skills.

Responsibilities

• Provide expert advice and support on Veeva QualityDocs implementation.
• Develop and share best practices for document management.
• Ensure compliance with FDA and EMA regulations.

Skills

Communication Skills

Problem-Solving

Team Player

Education

Bachelor’s or Master’s degree in Life Sciences, Quality Management, or a related field

Tools

Veeva QualityDocs

Job description

Direct message the job poster from Cpl Life Sciences

Location: United States (Remote)

About the Company: We are a recruitment company specializing in the life sciences industry. We are representing a leading life science company dedicated to providing innovative solutions and expert guidance to the global life sciences industry. Our client’s mission is to help bring medicines and therapies to patients faster by leveraging cutting-edge technology and industry best practices.

Job Summary: Our client is seeking a highly skilled and experienced Subject Matter Expert (SME) for Veeva QualityDocs. The ideal candidate will have extensive experience in the life sciences industry and a deep understanding of quality management systems and regulatory requirements. This role involves providing expert guidance, developing best practices, and ensuring the successful implementation and utilization of Veeva QualityDocs.

Key Responsibilities:

• Expert Guidance: Provide expert advice and support to clients on the implementation and use of Veeva QualityDocs.
• Best Practices Development: Develop and share best practices for document management and quality systems within the life sciences industry.
• Training and Support: Conduct training sessions and provide ongoing support to clients to ensure effective use of Veeva QualityDocs.
• Regulatory Compliance: Ensure that all document management practices comply with relevant regulatory requirements (e.g., FDA, EMA).
• Collaboration: Work closely with cross-functional teams, including sales, consulting, and engineering, to deliver high-quality solutions to clients.
• Thought Leadership: Participate in industry events, publish articles, and contribute to the company's thought leadership initiatives.

Qualifications:

• Education: Bachelor’s or Master’s degree in Life Sciences, Quality Management, or a related field.
• Experience: Minimum of 5 years of experience in the life sciences industry, with a focus on quality management systems and regulatory compliance.
• Technical Skills: Proficiency in using Veeva QualityDocs or similar document management systems.
• Communication Skills: Excellent verbal and written communication skills, with the ability to convey complex information clearly and concisely.
• Problem-Solving: Strong analytical and problem-solving skills, with the ability to develop innovative solutions to complex challenges.
• Team Player: Ability to work effectively in a team environment and collaborate with colleagues across different functions.

Preferred Qualifications:

• Experience with other Veeva products (e.g., Veeva Vault, Veeva RIM).
• Certification in quality management (e.g., ASQ, ISO).
• Experience in a consulting or client-facing role.
• Competitive salary and benefits package.
• Flexible work environment with the option to work remotely.
• Opportunities for professional growth and development.
• Be part of a mission-driven company committed to making a positive impact on the life sciences industry.

If you are interested, please apply or send your resume to [e-mail].

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Information Technology

• Industries

  Pharmaceutical Manufacturing

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