Job summary
Job post source
This job is from a recruiting firm hiring for a separate company.
Job overview
The Veeva QualityDocs Subject Matter Expert (SME) role involves providing expert guidance and ensuring successful implementation of Veeva QualityDocs to support quality management in the life sciences industry.
Responsibilities and impact
The SME will provide expert advice on Veeva QualityDocs, develop best practices, conduct training, ensure regulatory compliance, collaborate with cross-functional teams, and contribute to thought leadership.
Compensation and benefits
The position offers a competitive salary and benefits package, flexible remote work options, and opportunities for professional growth.
Experience and skills
Candidates need at least 5 years in life sciences quality management, proficiency with Veeva QualityDocs, strong communication and problem-solving skills, with preferred experience in other Veeva products and consulting roles.
Career development
The job offers opportunities for professional growth and development within a mission-driven company.
Work environment and culture
The company promotes a flexible work environment with remote work options and a mission-driven culture focused on impacting the life sciences industry positively.
Company information
The recruiting firm represents a leading life sciences company focused on innovative solutions and accelerating medicine delivery globally.
Job location and travel
The role is remote within the United States.
Application process
Applicants are instructed to apply or send their resume to the provided email address at the recruiting firm.
Unique job features
The role involves thought leadership activities such as participating in industry events and publishing articles, distinguishing it from similar positions.
Company overview
Cpl Life Sciences is a specialized recruitment agency that focuses on the life sciences sector, providing staffing solutions for pharmaceutical, biotechnology, and medical device companies. They generate revenue by offering recruitment services, including permanent, contract, and temporary placements, tailored to the specific needs of their clients within the life sciences industry. The company is part of Cpl Resources, a larger recruitment and outsourcing group with a strong presence in Europe. Cpl Life Sciences has built a reputation for its deep industry knowledge and expertise, making it a trusted partner for both job seekers and employers in the life sciences field.
How to land this job
Tailor your resume to emphasize your extensive experience with Veeva QualityDocs and your deep knowledge of quality management systems and regulatory compliance in the life sciences industry.
Highlight your expertise in providing guidance, developing best practices, and training clients on Veeva QualityDocs, as well as your ability to collaborate with cross-functional teams.
Apply through multiple channels including Cpl Life Sciences' corporate website, LinkedIn, and by directly emailing the contact provided to increase your chances of being noticed.
Connect with current employees or recruiters at Cpl Life Sciences who specialize in life sciences or quality management on LinkedIn; start conversations by commenting on recent company posts, asking about their experience with Veeva implementations, or inquiring about the company culture.
Optimize your resume for ATS by incorporating keywords such as 'Veeva QualityDocs,' 'quality management systems,' 'regulatory compliance,' 'training,' and 'document management' to ensure your resume passes initial screenings.
Use Jennie Johnson's Power Apply feature to automate applying across multiple platforms, tailor your resume with the right keywords, and identify relevant LinkedIn connections to network with, saving you valuable time during your job search.
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