Documentation / Data Lead

Valspec; Boston (MA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

ESOP

Premium medical coverage

401(k) with company match

Tuition reimbursement

Unique performance incentives

Job summary

Valspec is seeking a Documentation/Data Lead for the East Coast greenfield pharma/biotech program. You will own CQV documentation governance and data management across the project lifecycle, ensuring rigorous data integrity and compliant reporting.

The role focuses on managing document lifecycle processes, turnover packages, and readiness documentation, while supporting metrics, dashboards, and compliance tracking for large capital pharma/biotech projects.

Qualifications

• Strong CSV management and deliverable governance experience.
• Background in document review, resource planning, and quality systems oversight.
• Experience on large capital pharma/biotech or advanced manufacturing projects.

Responsibilities

• Manage document lifecycle processes
• Oversee turnover packages and readiness documentation
• Drive data integrity and reporting standards
• Support metrics, dashboards, and compliance tracking

Skills

CSV management

Documentation governance

Quality systems oversight

Data integrity & reporting

Job description

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

Documentation/Data Lead — East Coast (Greenfield Pharma/Biotech Program)

About the Role

Join a major greenfield pharmaceutical manufacturing program as Documentation/Data Lead, owning CQV documentation governance and data management across the project lifecycle.

What You'll Do

• Manage document lifecycle processes
• Oversee turnover packages and readiness documentation
• Drive data integrity and reporting standards
• Support metrics, dashboards, and compliance tracking

What We're Looking For

• Strong CSV management and deliverable governance experience
• Background in document review, resource planning, and quality systems oversight
• Experience on large capital pharma/biotech or advanced manufacturing projects

Location

East Coast (site-specific details shared during interview process)

Why Join Valspec?

At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including:

• Premium medical coverage
• 401(k) with company match
• Tuition reimbursement
• Unique performance incentives
• And more — all designed to support your growth, well‑being, and future.

Join a team where your contributions matter, your development is prioritized, and your success is shared.

Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.

Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.