Quality Operations Program Manager

Veeva Systems

Confirmed live yesterday High trust

Remote

Quick summary

Work type: Remote
Location: Remote
Salary: $85,000–$130,000 / yr
Posted: 71 days ago
Freshness: Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $178k

This role $108k

$70k most similar roles pay here $229k

This role pays less than 98% of similar roles. Most pay $152,150–$203,525 — the shaded band above. At the midpoint, this role pays about $108k versus about $178k for comparable roles.

Based on 240 similar postings.

Employer

About Veeva Systems

Veeva Systems is a cloud software company serving the global life sciences industry, providing CRM, clinical, regulatory, quality, and data applications used by pharmaceutical and biotech companies.

Veeva Systems currently has 93 open roles on FindRole.

Listed pay typically runs $80,000–$165,000 across 82 roles with salary data.

Most-posted roles

View all roles at Veeva Systems

At a glance

TL;DR · Quality Operations Program Manager

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The Quality Operations Program Manager joins the Quality & Security & Compliance team to ensure the integrity and management of processes within the Quality Management System. As a process owner for document control, you will manage the lifecycle of quality records, provide oversight on regulated activities like validation testing and product releases, and offer technical expertise regarding federal regulations and quality system requirements. You will also develop metrics to track the effectiveness of domain systems. This role requires experience in life sciences, Quality Management Systems, and electronic Document Management Systems or eQMS. Key competencies include a deep understanding of GxP regulations, 21CFR 11, ICH Q10, and QSR. You will utilize skills in process mapping and problem-solving to navigate the complexities of maintaining compliance within regulated product lines and systems.

Skills

QMS eDMS eQMS GxP 21CFR 11 ICH Q10 QSR ISO9001 Veeva Quality Cloud Veeva QualityDocs SDLC CSV ITIL ISO IEC IEEE

What you'll do

Act as a subject matter expert for the Document Control process area.
Manage the creation and lifecycle of quality processes and records.
Provide quality oversight on regulated activities, including validation testing and product releases.
Interpret federal regulations and provide direction regarding quality system requirements.
Develop metrics to track the effectiveness and productivity of domain systems.
Ensure the integrity and compliance of processes within the Quality Management System (QMS).
Maintain defined processes across multiple product lines and regulated domains.

What we're looking for

Hold a BS/BA in Science, Information Management, Engineering, or a related field.
Have 3+ years of experience in a regulated quality role within the Life Sciences industry.
Possess experience with Quality Management Systems including documentation, record management, training, change control, and CAPA.
Have experience with electronic Document Management Systems (eDMS) and/or electronic Quality Management Systems (eQMS).
Demonstrate a solid understanding of GxP regulations, 21CFR 11, ICH Q10, QSR, or ISO9001 frameworks.
Possess excellent process mapping, problem-solving, and communication skills to convey technical and regulatory concepts.
Experience with Veeva Quality Cloud solutions is preferred.
Knowledge of SDLC, CSV, and quality standards like ISO, IEC, IEEE, or ITIL is preferred.