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Lims Veeva Jobs (NOW HIRING)

Novo Nordisk

Associate, API Manufacturing

Boulder, CO

$70K - $82K/yr

Experience using NN software systems (SCADA, SAP, LIMS, Veeva) is preferred The base compensation range for this position is $70,400 to $82,500. Base compensation is determined based on a number of ...

AA2IT

Microbiologist

Durham, NC · On-site

Veeva Vault, IPI, LIMS. Personality: * Strong communication. * Collaborative. * Proactive. * Team Player. Responsibilities: - Large Molecule Analytical Sciences-Durham The Contractor in Analytical ...

Inteldot

Specialist QA 35382

Juncos, PR · On-site

Documentation platforms such as Veeva, Spotfire, LIMS, Maximo. * Use of artificial intelligence tools such as data analytics and large language models * Strong communication (both written and verbal ...

Actalent

Quality Training Assistant

Grove City, OH

$17.50 - $22/hr

Must have some experience in a LIMS (Laboratory Information Management System) such as Veeva, Power BI, Smartsheet, or Cornerstone. This role is primarily desk-based in a beautiful, state-of-the-art ...

FITS LLC

Specialist Quality Assurance

Juncos, PR · On-site

Data trending, statistical anlaysis, and electronic platforms (Veeva, Spotfire, LIMS, Maximo). The Personality Part: * Picture yourself in a lab... with all the equipment you need to put your ...

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How much do lims veeva jobs pay per year?

As of Jun 5, 2026, the average yearly pay for lims veeva in the United States is $178,207.00, according to ZipRecruiter salary data. Most workers in this role earn between $161,500.00 and $196,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by professionals working with LIMS Veeva, and how can they be overcome?

Professionals working with LIMS Veeva often encounter challenges related to system integration, data migration, and adapting to evolving regulatory requirements. Successfully navigating these issues typically involves collaborating closely with IT teams, staying up-to-date with Veeva platform updates, and participating in ongoing training. Additionally, clear communication with laboratory staff and stakeholders is essential for ensuring that workflows are optimized and compliant with industry standards. Continuous learning and proactive problem-solving are key to thriving in this dynamic environment.

What are LIMS Veeva jobs?

LIMS Veeva jobs typically refer to roles that involve working with Laboratory Information Management Systems (LIMS) in conjunction with Veeva, a cloud-based software platform widely used in the life sciences industry. Professionals in these roles may be responsible for implementing, configuring, supporting, or integrating LIMS with Veeva Vault Quality, Veeva Vault QMS, or other Veeva solutions. These jobs often require a background in laboratory processes, IT systems, and regulatory compliance. Key responsibilities can include managing data workflows, ensuring system validation, and supporting digital transformation initiatives in pharmaceutical, biotech, or healthcare settings.

What are the key skills and qualifications needed to thrive as a LIMS Veeva specialist, and why are they important?

To thrive as a LIMS Veeva specialist, you need a strong background in laboratory information management systems (LIMS), data management, and regulatory compliance, often supported by a degree in life sciences, IT, or a related field. Familiarity with Veeva Vault Quality Suite, LIMS platforms, SQL, and experience with validation or GxP environments are typically required. Strong problem-solving, attention to detail, and effective communication skills help professionals excel in collaborating with cross-functional teams and addressing user needs. These skills and qualities are crucial for ensuring accurate data management, regulatory adherence, and seamless digital workflow integration in laboratory environments.
Infographic showing various Lims Veeva job openings in the United States as of May 2026, with employment types broken down into 93% Full Time, 1% Temporary, 5% Contract, and 1% Nights. Highlights an 74% Physical, 6% Hybrid, and 20% Remote job distribution, with an average salary of $178,207 per year, or $85.7 per hour.
Executive Director, Analytical Development & Quality Control

Executive Director, Analytical Development & Quality Control

Ardelyx

Waltham, MA • On-site

$267K - $327K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

Description
Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact - both within our company and in the lives of patients we serve.
Position Summary:
The Executive Director, Analytical Development & Quality Control (AD/QC), is the enterprise leader accountable for Ardelex's analytical chemistry activities. Reporting to the Chief Technical Operations Officer, the Executive Director will provide oversight of Ardelyx's array of contract testing laboratories across the company's portfolio of development-stage projects and commercial products. The Executive Director will collaboratively build, improve, and scale a modern, inspection ready analytical chemistry capability that ensures reliable supply, strengthens compliance, and champions a proactive, high-engagement technical and quality culture across internal teams and external partners.
Responsibilities:
  • Provide strategic roadmap for the AD/QC department, aligning it with the overall company objectives and regulatory requirements
  • Partner with other functions (e.g. Supply Chain, CMC, Quality Assurance, and Regulatory Affairs) to develop and implement appropriate control strategies for all stages of product development and manufacturing
  • Lead and collaborate with other departments to implement quality and process improvement initiatives
  • Oversee the development, validation, implementation, and life-cycle management of analytical methods for the analysis of raw materials, intermediates, drug substance, and drug product
  • Ensure with functional leaders that all AD/QC activities are conducted in stage-appropriate accordance with current Good Manufacturing Practices (cGMPs) and relevant regulatory requirements
  • Author and review IND/NDA Module 3 sections, with primary responsibility for Characterization/Impurities, Analytical Methods/Validation, Batch Analysis, Specifications, and Stability
  • Manage and develop a team of skilled professionals, providing mentorship and fostering a culture of excellence, innovation, collaboration, and teamwork
  • Develop and maintain productive relationships with outsourced analytical testing partners, actively managing all associated activities
  • Allocate internal and external resources effectively to meet departmental and corporate timelines and objectives
  • Develop and monitor Key Performance Indicators (KPIs) for the AD/QC department
  • Collaborate with QA in the preparation and presentation of reports to management on quality-related metrics and compliance status

Qualifications:
  • An advanced degree (MS or Ph.D.) in Chemistry or a related discipline
  • 12+ years pharmaceutical industry experience, with a strong background in the AD and QC functions, phase-appropriate requirements, and at least 10 years of experience in a managerial role, or equivalent experience
  • Proven track record of successful collaboration with key stakeholder functions (e.g. Supply Chain, CMC, Quality Assurance, and Regulatory Affairs)
  • In-depth knowledge of current regulatory requirements and guidelines for analytical development and quality control (cGMP, ICH, FDA, etc.)
  • Direct experience as a lead author of relevant Module 3 sections and supporting regulatory authority inspections
  • Experience with computerized systems (e.g. LIMS, Veeva, etc.) and their associated compliance requirements
  • Strong technical problem-solving and decision-making skills with the ability to interface with a broad range of internal and external stakeholders at all levels of the organization

Work Environment:
  • The position may be based in either of Ardelyx's two locations (Waltham, MA or Newark, CA)
  • The ability to travel to Ardelyx's other locations and external testing labs is required (up to 20 %)

The anticipated annualized base pay range for this full-time position is $267,000 - $327,000. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.
Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.
Ardelyx is an equal opportunity employer.

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