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Q Pharma Jobs (NOW HIRING)

This role is central to the success of our Cell Q platform and commercial-scale QC operations. The ... Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug ...

Lead a crosssite team (CoE + domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems ... and pharma to tackle the world's biggest health challenges. Imagine being part of a team that ...

This role is central to the success of our Cell Q platform and commercial-scale QC operations. The ... Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug ...

Lead a crosssite team (CoE + domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems ... and pharma to tackle the world's biggest health challenges. Imagine being part of a team that ...

This role is central to the success of our Cell Q platform and commercial-scale QC operations. The ... Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug ...

Director Data AI & Analytics

Irvine, CA · On-site

$154.57 - $216.10/hr

Lead a cross-site team (CoE + domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems ... and pharma to tackle the world's biggest health challenges. Imagine being part of a team that ...

Lead a cross-site team (CoE + domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems ... and pharma to tackle the world's biggest health challenges. Imagine being part of a team that ...

PR · On-site

Lead SAT planning and execution coordination with C&Q and the System Turnover Lead. * Manage vendor ... Bachelor's degree in Mechanical, Chemical, or Industrial Engineering. * 12+ years of pharma/biotech ...

PR · On-site

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR · On-site

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR

$12.25 - $15.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR · On-site

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR · On-site

$12.50 - $16/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR · On-site

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

PR

$16 - $20.50/hr

Commissioning & Qualification (C&Q) * Resolve design issues and coordinate design changes with ... Experience in GMP or regulated environments (pharma/biotech) * Strong understanding of: * Warehouse ...

Showing results 41-60

Q Pharma information

See salary details

$5

$54

$91

How much do q pharma jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for q pharma in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $50.48 and $63.70 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Q Pharma position, and why are they important?

To thrive in a Q Pharma role, candidates typically need a background in pharmaceutical sciences, quality assurance, or regulatory affairs, often supported by a relevant degree. Familiarity with industry-standard tools and systems such as GMP (Good Manufacturing Practices), LIMS (Laboratory Information Management Systems), and FDA or EMA regulatory standards is crucial. Strong attention to detail, analytical thinking, and excellent communication skills help professionals excel in this position. These competencies ensure pharmaceutical products meet strict quality standards and regulatory compliance, safeguarding consumer safety and organizational reputation.

What is a Q Pharma?

A Q Pharma job typically refers to a position within the pharmaceutical industry that focuses on quality assurance, quality control, or regulatory compliance. Professionals in these roles ensure that pharmaceutical products meet industry standards, regulatory requirements, and safety guidelines. Responsibilities may include reviewing manufacturing processes, conducting audits, and maintaining documentation to comply with FDA and other regulatory bodies. These jobs are critical for maintaining product integrity and patient safety in the pharmaceutical sector.

What are the main responsibilities of someone working in a Q Pharma position?

In a Q Pharma role, your core responsibilities typically include monitoring product quality throughout the manufacturing process, conducting inspections and audits, maintaining meticulous documentation, and ensuring compliance with regulatory guidelines. You might also be involved in investigating quality issues, developing process improvements, and coordinating with production, R&D, and regulatory teams. The position often requires balancing multiple projects while supporting both routine operations and new product introductions. Success relies on close collaboration with cross-functional departments to ensure quality standards are consistently maintained.

More about Q Pharma jobs
Infographic showing various Q Pharma job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 2% Part Time, 9% Contract, and 1% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $113,000 per year, or $54.3 per hour.

$154.57 - $216.10/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

Position Overview Position Description

We are hiring a Director Data, AI and Analytics. The Director Data, AI and Analytics will own the strategy, platforms, operating model, and outcomes for Data, AI, and Analytics across three FUJIFILM life‑sciences businesses. In highly regulatedGxPenvironments, deliver a trusted data backbone, governed self‑service analytics, advanced analytics, bioinformatics pipelines, and agentic AI—meeting 21 CFR Part 11/EU Annex 11, ALCOA+, and CSV/CSA expectations. Lead a cross‑site team (CoE+ domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems, and ERP, and convert data and AI into measurable business value.

This position is hybrid in Irvine, CA.

Company Overview

At FUJIFILM Biosciences, we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world’s biggest health challenges.

Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture foster curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you’re ready to make an impact, your future belongs with us at FUJIFILM Biosciences.

Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description Responsibilities:
  • Define the multi‑year Data/AI roadmap for locations in California and Wisconsin; align to business priorities and compliance needs.
  • Stand up a Data, AI & Analytics Center of Excellence with domain‑aligned product squads (M&Q, R&D/Bioinformatics, Finance/SC).
  • Run governance: Data & AI Steering Committee, Model Risk & Compliance Board; assign data product ownership.
  • Own the enterprise data platform (lakehouse/warehouse), ingestion (ELT/CDC), orchestration, and semantic/metric layers.
  • Implement catalog/lineage, data quality rules, accesscontrols;drive data product SLAs and ownership.
  • Integrate core systems: MES (e.g., PAS‑X), QMS (ETQ/Veeva), LIMS/ELN (LabWare/Benchling), ERP (e.g., SAP/Oracle), OSI PI/AVEVA, and instrument data hubs.
  • Deliver executive and operational analytics (FPY/yield, OEE, deviation/CAPA TAT, batch release, QC throughput, inventory turns, cost‑to‑serve).
  • Enable governed self‑service (certified datasets/semantic models, KPI library, training, community of practice).
  • Lead data science programs for manufacturing quality, supply chain, and R&D.
  • Own bioinformatics analytics and pipelines (e.g., NGS/omics workflows, imaging pipelines, assay analytics) and integration with lab systems and data platforms.
  • Build responsible and agentic AI capabilities (assistants/co‑pilots, retrieval/grounding, task automation) with MLOps (experiment tracking, model registry, CI/CD, monitoring, retraining).Separate GxP vs non‑GxP AI; ensure intended use, explainability, validation/CSA, and periodic review for regulated models.
  • Embed compliance by design: 21 CFR Part 11, Annex 11, ALCOA+, data retention/archival, audit trails.
  • Partner with QA/CSV on risk‑based validation, test evidence, and inspections; maintain validated state for applicable analytics/data flows.
  • Coordinate with Corporate Security on classification, RBAC/least privilege, encryption, logging/monitoring, and incident response for data/AI workloads.
  • Govern AI safety: model cards, red‑team testing, bias/fairness checks, PHI/PII safeguards, vendor due diligence.
  • Prioritize a portfolio of use cases with quantified value; pilot, scale winners, retire low‑value work.
  • Publish a quarterly “Data & AI Outcomes” report (business impact, adoption, cost/performance, compliance posture).
  • Select and govern platform vendors (cloud, data/ML, BI, bioinformatics tools) and SIs; negotiate commercials, SLAs, exit terms.
  • Drive FinOps: usage visibility, rightsizing, tiered storage, and cost/performance optimization.
  • Hire and develop data/platform/analytics engineers, data scientists/ML engineers, bioinformatics engineers, and product managers.
  • Build cross‑site career paths and a culture of reliability, compliance, and measurable impact.
Required Skills/Education:
  • BS/BA (or equivalent) in Business, Computer Science or similar.
  • 10+ years leading Data/Analytics functions with 5+ years in regulated life sciences (biotech, pharma, CDMO); multi‑site/global experience.
  • Ownership of enterprise data platforms (lakehouse/warehouse), analytics programs, andMLOpsin production.
  • StrongGxP/CSV/CSA knowledge with practical application in analytics/AI and data flows; 21 CFR Part 11/Annex 11/ALCOA+.
  • Hands‑on familiarity with bioinformatics analytics/pipelines (e.g., NGS/omics, imaging, workflow orchestration) and integration with LIMS/ELN and lab systems.
  • Proven record converting Data/AI programs into business outcomes (e.g., cycle time, yield/FPY, cost, quality).
  • Cross‑functional leadership with QA/CSV, Manufacturing/Quality, R&D, Security, ERP/MES/QMS owners, and vendors.
  • Excellent executive communication and pragmatic technical guidance.
  • Platforms: Databricks/Snowflake/BigQuery; Azure/AWS data services; Spark; DBT; Airflow/Prefect; Kafka/EventHub.
  • BI: Power BI/Tableau; semantic/metrics layers; KPI governance.
  • MLOps/AI:MLflow/W&B,SageMaker/Azure ML; vector DBs/RAG; LLM orchestration; agent frameworks; feature stores.
  • Bioinformatics:Nextflow/Snakemake, CWL/WDL; common tools (e.g., GATK) or imaging/omics pipelines; HPC/containers.
  • Governance: Collibra/Alation/Atlan; model risk management/AI governance.
  • Certifications: GAMP 5/CSA, ITIL, cloud (Azure/AWS), or data governance certifications.
  • Ability to speak, read, and write in English.
  • Good verbal and written communication skills; effective presentation skills.
Salary and Benefits:
  • For California, the base salary range for this position is $154,565.00 - $216,100. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.).
  • Medical, Dental, Vision
  • Life Insurance
  • 401k
  • Paid Time Off

*#LI-hybrid

EEO Information

Fujifilm is committedto providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre‑employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (flbi@fujifilm.com).

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