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Nitto Avecia Jobs (NOW HIRING)

Nitto Denko Corp.

Project Manager

Milford, MA · On-site

$98K - $120K/yr

The Project Manager will work closely with all relevant departments within Avecia to ensure projects are delivered within a manner that meets both Avecia's and the customer's needs. Key ...

Nitto Denko Corp.

$98K - $120K/yr

The Project Manager will work closely with all relevant departments within Avecia to ensure projects are delivered within a manner that meets both Avecia's and the customer's needs. Key ...

Nitto Denko Corp.

$89K - $109K/yr

Preparation of Process Validation protocols / reports, CPV protocols and reports, PC&P reports, and VMP / VSR to enable Avecia's process validation programs to be executed efficiently. * Preparation ...

Avecia Pharma

ENG Staff Facilities, HY

Oceanside, CA · On-site

$127 - $150/hr

Create Alert Hydranautics is a part of the Nitto Group of companies and one of the global leaders in the field of integrated membrane solutions. We offer complete membrane solutions like reverse ...

Nitto Denko Corp.

$152K - $186K/yr

Provide periodic summaries to Quality and Digital leadership on relevant AI advancements, case studies, and potential applications applicable to Avecia operations * Identify opportunities where ...

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Nitto Avecia information

See salary details

$25K

$80.3K

$163.5K

How much do nitto avecia jobs pay per year?

As of Aug 16, 2026, the average yearly pay for nitto avecia in the United States is $80,287.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Nitto Avecia position?

To thrive at Nitto Avecia, which specializes in oligonucleotide manufacturing and pharmaceutical services, you need a background in chemistry, biology, or a related scientific field, often supported by relevant laboratory experience and education. Familiarity with analytical instruments such as HPLC, mass spectrometry, and GMP documentation systems is typically required. Strong attention to detail, excellent teamwork, and effective communication skills are essential for success in this collaborative and regulated environment. These skills ensure product quality, regulatory compliance, and smooth workflow in pharmaceutical manufacturing.

What does a typical workday look like for someone employed at Nitto Avecia?

A typical workday at Nitto Avecia involves working in state-of-the-art laboratory and cleanroom settings where you'll carry out oligonucleotide synthesis, purification, and analysis. Employees often collaborate closely with colleagues from quality assurance, regulatory affairs, and process development teams to meet production and documentation standards. The day may include routine instrument calibration, sample testing, and updating batch records to ensure compliance with GMP and client specifications. This dynamic environment provides opportunities to grow technical expertise and learn about various phases of pharmaceutical manufacturing through cross-functional teamwork.

What is a Nitto Avecia?

A Nitto Avecia job typically involves working in the pharmaceutical and biotech industries, specializing in oligonucleotide manufacturing and related services. Employees may work in areas such as research and development, manufacturing, quality control, regulatory affairs, or engineering. The company focuses on producing high-quality nucleic acid-based therapeutics for clients worldwide. Positions at Nitto Avecia require expertise in scientific, technical, or operational fields, depending on the role.

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Nitto Avecia jobs near you
Infographic showing various Nitto Avecia job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% Physical, and 8% Remote job distribution, with an average salary of $80,287 per year, or $38.6 per hour.

Digital Transformation Program Manager

Nitto Avecia

Milford, MA • On-site

Full-time

Re-posted 14 days ago

Job description

Job Summary:
Nitto Avecia is a company focused on digital transformation within the quality management domain. They are seeking a Digital Transformation Program Manager to oversee the planning and execution of cross-functional projects related to electronic quality management systems and AI initiatives, ensuring compliance and timely delivery across various teams.
Responsibilities:
• Manage end-to-end delivery of Quality digital projects, including eQMS, LIMS, eBR, and AI use cases
• Develop project charters, schedules, milestones, RAID logs, and communication plans
• Track scope, timelines, risks, and dependencies across multiple workstreams
• Ensure clear handoffs between design, build, validation, deployment, and sustainment phases
• Act on behalf of project owners to enforce agreed timelines, track commitments, and drive cross-functional teams toward timely completion and formal project closure
• Facilitate project meetings and working sessions across QA, QC, Manufacturing, Process Development, Analytical Development, Engineering, QA-Validation, IT, and vendors
• Drive alignment on requirements, priorities, and deliverables
• Escalate risks and issues in a timely, structured manner
• Support change management and user adoption activities
• Coordinate project activities to ensure compliance with data integrity, and CSV expectations
• Support validation planning, documentation readiness, and change control execution
• Maintain inspection ready project documentation
• Support implementation of AI-enabled initiatives (e.g., batch record review, deviation triage, enhanced Powerbi reporting)
• Coordinate activities between cross functional teams
• Track risks related to AI use in regulated environments and ensure appropriate governance steps are followed
• Provide periodic summaries to Quality and Digital leadership on relevant AI advancements, case studies, and potential applications applicable to Avecia operations
• Identify opportunities where emerging AI capabilities could improve efficiency, compliance, data integrity, or inspection readiness
• Prepare routine project status updates for Quality leadership
• Maintain dashboards and metrics on project health
• Ensure transparency on progress, risks, and decision points
Qualifications:
Required:
• Bachelor’s degree in Engineering, Life Sciences, IT, or related field
• 5+ years of experience as a Project or Program Manager in regulated industries (pharma, biotech, medical device)
• Demonstrated experience managing system implementation or upgrade projects (eQMS, LIMS, MES/eBR, or similar)
• Strong understanding of GxP environments and cross-functional Quality processes
• Proficiency with standard PM tools (MS Project, Smartsheet, Jira, or similar)
• Exposure to AI, Power BI, machine learning, or large language model projects
• Familiarity with AI governance, validation considerations, and risk assessments
• Experience working with vendors such as Veeva, TrackWise, Biovia, or Siemens
• PMP or equivalent project management certification
Company:
Oligonucleotides are giving rise to a new generation of therapeutics—and Nitto Avecia is helping lead the way. Founded in 1995, the company is headquartered in Milford, USA, with a team of 501-1000 employees. The company is currently Late Stage.

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