Nitto Avecia Jobs Hiring Now
Nitto Avecia is hiring for 7 open roles on Migrate Mate as of July 16, 2026, concentrated in biotech & life sciences and engineering (Non-Software), with listed salaries up to about $148,000. Migrate Mate updates Nitto Avecia's live openings daily. Nitto Avecia is a pharmaceutical and chemical manufacturing company that develops and produces active pharmaceutical ingredients and complex molecules for the life sciences industry.
Find Nitto Avecia JobsOverview
Nitto Avecia hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 7
- Top team
- Biotech & Life Sciences
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Milford
- Salary range
- $60,000–$148,000
Listed salaries for Nitto Avecia roles on Migrate Mate range from about $60,000 to $148,000 per year across 7 open roles, as of July 16, 2026.
Open Roles at Nitto Avecia
Showing 7 of 7+ Nitto Avecia jobs
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Regular Full Time
About this opportunity :
As a Quality Assurance Specialist III, you will be responsible for being a lead QA representative for Raw Materials and Batch Records functions.
Key Responsibilities:
Review and verify raw material documentation (e.g., Certificates of Analysis, Certificates of Compliance, and material specifications) for compliance with internal and regulatory requirements.
Perform QA-related entries and reviews in inventory management systems (e.g., SAP or LIMS) related to raw material status changes (quarantine/release/reject).
Assist in the documentation and investigation of raw material-related deviations, discrepancies, and OOS/OOT results in coordination with QA and QC teams.
Assist with Deviations and CAPAs for the Batch Record/Raw Material group.
Open and complete MRB DEVNs for raw material department.
Participate in the evaluation of changes related to raw materials (e.g., supplier, specification, or process changes) under the QA change control process.
Help track batch records and raw materials.
Help create and maintain metrics for batch records and raw materials.
Oversees the QA release meeting to ensure releases on track.
QA contact with Manufacturing and QC for all batch record issues, corrections, prioritizations, and requests.
Oversees training of new employees (batch record reviews, raw materials reviews)
Releases, tracks, prioritizes, and fills requests for raw materials.
Attend or lead all raw material meetings including interaction with other departments such as QC, Milford Supply Chain, Cincinnati Supply Chain, etc.
Responsible for ensuring MRBs for raw materials are initiated and completed in a timely manner.
Supports and reviews QA raw material/batch record CAPAs and Deviations.
Supports the QA Lead Supervisors.
Supervise others (as needed).
Perform walk-through of manufacturing suites (as needed).
Responsible for knowledge of SAP system for release/rejection of raw materials.
Prepare raw material-related documents and files for internal, customer, or regulatory audits. Participate in audit backroom as needed.
Lead internal audits.
Interface with Manufacturing, Purchasing, QC, Warehouse, and Supply Chain to ensure timely and compliant material release and disposition activities.
Provide assistance during cGMP compliance inspections of the Milford facility. This includes the retrieving of quality documents/records/trend data and any other documentation requested during these inspections.
Attend daily QA meetings.
Review and approved AA and HVAC Reports (as needed).
Required Skills/Abilities:
The job requires a BS/BA in science or equivalent work experience with 5 years’ experience in either Production or Quality Assurance.
Must be able to gown up and enter Manufacturing suites for walk-throughs and MRB labeling.
Must have deviation and/or MRB experience.
Provide sound decision-making and guidance on all aspects of batch record review and raw material release.
The annualized salary range for this role is $73,700.00 - $89,177.00.
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Regular Full Time
About this opportunity :
As a Quality Assurance Specialist III, you will be responsible for being a lead QA representative for Raw Materials and Batch Records functions.
Key Responsibilities:
Review and verify raw material documentation (e.g., Certificates of Analysis, Certificates of Compliance, and material specifications) for compliance with internal and regulatory requirements.
Perform QA-related entries and reviews in inventory management systems (e.g., SAP or LIMS) related to raw material status changes (quarantine/release/reject).
Assist in the documentation and investigation of raw material-related deviations, discrepancies, and OOS/OOT results in coordination with QA and QC teams.
Assist with Deviations and CAPAs for the Batch Record/Raw Material group.
Open and complete MRB DEVNs for raw material department.
Participate in the evaluation of changes related to raw materials (e.g., supplier, specification, or process changes) under the QA change control process.
Help track batch records and raw materials.
Help create and maintain metrics for batch records and raw materials.
Oversees the QA release meeting to ensure releases on track.
QA contact with Manufacturing and QC for all batch record issues, corrections, prioritizations, and requests.
Oversees training of new employees (batch record reviews, raw materials reviews)
Releases, tracks, prioritizes, and fills requests for raw materials.
Attend or lead all raw material meetings including interaction with other departments such as QC, Milford Supply Chain, Cincinnati Supply Chain, etc.
Responsible for ensuring MRBs for raw materials are initiated and completed in a timely manner.
Supports and reviews QA raw material/batch record CAPAs and Deviations.
Supports the QA Lead Supervisors.
Supervise others (as needed).
Perform walk-through of manufacturing suites (as needed).
Responsible for knowledge of SAP system for release/rejection of raw materials.
Prepare raw material-related documents and files for internal, customer, or regulatory audits. Participate in audit backroom as needed.
Lead internal audits.
Interface with Manufacturing, Purchasing, QC, Warehouse, and Supply Chain to ensure timely and compliant material release and disposition activities.
Provide assistance during cGMP compliance inspections of the Milford facility. This includes the retrieving of quality documents/records/trend data and any other documentation requested during these inspections.
Attend daily QA meetings.
Review and approved AA and HVAC Reports (as needed).
Required Skills/Abilities:
The job requires a BS/BA in science or equivalent work experience with 5 years’ experience in either Production or Quality Assurance.
Must be able to gown up and enter Manufacturing suites for walk-throughs and MRB labeling.
Must have deviation and/or MRB experience.
Provide sound decision-making and guidance on all aspects of batch record review and raw material release.
The annualized salary range for this role is $73,700.00 - $89,177.00.
Job Roles at Nitto Avecia
Working at Nitto Avecia
Nitto Avecia's 7 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are biotech & life sciences, engineering (Non-Software), and logistics & inventory. Nitto Avecia is a pharmaceutical and chemical manufacturing company focused on producing active pharmaceutical ingredients and complex molecules for the life sciences sector. Operations span supply chain, process development, quality assurance, and engineering functions. Most Nitto Avecia roles are based in Milford and Cincinnati.
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Browse jobs by roleNitto Avecia Jobs: Frequently Asked Questions
How many jobs is Nitto Avecia hiring for right now?
Nitto Avecia is hiring for 7 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in biotech & life sciences and engineering (Non-Software). Roles span supply chain, quality assurance, process development, and engineering. Migrate Mate pulls Nitto Avecia's current postings so the count reflects what is actively open.
What kinds of roles does Nitto Avecia hire for?
The most active teams are biotech & life sciences, engineering (Non-Software), and logistics & inventory. Nitto Avecia hires across scientific and technical disciplines, including chemists and process development scientists, as well as operational roles in supply chain, quality assurance, and engineering. Project management and talent acquisition positions also appear regularly. Most postings are across all levels, reflecting the specialized nature of pharmaceutical manufacturing work.
Are Nitto Avecia jobs remote or in-person?
Mostly on-site. About 0% of Nitto Avecia's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Milford. Each Nitto Avecia listing shows its work location so you can filter before applying.
How do I apply to a job at Nitto Avecia?
Find a role that fits on Migrate Mate, then follow the listing directly to Nitto Avecia's own careers page to complete the application. Nitto Avecia manages its own hiring process, including screening and interviews. Migrate Mate keeps listings current so the roles you see are ones Nitto Avecia is actively recruiting for.
What do Nitto Avecia jobs pay?
Listed salaries for Nitto Avecia roles on Migrate Mate range from about $60,000 to $148,000 per year as of July 16, 2026, with most postings at across all levels. Exact pay is set by Nitto Avecia and shown on each listing.
Does Nitto Avecia hire entry-level?
Most of Nitto Avecia's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Nitto Avecia listings for stated experience requirements.
Where is Nitto Avecia hiring?
Most Nitto Avecia roles are based in Milford and Cincinnati, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.