Quality Assurance Compliance Specialist II

Avecia Pharma; Milford (MA); On-site; USD 72,000 - 88,000; Full time

Job summary

Avecia Pharma is seeking a Quality Assurance Compliance Specialist II to support regulatory intelligence and auditing within the Quality organization. Responsibilities include inspection readiness, audits, CAPA management, and KPI data compilation.

The role requires 5+ years in a regulated/GMP setting, deep knowledge of cGMP/FDA guidance, and strong leadership and documentation skills to drive timely corrective actions.

Qualifications

• At least 5 years’ experience in a regulated/GMP industry.
• Regulatory inspection experience to lead inspection readiness.
• Knowledge of cGMP, FDA regulations, USP/IcH guidance; interpretation and implementation.
• Proficient with PC-based word processors and spreadsheets.
• Proficient with electronic quality management systems (eQMS).
• Intermediate understanding of ICH, ISO, cGMP, USP, EU regulatory guidance.
• Ability to work in a fast-paced environment with minimal oversight.
• Strong leadership, written communication, and KPI development abilities.
• Experience with cross-functional collaboration across departments.

Responsibilities

• Support inspection administration during Health Authority and client inspections.
• Support audits and CAPA management to identify risks and ensure timely closure.
• Organize and manage quality documents, records, and data for audit readiness.
• Assist in preparing responses to inspectional observations.
• Monitor CAPAs and track KPI data for quality reviews.
• Maintain Site Master File and issue Letters of Authorization.
• Support internal audits to identify risks and report findings.

Skills

Regulatory inspection

cGMP knowledge

FDA regulations

Quality systems

ICH guidance

eQMS

Documentation

Leadership

MS Word

MS Excel

Tools

MS Word

MS Excel

Job description

Quality Assurance Compliance Specialist II

Oct 9, 2026

Regular Full Time

About this opportunity :

The Quality Assurance Compliance Specialist is responsible to supporting the site’s regulatory intelligence compliance and auditing functions. This position provides regulatory compliance management within the Quality organization.

Key Responsibilities:

• Support inspection administration during Health Authority and client inspections.
• Support Avecia’s Health Authority and client audits to identify potential risks, including approval of any final reports and completion of identified CAPAs.
• Provide administrative and operational support within the Quality Assurance Department, including the retrieval, organization, and management of quality documents, records, and data to support and ad hoc documentation requests.
• Participate in the preparation or review of responses to Health authority and client inspectional observations.
• Support the execution of commitments identified during Health Authority and client audits and ensure that CAPAs are closely monitored and completed in a timely fashion.
• Support the compilation of Nitto Avecia’s KPI metric requirements and Management Review process by compiling, and trending quality data related to audit findings.
• Maintain Site Master File and issue Letters of Authorization
• Support Internal Audit Program: Perform and/or support Nitto Avecia internal audits to identify potential risks, including approval of any final reports and CAPAs, as needed.

Required Skills/Abilities:

• At least 5 years’ experience in a regulated/GMP industry required, with experience in Pharmaceuticals or Biotechnology preferred.
• This position requires a candidate with regulatory inspection experience to lead Nitto Avecia’s inspection readiness program.
• Comprehensive working knowledge of cGMP’s/FDA regulations, Quality systems, FDA Guidance documents, USP, ICH and other applicable laws and their interpretation, implementation
• Proficient with PC-based word processors and spreadsheets.
• Proficient with electronic quality management systems
• Intermediate understanding of ICH, ISO, cGMP, USP, EU, and other relevant regulatory guidance/requirements. Specific knowledge of 21 CFR 210, 21 CFR 211, ICH Q7, ICH Q9, ICH Q10, Eudralex – Volume 4, is desired.
• Ability to work in a fast-paced environment consisting of internal and external team members with minimal oversight.
• Problem-solving skills with the ability to adapt to changing priorities and timelines.
• Strong leadership and communication skills, including establishment of clear expectations and development of metrics and KQIs to monitor performance and ongoing activities.
• Demonstrated ability to write effectively, present ideas publicly, and proactively share knowledge with others to encourage team development.
• Ability to build positive working partnerships with other department management teams to successfully support validation and commissioning timelines.
• Experienced with making decisions through critical reasoning to solve standard and involved problems that may impact multiple departments.
• Experienced in the use of electronic systems such as eQMS
• Prior experience with clinical and commercial manufacturing is preferred.
• Requires the ability to gown into clean rooms and wear PPE.

The annualized salary range for this position is between $71,500.00 and $87,500.00.