Quality Assurance Specialist

PharmaEssentia U.S.A.; Burlington (MA); On-site; USD 81,000 - 102,000; Full time

Benefits offered by this job

Medical coverage

Dental and vision coverage

Paid time-off

401(k) retirement plan with company-mq

Job summary

PharmaEssentia USA in Burlington, MA, is seeking a Quality Assurance Specialist to manage the product quality system, review batch records, deviations, CAPA, complaints, recalls, and DSCSA compliance. You will partner with cross-functional teams and HQ QA to ensure timely, compliant product release.

The role requires a Bachelor's degree in life sciences and 3+ years in aGxP QA, with strong knowledge of FDA regulations, ICH guidelines and DSCSA. On-site work five days a week.

Qualifications

• Bachelor's degree in life sciences, pharmacy, biotechnology, chemistry, or related field.
• Three+ years of QA experience in pharmaceutical/biotech with aGxP exposure.
• Knowledge of FDA, ICH, GCP/GMP/GDP expectations.
• Working knowledge of DSCSA and serialization standards.

Responsibilities

• Manage QA processes in the QMS, including deviation, CAPA, change control and risk management.
• Review batch records and support product release.
• Collaborate with cross-functional units and HQ QA for investigations and audits.
• Oversee DSCSA serialization and product tracing compliance.
• Lead quality projects and participate in audits/inspections.

Skills

Quality Assurance

Regulatory knowledge

Cross-functional collaboration

Communication

Attention to detail

Education

Bachelor's degree in life sciences

Advanced degree preferred

Job description

About PharmaEssentia

It’s not often you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together.

PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology and oncology, with one product approved and a diversifying pipeline. We believe in the potential to improve both health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese-American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taiwan Stock Exchange (TWSE: 6446) and are expanding our global presence with operations in the U.S., Japan, Singapore, South Korea, and China, along with a world-class biologics production facility in Taichung.

Position Overview

The Quality Assurance Specialist reports to the senior manager of QA and will play a key role in managing the product quality system, including product release batch records review, deviation/CAPA, product quality complaints, recall and ensuring DSCSA (Drug Supply Chain Security Act) compliance together with supporting QA activities, such as supplier audits and authority inspections.

The key responsibilities of the position include, but are not limited to, the following:

Quality Management System

• Manage assigned QMS processes, including change control, deviations, investigations, corrective and preventive actions (CAPA), and quality risk management.
• Monitor quality records and follow up with process owners to support timely completion and effective closure.
• Prepare quality metrics, summaries, and trend reports for management review and continuous improvement.

Product Quality Complaints Management

• Collaborate with cross functional units including the call center, external partners, internal teams, and headquarters to manage product quality complaints in alignment with SOPs and regulatory requirements
• Ensure timely response and communication to resolve return/ replacement request arise from Product Quality Complaints
• Coordinate investigations with internal stakeholders and third-party vendors, ensuring root cause analysis and corrective actions are implemented.
• Complete and retain proper documentation of complaint details.
• Prepare complaint summaries and trend reports for management review.

DSCSA Compliance

• Oversee compliance with DSCSA serialization and product tracing requirements.
• Validate serialization systems and ensure data integrity across the supply chain.
• Coordinate investigations of suspect or illegitimate products, product defects, and DSCSA exceptions.
• Support product recalls or withdrawals, including communication with trading partners and regulatory authorities.
• Ensure timely submission of notifications to FDA as required by DSCSA policy.

Production Oversight

• Review batch records related to GDP (Good Distribution Practice) to support product release schedule, ensuring regulatory compliance, and delivery of products.
• Identify and resolve all GDP records discrepancies to prevent a regulatory impact.
• Collaborate with HQ QA to ensure an efficient and compliance process for product release.
• Ability to exercise independent judgement and critical thinking.

Cross-function collaboration and Quality Support

• Maintain effective communication with stakeholders to ensure compliance and timely resolution of quality issues.
• Lead assigned quality projects and coordinate activities across internal and external stakeholders.
• Participate in audits and inspections, providing documentation and responses as needed.

• Other QA-related duties as assigned by management.

Qualifications and Experience

• Bachelor's degree in life sciences, pharmacy, biotechnology, chemistry, or a related field; advanced degree preferred.

• Three or more years of Quality Assurance experience in the pharmaceutical or biotechnology industry, including experience in aGxP-regulated environment.

• Working knowledge of applicable FDA regulations, ICH guidelines, and relevant GCP, GMP, and GDP expectations.
• Working knowledge of DSCSA and global serialization standards (e.g., GS1, EPCIS).

• Experience with QMS processes, non-conformance investigations, CAPA, audits, andinspectionreadiness.

• Ability to communicate effectively, build collaborative relationships, and influence cross-functional stakeholders.
• Flexible schedule to maintain timelines, shifting priorities and accommodate occasional early/evening meetings with global teams.

Key Competencies

• Quality and compliance mindset
• Cross-functional collaboration
• Accountability and attention to detail

Location and Work Arrangement

This position is based in Burlington, Massachusetts, and requires the person to be on-site 5 days a week.

The expected salary range for this position based on greater Boston, MA location is $81,151 - 101,959. Actual salary pay will be based on multiple factors, including geographic location, experience, qualifications, and other job-related factors permitted by law.

Benefits of working with our team

• Comprehensive medical coverage
• Dental and vision coverage
• Generous paid time-off
• 401(k) retirement plan with competitive company match
• Medical & Dependent Care Flexible Spending Account
• Up to $150 monthly cell phone reimbursement
• Employee Assistance Program

At PharmaEssentia USA, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PharmaEssentia USA believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.

PharmaEssentia does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PharmaEssentia employees. PharmaEssentia is not responsible for any fees related to unsolicited resumes from staffing agencies.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.