Senior QA Associate – On-Site, Second Shift, Plant QA

Replimune-2; Framingham (MA); On-site; USD 99,500 - 128,500; Full time

Benefits offered by this job

Medical, Dental, Vision Insurance

401k Match

Flexible Time Off

Year-end Holidays

Job summary

Replimune Group, Inc. seeks a Senior Associate, Plant Quality Assurance to provide day-to-day quality oversight for Drug Substance, Drug Product, and Quality Control operations at our Framingham site.

You will ensure adherence to cGMP, GDP and regulatory requirements while partnering across Manufacturing, QA and QC teams. You will review records, support deviations and CAPAs, and help maintain a culture of quality with trained personnel and robust documentation practices.

Qualifications

• 3–5+ years of experience in the pharmaceutical/biotech regulated industry.
• Minimum of 3 years in QA, QC, Manufacturing, or GMP-regulated function.
• Working knowledge of cGMP regulations, GDP requirements, and quality systems.
• Ability to manage multiple priorities in a fast-paced manufacturing environment.
• Strong written and verbal communication skills.
• Experience reviewing GMP documentation and quality records.
• Demonstrated ability to work collaboratively across departments.

Responsibilities

• Provide on-floor Quality Assurance support during second shift to ensure compliance.
• Perform quality walkthroughs and inspections to maintain an inspection-ready environment.
• Support review and timely closure of quality records (deviations, CAPAs, change controls).
• Review production batch records, logbooks, and lab documentation for accuracy and compliance.
• Assist in authoring and revising quality system documents (SOPs, training materials, risk assessments).
• Provide guidance on cGMP, GDP, and quality system requirements to manufacturing and support teams.
• Participate in root-cause investigations and corrective/preventive actions.
• Escalate quality issues to management as appropriate.
• Support training on procedures and quality systems.
• Identify and execute continuous improvement initiatives.

Skills

Quality Assurance

GDP

cGMP

Quality Systems

Written & Verbal Communication

GMP Documentation

Cross-Functional Collaboration

Multi-Tasking

Education

BA or BS in a scientific discipline

Job description

Overview

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.

At Replimune, we live by our values:

United: We Collaborate for a Common Goal.

Audacious: We Are Bold.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.

Join us, as we reshape the future.

Summary of job description:

The Senior Associate, Plant Quality Assurance (PQA) reports to the Manager, Plant Quality Assurance and is responsible for providing day-to-day Quality oversight to support Drug Substance, Drug Product, and Quality Control operations in accordance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other applicable regulatory requirements.

This position works closely with Manufacturing, Quality Control, and other cross-functional teams to support compliance initiatives, batch record review, quality record review, and maintenance of a quality-focused culture. The Senior Associate serves as a key quality partner on the manufacturing floor and provides guidance to ensure activities are performed in compliance with established procedures and regulatory expectations.

• This position is based in our Framingham location and typically has a 5-day on-site expectation.

Key responsibilities:

• Provide on-floor Quality Assurance support during second shift operations to help ensure manufacturing and testing activities are performed in compliance with cGMP requirements and approved procedures.

• Perform quality walkthroughs and inspections to promote an inspection-ready environment and identify potential compliance concerns.

• Support the review and timely closure of quality records, including deviations, CAPAs, and change controls.

• Review production batch records, logbooks, and laboratory documentation for accuracy, completeness, and compliance with established procedures.

• Assist in authoring, revising, and reviewing quality system documents, including standard operating procedures, training materials, risk assessments, and validation related documentation.

• Provide guidance and support to manufacturing and support personnel regarding cGMP, GDP, and quality system requirements.

• Participate in root cause investigations and support development and implementation of corrective and preventative actions.

• Escalate quality issues and compliance risks to management as appropriate.

• Support training activities related to procedures, cGMP requirements, and quality systems.

• Identify, own, and execute continuous improvement initiatives, incorporating cross-functional input and driving projects to timely completion.

Other responsibilities:

• Support internal and external audits and regulatory inspections as required.

• Contribute to continuous improvement initiatives within the Quality Management System.

• Collaborate effectively with cross-functional teams to promote quality and compliance objectives.

• Perform other duties as assigned.

Educational requirements:

• BA or BS degree in a scientific discipline or related field, or equivalent combination of education and relevant experience.

Experience and skill requirement:

• 3–5+ years of experience in the pharmaceutical, biotechnology, or related regulated industry.

• Minimum of 3 years of experience in Quality Assurance, Quality Control, Manufacturing, or a related GMP-regulated function.

• Working knowledge of cGMP regulations, GDP requirements, and quality systems.

• Ability to manage multiple priorities in a fast-paced manufacturing environment.

• Strong written and verbal communication skills.

• Experience reviewing GMP documentation and quality records.

• Demonstrated ability to work collaboratively across multiple departments.

• Experience providing quality support within a GMP manufacturing environment preferred.

Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $99,500 -$128,500. The exact base pay offered for this role will depend on various factors, including but not limited to the selected candidate’s unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.

At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.

About Replimune

Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.