Replimune Group, Inc.

Sr. Associate, Serialization and Packaging

Replimune Group, Inc.$103K — $133K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 2-4 years of experience in a regulated GMP environment (pharmaceutical, biotechnology, medical device)
  • Associates Degree, Biotechnology Certificate, or Bachelor's Degree in Life Sciences, Engineering, Supply Chain, or related discipline preferred
  • Experience with commercial-stage pharmaceutical products
  • Hands-on experience with packaging and serialization operations
  • Knowledge of DSCSA compliance and serialization regulations

Responsibilities

  • Support the execution of packaging, labeling, and serialization activities
  • Perform setup, operation, and troubleshooting of packaging and serialization equipment
  • Serve as the primary resource for serialization processes and exception management
  • Ensure compliance with batch records, SOPs, and GMP during packaging operations
  • Monitor packaging line performance to identify efficiency and compliance improvements
  • Oversee and support serialization system operations and data integrity
  • Complete and review necessary documentation in compliance with GDP and cGMP standards

Benefits

  • Opportunities for professional development and training
  • Participation in continuous improvement initiatives
  • Exposure to advanced serialization technologies and equipment
  • Collaborative work environment with experienced professionals
Full Job Description
The Senior Associate, Serialization & Packaging is responsible for supporting the execution, coordination, and continuous improvement of commercial packaging and serialization operations at Replimune's Framingham facility. This role serves as a technical resource and subject matter expert for packaging line operations, serialization processes, and associated systems, including Antares serialization equipment, TraceLink serialization platforms, and Oracle transactions supporting commercial distribution.

Working closely with the Manager, Commercial Packaging & Serialization and Packaging team, this position supports daily packaging operations, batch execution, serialization activities, documentation review, training, troubleshooting, and operational readiness. The Senior Associate plays a critical role in ensuring products are packaged, serialized, documented, and transferred for distribution in compliance with cGMP, GDP, company procedures, and regulatory requirements.

The ideal candidate combines strong technical knowledge of packaging and serialization operations with hands-on execution experience in a commercial pharmaceutical or biotechnology environment.

Key Responsibilities:

Packaging & Serialization Operations
• Support the execution of commercial packaging, labeling, and serialization activities conducted at Replimune's Framingham facility.
• Perform setup, operation, line clearance, troubleshooting, and shutdown of packaging and serialization equipment.
• Serve as the primary operational resource for serialization processes including commissioning, aggregation, reconciliation, and exception management.
• Ensure packaging and serialization activities are executed in accordance with approved batch records, SOPs, and GMP requirements.
• Monitor packaging line performance and identify opportunities to improve efficiency, throughput, and compliance.
• Support product packaging activities through final shipment preparation and transfer to the 3PL.

Serialization Systems Support
• Serve as the site subject matter expert for serialization operations and associated business processes.
• Support operation and troubleshooting of Antares serialization equipment
• Monitor and support TraceLink transaction processing, EPCIS data exchange activities, and serialization data integrity.
• Execute and review Oracle transactions supporting packaging, inventory movements, and shipment activities.
• Support testing, implementation, validation, and deployment of serialization system updates and enhancements.
• Investigate and resolve serialization discrepancies, system exceptions, and operational issues.

Documentation, Compliance & Quality
• Complete and review batch records, forms, logbooks, and serialization documentation in accordance with Good Documentation Practices (GDP).
• Ensure all packaging and serialization documentation is accurate, complete, and inspection-ready.
• Support deviation investigations, CAPAs, change controls, and quality events related to packaging and serialization operations.
• Maintain compliance with cGMP, GDP, safety requirements, and internal procedures.
• Assist with internal audits, regulatory inspections, and inspection readiness activities.

Technical Leadership & Continuous Improvement
• Provide day-to-day guidance and technical support to Packaging Associates and other operational personnel.
• Support onboarding and training of new employees on packaging and serialization processes, SOPs, and equipment.
• Develop and maintain training materials, work instructions, and operational best practices.
• Analyze operational metrics and process performance to identify improvement opportunities.
• Lead or participate in continuous improvement initiatives focused on packaging operations, serialization compliance, equipment reliability, and operational efficiency.
• Prepare technical reports, presentations, and operational summaries as required.

Additional Skills/Preferences:
• Experience supporting commercial-stage pharmaceutical products.
• Experience operating within an in-house packaging and serialization environment.
• Experience with DSCSA compliance and serialization regulations.
• Experience training and mentoring manufacturing or supply chain personnel.
• Experience working with Antares serialization equipment or similar systems.
• Experience using TraceLink or equivalent serialization management platforms.
• Working knowledge of Oracle ERP transactions within operations environment
• Strong understanding of cGMP, GDP, and Good Documentation Practices.

Educational requirements:
• 2-4 years of experience in a pharmaceutical, biotechnology, medical device, or other regulated GMP environment.
• Associates Degree, Biotechnology Certificate, or Bachelor's Degree in Life Sciences, Engineering, Supply Chain, or related discipline preferred.
• High School Diploma or GED with relevant pharmaceutical or biotechnology industry experience may be considered.

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 $103,500 - $133,500. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.

About Replimune Group, Inc.

Replimune Group, Inc. is a clinical-stage biotechnology company focused on the development of oncolytic immunotherapies to treat cancer. The company's lead product candidate, RP1, is a selectively replicating version of herpes simplex virus 1 (HSV-1) that is designed to infect and destroy cancer cells. RP1 is currently being evaluated in multiple clinical trials for the treatment of various solid tumors. Replimune is also developing a pipeline of other oncolytic immunotherapies, including RP2, RP3, and RP-Abl, which are designed to target different types of cancer. The company was founded in 2015 and is headquartered in Cambridge, Massachusetts.
Learn more about Replimune Group, Inc.
Size
170 employees
Market Cap
$1.5 billion
Industry
Net Income
-$75.1 million
Founded
2015

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