Replimune Group, Inc.

Commercial Supply Chain Prod Pkg Associate II

Replimune Group, Inc.$73K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 2+ years in a regulated GMP environment (pharmaceutical, biotechnology, medical device).
  • Associate's degree, Bachelor's degree, or Biotechnology Certificate preferred.
  • Experience with pharmaceutical manufacturing packaging and serialization equipment.
  • Familiarity with cGMP and Good Documentation Practices (GDP).
  • Proficient in completing and reviewing batch documentation in a regulated setting.

Responsibilities

  • Set up, operate, and clean packaging equipment following approved procedures.
  • Execute compliant packaging activities ensuring safety and quality standards.
  • Document production activities accurately and contemporaneously as per company guidelines.
  • Verify equipment setup and packaging configurations against batch documentation.
  • Support serialization processes for product accuracy and traceability.
  • Perform quality checks and visual inspections of packaging components.
  • Communicate any equipment or quality issues to management immediately.

Benefits

  • Commitment to fair and equitable compensation practices.
  • Market competitive total compensation packages.
Full Job Description
Overview

The Commercial Supply Chain Packaging Associate is responsible for executing packaging and serialization activities for finished drug product at Replimune's Framingham facility in accordance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and company procedures. This role supports the packaging of commercial products while ensuring the highest standards of quality, compliance, and patient safety. The role requires strict adherence to approved procedures, accurate documentation practices, and effective collaboration across the Commercial Supply Chain and Quality teams.

Key responsibilities:
  • Perform the setup, operation, line clearance, shutdown, and cleaning of packaging and serialization equipment in accordance with approved SOPs and batch records.
  • Execute packaging activities while maintaining compliance with cGMP, GDP, and safety requirements.
  • Complete all required production documentation (e.g. batch records, forms, etc.) accurately, legibly, and contemporaneously in accordance with Replimune procedures.
  • Verify that equipment setup and packaging configurations match approved batch documentation and operational requirements.
  • Support serialization operations to ensure accurate printing, aggregation, and tracking of commercial product.
  • Perform in-process quality checks and visual inspection of cartons and finished product components during packaging operations.
  • Conduct visual inspection of drug product vials as required.
  • Escalate equipment issues, process deviations, product defects, and quality concerns immediately to management or Quality personnel.
  • Ensure products are packaged, labeled, and serialized in accordance with approved specifications and commercial requirements.
  • Move materials and finished drug product safely to designated storage locations.
  • Maintain adequate supplies of packaging materials and notify supervision of replenishment needs.
  • Support routine cleaning, organization, and maintenance of GMP manufacturing and packaging areas.
  • Maintain clean, safe, and organized workstations and production areas.
  • Handle and package materials requiring ultra-low temperature storage (up to -80°C) while utilizing appropriate PPE and handling procedures.
  • Follow all safety policies, procedures, and PPE requirements.
  • Demonstrate reliability, punctuality, and adherence to established work schedules.
  • Collaborate effectively with team members and cross-functional partners to achieve departmental objectives.
  • Participate in continuous improvement activities to enhance operational efficiency, quality, and compliance.


Preferred Experience / Education:
• 2+ years of experience in a pharmaceutical, biotechnology, medical device, or other regulated GMP environment.
• Associates degree, Bachelors degree, Biotechnology Certificate, or equivalent technical training.
• High School Diploma or GED with relevant pharmaceutical or biotechnology industry experience may be considered.
• Experience operating pharmaceutical manufacturing, packaging, labeling, or serialization equipment.
• Familiarity with cGMP and Good Documentation Practices (GDP).
• Understanding of pharmaceutical serialization processes and requirements.
• Experience reviewing and completing batch documentation in a regulated environment.
• Demonstrated ability to perform packaging operations with consistency, accuracy, and attention to detail.

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 $73,500 - $95,000. 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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