Commercial Supply Chain Production Packaging Associate II

Replimune; Framingham (MA); On-site; USD 73,500 - 95,000; Full time

Job summary

Replimune is seeking a Commercial Supply Chain Packaging Associate at our Framingham facility. You will execute packaging and serialization for finished drug products in alignment with cGMP, GDP, and company procedures, collaborating with Commercial Supply Chain and Quality teams.

Responsibilities include equipment setup, line clearance, documentation, and product verification. Preferred candidates have 2+ years in a GMP environment, related degrees, and a keen eye for quality and safety.

Qualifications

• 2+ years experience in a regulated GMP environment.
• Familiarity with cGMP and GDP.
• Experience operating packaging, labeling, or serialization equipment.
• Ability to review and complete batch documentation.

Responsibilities

• Set up, operate, and maintain packaging and serialization equipment per SOPs.
• Perform packaging activities while ensuring cGMP and GDP compliance.
• Complete batch records and related documentation legibly and contemporaneously.
• Verify equipment setup against approved batch documentation.
• Support serialization, printing, aggregation, and tracking of products.
• Conduct in-process quality checks and visual inspections of cartons and vials.
• Escalate issues promptly to management or Quality.

Skills

Attention to detail

Quality compliance

Team collaboration

Education

Associate's degree / Bachelor's degree / Biotechnology certificate

High School Diploma with relevant experience

Job description

Commercial Supply Chain Packaging Associate

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.
• Associate's degree, Bachelor's 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.

Compensation

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.

We are an Equal Opportunity Employer.