Manufacturing Associate I

Replimune; Framingham (MA); On-site; USD 50,000 - 80,000; Full time

Job summary

Scorpion Therapeutics in Framingham, MA is seeking a Manufacturing Associate I/II to support cGMP biopharma manufacturing of oncolytic platforms. The role emphasizes aseptic processing, equipment operation, and adherence to production schedules.

The candidate will author batch records, assist with process validation, and maintain GMP compliance while contributing to production readiness in a fast-paced facility.

Qualifications

• Bachelor's degree with 1-3 years or Associate's/High School Diploma with 3-6 years of cGMP biopharma manufacturing experience.
• Experience in cell culture, purification, or aseptic filling.
• Familiarity with single-use technologies.
• Strong organizational, communication, and teamwork skills.
• Proficiency in Microsoft Word and Excel.

Responsibilities

• Author SOPs and batch records
• Perform aseptic gowning
• Operate viral production equipment (e.g., tangential flow filtration, chromatography)
• Prepare buffers
• Perform visual inspection
• Assist with equipment setup, maintenance, and validation

Skills

Strong organizational skills

Effective communication

Teamwork

Microsoft Word

Microsoft Excel

Aseptic techniques

Education

Bachelor's degree in a relevant field

Associate's degree or high school diploma with cGMP manufacturing experience

Tools

Tangential flow filtration

Chromatography

Job description

Role:

Manufacturing Associate I/II supporting cGMP biopharma manufacturing of Replimune's oncolytic immunotherapies at the Framingham, MA facility.

Objectives:

execute manufacturing operations, ensure GMP compliance, support process validation, and maintain production readiness.

Responsibilities:

• author SOPs and batch records
• perform aseptic gowning
• operate viral production equipment (e.g., tangential flow filtration, chromatography)
• prepare buffers
• perform visual inspection
• assist with equipment setup, maintenance, and validation

Qualifications:

• Bachelor's degree with 1-3 years or Associate's/High School Diploma with 3-6 years of cGMP biopharma manufacturing experience
• experience in cell culture, purification, or aseptic filling
• familiarity with single-use technologies
• strong organizational, communication, and teamwork skills
• proficient in Microsoft Word and Excel

HighValue:

• biologics manufacturing
• viral vector or oncolytic platforms
• GMP environment
• equipment validation
• aseptic processing
• working in a cleanroom setting

Work setup:

primarily on-site with some weekend/holiday work depending on production needs.