Senior Manufacturing Associate I, Label & Packaging (Biotech Manufacturing)

Location: Norwood, Massachusetts, United States; onsite role. Only U.S. persons are eligible due to U.S. export control requirements.

Salary: $74,000–$118,400 per year, with potential bonus, incentive compensation, or equity subject to eligibility.

Company

hirify.global develops mRNA-based medicines, vaccines, delivery technologies, and manufacturing capabilities for infectious diseases, oncology, rare diseases, and cardiovascular diseases.

What you will do

• Execute and lead line setup, operation, changeovers, labeling, cartoning, kitting, aggregation, and case-packing activities.
• Perform line clearances, equipment readiness checks, controlled material staging, and label issuance, reconciliation, segregation, and disposition support.
• Conduct in-process inspections, barcode and label verification, vision checks, and print or scan verification.
• Complete batch records, logbooks, electronic manufacturing transactions, and other ALCOA+ documentation accurately and contemporaneously.
• Identify and escalate deviations, atypical events, equipment issues, and system problems; support investigations, CAPAs, change controls, and corrective actions.
• Train and coach associates while collaborating with QA/QC, MS&T, Engineering, Supply Chain, and Digital/Systems teams on readiness and process improvement.

Requirements

• High School Diploma or GED required; an Associate’s or Bachelor’s degree in a scientific or technical field is preferred.
• Typically 3–5 years of experience in GMP manufacturing or regulated operations; pharmaceutical or biotech labeling and packaging experience is strongly preferred.
• Experience with packaging batch records, line clearance, in-process checks, label control and reconciliation, and equipment or system troubleshooting.
• Ability to work in controlled environments, follow gowning and PPE requirements, stand for extended periods, perform repetitive tasks, and lift approximately 35 pounds.
• U.S. person status is required; the position cannot sponsor non-U.S. persons for an export control license.
• Ability to work different shifts, weekends, overtime, and off-hours as production needs require.

Nice to have

• Working knowledge of cGMP expectations, ALCOA+ principles, packaging batch records, logbooks, and electronic manufacturing or labeling systems.
• Experience providing peer coaching, training, escalation support, and shift-level problem solving.
• Strong attention to detail, communication, ownership, reliability, and commitment to safety and continuous improvement.

Culture & Benefits

• Healthcare and voluntary benefit programs.
• Fitness, mindfulness, and mental health resources.
• Family planning support, including fertility, adoption, and surrogacy benefits.
• Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
• Savings and investment programs plus location-specific benefits.
• Equal employment opportunity and reasonable workplace accommodations.