Mfg Assoc - Drug Product Label and Packaging

Randstad USA; Norwood (MA); On-site; USD 62,000 - 69,000; Full time

Benefits offered by this job

Medical, prescription, dental, vision

401(k) plan

Short-term disability

Life insurance

Job summary

Randstad USA in Norwood, MA is seeking a Contingent Manufacturing Associate II to support drug product labeling and packaging on a 100% onsite schedule. The role requires GMP experience and will involve line setup, labeling, box packing, and QA documentation.

Shift is Mon-Fri, day shift, with pay range $30–$33 per hour based on experience. Ideal candidates have 1–3 years in GMP manufacturing or pharma/biotech packaging, strong batch record discipline, and the ability to stand for long periods

Qualifications

• High School Diploma or GED; science/technical degree preferred.
• 2+ years experience in GMP manufacturing or regulated ops (pharma/biotech packaging/labeling preferred).
• Experience with batch records, line clearance, in-process checks, and label reconciliation.

Responsibilities

• Perform line setup, operation, and changeover support for labeling, cartoning, kitting, and case packing activities.
• Perform room/equipment checks, line clearances, and controlled material staging to keep production running smoothly and compliantly.
• Support label issuance, use, segregation, reconciliation, and documentation accuracy.
• Conduct vision checks, print/scan verifications, and barcode verifications to ensure flawless execution.
• Complete contemporaneous batch records and electronic logbooks using ALCOA+ principles.
• Partner with QA/QC, MS&T, Engineering, and Supply Chain to resolve issues and drive continuous process improvements.

Education

High School Diploma / GED

Associate's or Bachelor's degree in a scientific/technical field (preferred)

Tools

MES/eBR

Scanners

Electronic logbooks

Labeling systems

Job description

[Contingent] Manufacturing Associate II, Drug Product Label & Packaging

Location: Norwood, MA (100% Onsite)

Shift: M-F Day shift i.e 7-3, 8-4 Pay Rate: $30-33 per hour based on experience.

Make a Direct Impact on Next-Generation Therapeutics Are you an experienced GMP operator looking to take the next step in your biotech career? Join an innovative life sciences team in Norwood, MA, where your precision, dedication, and attention to detail directly ensure high-quality medicine reaches patients in need.

We are looking for a Manufacturing Associate to support cGMP labeling and packaging operations for parenteral drug product presentations, including vials and prefilled syringes.

What You Bring to the Table Basic Qualifications:

• High School Diploma / GED required; Associate’s or Bachelor’s degree in a scientific/technical field preferred.
• 1–3 years of experience in GMP manufacturing or regulated operations (pharma/biotech packaging/labeling experience strongly preferred).
• Experience with batch records, line clearance, in-process checks, and label reconciliation.
• Physical capability to stand for extended periods, wear required PPE/gowning, and lift up to ~35 lbs.
• Flexibility to work off-hours, weekends, or overtime to support production demands.

Preferred Skills:

• Solid understanding of cGMP regulations, SOP execution, and ALCOA+ documentation principles.
• Familiarity with digital manufacturing tools (MES/eBR, scanners, electronic logbooks, and labeling systems).
• Excellent communication and shift pass-down skills with a focus on timely escalation.
• solid commitment to team collaboration, safe work practices, and 5S/housekeeping standards.

Why Work With Us?

• Collaborative Onsite Culture: Our 100% onsite model fosters real-time mentorship, solid team connections, and hands-on learning.
• Continuous Growth: Build your expertise across work centers in a fast-paced, high-tech manufacturing facility.
• Mission-Driven Environment: Be part of a workplace dedicated to highest quality, safety, and operational excellence.

What You’ll Do

• Execute Core Operations: Perform line setup, operation, and changeover support for labeling, cartoning, kitting, and case packing activities.
• Ensure Line Readiness: Perform room/equipment checks, line clearances, and controlled material staging to keep production running smoothly and compliantly.
• Maintain Label Control: Support label issuance, use, segregation, reconciliation, and documentation accuracy.
• In-Process Quality Checks: Conduct vision checks, print/scan verifications, and barcode verifications to ensure flawless execution.
• Documentation Excellence: Complete contemporaneous batch records and electronic logbooks using ALCOA+ principles.
• Cross-Functional Collaboration: Partner with QA/QC, MS&T, Engineering, and Supply Chain to resolve issues and drive continuous process improvements.

Skills

• GMP
• cGMP
• labelling
• Drug Product Labelling
• Packaging

Qualifications

• Years of experience: 2 years
• Experience level: Entry Level

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Experience

• Entry Level
• 2 years

Education

• High School (required)