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Kit Packaging & Visual Inspection Associate
Job in
Billerica, Middlesex County, Massachusetts, 01821, USA
Listed on 2026-06-26
Listing for:
Randstad USA
Full Time
position Listed on 2026-06-26
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations
Job Description & How to Apply Below
Kit Packaging & Visual Inspection Associate
- Shift: 1st Shift (Overtime as required)
- Primary M-F 7-4
- Standard
Schedule:
Monday through Thursday (four 10-hour shifts). - Overtime:
Overtime is often required on Fridays as needed to meet production goals. - Environment:
Fast-paced, Team-oriented, cGMP Compliant
Delivering Excellence Globally
We provide life-saving diagnostic imaging agents to clinicians and patients worldwide. As a member of our Kit Packaging team, you play a vital role in ensuring that every pharmaceutical product is labeled, inspected, and packaged with the highest level of "pharmaceutical elegance" and accuracy before it reaches a patient.
The Role:Your Daily Impact
This is a hands-on, detail-oriented position where you will manage the final stages of the production lifecycle. You will balance manual craftsmanship with automated technology to maintain our world-class quality standards.
Key Responsibilities- Precision Packaging:
Execute the labeling and packaging of pharmaceuticals for worldwide distribution using both manual techniques and automated labeling machinery. - Visual Quality Inspection:
Perform critical visual inspections of filled vials to ensure product integrity and compliance with safety standards. - Technical Documentation:
Accurately follow manufacturing batch records and Departmental SOPs while completing standardized forms with high attention to detail. - Process Management:
Manage area clearances, product accountability, label control, and product segregation to prevent cross-contamination or errors. - Inventory & Systems:
Utilize BPCS/MRP or SAP software to perform inventory transactions, cycle counts, and resolve discrepancies.
- Compliance Mindset: A strong understanding of cGMP guidelines and a commitment to maintaining a safe, sterile, and organized work environment.
- Adaptability:
The ability to pivot quickly to changing production priorities and manage multiple tasks in a high-speed setting. - Communication:
Excellent interpersonal skills with the ability to instruct team members on procedures and participate actively in group problem-solving. - Technical Literacy:
Basic math and science skills relevant to manufacturing, along with a working knowledge of computer-controlled production equipment.
- Education:
High School Diploma with 0–3 years of manufacturing experience (Pharmaceutical environment preferred). - Alternative:
An Associate’s Degree with working knowledge of BPCS/MRP and SAP software systems.
- Proven success working in team-based environments requiring extreme accuracy and self-motivation.
Position Requirements
10+ Years
work experience
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