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Manufacturing Technician

Job in Delray Beach, Palm Beach County, Florida, 33483, USA
Listing for: Actalent
Per diem position
Listed on 2026-09-01
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Production Associate / Production Line
Salary/Wage Range or Industry Benchmark: 29000 - 30000 USD Yearly USD 29000.00 30000.00 YEAR
Job Description & How to Apply Below

Actalent is Hiring a Team of Lab Technicians/Manufacturing Technicians!! Both Day and Night Shift!

Responsibilities

  • Clean and sanitize equipment before and after use, following established procedures to maintain a controlled cleanroom environment.
  • Perform production operations in a GMP-regulated manufacturing setting, adhering to Standard Operating Procedures and documentation requirements.
  • Make and verify connections on flow panels to support purification and production processes.
  • Perform pH and conductivity measurements to ensure process solutions meet defined specifications.
  • Prepare and perform chemical and buffer additions according to batch instructions and safety guidelines.
  • Operate ultrafiltration systems and related purification equipment to support product processing.
  • Initiate product processes on the Process Automated System, including chromatography operations using columns up to 80 cm.
  • Take and prepare product samples for testing, ensuring proper labeling, handling, and documentation.
  • Order and maintain raw material inventories, including monitoring stock levels and coordinating replenishment as needed.
  • Complete batch records accurately and in a timely manner, ensuring compliance with cGMP documentation practices.
  • Assist in training other technicians by supporting the Group Leader in demonstrating procedures, processes, and best practices.
  • Follow cleaning and sanitization procedures for equipment, tools, and cleanroom areas to maintain compliance with GMP and FDA requirements.
  • Perform general production and material handling tasks, including unloading, moving, and staging materials.
  • Use tools such as calipers and other measuring devices as needed for production or inspection activities.
  • Communicate effectively with team members and other departments to coordinate activities, resolve issues, and achieve production goals.
  • Use Personal Protective Equipment (PPE) as required and follow all safety and environmental guidelines.
  • Stand, kneel, climb, lift, pull, and carry materials as part of daily production and warehouse-related activities.
  • Investigate and resolve inventory and delivery discrepancies by using computer systems, reading and preparing reports, and coordinating with warehousing staff.
  • Support occasional after-hours and weekend work as needed to meet production schedules or handle emergency shipments, deliveries, and receipts.
Additional

Skills & Qualifications
  • High school diploma or equivalent; an associate degree or equivalent experience is preferred.
  • Experience in a large-scale manufacturing cGMP environment working with SOPs and cGMP documentation practices (preferred but not required).
  • Previous experience in pharmaceutical, biopharmaceutical, medical device, or medical assembly manufacturing environments.
  • Preference for candidates with plasma fractionation or purification experience.
  • Experience operating ultrafiltration systems and chromatography equipment.
  • Familiarity with inspection activities and general production or general labor tasks in a GMP environment.
  • Experience using calipers and other measuring tools in a manufacturing or laboratory setting.
  • Prior experience with cleaning tools and chemicals in a regulated environment (preferred but not required).
  • Ability to manage stressors such as variable delivery frequencies, volume of work, interruptions, and occasional emergency shipments.
  • Interest in long-term growth opportunities supported by benefits such as tuition assistance, retirement plans, and professional development.
Work Environment

This role is based in a GMP- and FDA-regulated manufacturing facility that operates 24/7/365. The environment includes cleanroom and laboratory areas, as well as warehouse and general production spaces. The position is primarily for the night shift, with typical hours of 7:00 p.m. to 7:00 a.m. on a schedule of 5 days on and 2 days off, working in 2–3 day intervals.

There may be occasional after-hours and weekend work depending on production needs. The physical demands include sitting at a desk approximately 10–15% of the time to operate computers, use related software, investigate and resolve inventory and delivery discrepancies, read and prepare reports…

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