Production Technician
Job in
Allentown, Lehigh County, Pennsylvania, 18101, USA
Listed on 2026-09-02
Listing for:
B. Braun
Full Time
position Listed on 2026-09-02
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Production QC/QA, Production Associate / Production Line
Job Description & How to Apply Below
B. Braun is seeking a Production Technician for our Yellow Team night shift (6pm-6am) in our biotechnology and pharmaceutical manufacturing facility. In this role, you'll operate and monitor automated equipment, perform setups and basic maintenance, and complete in-process quality checks to ensure safe, sterile, and compliant products. You'll follow strict cGMP and FDA guidelines, accurately document production data, and support continuous improvement.
B. Braun offers a collaborative, safety-focused culture with strong training and opportunities for growth in a dynamic, innovation-driven environment.
Responsibilities
- Operate and monitor pharmaceutical production equipment on the Yellow Team night shift (6pm-6am) to ensure safe, efficient output.
- Follow strict c
- GMP, FDA, and ISO guidelines, documenting all production data accurately in batch records and logs.
- Perform routine equipment setups, changeovers, and basic preventive maintenance to minimize downtime.
- Conduct in-process quality checks, inspections, and sampling to verify products meet quality and sterility standards.
- Troubleshoot minor equipment or process issues, escalating complex problems to maintenance or supervision.
- Handle raw materials, components, and finished products following safety, aseptic handling, and labeling procedures.
- Collaborate with quality, maintenance, and engineering teams to support continuous improvement and process optimization.
- Maintain a clean, organized, and safe production area by following 5
- S and all EHS policies and procedures.
- Participate in training, cross-training, and skill development to support flexible staffing and career growth.
- Report deviations, nonconformances, and safety concerns promptly and support root-cause investigations and CAPA activities.
Required Skills
- Pharmaceutical manufacturingc
- GMP compliance
- Batch record documentation
- Aseptic handling
- Automated production equipment operation
- In-process quality inspection
- Basic mechanical troubleshooting
- SOP adherence
- FDA and ISO regulations awareness5
- S and safety practices
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