Aseptic Manufacturing Technician
Trident Consulting · Indianapolis, Indiana, United States
FULL TIMEpermanent
Job Description
Trident Consulting is seeking a " Production Technician II" for one of our clients in "Indianapolis, IN” A global leader in business and technology services.
Learn more about the general tasks related to this opportunity below, as well as required skills.
Role: Production Technician IILocation: Indianapolis, IN 46268Pay Rate: $21.50/hr w2 Shift: Monday–Friday, 7:00 AM–3:30 PM (Overtime possible)Work Mode: 100% Onsite
Job SummarySeeking a Production Technician II with experience in aseptic pharmaceutical manufacturing, cGMP compliance, packaging, and product inspection. Vial washing and capping experience are preferred.Key ResponsibilitiesPerform vial washing, capping, component preparation, packaging, and inspections.Set up equipment and replenish production supplies.Follow batch records, SOPs, and cGMP requirements.Verify scale calibration and inspect products for quality.Handle and dispose of hazardous chemicals safely.Operate production equipment with minimal supervision.Required QualificationsHigh school diploma or equivalent.2+ years of aseptic manufacturing experience in a cGMP pharmaceutical facility.Working knowledge of GMP regulations and SOPs.Strong communication and attention to detail.Ability to lift up to 50 lbs and work onsite.Preferred: Vial washing, capping, packaging, inspection, and Microsoft Word/Excel experience. xzbcwsv Interview Process: Virtual interviews.
Learn more about the general tasks related to this opportunity below, as well as required skills.
Role: Production Technician IILocation: Indianapolis, IN 46268Pay Rate: $21.50/hr w2 Shift: Monday–Friday, 7:00 AM–3:30 PM (Overtime possible)Work Mode: 100% Onsite
Job SummarySeeking a Production Technician II with experience in aseptic pharmaceutical manufacturing, cGMP compliance, packaging, and product inspection. Vial washing and capping experience are preferred.Key ResponsibilitiesPerform vial washing, capping, component preparation, packaging, and inspections.Set up equipment and replenish production supplies.Follow batch records, SOPs, and cGMP requirements.Verify scale calibration and inspect products for quality.Handle and dispose of hazardous chemicals safely.Operate production equipment with minimal supervision.Required QualificationsHigh school diploma or equivalent.2+ years of aseptic manufacturing experience in a cGMP pharmaceutical facility.Working knowledge of GMP regulations and SOPs.Strong communication and attention to detail.Ability to lift up to 50 lbs and work onsite.Preferred: Vial washing, capping, packaging, inspection, and Microsoft Word/Excel experience. xzbcwsv Interview Process: Virtual interviews.
Details
| Company | Trident Consulting |
| Location | Indianapolis, Indiana, United States |
| Type | FULL TIME |
| Niche | general |
| Experience | permanent |

