Specialist I, Sterile Manufacturing Operator (M-F, 7am to 3:30pm)

MannKind Corporation•Danbury, CT

6h•$29 - $43•Onsite

About The Position

The Manufacturing Specialist I is a developmental role responsible for learning and performing sterile manufacturing activities under direct guidance. The incumbent progresses through a structured qualification program covering the complete process train and may independently perform only those tasks for which current qualification has been documented. This is a 1st Shift role; Monday to Friday from 7:00am to 3:30pm.

Requirements

HS/GED with 6-8 years’ experience or BA with 1-3 years’ experience in a scientific/technical area or the combination equivalent of training and experience.
0-1 year of manufacturing experience.
Strong attention to detail and commitment to patient safety, product quality, and reliable execution.
Ability to read, understand, and execute technical procedures and batch instructions.
Mechanical aptitude and ability to learn automated equipment, HMIs, alarms, sensors, and basic troubleshooting.
Ability to perform accurate calculations and complete clear, compliant documentation.
Ability to communicate effectively, work collaboratively, accept coaching, and escalate concerns promptly.
Ability to distinguish relevant defects for visual inspection after successful completion of required qualification and periodic requalification.
Ability to work in classified cleanroom environments and wear required gowning and personal protective equipment for extended periods.
Ability to stand, walk, reach, bend, and perform repetitive tasks for extended periods.
Ability to pass a visual acuity check for qualification of visual inspection to meet 20/20 near vision (natural or corrected)
Ability to lift and move materials within company-defined safe-lifting limits, with assistance or mechanical aids when required.
Ability to work around cleaning agents, sanitizers, disinfectants, and VHP-controlled equipment in accordance with approved safety procedures.
Ability to work the assigned schedule and modified schedules during qualifications, media fills, campaigns, shutdowns, or business-critical events.

Nice To Haves

Relevant technical certificate or associate degree preferred.
Pharmaceutical, biotechnology, medical device, food, semiconductor, or other controlled manufacturing experience is preferred but not required.

Responsibilities

Perform assigned operations in accordance with approved SOPs, batch records, work instructions, safety requirements, and cGMP expectations.
Support drug product formulation, including material staging, dispensing support, solution preparation, mixing, sampling, pH adjustment, filtration, and transfer as qualified.
Clean, wash, inspect, assemble, wrap, load, sterilize, unload, and store product-contact change parts and equipment components as qualified.
Set up the robotic isolator and filling line, load components, perform approved pre-use checks, initiate and monitor VHP cycles, and support line clearance and readiness activities as qualified.
Operate and monitor prefilled syringe filling operations, respond to alarms within qualification, perform in-process checks, reconcile components, and document interventions.
Operate automated visual inspection equipment and perform qualified manual visual inspection of AVI ejects in accordance with approved defect standards and inspection procedures.
Operate the auto-injector assembly system, including component loading, recipe verification, in-process checks, reject handling, reconciliation, and line clearance as qualified.
Complete batch records, logbooks, forms, labels, and electronic entries accurately and contemporaneously.
Immediately report safety, quality, equipment, environmental, documentation, and process concerns.
Participate in cleaning, environmental and personnel monitoring support, media fills, validation activities, preventive maintenance support, and continuous improvement activities as assigned.
Follow approved procedures and maintain good documentation and data integrity practices.
Identify and promptly escalate deviations, atypical conditions, errors, defects, alarms, and potential product-quality risks.
Support investigations, CAPAs, change controls, risk assessments, procedure revisions, and inspection readiness activities at a level appropriate to qualification and experience.
Maintain all required curriculum, gowning, aseptic, equipment, safety, and visual inspection qualifications.