Associate II, Manufacturing Operator; Shift - Wed, Thurs, Fri & Sat
Listed on 2026-02-18
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Manufacturing / Production
Manufacturing Production, Manufacturing Engineer, Operations Engineer, Pharmaceutical Manufacturing
Job Title
Position: Associate II, Manufacturing Operator (12 Hour Shift - Every Other Wed, Every Thurs, Fri & Sat)
LocationLocation: Danbury, CT
CompanyMann Kind
Mann Kind Corporation (Nasdaq: MNKD) is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions. With a focus on cardiometabolic and orphan lung diseases, we develop and commercialize treatments that address serious unmet medical needs, including diabetes, pulmonary hypertension, pulmonary fibrosis, nontuberculous mycobacterial (NTM) lung disease, and fluid overload associated with heart failure and chronic kidney disease.
At Mann Kind, our employees are our greatest asset. We foster a close‑knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Job SummaryExecutes quality and manufacturing procedures in order to meet production demands and regulatory requirements. Responsibilities include on‑time manufacture of intermediate, semi‑finished and finished pharmaceutical products that meet quality standards. Assists with establishing equipment operating specifications, standard operating procedures and improving manufacturing techniques. Assists with equipment maintenance, calibration and resolving technical issues.
ScheduleEvery Other Wednesday, but every Thursday, Friday and Saturday, 6:00 am to 6:30 pm. with a 5% Shift Differential
Key Responsibilities- Works on assignments that are semi‑routine in nature where some judgment is required in resolving problems and making routine recommendations.
- May provide guidance on assignments to other lower‑level personnel.
- Execute manufacturing operations as required by Manufacturing Records according to Current Good Manufacturing Practices and Standard Operating Procedures in a clean room environment.
- Performs manufacturing area and equipment setup, cleanup and teardown and sanitization with supervision.
- Operates manufacturing production equipment, under supervision, as required by Manufacturing Records and Standard Operating Procedures.
- Performs in‑process inspection and testing, under supervision, as required by Manufacturing Records and Standard Operating Procedures.
- Accurately and completely documents manufacturing activities in appropriate Manufacturing Records, Controlled Forms Product Container Labels and Logbooks.
- Verifies and documents manufacturing steps performed by other Manufacturing Associates as correct in Manufacturing Records and / or Logbooks.
- Responsible for observing all Company, Health, Safety and Environmental guidelines.
- Fully qualified and able to operate approximately 50% of manufacturing equipment.
Duties and responsibilities are not limited to the work listed above and may include other assignments as necessary.
Minimum Qualifications- High School/GED with minimum of 2 - 4 years related experience or the equivalent combination of experience and training.
- Must be willing and able to receive medical clearance to wear a respirator (i.e., Powered Air Purifying Respirator) for entire working shift.
- Must be physically able to gown and de‑gown (including the use of a decontamination fogging shower) in up to three layers of clean room and potent compound facility gowning (i.e., Tyvek jumpsuit).
Pay Range: $25 - $37 per hour
How to ApplyApply for this Position
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