Operator I (Manufacturing)- Pharmaceutical
NLB Services, Florida, NY, United States
Shift:
Monday – Friday | 10:00 PM – 6:30 AM EST
Employment Type:
Temp to Perm (based on performance & openings)
Job Summary
We are seeking a
Manufacturing Operator I
to support production operations in a regulated environment. The role involves operating equipment, maintaining batch records, monitoring product quality, and ensuring compliance with
cGMP and safety standards .
Key Responsibilities
Operate and set up manufacturing equipment for production processes
Monitor processes and make adjustments to meet batch specifications
Maintain accurate
batch records, logs, and documentation
Perform
in-process testing and product quality checks
Conduct
batch reconciliations and label verification
Troubleshoot minor equipment or process issues and report concerns
Clean and maintain equipment and production areas
Follow SOPs, safety policies, and regulatory requirements (FDA, cGMP)
Core Requirements
High School Diploma or GED
0–1 year of manufacturing experience (pharma preferred)
Strong English communication (reading, writing, speaking)
Basic math and documentation skills
Willingness to work overtime (varies weekly)
Stable work history (longevity in roles preferred)
Screening Requirements
11-Panel Drug Test + Fentanyl
Medical Screening including:
Vital signs & urine analysis
Hearing test (audiogram)
Physical ability (lifting up to 30–35 lbs)
Work Environment & Physical Requirements
Manufacturing environment with moderate to high noise levels
Requires standing, walking, lifting, and equipment handling
May require respirator use and pulmonary function testing
Preferred Knowledge & Skills
Familiarity with
cGMP, FDA regulations
Basic understanding of manufacturing processes
Strong attention to detail and documentation accuracy
#J-18808-Ljbffr
Monday – Friday | 10:00 PM – 6:30 AM EST
Employment Type:
Temp to Perm (based on performance & openings)
Job Summary
We are seeking a
Manufacturing Operator I
to support production operations in a regulated environment. The role involves operating equipment, maintaining batch records, monitoring product quality, and ensuring compliance with
cGMP and safety standards .
Key Responsibilities
Operate and set up manufacturing equipment for production processes
Monitor processes and make adjustments to meet batch specifications
Maintain accurate
batch records, logs, and documentation
Perform
in-process testing and product quality checks
Conduct
batch reconciliations and label verification
Troubleshoot minor equipment or process issues and report concerns
Clean and maintain equipment and production areas
Follow SOPs, safety policies, and regulatory requirements (FDA, cGMP)
Core Requirements
High School Diploma or GED
0–1 year of manufacturing experience (pharma preferred)
Strong English communication (reading, writing, speaking)
Basic math and documentation skills
Willingness to work overtime (varies weekly)
Stable work history (longevity in roles preferred)
Screening Requirements
11-Panel Drug Test + Fentanyl
Medical Screening including:
Vital signs & urine analysis
Hearing test (audiogram)
Physical ability (lifting up to 30–35 lbs)
Work Environment & Physical Requirements
Manufacturing environment with moderate to high noise levels
Requires standing, walking, lifting, and equipment handling
May require respirator use and pulmonary function testing
Preferred Knowledge & Skills
Familiarity with
cGMP, FDA regulations
Basic understanding of manufacturing processes
Strong attention to detail and documentation accuracy
#J-18808-Ljbffr