Actalent
Job Title: QA Inspector I
Job Description
As a QA Inspector I, you will be responsible for ensuring the quality and compliance of manufacturing processes in a pharmaceutical environment. You will play a crucial role in maintaining the integrity of the production lines by performing thorough inspections and documentation.
Responsibilities
Perform room and equipment cleaning checks before commencing any activities.
Conduct daily rounds of the warehouse to ensure compliance.
Document cleaning activities in logbooks and checklists.
Physically release materials upon receiving and reviewing release reports from QA.
Verify that materials match incoming documents, release documents, and material labels.
Monitor and maintain the reject cage.
Perform daily verification of balances.
Monitor temperature and humidity according to SOP.
Maintain and file documents appropriately.
Adhere to company policies, safety requirements, cGMP, and SOPs.
Perform other duties as assigned by the supervisor.
Essential Skills
Experience in quality assurance, line inspection, and document review.
Familiarity with line clearance in a manufacturing or production environment.
Experience with batch record review and quality inspection.
1-5 years of QA experience, with a recent background in pharmaceuticals.
Ability to understand and adhere to GMP standards and regulations.
High school diploma and the ability to understand SOPs.
Additional Skills & Qualifications
Experience in a pharmaceutical environment is highly preferred.
Work Environment
The role is situated in a manufacturing environment within a pharmaceutical company. The facility, located in Central Islip, is a brand new setup where inspectors oversee the packaging lines, managing 1-3 lines simultaneously. There are three openings available: one in Central Islip and two in Hauppauge. The position operates on the 2nd shift from 3:00 PM to 11:30 PM, with potential variations based on business needs. This essential business offers holiday pay and overtime opportunities, ensuring continued operation during shutdowns.
Job Type & Location
This is a Permanent position based out of Central Islip, New York.
Pay and Benefits
The pay range for this position is $41600.00 - $49920.00/yr.
benefits start day 1 and they are eligible for 2 weeks vacation, 56 hours sick and wellness add 2 days mental health days
Workplace Type
This is a fully onsite position in Central Islip,NY.
Application Deadline
This position is anticipated to close on Oct 16, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
As a QA Inspector I, you will be responsible for ensuring the quality and compliance of manufacturing processes in a pharmaceutical environment. You will play a crucial role in maintaining the integrity of the production lines by performing thorough inspections and documentation.
Responsibilities
Perform room and equipment cleaning checks before commencing any activities.
Conduct daily rounds of the warehouse to ensure compliance.
Document cleaning activities in logbooks and checklists.
Physically release materials upon receiving and reviewing release reports from QA.
Verify that materials match incoming documents, release documents, and material labels.
Monitor and maintain the reject cage.
Perform daily verification of balances.
Monitor temperature and humidity according to SOP.
Maintain and file documents appropriately.
Adhere to company policies, safety requirements, cGMP, and SOPs.
Perform other duties as assigned by the supervisor.
Essential Skills
Experience in quality assurance, line inspection, and document review.
Familiarity with line clearance in a manufacturing or production environment.
Experience with batch record review and quality inspection.
1-5 years of QA experience, with a recent background in pharmaceuticals.
Ability to understand and adhere to GMP standards and regulations.
High school diploma and the ability to understand SOPs.
Additional Skills & Qualifications
Experience in a pharmaceutical environment is highly preferred.
Work Environment
The role is situated in a manufacturing environment within a pharmaceutical company. The facility, located in Central Islip, is a brand new setup where inspectors oversee the packaging lines, managing 1-3 lines simultaneously. There are three openings available: one in Central Islip and two in Hauppauge. The position operates on the 2nd shift from 3:00 PM to 11:30 PM, with potential variations based on business needs. This essential business offers holiday pay and overtime opportunities, ensuring continued operation during shutdowns.
Job Type & Location
This is a Permanent position based out of Central Islip, New York.
Pay and Benefits
The pay range for this position is $41600.00 - $49920.00/yr.
benefits start day 1 and they are eligible for 2 weeks vacation, 56 hours sick and wellness add 2 days mental health days
Workplace Type
This is a fully onsite position in Central Islip,NY.
Application Deadline
This position is anticipated to close on Oct 16, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.