Salary: $18 - 26 per hour + none
Reference: AB_4785674
Randstad is currently seeking a dedicated and detail-oriented Quality Assurance Inspector II for our client, a reputable pharmaceutical manufacturer based in Hauppauge, NY. This is a full-time, onsite position ideal for candidates with hands-on experience in in-process quality assurance, sampling, and GMP compliance in a regulated pharmaceutical production environment.
This is a great opportunity for professionals with industry knowledge, ideally with schooling or formal training in pharmaceutical sciences, chemistry, or related fields.
salary: $18 - $26 per hour
shift: First
work hours: 8 AM - 4 PM
education: High School

Responsibilities

• Conduct real-time in-process quality checks during manufacturing and packaging in accordance with batch manufacturing records and SOPs.
• Verify raw materials during dispensing and approve printed packaging materials before issuance.
• Perform and document blend uniformity (BU) sampling and ensure cleanliness of associated tools and sampling equipment.
• Collect validation, in-process, and finished product samples accurately and according to protocols.
• Ensure line clearance and proper cleaning of manufacturing and packaging equipment prior to and after production runs.
• Review production documentation, equipment logbooks, calibration, and maintenance records to verify compliance.
• Input transactions into SAP (ERP system) for materials, samples, and inventory traceability.
• Participate in and support investigations of OOS (Out of Specification), OOT (Out of Trend) results, Deviations, and other quality issues.
• Conduct daily GMP compliance rounds in production areas and escalate any discrepancies to QA Management.
• Verify appropriate isolation and documentation of any non-conforming materials.
• Support completion of logbooks, quality forms, and documentation required to maintain compliance.
• Assist with review of engineering records (temperature, humidity data, calibration reports, etc.).
• Follow all company policies, cGMP, SOPs, and applicable FDA regulations.

Skills

• Quality Control

Qualifications

• Years of experience: 3 years
• Experience level: Experienced

Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you’re looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days

• Conduct real-time in-process quality checks during manufacturing and packaging in accordance with batch manufacturing records and SOPs.
• Verify raw materials during dispensing and approve printed packaging materials before issuance.
• Perform and document blend uniformity (BU) sampling and ensure cleanliness of associated tools and sampling equipment.
• Collect validation, in-process, and finished product samples accurately and according to protocols.
• Ensure line clearance and proper cleaning of manufacturing and packaging equipment prior to and after production runs.
• Review production documentation, equipment logbooks, calibration, and maintenance records to verify compliance.
• Input transactions into SAP (ERP system) for materials, samples, and inventory traceability.
• Participate in and support investigations of OOS (Out of Specification), OOT (Out of Trend) results, Deviations, and other quality issues.
• Conduct daily GMP compliance rounds in production areas and escalate any discrepancies to QA Management.
• Verify appropriate isolation and documentation of any non-conforming materials.
• Support completion of logbooks, quality forms, and documentation required to maintain compliance.
• Assist with review of engineering records (temperature, humidity data, calibration reports, etc.).
• Follow all company policies, cGMP, SOPs, and applicable FDA regulations