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Job summary
A pharmaceutical company in Central Islip, NY is seeking a full-time QA Inspector I for the 1st Shift to monitor product quality throughout manufacturing processes. In this role, you will verify raw materials, conduct in-process checks, and ensure compliance with Good Manufacturing Practices. Candidates should have 1-2 years of experience in pharmaceutical manufacturing and possess strong organizational skills. This position offers competitive compensation and requires onsite work.
Qualifications
1–2 years experience in pharmaceutical manufacturing or packaging.
Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Ability to read, write, and communicate effectively in a fast-paced environment.
Responsibilities
Verify raw materials during dispensing and post dispensing.
Conduct in-process checks during batch manufacturing.
Perform daily shop floor quality rounds to maintain GMP compliance.
Skills
Knowledge of Good Manufacturing Practices (GMP)
Ability to read, write, and communicate effectively
Self-motivated with strong multitasking skills
Basic computer skills (Microsoft Word, Excel)
Education
High School Diploma
Tools
SAP
Microsoft Word
Microsoft PowerPoint
Microsoft Excel
Job description
A pharmaceutical company in Central Islip, NY is seeking a full-time QA Inspector I for the 1st Shift to monitor product quality throughout manufacturing processes. In this role, you will verify raw materials, conduct in-process checks, and ensure compliance with Good Manufacturing Practices. Candidates should have 1-2 years of experience in pharmaceutical manufacturing and possess strong organizational skills. This position offers competitive compensation and requires onsite work.