Inspection Associate, 2nd shift

Inspection Associate Summary

INCOG Bio Pharma Services is seeking a subject matter expert (SME) with capabilities in the inspection of sterile drug products. The Inspection Associate is a key role within the organization. The ideal candidate must have experience in the inspection of pharmaceutical drug products.

The primary responsibility of the Inspection Associate is to perform continuous inspection to identify and remove critical, major, and minor defects from finished product according to standard procedures. They will be responsible for meeting or exceeding production standards, maintaining product quality, and minimizing or preventing equipment downtime. The incumbent will ensure compliance with quality systems, policies, procedures, and cGMP practices and collaborate effectively with internal partners, clients, and vendors.

The hours for the Inspection Associate, 2nd Shift are 2:00 pm – 10:30 pm.

• Follow production and manufacturing procedures.
• Inspect filled product containers for cosmetic, particle, and integrity defects.
• Assist in writing and implementing area’s process documents.
• Operate equipment in compliance with SOPs.
• Assure compliance with cGMP requirements (current good manufacturing practices).
• Perform label and packaging activities for finished product.
• Complete and review associated production records.
• Train new inspectors in accordance with inspector certification procedures.
• Assist other manufacturing functions (Formulation, Fill, Materials) as required.
• Perform duties gowned in Grade C, D, and controlled non‑classified clean rooms.
• Perform cleaning and sanitization activities as needed.
• Collaborate and communicate with cross‑functional teams.
• Work flexible hours to ensure production facility coverage.

• High school diploma required, minimum 1 year of GMP pharmaceutical experience in drug product inspection and/or packaging.
• Must pass a health and visual check and yearly eye inspections for visual acuity and color blindness. Failure in the vision test or annual recertification could result in termination.

• Good math and documentation skills.
• Ability to perform repetitive tasks.
• Ability to learn and adapt to innovative ideas.
• Good observation skills.
• Initiative‑taking and collaborative mindset.
• Effective organization skills and diligence.
• Ability to work with minimal supervision.

INCOG Bio Pharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG Bio Pharma are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.

We will not tolerate discrimination or harassment based on any of these characteristics.

Qualified applicants must be authorized to work in the United States on a full‑time basis. INCOG will not provide sponsorship or support for work authorization or visas for this role, including but not limited to F‑1 CPT, F‑1 OPT, F‑1 STEM OPT, J‑1, H‑1B, TN, O‑1, E‑3, H‑1B1, or L‑1.

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