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Qa inventory associate - 2nd shift

Lancaster
Nutramax Laboratories
Posted: 13 October
Offer description

Job Description

The hours for this position are Monday - Thursday 3:15pm - 11:30pm and Friday 3:15pm - 10:15pm.

Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check, drug screen (subject to applicable law) and reading comprehension test.


Responsibilities

* The Quality Assurance Incoming Associate (QAIA) will follow current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP) to record all procedures in a timely manner. The QAIA will understand and follow Standard Operating Procedures (SOP) in all functions executed and report any deviations where necessary.
* The QAIA will inspect all incoming materials for identity, quantity, and damages. The QAIA will be responsible for reporting any discrepancies throughout the receiving process.
* The QAIA is responsible for receiving materials using a Powered Industrial Vehicle (forklift, pallet jack).
* The QAIA is responsible for reading and understanding all accompanying paperwork, which includes, but is not limited to: packing slip, bill of lading, Certificate of Analysis (CofA), and Certificate of Compliance (CofC).
* The QAIA will be responsible for inspecting and sampling incoming materials to ensure they meet quality standards. All materials will be inspected and sampled according to the material specifications, component specifications and master proofs.
* The QAIA will be responsible for using the appropriate documents and software programs during the receiving, inspection, and releasing process. This includes, but is not limited to, inspection forms, AQL forms, disposition labels, Microsoft Suite (Excel, Word), LIMs, and SAP.
* The QAIA will be expected to work independently and/or with other QAIA’s with minimal supervision.
* Maintaining a safe working environment by following all safety guidelines/regulations and wearing Personal Protective Equipment (PPE) as appropriate. This person will ensure that all equipment and work area used is clean, calibrated, and properly maintained.
* Regular attendance is required.
* Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives.
* Communicate effectively with your team, supervision and other departments within the organization and function within a team, promoting positive work environment.


Minimum Requirements

Proficient in computer work processing and Microsoft Office applications. Ability to lift (up to 55lbs or by team lift) and maneuver material up to 110 lbs. Good written and oral communication skills that enable them to communicate well with other QAIA’s and other departments.


Education and Experience

Equivalent combination of college level coursework with one-year experience in a regulated cGMP environment.


Supervisory Responsibilities

None


Job Details

* Seniority level: Entry level
* Employment type: Full-time
* Job function: Quality Assurance and Manufacturing
* Industries: Manufacturing
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