QA Incoming Associate (2nd shift) at Nutramax Laboratories

Lancaster, South Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

07 Jul, 26

Salary

0.0

Posted On

08 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, cGMP, cGDP, SOP, Forklift Operation, Pallet Jack Operation, Material Inspection, Sampling, Microsoft Office, Excel, Word, LIMS, SAP, Documentation, Safety Compliance, Communication

Industry

Manufacturing

Description

Description The hours for this position are 3:15pm - 11:30pm, Monday - Friday. Roles and 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. o The QAIA is responsible for receiving materials using a Powered Industrial Vehicle (forklift, pallet jack). o The QAIA is responsible for reading and understanding all accompanied 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 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 and drug screen (subject to applicable law).

Responsibilities

The QA Incoming Associate is responsible for inspecting, sampling, and receiving incoming materials while adhering to cGMP and cGDP standards. They must operate industrial vehicles and utilize software programs like SAP and LIMS to document and release materials accurately.