In-process line QA Associate Position Available In Middlesex, New Jersey

In-process line QA Associate Aviva Naturals New Brunswick, NJ 08901 Aviva is a manufacturer of vitamins & dietary supplements. We have an exciting opportunity available for an energetic and motivated In-Process line QA Associate to join our team for our Contract Manufacturing and Packaging facility for Dietary Supplements. This is a full-time on-site position at our manufacturing facility in New Brunswick, NJ.

Responsibilities:

ROLE AND RESPONSIBILITIES

The In-Process line QA is responsible for the assurance of the manufacturing activities within Aviva Naturals. The employee in this position should reports to QA supervisor and is responsible for working in warehouse, process & packaging rooms and evaluates all activities meets the acceptance criteria. Sample, inspect incoming raw materials, components, in-process, intermediates, and finished products and submit samples to the QC laboratory for analysis. Inspect the manufacturing equipment/rooms and packaging lines/ equipment for cleanliness and approve them for use prior to the start of the operation. Perform QA in-process checks (Beginning, Middle and End) for manufacturing/packaging operations and determine the results meets against pre-determined standards and batch record. Conduct AQL inspections on incoming materials and finished dosage forms against pre-determined Quality attributes. Collect and maintain QA Retain samples from all products manufactured. Assure that all retains are stored in an appropriate manner for accountability, annual inspection. Sample and proofread all pharmaceutical labeling for conformance to the standard. Issues approved labels to the packaging lines for use. Inform immediately any manufacturing/packaging issue to the QA supervisor. Assure all activities are in accordance with the batch records, departmental

SOP & GMP.

Review of batch records in terms of completeness of signatures, entries, and actual reconciliation / yields. Ensure the proper isolation of rejected or defective product/ material generated during batch process and accountability in the batch record. Monitor facility and product environmental operating conditions. Provide necessary support to conduct root cause analysis for any incidents generated at the facility during all phases of the production and packaging process. Perform other QC duties as assigned.

Qualifications:

QUALIFICATIONS AND EDUCATION REQUIREMENTS

Minimum 2 years of experience in a nutraceutical field. Excellent communication skills Attention to detail is paramount Desire to achieve high quality of work and diligent about following Standard Operating Procedures Knowledge of Good Manufacturing Practices(GMP)

Job Type:

Full-time Pay:

$17.00 – $18.00 per hour Expected hours: No less than 40 per week

Schedule:

Monday to

Friday Work Location:

In person