One of our bioscience clients is looking for a Technician to join their Manufacturing team. This individual is responsible for executing the company's manufacturing and packaging processes while adhering to current Good Manufacturing Practices (cGMP). The role focuses heavily on inspection, labeling, packaging, and documentation of finished products in a regulated environment.This is a second shift opening (Monday - Friday, 2 - 10:30 PM) and 6-month contract with potential for extension and conversion at the conclusion of the contract.Required Skills & Experience2+ years of experience in manufacturing, inspection, packaging, or a related environmentExperience with inspection, labeling, packing, and documentationStrong attention to detail and qualityLegible handwriting required for GMP documentation and basic computer skillsNice to Have Skills & ExperiencePrior GMP experienceBackground in regulated manufacturing environments (pharmaceuticals, bioscience, or food production)Experience inspecting or packaging finished goodsKey ResponsibilitiesManufacturing & Processing:Support manufacturing operations including processing, filling, and packaging of bioscience productsRetrieve and handle product from freezers (-20°C) as part of production workflowFollow established procedures to ensure product quality and complianceRelease production lots within required timelinesInspection & Quality:Inspect finished products for label deformities, particles, and defectsPerform inspections after required wait times (e.g., post‑fill and post‑freeze)Spend approximately 80% of time performing product inspectionsEnsure products meet quality standards before labeling and packagingLabeling & Packaging:Label frozen and inspected bottles for main productionOperate manual labeling equipment and inspect products during labelingPackage smaller bottles into boxes and verify labeling accuracyPerform final inspection of labeled and boxed productsSpend approximately 20–25% of time on labeling and packaging activitiesDocumentation & Systems:Complete GMP documentation accurately and legiblyMaintain clear, compliant handwritten recordsUse basic computer systems, including laptops and barcode scanners, to scan and track product lotsFollow documentation requirements in a regulated manufacturing environment