What are the responsibilities and job description for the IN-Process Quality Assurance Technician(2nd & 3rd Shift) position at Granules?
Description:The QA Technician compliance with cGMP and SOP’s and systems. This position is responsible for daily floor monitoring., water sampling for testing, swab collection. In-process testing, line clearance. Monitor manufacturing personnel follow and adhere to SOP pertaining to Manufacturing floor activities.Job Description/ResponsibilitiesPerform line clearance, material verificationsCollect purified water sample for testing, Trending the resultsCo-ordinate Environmental monitoring in GMP area.Log book and Batch record reviewCheck the equipment cleanliness and Equipment Swab collection, Equipment release to the operations.In process QA testing.Archival of SOP’s, Batch documentation.Review the In-process SOP’s and identify the gapsInitiation of Change control/IncidentsMaintain the employee training recordsPerform Any other activity as assigned by the Supervisor.Minimum RequirementsA background in cGMP compliance within the pharmaceutical manufacturing industry is required.Experience in maintaining cGMP documentation.Ability to manage multiple priorities and re-prioritize tasks, as required.Flexible and able to adapt to company growth and evolving responsibilitiesStrong attention to detail and excellent organizationMinimum Education/ExperienceHigh School diploma, or Associate degree.At least 1 to 2 years’ experience in pharmaceutical/food industry.Benefits:401(k)401(k) matchingDental insuranceDisability insuranceEmployee assistance programHealth insuranceHealth savings accountLife insurancePaid time offReferral programVision insuranceRequirements:Required Qualifications:Quality assurance within Pharmaceutical Industry: 2 years highly preferredManufacturing: 2 years (Preferred)Document management: 2 years (Preferred)Knowledge & SkillscGMP compliance within the pharmaceutical manufacturing industry.Writing and maintaining cGMP documentation.Analyze data/information and resolve complex issues.Verbal and written communication skills.Work and communicate with cross-functional teams.Multiple priorities and re-prioritize tasks.Experience & EducationAt least 2 -3 years of experience in a quality assurance role in a cGMP-regulated environment.A college Degree preferably in sciences (i.e., Biology, Chemistry etc.), or related discipline