Quality Inspector Lead - 1st Shift (Ventura County)

Quality Inspector Lead - 1st Shift (Ventura County)

18 Feb 2024
California, Ventura county 00000 Ventura county USA

Quality Inspector Lead - 1st Shift (Ventura County)

Vacancy expired!

Volt is searching for a Lead Quality Inspector for an amazing pharmaceutical company in Camarillo. See the description below and apply today!Shift: Monday - Friday, 6:00am - 2:30pm (plus overtime as needed)Pay: $21.00/hourGeneral Duties and Responsibilities:Reads and understands written instructions and SOPs.Knows and understands quality-related SOP requirements that determine appropriate process for conducting job performance.Provides appropriate information regarding Quality activity & requirements in response to Packaging personnel questions.Rejects product that do not conform to required specification and follow up on any requirements to obtain product conformance.Conducts investigation regarding product deviations & prepares relevant Deviation Report or Change Control Report.Pulls Batch Record sampling for Annual Review and prepares statistical analysis.Evaluate retained product samples for Annual Review and prepares statistical analysis.Reviews and verifies Clean Log information to ensure it is complete.Reviews and verifies temperature & humidity logs.Reviews and verifies Air Pressure Records, Air Compressor Logs, Scale Calibration, and other associated Facilities forms requiring Quality verificationTrains new Quality Inspector personnel.Act as informational resource for Quality Inspector I personnel.Intermittently perform Quality Assurance Supervisor responsibilities as assigned when Quality Assurance Supervisor is not available.Including Duties within the Quality Inspector I structure:Makes sure relevant activities fall within SOP and regulatory requirements to ensure product conformity.Prioritizes multiple tasks simultaneously & completes tasks in timely manner.Reviews Master Batch Record for accuracy prior to packaging run.Checks/verifies/approves component release for production.Checks product lot number information.Reviews outserts & product sample for accuracy.Reviews and approve tray & box labels for accuracy.Issues correct labels for production run.Conducts line verifications.Conducts product in-process inspections at designated intervals.Performs final QA inspection for finished product release.Verifies Packaging Personnel reconciliation for accuracy on finished product release.Prepares & print outer box release tags when finished product is approved for release.Inspects Packaging Room Clean/Clear status & approve its use for next packaging run.Ensures required approved forms are available in vestibules for packaging personnel use.Reviews and disposes customer returns (return to inventory or morgue product).Performs quality and compliance-related duties as assigned.Physical/Cognitive Requirements:One to three years in pharmaceutical manufacturing preferred.Quality auditing experience required, either in Quality Assurance or Quality Control. Knowledge of federal and state laws and regulations, and accreditation standards.Through knowledge of knowledge of quality system regulations/requirements (i.e. ISO – International Organization for Standardization, FDA – Food and Drug Administration, and GMP – Good Manufacturing Practices.Knowledge of manufacturing processes and relevant statistical techniques (Six Sigma, Statistical Process Control (SPC).Effective communication skills at all levels both written and verbal.Effective skills in analytical thinking and problem solving.Ability to perform multiple tasks and ability to effectively manage conflict.Ability to work in teams to obtain results.Must be a self-starter than can work independently on assigned project but know how to ask for help when needed.Can effectively cope with change and is comfortable changing direction.Time management and planning skills are essential, as well as excellent interpersonal skills in order that the incumbent may work effectively with the auditee and assure timely implementation of corrective measures following audits.Excellent computer skills and strong internet research skills is required.Job involves extensive periods of sitting, a lot of reading and analyzing of information. Must have the ability to adapt work through conflicts and persuasively influence outcomes.Can effectively cope with change and is comfortable changing direction and acting without complete information.Ability to develop and deliver effective presentations and written/oral communications.Strong organizational and prioritization skills.Team player works with others effectively respectfully and cordially.Executes plans to resolve basic to moderately complex problems.Capable of resolving sensitive concerns that present minimal risk to the business.May be required to work longer than the typical 8-hour work day.Regularly required to stand; walk; use hands to fingers, handle, or feel; reach with hands and arms; and stoop, kneel, crouch, or crawl.Frequently required to sit.Specific vision abilities required includes close vision, distance vision, color vision, peripheral vision, depth vision, depth perception, and ability to adjust focus.Perform light physical duties in keeping personal work station clean organized, and presentable.Volt is an Equal Opportunity Employer

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