Quality Control Inspector

**Job Overview**
The Quality Control Inspector’s role is to ensure that the products and services of a company are up to standard.

**Reports to**:
Quality Control Manager

**Duties and Responsibilities**
- To assure the quality of manufactured products through document review and control, investigation, reconciliation, master batch production record review, product audits, and inspection.
- Conducting regular internal audits per the yearly audit schedule
- Perform batch record reviews, investigations, and audits.
- Conduct line inspection and approve line standards.
- Handling issues and non-conformances such as preparing NCR and CAPA Report
- Perform line clearance check and ensure compliance with SOPs.
- Assessment of drug product and cosmetic quality and conformance to specifications by reviewing batch production and testing/inspection records; reviews and evaluates quality-related data from inspection activities and reports these data using statistical techniques.
- Review batch production records and other QA documentation and report any deviations to the Quality Assurance Manager and affected departments.
- Clarify information and address deviations.
- Reviews reconciliation calculations for drug items as part of batch production record review prior to release of finished goods.
- May assist production in doing the calculations, Complete product inspection reports, and release products after review of documents and related test parameters.
- Gathers all batch production documents and keeps them as batch production packets; does overall review and completion.
- Responsible for FG product releases and ensures that batch production records are complete, accurate, and in compliance; Releases products for shipment according to specifications and keeps track of drug products produced.
- Provides information on the latest standards, specifications, procedures, and requirements related to existing and new products.
- Provides necessary specification documents and inspection forms to Production before filling and packing of drug products, issues & reviews batch cards for drug products and cosmetics.
- Prepare Micro samples to be sent to the micro testing lab.
- Conduct incoming inspection on cosmetic components and labels following the sampling plan.
- Collect bulk samples, perform bulk testing, and prepare a certificate of analysis.
- Assist in conducting root cause analysis for internal quality issues. Recommends corrective and preventive measures and maintains records. Ensure root cause/preventive measures are identified and corrective actions are taken.
- Assists in writing and reviewing SOPs according to GMP requirements.
- Assists in conducting regular internal Quality/GMP audits according to the self-improvement program (SIP) and according to GMP requirements. Prepares audit reports and action plans.
- Assist in monitoring the calibration program of the site by maintaining the calibration log and certificates.
- May assist in any QA/QC activities as required.
- Follow safety rules and regulations at all times.

**Qualifications**
- Bachelor/Diploma in Chemistry, Chemical Engineering, Chemical Technician, or any related science field.
- 2 years experience as a quality technician/Quality Inspector
- Self-motivated, highly organized, and with good documentation skills
- A process-oriented person with GMP awareness and strong interpersonal and communication skills to handle production questions and concerns and to initiate necessary actions.

Pay: $45,000.00-$50,000.00 per year

**Benefits**:

- Dental care
- Extended health care
- Life insurance
- Vision care

Schedule:

- 8 hour shift
- Day shift
- Monday to Friday

Work Location: In person

Application deadline: 2024-11-14
Expected start date: 2024-11-18