H-1B Visa Quality Control Inspector Jobs

Job Title: QC Inspector Compounding

Location: GuruNanda LLC - 6645 Caballero Blvd, Buena Park, CA 90620
Department: Quality Control
Reports To: QC Manager
Job Type: Full-Time

Position Summary:

We are seeking a knowledgeable and hands-on QC Inspector to oversee quality activities within the Compounding Department, ensuring real-time compliance with cGMP requirements and internal SOPs. The ideal candidate will have strong experience in in-process quality control, including pre-weigh verification, compounding and mixing operations, batch record review, documentation control, line clearances, and manufacturing process monitoring. Experience in the production of cosmetics, OTC drug products, dietary supplements, and preferably medical devices, is highly desirable. The successful candidate will play a key role in maintaining product quality, regulatory compliance, and operational excellence throughout the manufacturing process.

Key Responsibilities:

• Conduct in-process quality inspections during pre-weighing, batching, and mixing operations.

• Perform line clearance activities prior to mixing, ensuring the correct ingredients are available, equipment is cleaned and sanitized, and water quality meets established specifications.

• Monitor and test water quality on a daily basis.

• Perform equipment swabbing to verify cleaning and sanitization effectiveness.

• Collect batch samples and perform testing of bulk batches in accordance with approved specifications and test methods.

• Ensure all pre-weighing and mixing activities are conducted in compliance with cGMP requirements and internal SOPs.

• Complete batch records accurately and in a timely manner to maintain compliance and data integrity.

• Identify, segregate, and control non-conforming materials or products, and complete the required non-conformance documentation.

• Support root cause investigations and assist in the implementation of corrective and preventive actions (CAPAs) for production-related quality issues.

• Collaborate closely with Production, R&D, and QA teams to resolve quality concerns and support continuous improvement initiatives.

• Ensure retain samples and samples required for third-party testing are collected during blending activities in accordance with established requirements.

• Maintain and update QA/QC production logs in a timely and accurate manner.

• Support regulatory, customer, and internal audits as required.

• Perform any other duties and responsibilities assigned by management.

Qualifications

• Minimum 2–3 years of progressive experience in Quality Control and/or Assurance within OTC Drug and Dietary Supplement manufacturing

• Experience with line clearance, in-process QC checks in blending, swabbing and batch record completion.

• Excellent interpersonal, documentation, and communication skills

• Ability to lead by example and drive quality culture on the production floor

• High School Diploma or equivalent

• Responsibilities may be shifted based on the department and company’s demand

Preferred Qualifications:

• Familiarity with cGMP requirements for Cosmetic, OTC drug, Dietary supplements & Medical device products.

• Use of ATP swabs to ensure equipment is cleaned and sanitized.

• GMP and Social Compliance audit experience

• Flexibility in work schedule

Pay: $25.00 - $30.00 per hour

Benefits:

• Dental insurance

• Employee assistance program

• Health insurance

• Life insurance

• Paid time off

• Vision insurance

Application Question(s):

• How many years of experience you have in Quality Control and/or Assurance within OTC Drug and Dietary Supplement manufacturing?

• Do you have experience with line clearance, in-process QC checks in blending, swabbing and batch record completion?

Education:

• High school or equivalent (Preferred)

Experience:

• Cosmetic, OTC drug, Dietary supplements & Medical device: 2 years (Required)

• GMP and Social Compliance audit: 2 years (Required)

Ability to Commute:

• Buena Park, CA 90620 (Required)

Work Location: In person