Quality Inspector I (Entry-Level) (3rd shift Sunday night- Friday morning 10pm-6:30 am)

THE ROLE: 

The 3rd  Shift MQA Technician I is responsible for conducting quality control checks of materials, products and documentation before, during and after batch production activities.

HOW YOU WOULD CONTRIBUTE: 

• Perform pre-batch inspection activities (e.g., verify line clearance, review of staged materials, review of batch-related documentation, inspection of initial units, line release, etc.), swabbing of equipment to verify cleanliness before use, and in-process quality control checks for low-speed Powder and Tea packaging lines
• Perform swabbing of manufacturing equipment to verify cleanliness
• Perform in-process quality control checks
• Ensure batch-related documentation is completed accurately and completely in real-time
• Change the status of production materials to released, rejected, hold, etc.
• Detail quality-related incidents using appropriate GMP documentation (e.g., nonconforming materials report, unplanned deviation report, quality incident report, etc.)
• Review production-related GMP documentation (e.g., production logbooks) to ensure they are being completed accurately and completely.
• Report any violations of GMP procedures or company policy to MQA management
• Performs other related duties as assigned by management.

SUPERVISORY RESPONSIBILITIES: 

None

SKILLS AND BACKGROUND REQUIRED TO BE SUCCESSFUL: 

Skills:

• Attention to detail
• Good interpersonal and communication skills
• Ability to communicate effectively verbally and in written English
• Digital literacy, with solid PC and software experience
• Ability to lift a minimum of 30 lbs
• Strong ability to work independently and as a team member under the pressure of manufacturing
• This position will require the employee to operate a motorized powered lift i.e. Forklift, Scissor lift, one man lift, etc. A MVR (Motor Vehicle Report) will resolve an employee’s eligibility to operate these lifts.

Experience:

• A minimum of 1 year of experience in FDA or GMP regulated industry

Education:

• High-school diploma (or equivalent)

Additional Information

Final candidates must successfully complete a pre‑employment drug screen and background check as a condition of hire.

PREFERRED QUALIFICATIONS: 

• Experience with food, supplement or pharmaceutical manufacturing
• Knowledge and understanding of GMP quality systems

PHYSICAL DEMANDS: 

In general, the following physical demands are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to allow otherwise qualified individuals to perform the essential functions of the job.

• Must be able to see, hear, speak and write clearly in order to communicate with employees and/or other customers.
• Manual dexterity required.

Moderate: Mostly standing, walking, bending, frequent lifting 

WORK ENVIRONMENT:  

In general, the following conditions of the work environment are representative of those that an employee encounters while performing the essential functions of this job.  Reasonable accommodations may be made to allow differently-abled individuals to perform the essential functions of the job within the environment.

• The manufacturing facility is clean, orderly, properly lighted and ventilated
• Noise levels are considered low to moderate, with some areas requiring hearing protection

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