Quality Control Inspector I

Industry

Pharmaceuticals

Advert ID

USA_498592

Location

Merrimack

Job Type

Contract

Hours

Full-Time

Salary Range

USD17.00-20.00/hr

No. of Openings

1

Branch Information

Manchester, NH - (USA) 80 Canal Street NH Manchester , NH 03101

Branch Phone Number

603-625-6994

Job Description

Our Client in Merrimack NH is looking for a Quality Control Inspector to join their team! This is a temp to perm position for the right Candidate!



Job Description:

To provide support in carrying out all quality control functions to ensure that quality requirements are met, and perform quality control assignments as required.



Job Functions: (Primary "essential" duties and responsibilities)

* Performs in-process inspection/testing using approved test procedures, quality procedures and visual aids, and documents the results.

* Assists in data entry and performs various electronic transactions.

* Reviews Device History Records (DHRs) for completion and release of non-sterile product.

* Performs destructive testing.

* May perform other various QC testing as needed.

* Contributes to team effort by accomplishing related duties as requested.

* Inspection of some finished goods components per specifications using various measuring devices and documents.



Job Functions (continued): (Primary "essential" duties and responsibilities)

* Provide input to documentation gaps, process improvements.

* Reacts to changing priorities and manufacturing inspection needs with little supervision.

* Assists in special projects as needed.



Required Knowledge, Skills and Abilities: Soft skills and technical requirements to be listed here.

* Demonstrated ability to learn and understand QC core structure (inspection, testing, using various measuring devices, documentation of results, ability to follow DMR).

* Must have a high commitment to safety.

* The ability to perform repetitive tasks with a high level of accuracy.

* Able to work in a controlled clean environment.

* Self-motivated and able to take direction to perform all necessary duties.

* Ability to work cross-functionally with different departments.

* Capable of working in a fast paced, dynamic environment.

* Demonstrates ability to manage time efficiently.

* Strong analytical skills.



Minimum Requirements: minimum requirements for the position.

* High School Diploma or equivalent.

* Minimum of one year of experience working in a QC/GMP/GLP/Manufacturing environment.

* Good computer skills with MS Office applications (Word/Excel).

* Strong communication skills (English)



Quality Requirements (Required language- Please do not edit):

* Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

* Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).

* Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function).

* Attend all required Quality & Compliance training at the specified interval.

* Adopt the "Beyond Compliance Quality Culture" in the work environment; always meet and exceed requirements.



Environmental/Safety/Physical Work Conditions:

* Duties may be performed in a manufacturing/clean room environment.

* Personal protective equipment may be required as dictated by work environment.

* Must have the ability to work while standing/sitting for long periods of time.