QC Inspector I - 2nd Shift

Getinge•Merrimack, NH

About The Position

The QC Inspector I supports quality control functions to ensure quality requirements are met and carries out quality control assignments as needed. The position performs in-process inspections and testing using approved procedures and visual aids, documents results, assists with data entry and electronic transactions, reviews Device History Records (DHRs) for completion and release of non-sterile product, and performs destructive testing and other QC tests as needed. The role also inspects certain finished-goods components against specifications using measuring devices, contributes input on documentation gaps and process improvements, and responds to changing priorities and manufacturing inspection needs with little supervision. The position requires good manufacturing practices, including accurate recordkeeping, and is performed in a manufacturing environment, potentially in a controlled clean environment. Personal protective equipment may be required.

Requirements

High school diploma or equivalent.
Strong English communication skills.
Ability to learn and understand QC fundamentals, including inspection, testing, use of measuring devices, documentation of results, and following DMR.
High commitment to safety.
Ability to perform repetitive tasks accurately.
Ability to work in a controlled clean environment.
Self-motivated and able to take direction to perform necessary duties.
Ability to work cross-functionally with different departments.
Ability to work in a fast-paced, dynamic environment.
Ability to manage time efficiently.
Strong analytical skills.
Good computer skills, including MS Office (Word/Excel).
Ability to teach and educate employees to improve processes and productivity.

Nice To Haves

At least one year of experience working in a QC or manufacturing environment.
Working knowledge of GMP, FDA, and ISO standards.

Responsibilities

Perform in-process inspections and testing using approved test procedures, quality procedures, and visual aids, and document results.
Assist with data entry and perform electronic transactions.
Review Device History Records (DHRs) for completion and release of non-sterile product.
Perform destructive testing and other QC testing as needed.
Inspect finished-goods components against specifications using measuring devices and document results.
Provide input on documentation gaps and process improvements.
Respond to changing priorities and manufacturing inspection needs with little supervision.
Demonstrate good manufacturing practices, including recordkeeping.
Contribute to team efforts by completing related duties as requested.
Maintain professional and respectful relationships with internal and external customers.