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QA AuditorHamilton Connection • United States
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QA Auditor

Hamilton Connection
  • US
    United States
  • US
    United States
Postuler Maintenant

À propos

Job Description
Hamilton Connections has a
QA associate
position on
2nd shift
at a Pharmaceutical company in Clinton, CT available. Pay range starting at
55k . Temp to hire positions available. Fast-paced blending keeps products moving!
POSITION SUMMARY for QA:
This is a 2nd shift, minimum hours will be Monday to Friday, 3:50PM to 12:20AM.
Responsible for the enforcement of Tower Laboratories, Ltd. quality system, which ensures production of a consistently high quality product.
Work closely with production staff to ensure that our effervescent tablets and powders are manufactured in accordance with applicable procedures, specifications and in a cGMP (current
Good Manufacturing Practices) compliant manner. Partners with manufacturing throughout production life cycle to assure that procedures are followed and activities are appropriately documented.
ESSENTIAL FUNCTIONS: Perform product manufacturing audits throughout process through observation and by conducting in-process testing to ensure product meets specifications. Conduct packaging audit ensuring final product meets packaging specifications and is within the allowed accepted quality limits (AQL); inspect all incoming packaging components, ensuring specifications are met by performing appropriate tests following determined component specifications. Conduct investigations as directed and collect information to assess root causes when product or processes are not meeting specifications. Assist in the conduct of internal audits of cGMP to ensure compliance to cGMP and internal procedures and policies. Audit finished/completed batch production documents for procedural or mathematical errors prior to final review and release of product by the QA Manager. Communicate identified manufacturing deficiencies to key personnel (Machine Operator, Quality Supervisor/Manager, Production Manager, etc.). Verify that all instrumentation used are calibrated and perform equipment calibrations as identified. Work as a team member; be cooperative with all departments and staff to meet company objectives. Perform all work in accordance with established Safety, cGMP and company procedures. Other responsibilities as assigned. ESSENTIAL SKILLS AND EXPERIENCE:
Minimum of 2 years' experience in either pharmaceutical, food/beverage, nutritional supplement or another highly regulated environment. Demonstrated strong attention to detail. Knowledge of cGMP regulations highly preferred. Working knowledge of MS Word and MS Excel. Must be able to read and follow directions, complete paperwork and communicate effectively in English. Excellent organizational skills. Good interpersonal skills; ability to communicate effectively with all levels of plant personnel. Strong team player, demonstrated team attitude and behaviors. PHYSICAL DEMANDS:
QA will Lift, push, pull up to 25lbs. on occasional basis Climb stairs, walking throughout manufacturing/warehouse areas Must be able to wear safety shoes & safety glasses when in manufacturing/warehouse areas Must be able to wear sanitary attire such as gloves, hairnet, face mask and lab coat.
Additional Information
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  • United States

Compétences linguistiques

  • English
Avis aux utilisateurs

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