2nd Shift QC Inspector at LIFE SCIENCE OUTSOURCING INC

Somersworth, New Hampshire, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Mar, 26

Salary

0.0

Posted On

18 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Attention To Detail, Communication, Organizational Skills, Customer Service, Team Player, Problem Solving, Quality Assurance, Manufacturing Knowledge, Regulatory Compliance, Testing Procedures, Documentation, Device History Records, Caliper Use, Good Manufacturing Practice, Quality Management Systems, Microsoft Office Suite

Industry

Medical Equipment Manufacturing

Description

Job Details Level: Experienced Job Location: LSO East NH - Somersworth, NH 03878 Life Science Outsourcing, Inc. (“LSO”) (www.lso-inc.com) is a contract manufacturing organization focused on assembly, packaging, sterilization, and packaging with over 25 years of experience. The Company serves orthopedic, cardiovascular, diagnostic, dental and a variety of other medical specialties. Our unique model is focused on in-house end-to-end portfolio processes and service offerings with deep regulatory knowledge. This provides the agility and flexibility that customers need to accelerate their go-to-market launches while standardizing their supply chain and mitigating risk. Clients rely on LSO to perform all activities required to introduce their products to market, from procurement to final packaging and shipping. LSO’s is headquartered in Brea, CA (North Orange County). In January 2023, the Company added its east coast facility in Somersworth, New Hampshire (formerly J-Pac Medical). We are currently seeking a self-motivated Customer Service Specialist with positive, engagement and collaborative energy to join our team and support the continued growth of the New Hampshire Facility. The Quality Inspector is responsible for quality assurance and quality manufacturing functions such as generating certificate of compliance, inspection and testing, disposition of product, incoming inspection, in-process and final inspection, review of DHRs (device history records). Essential Duties and Responsibilities include the following: (NOTE: Other duties may be assigned) Following written procedures for testing and legibly and accurately documenting all test data. Communicate test data results and findings that are outside specified limits Maintaining compliance to appropriate US FDA regulations and ISO 13485 Quality Management System standards by following written procedures. Submitting and maintaining test result documents Working directly with manufacturing and engineering personnel to test and inspect components and materials Promoting the smooth flow of products through quality control to disposition Providing test and inspection support to all new process developments Reviewing Device History Records (DHR) Reviewing all lab results and approve product release. Working in a team environment with all quality control inspection personnel The ability to use manual dexterity to measure, using rulers, calipers, micrometers, and other instruments. Special projects as necessary Education and Experience High school degree or GED equivalent required. Not Required but preferred: 2 years of experience in a medical device manufacturing or pharmaceutical environment, or 5 years’ experience in a general manufacturing environment. Knowledgeable in applications of caliper use, calibration and verification of tools, basic math skills and blueprints/drawings comprehension, IQ/OQ/PQ and quality principals. Basic knowledge of Good Manufacturing Practice. Basic knowledge in Quality Management Systems applicable to the medical device industry. Proficient in Microsoft Office Suite skills including electronic mail, record keeping, routine database activity, word processing, spreadsheets, graphics, etc. Skills and Abilities The Quality Inspector will have the following personal skills and attributes (in addition to the technical requirements for the job already mentioned): Attention to detail in a fast-paced environment Ability to work independently and take initiative Good interpersonal, communication (both verbal and written) Strong verbal and written communication skills Excellent organizational skills with the ability to handle multiple projects Passion for customer service and business growth Displays courtesy, tact and patience during interactions with all employees and customers Confident and creative Acts in an ethical manner at all times and demands the same in others Experience in process troubleshooting and timely resolution of issues. Eager to be a team player Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Individual will need to sit (at times for extended periods) or stand as needed. May require walking primarily on a level surface during the workday. Reaching above shoulder heights, below the waist or lifting as required to file documents or store materials during the workday.

Responsibilities

The Quality Inspector is responsible for quality assurance and quality manufacturing functions, including generating certificates of compliance, inspection and testing, and product disposition. They will work directly with manufacturing and engineering personnel to ensure compliance with FDA regulations and ISO standards.