Coder Salary at Lanhelper BETA

Bell International Laboratories is a complete solution and innovator, as experts in formulating and manufacturing high-quality products, including sun care, skin care, and consumer health products. Located in the Minneapolis/St. Paul metropolitan area, Bell International Laboratories is home to state-of-the-art manufacturing, warehousing, and laboratory facilities. More than 300 employees work in the facility, all dedicated to producing the highest quality products available. Position Summary: The Quality Assurance Document Control Specialist is a quality focused individual who ensures documentation and record keeping processes conform to cGMP and regulatory requirements as well as Bell International Laboratories approved procedures and output documents are accurate. The individual will assist in the day to day record management activities within Bell Labs complying with company and regulatory requirements. Responsibilities Perform QA document control functions, including document logi

A medical device manufacturer which specializes in precision injection molding and microelectronics is in need of an Automation Engineer to create and improve automated manufacturing processes. They are experiencing significant growth and pride themselves on fostering a collaborative environment where employees can grow within the company for many years. Your responsibilities will include: Design, evaluate, and improves automated manufacturing equipment, tooling, and processes. Lead workflow optimization, equipment layout planning, and cost/time estimation to support efficient production. Coordinate with cross-functional teams, vendors, and customers on project requirements and equipment specifications. Support automation acceptance (SAT/FAT), process validation (IQ, OQ, PQ, FMEA), and continuous improvement through data analysis (SPC, OEE). Prepares technical documentation, and contributes to engineering changes May provide training and mentorship to team members. Experience needed to

As a Project Engineer at GEA Group’s LPT division, you will support projects from initial customer meetings to commissioning and startup. You’ll develop technical solutions, specify equipment, and ensure timely, budget-compliant execution. Collaborating with global teams, you’ll assist with planning, documentation, compliance, and troubleshooting to deliver high-quality process solutions. Responsibilities / Tasks Participates in all phases of a project as required from initial customer meetings through pre-award sales support, cost estimation, proposal generation, engineering, commissioning and start up. As assigned by the Project Manager is responsible for specific technical areas of the project, engineering / sizing / specifying technical solutions and equipment which meet customer expectations/specifications within the time and budget constraints of the contract. Works with GEA Centers of Competency and Beverage Application Centers (worldwide) to deliver process solutions for GEA No

Job Description Job Description TTF is recruiting for a full time Coding Auditor with strong experience with DRG's, inpatient coding, auditing, revenue integrity and clinical documentation. This is a remote position and can be anywhere in the United States. The starting salary will depend on experience, with a alary range that will be $90,000-$110,000 per year with good benefits. Qualified candidates must have experience with DRG's, revenue integrity, and working within CDI and inpatient claims. A coding certificate with CCS, RHIT, or a CCDS is preferred. Please send your resume to Chelle at cbodnar@ttfrecruit.com for consideration. TTF is a healthcare search and staffing firm that works with the outstanding companies to find the best talent. Our service is free to all candidates and all conversations are kept confidential. We place candidates in areas such as Clinical Documentation Improvement (CDI), Coders, Coding Auditors, Nurse Auditors, Revenue Integrity Auditors, and DRG Auditors

Job Description Job Description Please join our company that is experiencing tremendous growth! We continue to grow and need your qualifications to fulfill our customer's needs. The starting pay listed INCLUDES a very generous bonus pay program, and could be higher if business continues to grow at the current pace. Our company manufactures products for use in the telecommunications and utility industries. Yes, we make products for companies that make sure we are all connected, whether it's pulling cable for internet or some other infrastructure...we are the company that supplies what they need. So not only will you be earning money working with a great group of dedicated people, you will be making a difference in making a better connected world! Core duties: · With basic knowledge of production processes, performs duties for the manufacture of chemical products and lubricants. · Ensure quality and consistency in production processes by operating and monitoring production equipment such

Job Description Job Description Position Summary: The Quality Assurance Document Control Specialist is a quality focused individual who ensures documentation and record keeping processes conform to cGMP and regulatory requirements, approved procedures, and ensures completed records are accurate and compliant. Assist in the day-to-day record management activities within Bell International Laboratories complying with company and regulatory requirements. Key Responsibilities: Perform QA document control functions, including document logging, tracking, processing, review, distribution, release and archiving of documents. Review, approve and formally release batch records that comply with requirements. Coordinate the revision, review, and approval and obsoleting of SOPs and other GMP documents. Responsible for ensuring compliance with document control requirements, such as periodic review of documents. Facilitate improvements to procedures by working with document owners to resolve conflict

A Senior Process Automation Engineer acts as a key member of the automation engineering team supporting Service Project upgrades within the Liquid and Powder Technologies Division of North America. The individual designs, tests, and commissions industrial process automation systems. The engineer will take a lead role and be able to work independently on their portion of the project. Projects may be comprised of different technologies consisting of Food, Dairy, Beverage, Brewery, Chemical, Pharmaceutical, and New Food business units. Responsibilities / Tasks Essential Duties/Responsibilities: Support sales to drive the automation upgrade and digital service products business. Participate in the sales phase of projects including customer meetings, pre-sales support, cost estimation, and proposal generation. Generates detailed process Functional Descriptions (FDs) from general process descriptions. Coordinates with the product departments to ensure the programming meets requirements. Coor

A Health, Beauty and Cosmetic Manufacturing Client is looking for a direct hire, Quality Engineer onsite in Eagan, Minnesota. The objective of this role is to improve quality within production to meet our customer’s needs and expectations. This Quality Engineer will focus on process and equipment improvements, develop quality control systems and processes, and attack quality system failures using effective root cause analysis methods. Additionally, this role will concentrate on continuous improvement through the implementation of effective Corrective and Preventive Actions (CAPA). The Quality Engineer will play a key role in ensuring that products meet industry standards, regulatory requirements, and internal quality objectives, while promoting a culture of compliance and continuous improvement across the organization. Responsibilities Lead quality-related problem-solving and root cause analysis in manufacturing to prevent recurrences. Lead process validation, equipment qualification,