Quality Auditor Salary at Tyndale Usa BETA

job summary: A worldwide manufacturer in Eastern PA is looking a Quality Engineer to support their supplier programs. Candidates must have a Bachelor's degree in Engineering or related discipline. Will need 5 years' of experience in a Supplier Quality Engineering role with demonstrated success in supplier qualification, management, correction, and development. Could be up to 50% travel. Relocation assistance, salary, bonus and benefits. location: EASTON, Pennsylvania job type: Permanent salary: $110,000 - 118,000 per year work hours: 8am to 4pm education: Bachelors responsibilities: Working with Sourcing and other functional groups, the incumbent will drive the Supplier Qualification Process for all existing and prospective suppliers in-country, in accordance with corporate procedures. Responsible for supplier qualification in conjunction with Sourcing and other applicable groups for the introduction of new suppliers, products, and production processes. Responsible for supporting all e

Supports the Senior Quality Manager in directing the quality assurance program for the plant. Performs duties relating to inspection, laboratory testing, statistical process control and salvage operations. Implement, maintain and modify as appropriate the companies/plant's quality management system to improve business operating systems and meet the requirements of customer and best practice audits. Lead/assist with the corrective action of quality related problems at the plant and/or customer location and start-up of new products/processes. Assist in troubleshooting technical problems. Drives the Global Food Safety Initiative program compliance. ESSENTIAL DUTIES AND RESPONSIBILITIES: Ensures operations are completed in accordance with Amcor Rigid Plastic’s safety procedures and ensures team members are working in a safe manner. Identifies and corrects unsafe work practices and procedures. Communicate with and visit customer to understand the performance of our product and evaluate thei

We are global, we are impacting the lives of millions every day, we are making a difference! At Amcor we are inspired to change the packaging industry and are taking on the aspirational challenge to make all our products recyclable or reusable by 2025. Through our products and global footprint, we are in a unique position to truly make a difference in the packaging space. Our products impact the lives of millions of people across the globe every day from food, beverage, pharmaceutical, medical, home- and personal-care, and other essential products. Amcor is a thriving S&P 500 organisation listed both on the NYSE (AMCR) and ASX (AMC) with US$13 billion in sales. We have a proud history dating back to the 1860's and come a long way from a single paper mill based in Melbourne to becoming the global leading packaging company. Today, Amcor is an international organisation empowering its 50,000 employees in over 40 countries and across 250 sites. Will you be next to join our journey towards

Quality Assurance Manager (Pharmaceutical) Strong working knowledge of cGMP and FDA regulations Experience with GMP & GCP audits preferred ASQ Quality Auditor Certification preferred Are you looking to make a career change to a rapidly growing company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance and paid PTO. Does this position match your future career goals? Then this opportunity could be the right fit for you Why should you apply for Quality Assurance Manager (Pharmaceutical) position? A positive workplace culture Competitive Salary Career Advancement opportunities Financial Growth Education and Experience Requirements: Bachelor's degree in Science Strong working knowledge of cGMP and FDA regulations Experience with GMP & GCP audits preferred ASQ Quality Auditor Certification preferred Internal and External auditing. Perform batch record reviews and manage product disposition tasks as needed. A

RLG Healthcare, a division of Resource Label Group, LLC, leads the way in providing innovative packaging solutions to the Healthcare market. RLG Healthcare provides a one-stop shop for all pharmaceutical packaging needs including labels, folding cartons and boxes, inserts, outserts, IFUs and DFUs, Med Guides, and physician support literature. Our industry-best lead times are made possible by our coast-to-coast manufacturing footprint and our dedicated team of packaging specialists with a passion for quality and service. We are currently seeking a highly motivated and experienced Quality Assurance Manager to lead our commitment to quality, operational efficiency, and excellence at RLG Healthcare in Windsor, NJ. As the QA Manager, you will be responsible for developing, implementing, and maintaining a comprehensive Quality Management System and play will play a key role in fostering a culture of quality, efficiency, and continuous improvement at the facility. Responsibilities: Develop, i

About Orchestra BioMed Orchestra BioMed is a biomedical innovation company accelerating high-impact technologies to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s vision is to accelerate medical innovation to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s partnership-enabled business model focuses on forging strategic collaborations with leading medical device companies to drive successful global commercialization of products it develops. Orchestra BioMed is led by a highly accomplished, multidisciplinary management team and a board of directors with extensive experience in all phases of therapeutic device development. Orchestra’s business was formed in 2018 by assembling a pipeline of multiple late-stage clinical product candidates originally developed by its founding team. Its flagship product candidates are BackBeat CNT for the treatment of hypertension, the lead

Carbel, part of Arvato, is a full-service 3PL provider serving national and international clients across various industries, with a strong focus on fashion and retail. The Inventory Quality Auditor is required to verify units being shipped out and ensure they follow the correct SOP. Ability to use Microsoft Office, Outlook and Access. Auditors pull parcels off the line and verify the shipping label, pack slip, units match the pack slip, verify packing requirements are met for each client. All audits are captured via database and reported back to the client. YOUR TASKS Unpack returned merchandise, inspect package condition and assess paperwork sent in with return instructions for proper return procedures Ensure that all shift personnel receive proper training, skill development, and assessment per company guidelines Receive merchandise, following all security and safety return procedures for each product type Distribute returned items to their proper location considering all factors inc

With Staff Management | SMX, you'll get a weekly paycheck, learn new skills, meet new people, and work with a great management team in a clean and safe environment. In this role, the QA Technician enables conformance to Mars Quality and Food Safety specifications and compliance to all regulatory requirements through the verification and execution of quality control protocols and monitoring of sampling and testing plans applied to packaging and product. The QA Technician contractor is a member of the Chalfont, PA site Q&FS team and is an on site position. . Perks & Benefits: Casual Dress Code, Paid Training, Weekly paychecks. Shifts: 1st Shift. Employment Types: Full Time. Pay Rate: $20.00 - $22.50 / hour Duties: 0-2 years of relevant experience in manufacturing or experience in a technical support area (2+ years preferred) Associate degree preferred Excellent analytical and troubleshooting skills to discover issues and to verify the accuracy of information, results, and data General kn