The Quality Engineer will be an active and integral participant in all phases of our manufacturing processes and the quality systems. Understand and comply with ISO/GMP quality standards; demonstrate behaviors in support of quality work processes. Bachelor’s degree or higher in Engineering with an e...
Here at Appian, our core values of Respect, Work to Impact, Ambition, & Constructive Dissent & Resolution define who we are.In short, this means we constantly seek to understand the best for our customers, we go beyond completion in our work, we strive for excellence with intensity, & we embrace can...
The candidates will be reviewing technical files from a quality perspective. ...
The candidates will be reviewing technical files from a quality perspective. ...
Job Title: Supplier Quality Engineer. Quality Assurance or Engineering in the passenger rail car business or a closely related field, plus. Generate necessary reports with follow up to closure on task open at Suppliers facility relating to quality. Assist in review, development, and implementation t...
The Quality Management Systems Engineer is responsible for supporting Spellman QMS for adherence to ISO Standards and other quality engineering functions as assigned. Other Quality Engineering functions as assigned. Spellman High Voltage Electronics Corporation, a family owned business for over 75 y...
Notifies Quality Improvement Specialist when abstraction is completed. ...
Manufacturing Engineers develop and improve manufacturing processes by studying products and manufacturing methods. Manufacturing Engineers design, control, and improve the manufacturing process and system design through a collaborative effort with the value stream team. They provide engineerin...
Onsite position Monday to Friday located in Syosset, New York.Responsible to lead the supplier approval program at the company's co-manufacturing and co-packaging facilities for compliance to QA/QC policies and standards.Work along-side multiple departments with all aspects of product roll-out and c...
Process Development Engineer III: Upstream Development Gene Therapy. A Typical Day in the Role of Process Development Engineer III Might Look Like:. Masters degree with 5-7 years of experience in either Chemical Engineering, Biochemical Engineering, Biochemistry, or related field. Regeneron's Precl...
Judge Direct Placement is seeking a Quality Assurance & Safety Manager in Orangeburg, NY area! The qualified individual will ensure consistent production of quality, safe product by following government and corporate guidelines. They will supervise all Quality Assurance associates. The QA Manager wi...
Coaches, mentors, and leads all employees in the Quality Assurance Manager’s areas of responsibility to achieve goals and objectives related to quality control, quality assurance, customer demands, and customer specifications. Creates and implements KPI’s for quality assurance and quality control. C...
The Radiology Quality and Safety Manager serves as a role model and works collaboratively with departmental leaders and staff to ensure a smooth functioning, high-quality (efficient and effective) patient care operations with evidence-based practices that support all quality pillars within the Depar...
Support integration and test, evaluate test results, investigate discrepancies, provide technical assessment of anomalies, and drive issues to resolution. You'll be part of a small agile team of other engineers working with other similar teams to build products larger than you thought possible w...
Within this role you will be responsible for the administration, configuration, implementation, maintenance and ongoing support of various Manufacturing equipment specific applications and Systems in a cGMP environment. As a Automation Engineer, a typical day might include, but is not limited to, th...
Knowledge of extrusion processes or polymer processing unit operations. Our hiring client is providing R&D Process Development expertise to these manufacturing companies. Engage in cutting-edge chemical technology development, in this environmentally friendly “green” process development effort. The ...
Country Manager (Production, Sourcing & Quality) . Team! This person is expected to lead the Sourcing, Production, and Quality strategy definition and execution for both, our Apparel and our Beauty businesses, maximizing factory compliance, quality standards, and on-time productions, to achieve our ...
QA experience in pharmaceutical industry (OTC preferred) with a thorough knowledge of Quality Systems, Quality Assurance, and Quality Control in a cGMP environment. Manager will hold a key position in our Quality & Regulatory Affairs Department. This individual will support existing products and new...
Maintains a leadership role in providing Quality and Compliance oversight of site operations inclusive of but not limited to Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requir...
Knowledge of extrusion processes or polymer processing unit operations. Our hiring client is providing R&D Process Development expertise to these manufacturing companies. Engage in cutting-edge chemical technology development, in this environmentally friendly “green” process development effort. The ...
Under general supervision, the selected candidate will perform environmental engineering work of moderate difficulty and responsibility in the office and field and will receive training in engineering work. A baccalaureate degree in environmental, chemical, mechanical, petroleum, aeronautical, or ma...
Quality Control Inspector (Level 1) . Quality Control Inspector is primarily responsible for inspections of the product throughout the manufacturing process, including cleanroom and carton room. Immediate reporting of all non-conformances observed as well as any compromises to quality to Quality Ass...
Quality Compliance Specialist - Change Control. Quality Compliance Specialist - Change Control. Quality Assurance Change Control Team. Knowledgeable in Biotech/ Pharmaceutical Quality systems inclusive of cGMP, FDA regulations and familiarity with ICH guidelines and global regulatory. ...
Participates in preparation of Performance Improvement reports for care services presentation at committee meeting; reports to Hospital Quality Management for external benchmarking as needed. Participates in special projects related to quality issues; assists in recommendations and coordinating impl...
The Area Manager Quality will lead our QA teams to ensure Good Manufacturing Practices (GMPs) & sanitation meet our high-quality standards to provide the best service to our customers. Report defective materials or questionable conditions QA Manager. Update quality numbers in the computer system; ca...