- Abbott (Alameda, CA)
- …Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures. + Collects, organizes, and monitors information ... related to quality and process improvement. + Participates in internal &...experience in regulated environment such as medical devices or pharmaceutical products. + Knowledge of medical device standards including… more
- Kerry (Blue Earth, MN)
- …world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier ... About the role Role Description, Skills, Experience and Qualifications required: The Quality Control Technician is responsible for adherence to and compliance with… more
- Charles River Laboratories (Cleveland, OH)
- …to reduce error and deviations. Assist with implementing and monitoring quality control (QC) standards, methods, and procedures. Essential Duties and ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more
- Integra LifeSciences (Mansfield, MA)
- …* Working knowledge of DFSS techniques * 8 years of experience in a Quality Assurance role for medical device or pharmaceutical product development * Fluent ... standards of care. This **Staff Design & Reliability Assurance Quality Engineer** is a key functional role within the...2019), MDD (Medical Device Directive), IEC 62366, ISO 13485 ( Quality Management Systems), FDA QSR and cGMP. * Strong… more
- ThermoFisher Scientific (St. Louis, MO)
- …areas when production is on-going to coordinate activities from a quality perspective and provide QA-related input. + Perform manufacturing batch record ... team need to acquire agreement and collaboration to address issues and uphold quality culture and standards in Operations without direct authority. Using tact and… more
- Kelly Services (West Chester, OH)
- **Kelly Science & Clinical has a new temp-to-hire opportunity for a Quality Technician in West Chester, OH!** **A Temp to Hire Opportunity** **Shift:** M-F | 9am-5pm ... documentation practices + Maintain complete records in laboratory notebooks and quality records. + Conduct visual inspections and routine sampling using… more
- Actalent (Vacaville, CA)
- …of inspection readiness at all times. Key Requirements: - 1-3 years of Quality experience in the pharmaceutical or biopharmaceutical industry, preferably in a ... Description: We are looking for a motivated and experienced Quality Systems Support Specialist to join our team in...CA. This role involves providing vital support to our Quality System Management process through document control and PQS… more
- Merck (Rahway, NJ)
- …packaging & device development and technology teams, supply chain, operations, quality , analytical, regulatory, and project leaders. The successful candidate will ... platforms (eg syringes, auto injectors, bottles, blisters) meet safety, efficacy, quality , and robust supply standards. + Drive proactive risk management activities,… more
- Gilead Sciences, Inc. (Frederick, MD)
- …global regulatory requirements, marketing authorization holder expectations, and internal quality standards. + Manages QA personnel, including organizing and ... processes, procedures and controls to ensure that performance and quality of products conform to established standards and agency...PhD with 8+ years of relevant experience in the pharmaceutical industry OR + Master's degree with 10+ years… more
- Actalent (Riverside, CA)
- Job Title: Quality Assurance Documentation Specialist Job Description The Quality Assurance Documentation Specialist will organize and maintain GMP, ISO, and ... Skills + 1-2 years of QA experience, preferably in the nutraceutical or pharmaceutical industry. + Strong experience in documentation within a related industry. +… more