- ThermoFisher Scientific (Greenville, NC)
- …unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo ... responsibilities:** + Coordinate and align with activities related to pharmaceutical development projects, ensuring flawless execution of reception, storage,… more
- Quality Consulting Group (Villalba, PR)
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... USA. Responsibilities: + Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including… 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
- Actalent (St. Louis, MO)
- …and being front-facing in audits and inspection readiness. + Experience with Quality Systems, including change control , root cause analysis, deviations, ... Quality Engineer III/Regulatory Compliance Specialist Job Description The...role. + BS Degree in STEM. + Experience in pharmaceutical or medical device industry, with preference for pharmaceuticals.… 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
- United Therapeutics (Morrisville, NC)
- …**Who You Are** Are you passionate about creating processes to support combination product quality control testing? In this role you'll be part of a 'greenfield' ... We Are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public...+ Technical and leadership experience in GMP, combination products Quality Control laboratory + Experience reviewing new… more
- Actalent (Waunakee, WI)
- Quality Assurance Specialist Shift available: 3rd shift, rotating 3 on/2 off/2 on/3 off; 4pm-4am Job Description The QA Specialist will primarily be active on the ... specific gowning requirements in designated areas. Essential Skills + Experience in quality assurance within a regulated industry. + Familiarity with GMP, FDA, and… more
- Actalent (Grand Rapids, MI)
- Job Title: Quality Assurance Associate Job Description The Regulatory Affairs Specialist plays a crucial role in overseeing regulatory affairs activities for a ... for FDA approved commercial products for Cares Act Reporting. + Facilitate quality agreements with clients, ensuring alignment with regulatory requirements. + Submit… more
- Mentor Technical Group (Juncos, PR)
- …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... Mexico, Germany, Canada, and South America. Responsibilities: + Expertise in Quality Systems such as Deviations (Non-conformities, CAPA, and Change Control… more
- Genentech (South San Francisco, CA)
- …on best practices for data collection, propose innovative solutions, and ensure high- quality , compliant data. + Use surveillance tools to review data at an ... aggregate level, identifying patterns or anomalies to ensure high- quality results. + Organize and integrate data from various sources, maintaining its value through… more