- Lilly (Lebanon, IN)
- …of regulatory requirements in GMP (Good Manufacturing Practice), such as FDA regulations for pharmaceutical manufacturing. + Solid knowledge of Computer System ... Validation process. + Excellent problem-solving skills to address complex IT issues and implement effective solutions in a timely manner. + Strong customer service and communication skills to maintain high end-user satisfaction. + Proficiency in handling IT… more
- Boehringer Ingelheim (Indianapolis, IN)
- …based. + Performs all Company business in accordance with all regulations (eg, EEO, FDA , DEA, OSHA, PDMA, EPA, PhRMA, etc.) and Company policy and procedures. When ... violations are noted/observed they are to be immediately reported to management. Demonstrates high ethical and professional standards with all business contacts in order to maintain BIPI's excellent reputation within the medical and pharmaceutical community.… more
- Abbott (Altavista, VA)
- …equipment issues You'll be accountable for meeting our compliance standards including FDA , OSHA and Abbott policies and procedures. **Shift** This is for the ... night shift. Example of shift: **Shift Hours:** 6am to 6:30 pm, on a rotating basis. **Week One:** Mon - On / Tues - On / Weds - Off / Thurs - Off / Fri - On / Sat - On / Sun - On **Week Two:** Mon - Off / Tues - Off / Weds - On / Thurs - On / Fri - Off / Sat… more
- Nestle (Gaffney, SC)
- …at all times. Unauthorized deviations are strictly forbidden + Comply with all FDA rules, procedures, and work practices + Follow all Nestle and GMP procedures ... + Maintain confidential information on recipes + Report all deviations from the recipe _Operations:_ + Responsible for accurately and efficiently preparing all media to be used in the micro lab + Maintain inventories of all in-house prepared media used for… more
- Lilly (Lebanon, IN)
- …+ Basic computer skills (desktop software) are required. + Solid understanding of FDA guidelines and cGMP requirements. + Strong organizational skills and ability to ... handle and prioritize multiple requests. + Strong technical aptitude and ability to train and mentor others. + Ability to work with a team, make independent decisions, and influence diverse groups. + Ability to instill teamwork within the shift and demonstrate… more
- Boehringer Ingelheim (Ridgefield, CT)
- …the adherence of facilities, operations, studies, reports and practices to regulations (eg FDA , EMEA, NRC, DEA USDA) as well as to BIPI Standard Operating Procedures ... (SOPs), BIPI policies, regulatory guidelines and good scientific and documentation practices. He / she will inform BIPI Management of deviations from the cGMP, GLP, other Regulations observed during audits/inspections, to recommend appropriate corrective… more
- Actalent (Lake Mary, FL)
- …Skills + Strong verbal and written communication skills + Knowledge of FDA Health Regulations + Proficiency in managing processes and ensuring legal compliance ... + Attention to detail and focus on quality Additional Skills & Qualifications + Minimum 1-2 years of experience as a Pharmacist in a retail or specialty pharmacy setting. + Bachelor of Science in Pharmacy degree required, PharmD preferred. + Current and valid… more
- United Therapeutics (Raleigh, NC)
- …daughter's pulmonary arterial hypertension( **PAH)** . Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... lung disease ( **PH-ILD** ) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis ( **PF** ). The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many… more
- ManpowerGroup (Chicago, IL)
- …in canned goods manufacturing. + Thermal Processing Experience and knowledge of FDA regulations. + Strong leadership and project management skills. + Ability to ... travel to the Milton, PA facility as needed (less than 20%). **What's in it for me?** + Opportunity to innovate and improve quality programs. + Work with a team of dedicated professionals in a reputable company. + Chance to develop and lead your own team in… more
- J&J Family of Companies (Santa Clara, CA)
- …compliance with the company's Design Control requirements and consistent with FDA , ISO, and MDD requirements. + Participate on cross-functional development teams ... that manage projects from concept through commercialization. + Responsible for knowing and planning activities consistent with the company's quality policy and quality objectives. + Responsible for ensuring lab notebooks are documented in a timely manner and… more
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