- Charles River Laboratories (Houston, TX)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your ... quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.… more
- Houston Methodist (Houston, TX)
- …conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than 1,387 clinical research ... protocols and $70.3 million in extramurally funded translational research programs. Houston Methodist is an Equal Opportunity Employer. more
- POWER Engineers (Houston, TX)
- …process safety requirements and environmental concerns such as OSHA PSM, EPA RMP, FDA GMP regulatons, etc. + Software use knowledge with AutoCAD software suites, ... Revit, Navisworks, Plant P&ID, AspenPlus, MS Projects, etc. + Hands on experience developing process simulations such as Aspen Plus + Production experience is a plus + Ability to participate in a design team environment roles + Ability to delegate and mentor… more
- Medtronic (Fort Worth, TX)
- …with sourcing and/or supplier management for products or services within an FDA -regulated medical device, biotechnology, or pharmaceutical industry is a strong plus. ... + Strong communication skills (verbal/written) and internal/external partnering skills. + The ability to negotiate with suppliers to reach agreement on optimal contract terms and conditions. + Strong working knowledge of contract documentation, interpretation,… more
- Actalent (Fort Worth, TX)
- …position is onsite What You'll Do: + Educate and counsel patients on FDA -mandated REMS medications + Support medication adherence, refill scheduling, and side effect ... management + Collaborate with pharmacy teams to ensure timely drug delivery + Maintain accurate documentation and ensure compliance with REMS protocols + Report adverse events and product complaints as required What We're Looking For: + Active Texas RN license… more
- Fujifilm (College Station, TX)
- …objectives. + Strong understanding of 21 CFR Part 11 and Annex 11 regulations, FDA , GMP, GAMP and ISPE.Develop staff to maximize contributions to the team and the ... company. + Ability to multitask and easily prioritize work. + Ability to work independently with little supervision. + Proficient in Microsoft Excel, Word and PowerPoint. + All candidates must have a working knowledge of cGMP regulations for the production of… more
- Houston Methodist (Houston, TX)
- …conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than 1,387 clinical research ... protocols and $70.3 million in extramurally funded translational research programs. Houston Methodist is an Equal Opportunity Employer. more
- Urology Clinics of North Texas (Dallas, TX)
- …terminology (Oncology and Urology preferred). + Knowledge of good clinical practice, FDA , OHRP, HIPAA policies. + Proficiency with the Microsoft Office Suite, Google ... Docs, SharePoint. + Meticulous attention to details Qualifications Job Qualifications: + At least 1 year of experience in a clinical research setting, often transitioning from an assistant role + Prior experience in an oncology or urology setting preferred +… more
- OTG (Houston, TX)
- …a plus. + Experience working with unionized employees preferred. + Knowledge of FDA and/or major US metropolitan city health code adherence. + Proficiency in food ... costing, menu planning, inventory management, and procurement. + Strong written and verbal communication. + Proficiency with Microsoft Suite and kitchen management software. + Must be able to work varied hours/days, nights, weekends, holidays, and during… more
- Cardinal Health (Austin, TX)
- …False Claims Act, Civil Monetary Penalties Law, Stark, Beneficiary Inducement Statutes), FDA regulation (Food, Drug & Cosmetic Act), and privacy (HIPAA). * Draft, ... negotiate and review a wide range of agreements, including complex matters relating to manufacturer supply agreements and co-marketing arrangements. * Advise and ensure that internal clients receive sound, practical and timely legal advice on a wide variety of… more