- Charles River Laboratories (Wilmington, MA)
- …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
- Lilly (Pleasant Prairie, WI)
- …or directly supporting a pharmaceutical manufacturing operation + Strong understanding of FDA guidelines and cGMP requirements + Must pass a post offer physical ... exam. + Must pass eye exam and not be color blind. + Must be able to work in shift structure **Additional Skills/Preferences:** + Bachelor's Degree in a life science, engineering, or technical field + Excellent interpersonal, written and oral communication… more
- Actalent (Madison, WI)
- …Experience in quality assurance within a regulated industry. + Familiarity with GMP, FDA , and ISO standards. + Proficiency in batch record review, document control, ... and CAPA. + Ability to conduct audits within the pharmaceutical sector. Additional Skills & Qualifications + Bachelor's degree in any science discipline preferred. + For Specialist: Minimum of 2+ years of experience in a regulated industry. + For Sr.: Minimum… more
- Boehringer Ingelheim (Dayton, OH)
- …Performs all Company business in accordance with all regulations (eg, EEO, FDA , etc.) and Company policy and procedures. + Immediately reports noted/observed ... violations to management. + Manages an assigned territory. + Responsible for the sales and marketing objectives for the assigned territory under the direction of the TBM/Sr.TBM. + Works effectively with all customer-facing roles (ie, Account teams, Medical… more
- Imperative Care (Campbell, CA)
- …catheters, endovascular or neurological devices. + Working knowledge about quality system requirements ( FDA 21 CFR Part 820 and/or ISO 13485), as they relate to ... quality control processes and good manufacturing practices. + Strong communications skills (written and verbal). + Strong ability to perform multiple tasks concurrently with high level of accuracy. + Proficiency with Microsoft Office products. Employee… more
- ManpowerGroup (Vadnais Heights, MN)
- …PQ validation activities. + Working knowledge of ISO 13485 and applicable FDA quality system requirements. + Experience supporting customer audits and quality ... discussions. + Strong root cause analysis and corrective action experience. + Ability to manage multiple projects concurrently. + Strong understanding of print reading, cGMP/cGDP, GD&T, and cosmetic specifications. + Experience with Epicor or similar ERP… more
- Abbott (Abbott Park, IL)
- …in Computer Science, IT, MIS, or related field. + Experience in FDA -regulated environments. + Familiarity with risk-based planning and project management best ... practices. + Strong vendor management and stakeholder engagement skills. **Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** www.abbottbenefits.com Follow your career aspirations to… more
- Owens & Minor (Forest Park, GA)
- …Training Program. + Must meet job-related requirements to comply with DOT, FDA and standards of accrediting body. **Language Skills** + English (reading, writing, ... verbal). **PHYSICAL DEMANDS** While performing the duties of this job, the employee uses his/her hands to finger, handle or feel objects, tools or controls; reach with hands and arms; stoop, kneel, or crouch; talk or hear. The employee uses computer and… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …robust field action solutions. + Familiarity with CAPA, risk management, and FDA documentation. + Strong writing and organizational skills. + Detail-oriented and ... comfortable working in a fast-paced environment. + Knowledge of ISO 14971, ISO 13485, ISO 9001, 21 CFR Part 820 At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential… more
- Novo Nordisk (Plainsboro, NJ)
- …governing the CMR organization's functions, including fraud-and-abuse laws, FDA regulations, ICH guidelines GxP requirements, pharmacovigilance, and relevant ... privacy laws and regulations + Provide general legal support, when required, to other North American affiliates, including on a broad range of collaboration activities, research-operations matters and strategic-business initiatives + Collaborate with Legal… more