- Fotona (Philadelphia, PA)
- …States, in accordance with Fotona-approved protocols and guidelines. + Strictly adhere to FDA clearances and compliance. + Successful completion of 6 to 8 trainings ... per month. + Act as a key point of contact for customers and colleagues on medical inquiries, product protocols, and clinical applications. + Contribute to creating a positive internal working environment and successful business relationships between Fotona… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …or equivalent experience in leading projects. + Knowledge of the FDA medical device quality system regulations and international quality system standards/regulations ... (eg ISO 9001, ISO 13485) as it relates to the design and continued support of BD products. + Can develop strategy, plan projects, and drive the completion of long-term goals and objectives. + Able to use judgement to influence within and across functions to… more
- Integer Holdings Corporation (Chaska, MN)
- …Environmental and Security Management Systems, US Food and Drug Administration ( FDA ) regulations, company policies and operating procedures, and other regulatory ... requirements. * Operates and sets up CNC shop equipment with minimal assistance. * Accountable for meeting cycle time and yield expectations. * Ability to simultaneously operate more than one machine as required. * Sharpens and changes tooling as needed to… more
- Astrix Technology (Piscataway, NJ)
- …projects to support product and process integrity. + Ensure ongoing compliance with FDA , EMA, ICH, and other global regulatory standards. + Provide leadership and ... mentorship to quality team members; foster collaboration across manufacturing, validation, and regulatory teams. + Support audits, inspections, and regulatory reviews, ensuring readiness and robust documentation. + Drive continuous improvement initiatives,… more
- Charles River Laboratories (Spencerville, OH)
- …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
- Veterans Affairs, Veterans Health Administration (Brownsburg, IN)
- …needed. Research a. Participation in research activities must be in accordance with FDA guidelines and regulations and VHA policy. b. Coordinates the receipt and ... distribution of all drugs in an investigational and/or clinical evaluation status and maintains appropriate records regarding their use as applicable. c. Serves as primary investigator for pharmacy resident and/or student research projects as necessary. Work… more
- Actalent (St. Paul, MN)
- …+ Proficiency in APQP, PPAP, and SPC. + Experience with ISO9001, ISO13485, or FDA . + Familiarity with Epicor or similar ERP systems. + Experience in print reading, ... cGMP/GDP, GD&T, and cosmetic specifications. + Ability to manage multiple projects concurrently. + Excellent verbal and written communication skills with proficiency in Microsoft Suite. + Experience with change control, revision change, and documentation. Job… more
- Charles River Laboratories (Mattawan, MI)
- …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
- Arvinas (New Haven, CT)
- …mutations. On August 8 th 2025, the US Food and Drug Administration ( FDA ) accepted the New Drug Application (NDA) for vepdegestrant- an investigational, orally ... bioavailable PROTAC estrogen receptor degrader- for its use as a monotherapy in the treatment of adults with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer… more
- Actalent (Wharton, NJ)
- …tools. Minimum 3+ years of experience in a regulated industry (eg, FDA , EPA, ISO), preferably in manufacturing or quality assurance roles. Demonstrated experience ... performing in-process quality inspections, line clearances, material disposition, and documentation review. Experience supporting trials, validations, rework activities, and sample collection for customers, retains, or stability programs. Prior exposure to… more