- Penn Medicine (Philadelphia, PA)
- …with all applicable federal, state, and local regulatory standards (eg, TJC, DOH, FDA , HIPAA, HCFA, DPW, LCGME, SCGME). + Be flexible and readily adopt new ... processes and engage in practice operation changes. Credentials: + Epic Certifications (Required) + Must successfully complete/pass EPIC schedgistration training/tests Education or Equivalent Experience: + HS Diploma/GED (Required) + Associate of Arts or… more
- JBS USA (Souderton, PA)
- …operations. + Familiarity with regulatory requirements and industry standards (eg, USDA, FDA , and OSHA) related to sanitation, safety, and food handling in the ... meat packing industry. + Excellent attention to detail and the ability to identify potential hazards or non-compliance issues in a fast-paced production environment. + Strong communication and interpersonal skills to effectively train and educate employees on… more
- Aerotek (York, PA)
- …their expertise in conductive printing, ablation, biosensors, and drug devices, adhering to FDA , ISO, and ISO 9001 standards. We are seeking machine operators who ... can contribute immediately, especially those with previous printing experience. **Responsibilities** + Operate semi-automatic and automatic press equipment. + Set up and operate various printing support machinery for pre and post-print applications. + Operate… more
- J&J Family of Companies (Horsham, PA)
- …Marketing and/or Sales Management). + Knowledge of pharmaceutical marketing including FDA regulatory and legal environment and compliance regulations is required. + ... Proven commercial experience, preferably within marketing education, demonstrating ability to drive business growth and strategic initiatives + Proven ability to understand business strategy and translate it into education solutions that support the company's… more
- CSL Behring (PA)
- …or policy work is beneficial. + Previous interaction with regulatory agencies such as FDA is a plus. **BENEFITS** + Medical, Dental Vision + 401K + Paid time ... Off \#LI-Hybrid **Our Benefits** CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …pharmaceutical and biotech industries + Knowledge and experience in cGMP and FDA regulated working environments is desirable + Quotations/QARs to completion, with ... coaching and support as needed + Use of manual dexterity is required + The employee is required to talk and hear **Why you should join Catalent** + Defined career path and annual performance review and feedback process + 152 hours of PTO + 8 paid holidays +… more
- J&J Family of Companies (Horsham, PA)
- …biologic / biotech, or medical device sales experience defined as selling FDA approved pharmaceutical or device product(s) to licensed healthcare professionals (ie ... MD, NP, RN, etc.) Preferred Qualifications: . Participation and/or completion of aJ&J Management Development Program (Field Development Program, DM Prep Program) or prior management experience required in lieu of FLDP or DMPP . Management and/or supervisory… more
- Charles River Laboratories (Wayne, PA)
- …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
- ManpowerGroup (Milton, PA)
- …or experience with thermal processing validation (retort, UHT). + Strong knowledge of FDA low-acid canned food (LACF) and aseptic regulations (21 CFR Part 113 & ... 114). + Experience with GFSI schemes (SQF, BRC, FSSC 22000) and audit procedures. **What's in it for me?** + Opportunity to lead and influence quality assurance practices in a dynamic environment. + Engage in continuous professional development and training. +… more
- Pfizer (Collegeville, PA)
- …+ Strong knowledge of clinical procedures, ICH guidelines,GCP and familiarity with FDA , EMA, and global regulations. + Strong scientific writing skills and ... communication skills (written and verbal) + Clinical document writing experience (eg, protocol, ICD, IB, IND), as well as understanding complex data analysis. + Track record of scientific productivity as evidenced by publications, posters, abstracts and/or… more