- Merck & Co. (Rahway, NJ)
- …technical strategies related to upstream processing and recombinant expression of drug candidates in early- and late-stage development .- Responsibilities include ... actively share expertise; guide career development; build strong, collaborative teamsChampion compliance and safety; promote a culture of diversity, inclusion, and… more
- Tris Pharma (Monmouth Junction, NJ)
- …Generics Leadership and team members, the incumbent follows proper protocols and compliance with regulatory and company requirements to handle and support standard ... tracks sales data and reports for the Generics team to ensure customer compliance , performance to budget and optimized sales efforts for existing and new… more
- Merck & Co. (Rahway, NJ)
- …strategies related to upstream processing and recombinant expression of drug candidates in early- and late-stage development.Responsibilities include, but are ... the functional area; guide career development; build strong, collaborative teams.Champion compliance and safety while promoting a culture of diversity, equity, and… more
- Merck & Co. (Rahway, NJ)
- …of actions.Experience in analysis of various Biologic modalities (eg, mAb, antibody- drug conjugate, fusion protein).Knowledge and experience in Antibody Drug ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Merck & Co. (Durham, NC)
- …our Intermediate Adjuvant manufacturing process and Sterile Supply manufacturing for Bulk Drug Substance. Focused areas of responsibility include but are not limited ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Merck & Co. (North Wales, PA)
- …analysis and reporting and submission standards that can be used for drug and/or vaccine projects across all therapeutic areas.Adheres to standard operating ... statistics, clinical trial, and data management concepts as applied to drug /vaccine development.Expertise in applying SAS for clinical trial programming including… more
- Legend Biotech USA, Inc. (Chicago, IL)
- …All KCM interactions are always within label, and consistent with commercial, compliance , legal and regulatory guidelines.The KCM will work closely, and within ... travel 75 - 85%.Must work within label, and regulatory and legal compliance guidelines.Required to exercise sound judgment and discretion, independently assess and… more
- Merck & Co. (North Wales, PA)
- …Activities:Provide support to statistical programming activities for late-stage drug /vaccine clinical development projects. Develop and execute statistical analysis ... have experience in CDISC and ADaM standards and in ensuring process compliance and deliverable quality.Significant expertise in SAS and clinical trial programming… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …and resolve manufacturing issues.Key Responsibilities Partner closely with Quality, Compliance , and technical experts to drive accelerated, robust, and consistent ... would provide reduction in COGs, increase throughput, capacity and quality compliance .Build strong partnerships with Manufacturing, Engineering and Quality to ensure… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …assign individuals their daily production task to execute and ensure compliance and successful completion of work-related tasks.Work closely with operations ... citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.Legend Biotech maintains a drug -free workplace. more
