- Merck & Co. (Rahway, NJ)
- …projects while adhering to management-approved strategic plans, corporate policies , and providing clear communication to cross-functional stakeholders, including ... external suppliers. Proactively resolve project obstacles and challenges and communicate device development strategy and design controls approach within Device Development and with external suppliers. Understand and apply regulatory / compliance requirements… more
- Aequor (Charles City, IA)
- …lab equipment, instrumentation and facility Following all Quality Standards, Policies and Procedures Providing minimum input for laboratory investigations (LIR), ... minimal project support Understanding of the QC software packages used during routine work Understanding of MODA EM software and zLIMS/SAP software Pipette work Preparation of media and reagents Media Fill inspections Equipment Monitoring Following Safety… more
- Cipla (Fall River, MA)
- …their working area is clean. Adhere to CIPLA's Safety, Health, and Environmental policies . Other duties assigned as required by Reporting management / Dept. Head. ... Education QualificationsBachelor's degree in pharmaceutical sciences/ electrical/ mechanical / production or related fields of study.Experience5-11 years of experience in packaging, operations, team management. Preference will be given to candidates with… more
- Cipla (Fall River, MA)
- …all cGMPs, compliance/regulatory mandates and quality requirements. Complying with company policies and procedures. Performing duties through the proper safe use of ... equipment, according to Health & Safety procedures and Equipment Manuals. Performing other related duties assigned. Other Responsibilities: Maintaining 100% cGMP & Compliance during complete operation hours. Must follow the Departmental SOPs. Reporting all… more
- Merck & Co. (North Wales, PA)
- …with virtual meeting platformsConsistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field ... standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilitiesPreferredField-based medical experienceResearch ExperienceDemonstrated record of scientific/medical publication#eligibleforERPRequired… more
- Lundbeck (New Orleans, LA)
- …quality of work from self and others. Assures adherence to all standards, policies , procedures and guidelines as set forth by the organization. REQUIRED EDUCATION, ... EXPERIENCE and SKILLS: Bachelor of Arts or Bachelor of Sciences degree from an accreditedcollege or university External Candidates: Minimum of 3+ years sales management experience in Pharmaceutical, Biopharmaceutical's, Biologics or related experience.… more
- Lundbeck (Phoenix, AZ)
- …pharmaceutical and regulatory environment, including accountability and adherence to Lundbeck policies and procedures and FDA regulations regarding the promotion of ... pharmaceutical and medical products. REQUIRED EDUCATION, EXPERIENCE and SKILLS: Bachelor of Arts or Bachelor of Sciences degree from an accredited college or university 4+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …batch related records.Perform tasks in a manner consistent with the safety policies , quality systems and cGMP requirements.Review and approve SOPs, and other ... documentation.Drive continuous improvement.Have advanced computer skills to increase department's productivity, as well as broadening technical and scientific knowledge.Works in a collaborative team setting with quality counterparts that include Manufacturing… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …preventive actions (CAPA).Perform tasks in a manner consistent with the safety policies , quality systems and cGM Prequirements.Works in a collaborative team setting ... with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development. RequirementsA minimum of a Bachelor's Degree in Science, Engineering or equivalent technical discipline is required.A Minimum of 4 years… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …to help the team, in a manner consistent with safety policies , quality systems, and cGMP requirements.Support manufacturing investigations, create/revise operational ... procedures, including manufacturing work instructions, master batch records, forms, and support and manage change controls.Work closely with Operations Manager to help oversee the development of production personnel, provide input on personnel… more
