- Merck & Co. (Rahway, NJ)
- …strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects.- Positions may ... of inspection results and maintain accurate records of findings in an electronic system.- Knowledge of PAS-X is preferable.GMP: Follow established inspection batch… more
- Merck & Co. (Rahway, NJ)
- …strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects.- Positions may ... maintain good manufacturing practice (GMP) operations, using paper-based and electronic systems.Maintains detailed knowledge of process equipment and operations.-… more
- Merck & Co. (Rahway, NJ)
- …strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects.- Positions may ... of inspection results and maintain accurate records of findings in an electronic system.- Knowledge of PAS-X is preferable.GMP: Follow established inspection batch… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …labels and documents prior to use on the manufacturing floor.Utilize multiple electronic quality systems, batch records and SAP.Work in a team based, ... the assigned tasks.Strong proficiency utilizing relevant manufacturing applications (SAP), electronic batch records (EBR), and quality systems.Utilizes tools within… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …procedures.Support Document Management system users with workflow handling and electronic system usage.Manage the periodic review process for procedures.Issuance of ... EU GDP/GMP, Part 11/Annex 11, PIC/S, MHRA).Operational experience with electronic quality systems.Experience with Document Management Systems (TruVault/Veeva) is… more
- Eisai, Inc (Nutley, NJ)
- …for all of Eisai's products.Maintain centralized labeling repository within Eisai's electronic document management system for all global labels at various stages ... approval. Manage labeling development, review and approval workflows within the electronic documents management system and track the timely and consistent… more
- Insmed Incorporated (NJ)
- …Vault, and other similar software platformsKnowledge of 21 CFR Part 11, Electronic Records and Electronic SignaturesExperience with GAMP 5 guidelines and ... validation lifecycle processesIT System Project managementExperience managing vendor relationships for multiple software platformsWhere You'll WorkThis is a hybrid role based out of our Bridgewater NJ HQ office. You'll have the option to work remotely most of… more
- ALPCO (CA)
- …and documentation. Contribute to technical manuals, troubleshooting guides, and electronic reference resources. Apply strong analytical skills to resolve complex ... 5-10 years of experience diagnosing and repairing electromechanical or electronic laboratory equipment. Prior applications, field applications scientist (FAS), or… more
- Cipla (Fall River, MA)
- …SDS, FS, validation plan, FAT, SAT, IQ, OQ,PQ, validation certificate, PIR,RTM, electronic signature, electronic reports. Knowledge of 21 CFR and implementation. ... Knowledge of automation of pharmaceutical equipment. Education and Experience Associate's degree with 4-6 years knowledge and experience of GMP documentation required. Bachelor's degree in science, biochemistry, pharmaceutical engineering, Pharmaceutical… more
- Move Forward Counseling (Pittsburgh, PA)
- …client referrals Administrative support At least monthly clinical supervision Electronic health records system Opportunities for professional development Work ... Environment: Complimentary snacks and beverages Relaxed dress code Regular team social events Collaborative culture where your voice matters Work-Life Balance: Choose your own schedule (based on office availability) Hybrid schedule; work from home and office… more
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