| URGENT :: Process Engineer (Pharmaceutical GMP) :: Parsippany, NJ :: at Parsippany, New Jersey, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2330106&uid= From: UTTAM BARMAN, SONITALENTCORP [email protected] Reply to: [email protected] Job Title: Process Engineer (Pharmaceutical GMP) Location: Parsippany, NJ - Onsite - Local Duration of project: 12 months Required visa: Any visa (Excepet H1B and CPT) Mode of Interview: Video End Client Name: Confidential Important Notes Below: I hope this is a hands-on process engineer that has spent the last 4 to 8 years on site at a manufacturing Pharmaceutical company with 100% hands on Equipment experience THIS IS NOT A VLADIOTION ROLE PLEASE DO NOT SEND VALIDATION, only people that have done this job 100% onsite And please do not forget the references for current assignment or last assignment, I am sure they can supply a reference from the last or current client project client reference NOT a consultant Position Description: - - experience with lyophilizers & autoclaves The ideal candidate will possess a strong technical background in pharmaceutical manufacturing processes, with specific expertise in autoclaves, lyophilizers, and fillers. This role requires a hands-on approach to providing technical support, troubleshooting complex issues, and driving solutions to ensure efficient and compliant manufacturing operations. Responsibilities: Provide hands-on technical support for pharmaceutical manufacturing equipment, including autoclaves, lyophilizers, and fillers, to ensure optimal performance and minimize downtime. Troubleshoot and resolve process deviations and equipment malfunctions, conducting root cause analysis and implementing corrective and preventative actions (CAPA). Develop and optimize manufacturing processes, ensuring compliance with cGMP regulations and company standards. Design and execute process validation studies, including IQ/OQ/PQ protocols and reports. Develop and maintain process documentation, including standard operating procedures (SOPs), batch records, and technical reports. Identify and implement process improvements to enhance productivity, reduce costs, and improve product quality. Provide technical training to manufacturing personnel on equipment operation and process procedures. Manage and execute equipment related change controls. Qualifications: 4 years of experience in pharmaceutical manufacturing process engineering. Strong technical knowledge of autoclaves, lyophilizers, and fillers, including their operation, maintenance, and troubleshooting. Experience with process validation and cGMP regulations. Proven ability to troubleshoot complex technical issues and implement effective solutions. Hands-on experience with pharmaceutical manufacturing equipment and processes. Education & Certifications: Bachelor's degree in a relevant field (e.g., Computer Science, Engineering, Information Technology) preferred. Thanks & Regards Uttam Barman, Technical Recruiter LinkedIn: https://www.linkedin.com/in/uttam-barman-b494b1254/ Email: [email protected] Contact: 8599464061 Keywords: access management New Jersey URGENT :: Process Engineer (Pharmaceutical GMP) :: Parsippany, NJ :: [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2330106&uid= |
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| 12:43 AM 10-Apr-25 |