312 Piramal Pharma Jobs
Executive - Process Engineering
Piramal Pharma
posted 23hr ago
Flexible timing
Key skills for the job
Bachelor s Degree in Engineering or a similar discipline is required with at least 0-3 years of relevant experience.
candidate needed basic knowledge on process engineering document activities including preparation of PFD, PID, HAZOP studies , Scaleup, incident investigation etc
Responsible for working with Technology Transfer, Production, and the Client to generate, revise, and approve master production records (MPRs) and any other documents associated with the commercial products in the manufacturing, e. g. , SOPs, material specifications, technical reports, etc.
Preparing unplanned and planned deviations for responsible processes and forming the investigation team.
Collaborates with Process Development (PD), Technology Transfer (TT), Operations, Quality Control (QC), and Quality Assurance (QA) in problem-solving activities, including deviation writing and CAPA closure.
Work with project and engineering teams to replace existing/modify or buy equipment s for continuous improvement or capacity enhancement
Functions as the technical interface between PPS-Riverview and the Client, focusing on providing technical advice and support, engineering solutions, overseeing GMP runs in the plant equipment, analyzing production data to evaluate process performance, and writing production summaries.
Will require solid understanding of manufacturing processes, GMP guidelines, site and corporate policies and procedures, hands-on experience, and complete understanding of production processes in the GMP environment as laid out at PPS-Riverview. Willingness to work flexible hours and shifts when there is a need.
Responsible for providing independent production support during off-hours as needed.
Ability to travel as needed.
Ensures process data is being updated monthly and analysis manufacturing KPI performance for improvement and discussion with the client.
Takes part in Operational Excellence activities for the plant.
Compliance:
Compliance with 21 CFR - Parts 210/211, EU Directives 91/356/EEC and ICH Q7.
Compliance with SOPs, batch records, forms, logs of use and Quality Agreements.
Recognizes common sources of failure and improves documentation to reduce deviations and errors.
Works with Operations Personnel to improve compliance.
Ensures work is in compliance with all state and federal regulations, including but not limited to OSHA, GMP, DEA, FDA, etc.
Assists in the formulation of corrective procedures when needed.
Uses appropriate PPE while inside a manufacturing area.
Assumes responsibility for safety and knows appropriate emergency procedures in case of emergency.
Knows the location of SDS binders and understand how the guidelines pertain
Employment Type: Full Time, Permanent
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