Manufacturing Engineer

Manufacturing Engineer (Chemical/ Production/ Pharma)6 Months Contract Location: Gul Circle Up to $6,000 depending on experience Industry: Pharmaceutical IMMEDIATE VACANCY Our client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address vaccine business challenges Job Summary: Responsible for designing, implementing, and reviewing the procedures involved in manufacturing processes. Establishes procedures and proper documentation control as well as performs risk analysis and HAZOPs to ensure that safety, quality, delivery and productivity goals are fulfilled. Conducts or participates in productivity improvement activities including equipment/ fixture selection, design and commissioning. This role is integral in driving continuous improvement processes, utilizing problem-solving techniques, and ensuring that operations align with company goals and standards. Responsibilities: Support all API manufacturing activities to deliver to the business production plan, while ensuring compliance with QHSE standards. Liaise with Process & Technology department and Engineering Maintenance department to ensure the design of appropriate process/ engineering modifications for the continuous improvement activities/ operational yield improvement initiative for the manufacturing department/ facilitate the introduction of new products. Lead the change management process for continuous improvement; plant modification and improvement projects, validation planning and cost-saving projects and equipment qualifications including generating the appropriate documentations (IQ, OQ and PQ). Other Activities: Work with all the support function to lead/ facilitate any trouble shooting activities resulting in timely closure of investigation and CAPA using problem solving tools such as Ishikawa, FMEA, 5 Whys Ensure accountability and commitment in achieving the goals of continuous improvement of Safety performance through participation/ leading in HAZOPs. Create, review and revise manufacturing documents such as batch records, SOPs, etc. to meet cGMP and safety compliance. Perform gap and technical assessments for global standards and procedures (GSPs and SOPs). Serve as risk lead or subject matter expert in support of risk assessments and hazards analysis e.g. microbial control risk assessments Develop technical training material and conduct technical training for production staff. To train and coach production team on the equipment and process. As a Key point of contact for any equipment or production issues. Develop technical reports and engineering documents such as URS, FS, P&IDs, etc. Support performance of reliability study of equipment. Ensure company life savings rules are understood and applied and being proactive in identifying, addressing and resolving issues in a timely manner. To support/lead internal and external quality and HSE compliance audits. Develop cleaning validation strategy. Perform simple use test in laboratory to assist in deviation investigation. Contribution to continuous improvement loops: Power continuous improvement loops with problems encountered and use problem-solving techniques to identify root causes Have the appropriate level in problem solving, e.g. GPS3, to be able to effectively coordinate problem solving groups and ensure the use of appropriate tools. Requirements: Bachelor's Degree in Chemical Engineering or equivalent. Minimum of 3 to 7 years of pharmaceutical or industrial manufacturing experience . Ability to quickly know products and processes to assess performance issues. Good knowledge of GxP requirements and regulations. #J-18808-Ljbffr