A reputable Jordanian Pharmaceutical is seeking to recruit highly motivated candidate for the following position Job Title Validation and Stability Supervisor / QC Department Responsibilities ( Ref 001 ) * Plan and perform analytical method validation at an advanced level. * Plan, Manage and oversee the daily operations of the QC Stability Program. * May represent QC in Quality , Customer, and Regulatory Audits/meetings Qualifications: Bachelors Degree in Chemistry/Pharmacy- three years of relevant cGMP lab Job Title Quality Assurance Senior (Ref 002) Job Summary The QA Supervisor will be responsible for the successful development, deployment and implementation of Supplier Quality Management and New Product Introduction strategies and associated policies, procedures, programs and initiatives that deliver quality, compliance, and cost and/or benefit to the supply chain. He/she will supervise the development and monitoring of processes and controls ensuring that the performance and quality of raw material, packaging suppliers, and new products are in compliance with all standards set at the manufacturing facility including cGMP, JFDA, etc. Provide guidance and training to related teams to ensure that compliance and quality requirements are adhered to during product development, scale up and validation and regulatory requirements throughout the development process. Qualifications A minimum of 4-7 years of experience in a pharmaceutical manufacturing plant is required including a broad and deep working knowledge of the pharmaceutical product operating functions of quality and compliance. Experience with documentation and regulation/compliance environment, is required. Prior experience with JFDA inspections is desirable. - Job Title Compliance Officer (Ref003) Job Summary: The Compliance Officer is responsible for ensuring all procedures comply with policies, standards, and regulations and according to set SOPs. He/she will undertake internal quality audits on all departments related to product development, manufacturing, and procurement and ensure all materials and new products comply with regulations. Liaise between all the aforementioned departments as well as Regulatory Affairs to ensure that SOPs are being implemented and all related product/material information is being communicated on a timely and accurate basis Qualifications: A minimum of 3 years of experience in a pharmaceutical manufacturing plant is required. Experience with documentation and regulation/compliance environment, is required. Prior experience with JFDA inspections is desirable. Job Title Maintenance Engineer (Ref 004) Duties will include but are not limited to: Supervision on the Maintenance Technicians, Carry out Preventive and Corrective Maintenance, Documentation System and Follow up. Qualifications: BSc Degree in Mechatronics or Mechanical Engineering,( 2-4 ) years industrial sector experience Job Title Security Supervisor (Ref005) * Only qualified candidates who meet the above requirements are invited to send their CVs to Pharmadept.hr@gmail
Posted on: Thu, 15 Aug 2013 18:01:42 +0000
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