.. audits from planning to execution. Create and implement the global risk, compliance and audit framework. Transform the risk control culture by designing, implementing and improving the risk framework, strategy, policies and processes. Present risk tolerance and appetite statements to the Board for review .. read more
About PSC Biotech Who we are? PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients. ‘Take your Career to a new Level’ PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting. Employee Value Proposition Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met. The Quality Specialist provides direct Quality support to a production area as part of a Quality IPT (Integrated Product Team). With guidance from the Associate Director of Quality Operations, the Quality Specialist ensures quality and compliance of products manufactured by the functional area, adherence to Good Manufacturing and Documentation Practices, and represents quality on the shop floor. The Quality Specialist performs review of process documentation/data for accuracy, completeness, and data integrity compliance. The incumbent may support the completion of batch disposition activities for release of product and may assist in conducting investigation of deviations. Additionally, the Quality Specialist spends significant time on the shop floor in a team environment to provide quality coaching and guidance, to enable documentation to be completed right the first time, and to ensure compliance with cGMPs and regulatory requirements. Requirements Responsibilities Participates as the quality member on cross functional projects. Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records Reviews executed production documentation such as electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures and ensures completion of proper remediation of errors. Provides presence on the shop floor to support compliance and data integrity. Review & approve new and updated SOPs/ Work Instructions and Controlled Job Aides Actively participates in the Tier process and use this forum to make concerns visible and to partner with the functional area on resolution. Q A support, review and approval of Commissioning and Qualification lifecycle documents for capital projects and new equipment. Will serve as the Quality SME for Performance qualification (PQ) activities across the site including but not limited to: Equipment, Facility and Utility PQ studies, Cleaning Validation, SIP, process validation, Support sustaining activities such as Change Management, Deviations, CAPAs, Equipment Requalification and Periodic review, Site Maintenance & Calibration Program. Provides support to internal audits and regulatory inspections. Collaborates with cross-functional team members in the identification and implementation of continuous improvement initiatives and action plans. Required Education · Bachelor degree, in a scientific or engineering field (preferred); candidates with degrees in other fields will be considered if accompanied by significant relevant experience Experience and Skills : Required: · Minimum 5 years of relevant post-degree work experience in GMP Manufacturing or Laboratory environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing or laboratory operations, or related industry experience in a laboratory, manufacturing, science related or regulated setting. · Evidence of leadership skills coupled with good oral and written communication skills. · Understanding of cGMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area. · Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment. Preferred: · Quality systems, pharmaceutical manufacturing, or laboratory processes, authoring and approving GMP documents. · Demonstrated analytical aptitude, critical thinking skills and problem-solving skills. · Demonstrated ability to upskill/coach others. · Experience working on manufacturing shop floor · Familiarity with GMP documentation review and/or shop floor auditing #LI-DM2