About PSC Biotech
Who are we
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 cloudbased 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 likeminded 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 diversecultural work setting.
Employee Value Proposition
Employees are the heartbeat of PSC Biotech we provide unparalleled empowering career development though Learning & Development inhouse 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.
Overview
- Provide quality oversight and direction for the introduction of new products and materials as well as manage external parties.
- Serve as the point of contact for quality at both the site level and with external inputs coordinating and attending Quality working group meetings.
- Participate as a functional expert in the crossfunctional team responsible for introducing products and materials at Carlow.
- Conduct quality reviews and approvals of engineering/validation/automation/utilities commissioning and qualification activities.
- Author review and approve protocols and reports for technology transfer od qualification and od validation.
- Review doentation ociated with new product and material introduction such as Material Packs QC Test Specifications BOMs and MES doentation.
- Develop and monitor supplier performance metrics participate in material review boards and quarterly reviews of key suppliers and actively engage in crossfunctional forums as needed.
- Maintain the approved supplier management list within the qualified Supplier Management system ensuring correct setup of suppliers and materials used at Carlow.
- Support deviation and atypical closeout as well as initiate and follow up on corrective and preventive actions.
- Facilitate compliance direction for the site by adhering to divisional policies guidelines and regulatory requirements. Proactively evaluate site compliance against emerging trends and initiate major compliance initiatives for improved status and operational efficiency. Actively participate in Plant/Quality committees and collaborate with other site functional groups.
Requirements
- A minimum of 35 years of experience in a quality role ideally in a pharmaceutical manufacturing environment.
- Knowledge of regulatory/code requirements related to Irish European and International Codes Standards and Practices.
- Familiarity with cGMP (current Good Manufacturing Practice) and GDP (Good Distribution Practice) is preferred.
- Strong report standards and policy writing ss.
- Experience with equipment and process validation.
- Familiarity with sterile filling processes and equipment.
- Proficiency in Microsoft Office and jobrelated computer applications.
- Experience or familiarity with Lean Six Sigma odology is desired.
- Good collaboration ss and the ability to work effectively as part of a team to determine priorities.
- Demonstrated ability to work independently and take ownership of improvement initiatives with a moderate level of guidance.
- Proven ability to drive the completion of tasks.
- Strong decisionmaking capability with a sense of accountability and responsibility.
- Demonstrated problemsolving ss
Qualification & Education
A Bachelors degree or higher in a related Science discipline is preferred.
Bring energy, knowledge, innovation and leadership to carry out the following: Lead SAP master data build and data approval activities including hypercare, sustainment materials build, BOMs and Recipes. Participate daily on cross-functional teams collaboratively and actively to address compliance issues and achieve project milestones. Support implementation and training for site Quality Systems and site GMP readiness activities. Support creation, maintenance and continuous improvement of Quality Management Systems (QMS) and ociated doentation. Provide QA review and approval of Change Controls, Deviations/CAPAs, SOPS and related doentation for compliance to GMP and site requirements at the start-up facility. Support other QA colleagues, as required. Work collaboratively to foster strong relationships with management and colleagues and to drive a safe and compliant culture. Support gathering of site metrics Ensure the escalation of risks to management in a timely manner.