Fill Finish Process EngineerPre-Filled Syringe SME

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:

• Our Engineers help ensure that internal and external manufacturing operations remain operational continuously improve and innovate. With our extensive range of facilities and environments our Engineers have opportunities across many diverse areas including Biological Chemical Automation Capital Projects Maintenance Safety Process Development Technical Services Utilities and Validation.
  
• The External Manufacturing (ExM) Technical Operation organization is seeking a highly motivated individual for a this support position. ExM Tech Ops is accountable for technology transfers and commercial production of sterile drug product at our External Partners (EPs).
  
• This person will have the opportunity to participate in all these areas. This may include supporting the execution of technology transfers providing manufacturing process support to resolve commercial production issues and to provide support for process and capacity optimization.
  
  

Requirements

Responsibilities include:

• Work with External Partners to achieve business goals and to establish a common culture that benefits our company External Partners and patients.
  
• Responsible for technical activities for the commercial manufacturing process at the External Partner which includes authorship of change control management of process improvement projects statistical analysis of process performance and investigation of atypical events.
  
• Responsible for technical transfer activities as applicable through authorship and/or review of required GMP documentation (Master Batch Records change control protocols reports qualifications etc.) and regulatory filings.
  
• Provide onsite coverage at External Partner in support of Commercial and / or Technology Transfer PersonInPlant Activities.
  
• Translate understanding of GMP requirements and current regulations and develop standardized work to meet these requirements by partnering with Operations Quality and External Partners.
  
• Ensure that External Partners are inspection ready for all routine inspections and / or inspections related to new product introductions or transfers in concert with Operations Quality and Regulatory.
  
• Responsible for participation in creating sharing and adopting best practices and business process strategies.
  

Education Minimum Requirement:

• Must have fill finish PreFilled Syringe experience for this role (Minimum 35 years)
  
• Bachelor s degree in Chemical/Biochemical Engineering Pharmaceutical Science or Chemistry/Biology or other related science or engineering field.
  

Required Experience and Skills:

• Minimum of 4 years postbachelors degree experience in a GMP functional area or support of a GMP functional area such as Operations Technical Operations Technology Engineering and/or Maintenance
  
• Travel will be a requirement of this position at approximately 2550%
  
• Strong communication and teamwork skills
  

• Preferred Experience and Skills:
  Experience in Fill Finish activities (Vial / Syringe finish Sterilization cleaning aseptic manufacturing etc.)
• Demonstrated ability to independently manage projects/work to schedule/deadlines
  
• Statistics experience (including Proactive Process Analysis and Continuous Process Verification)
  

• Experience in deviation management and/or change control and/or equipment support and/or project management.
  

#LIEL1