Sales Enablement Manager

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.

Job Description:

Role Functions:

• Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same.
  
• Operate as part of the QC team performing the allocated testing/inspection and laboratory based duties.
  
• Where applicable, review, approve and trend test results.
  
• Peer review other analysts documentation, ensuring QC Right First Time KPIs are achieved.
  
• Participate in QC daily meetings and ensure effective communication of testing progress, deviations etc.
  
• Ensure that all Quality Systems within the department are adhered to on a daily basis.
  
• Complete all documentation in compliance with GMP and GxP standards.
  
• Participate in the laboratory aspects of deviation investigations.
  
• Problem solving to get to root cause of issues.
  
• Provide support with audit/inspection requirements to ensure department compliance/readiness.
  
• Collaborating with others by sharing your skill-set and expertise
  
• Drive continuous improvement, perform root cause analysis on system failures e.g., FMEA, Fishbone diagrams, 5 whys etc,
  
• Drive compliance with Client s site Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, including maintenance of accurate records.
  

Requirements

Experience, Knowledge & Skills:

• 1 - 3 years experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
  
• Previous Analytical Experience
  
• Demonstrated ability to work independently and fully realize improvement initiatives with a moderate level of guidance
  
• Good communication, interpersonal skills and ability to work across teams.
  

Qualifications & Education:

• Degree in Science, Engineering or similar
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