General Manager of the Power Plant - Buraydah, المملكة العربية السعودية - NOMAC

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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.

Role Description:

Downstream Manufacturing Engineer working with Days Operations support team.

Role Functions:

• Work as a key team member within the Downstream (DS) Integrated Process Team (IPT) to ensure on-time delivery of the production schedule while maintaining alignment with site safety and quality standards.
  
• Provide oversight on material management, ensuring quality and delivery metrics related to material management are maintained at all times.
  
• Complete downtime analysis and trending for respective area and drive improvement projects in conjunction with the technical operations team.
  
• Provide oversight on day-to-day production quality metrics ensuring on-time documentation closure, line clearance and material management as per area SOPs.
  
• Drive continuous improvement projects related to schedule, equipment and delivery capability within the DS IPT.
  
• Act as a link between the shift operations team and days team, ensuring standardisation and integration between all IPT teams.
  
• Support audit readiness in the BDS and drive a permanent audit readiness culture within the team.
  
• Direct Root Cause Analysis (RCA) sessions for both safety and quality related events, driving actions to closure with appropriate corrective/preventive measures.
  
• Drive MPS standards within the area and ensure team alignment on same.
  
• Lead/support area change controls, CAPAs, QSAT actions as relevant per work stream as well as completing documentation updates as required.
  
• Manage and update BOMs per assigned workstream.
  
• Provide ongoing coaching and support to cross functional team members, to share process and operational best practices.
  

Requirements

Key Competencies & Experience:

• A Level 7 Degree in Science, Engineering or other relevant disciplines/ relevant experience.
  
• At least 3 years experience in the Pharmaceutical industry (preferably in Drug Substance)
  
• Experiences across multiple site functions (including but not limited to Quality, Engineering, or Supply Chain) desirable but not required.
  
• Experience in change management in a GMP environment.
  
• Proven track record of delivering high performance through development and coaching of a team.
  
• Desirable evidence of Continuous Professional Development.
  
• Self-motivated with excellent organizational skills
  
• Excellent verbal and written communication skills
  
• Ability to work independently and as part of a team in a cross functional collaborative environment
  
• High level of attention to detail
  
• Experience working with GMP Documentation Management Systems
  
• Proficient in Microsoft Office Tools (word/excel/PowerPoint )
  
• Good interpersonal skills
  
  

Qualifications & Education:

Qualifications:

• At minimum level 7 in a relevant Qualification
  

#LI-SO1

Key Competencies & Experience: A Level 7 Degree in Science, Engineering or other relevant disciplines/ relevant experience. At least 3 years experience in the Pharmaceutical industry (preferably in Drug Substance) Experiences across multiple site functions (including but not limited to Quality, Engineering, or Supply Chain) desirable but not required. Experience in change management in a GMP environment. Proven track record of delivering high performance through development and coaching of a team. Desirable evidence of Continuous Professional Development. Self-motivated with excellent organizational skills Excellent verbal and written communication skills Ability to work independently and as part of a team in a cross functional collaborative environment High level of attention to detail Experience working with GMP Documentation Management Systems Proficient in Microsoft Office Tools (word/excel/PowerPoint ) Good interpersonal skills Qualifications & Education: Qualifications: At minimum level 7 in a relevant Qualification #LI-SO1