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

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About PSCBiotech

Whoweare?

PSCBiotech is a leading Biotech Consultancy firm founded in 1996,headquartered in Pomona, California, USA, with Global operations inIreland, India, Singapore, Australia and the US, serving 350clients in more than 23 countries worldwide. We provide cloud-basedsoftware solutions for Quality Management and RegulatoryInspections, pharmaceuticals contract manufacturing professionals,and metrology services to ourclients.

Take your Career to a new Level

PSCBiotech disrupts the conventional consultancy model by aligning ourEVP as one of the unique selling point which includes theopportunity to work with the most talented cohort of like-mindedprofessionals operating in the Pharma/ Biotech Industry. We offer apermanent contract of employment giving exposure of working in TopPharmaceutical client sites in a diverse-cultural worksetting.

EmployeeValueProposition

Employeesare the heartbeat of PSC Biotech, we provide unparalleledempowering career development though Learning & Developmentin-house training mentorship through constant guidance tofacilitate career progression. We believe in creating highperforming teams that can exceed our client s expectations withregards to quality of all scalable and business unit deliverables,staying under budget and ensuring timelines for our deliverablesare beingmet.

RoleDescription:

DownstreamManufacturing Engineer working with Days Operations supportteam.

RoleFunctions:

• Workas a key team member within the Downstream (DS) Integrated ProcessTeam (IPT) to ensure on-time delivery of the production schedulewhile maintaining alignment with site safety and qualitystandards.
  
• Provideoversight on material management, ensuring quality and deliverymetrics related to material management are maintained at alltimes.
  
• Completedowntime analysis and trending for respective area and driveimprovement projects in conjunction with the technical operationsteam.
  
• Provideoversight on day-to-day production quality metrics ensuring on-timedocumentation closure, line clearance and material management asper areaSOPs.
  
• Drivecontinuous improvement projects related to schedule, equipment anddelivery capability within the DSIPT.
  
• Actas a link between the shift operations team and days team, ensuringstandardisation and integration between all IPT teams.
  
• Supportaudit readiness in the BDS and drive a permanent audit readinessculture within theteam.
  
• DirectRoot Cause Analysis (RCA) sessions for both safety and qualityrelated events, driving actions to closure with appropriatecorrective/preventivemeasures.
  
• DriveMPS standards within the area and ensure team alignment onsame.
  
• Lead/supportarea change controls, CAPAs, QSAT actions as relevant per workstream as well as completing documentation updates asrequired.
  
• Manageand update BOMs per assignedworkstream.
  
• Provideongoing coaching and support to cross functional team members, toshare process and operational bestpractices.
  

Requirements

KeyCompetencies &Experience:

• ALevel 7 Degree in Science, Engineering or other relevantdisciplines/ relevantexperience.
  
• Atleast 3 years experience in the Pharmaceutical industry (preferablyin DrugSubstance)
  
• Experiencesacross multiple site functions (including but not limited toQuality, Engineering, or Supply Chain) desirable but notrequired.
  
• Experiencein change management in a GMPenvironment.
  
• Proventrack record of delivering high performance through development andcoaching of ateam.
  
• Desirableevidence of Continuous ProfessionalDevelopment.
  
• Self-motivatedwith excellent organizationalskills
  
• Excellentverbal and written communicationskills
  
• Abilityto work independently and as part of a team in a cross functionalcollaborativeenvironment
  
• Highlevel of attention todetail
  
• Experienceworking with GMP Documentation ManagementSystems
  
• Proficientin Microsoft Office Tools (word/excel/PowerPoint)
  
• Goodinterpersonalskills
  
  

Qualifications&Education:

Qualifications:

• Atminimum level 7 in a relevantQualification
  

#LI-SO1

Key Competencies & Experience: A Level 7 Degree in Science,Engineering or other relevant disciplines/ relevant experience. Atleast 3 years experience in the Pharmaceutical industry (preferablyin Drug Substance) Experiences across multiple site functions(including but not limited to Quality, Engineering, or SupplyChain) desirable but not required. Experience in change managementin a GMP environment. Proven track record of delivering highperformance through development and coaching of a team. Desirableevidence of Continuous Professional Development. Self-motivatedwith excellent organizational skills Excellent verbal and writtencommunication skills Ability to work independently and as part of ateam in a cross functional collaborative environment High level ofattention to detail Experience working with GMP DocumentationManagement Systems Proficient in Microsoft Office Tools(word/excel/PowerPoint ) Good interpersonal skills Qualifications& Education: Qualifications: At minimum level 7 in a relevantQualification #LI-SO1