HR Intern- Global Sales

2 weeks ago


Dubai, Dubai, United Arab Emirates Energy Jobline Full time

AboutPSCBiotech

Whoweare?
PSCBiotech is a prominent Biotech Consulting firm established in 1996, based in Pomona, California, USA, with operations globally in Ireland, India, Singapore, Australia, and the US. We serve over 350 clients across 23 countries, providing cloud-based software solutions for Quality Management, Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services.Enhance your Professional Journey
PSCBiotech revolutionizes the traditional consultancy approach by offering an exceptional Employee Value Proposition. This includes the opportunity to collaborate with a highly skilled group of professionals in the Pharma/Biotech sector. We provide a secure employment contract that exposes you to working at top-notch Pharmaceutical client sites within a diverse cultural environment.EmployeeValueProposition
Employees are the core of PSC Biotech. We offer unparalleled career advancement opportunities through in-house training, mentorship, and continuous guidance to support your professional growth. Our focus is on fostering high-performing teams that surpass client expectations in terms of quality, scalability, budget adherence, and timely project completion.
Role:Senior Associate Quality Assurance
JobDescription:
  • The Senior Associate in Quality Assurance (QA) will play an active role within the QA team, specifically focusing on the IQA Quality functional area responsible for inspecting and approving primary packaging components.
  • Reporting to a QA Senior Manager, the Senior Associate in Quality Assurance will act as the Quality point of contact for Incoming Inspection of primary and packaging components.
The facility emphasizes continuous enhancement of work processes and practices. Hence, IQA Senior Associates may be tasked with additional responsibilities to support ongoing site improvement efforts.

IncomingQuality Assurance Sr. Associate KeyResponsibilities:

• Testing primary and secondary components for aseptic product manufacturing.
• Sampling Excipients and Drug Substance under Grade C conditions.
• Reviewing and approving documentation related to component testing for further QA Specialist or Qualified Person actions.
• Managing minor NCs and CAPAs to ensure compliance and effective resolution of root causes within set timelines.
• Providing training and guidance on component and packaging testing to staff.
• Participating actively in audits and their preparations.
• Ensuring compliance with cGMP records and approving Standard Operating Procedures as per policies.
• Performing all activities in line with safety standards and SOPs.
• Supporting Operational Excellence initiatives and continuous improvement efforts.
• Undertaking any other assignments or projects as requested by the manager.

Requirements
BasicQualifications &Experience:
• Successful completion of Eye-Tests essential for Visual Inspection.
• Possession of a university degree, preferably in an Engineering or Science-related field.
• Minimum 4 years of relevant experience in the pharmaceutical or biotechnology industry or equivalent combination of experience and education.

PreferredQualifications &Experience:
• Outstanding written and verbal communication skills.
• Experience collaborating with diverse cross-functional teams and displaying strong decision-making abilities.
• Strong organizational skills with a commitment to seeing tasks through to completion.
• Proven problem-solving skills and experience in managing Root Cause Analysis, Non-Conformance, and Deviation investigations.
• Background in aseptic operations, protein formulation, vial, and syringe filling.

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