QC Analyst

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 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.

Overview:

• An exciting opportunity for a motivated and enthusiastic
  QC Analyst to join our amazing and fast-paced QC Department .You will help with
  carrying out analytical testing on finished products, raw materials and
  stability using the correct procedures to comply with GMP, Health and Safety,
  SOP’s and environmental and regulatory requirements while ensuring we meet our
  customer’s needs.
  
• This position is offered as a 12-month fixed-term
  contract.
  
• 5-Days onsite
  

Requirements

Responsibilities:

• As a QC Analyst, you will play a vital role in ensuring
  the quality and compliance of our materials and products through precise and
  timely testing. Your key responsibilities will include:
  
• Conducting physical and chemical testing of raw
  materials, finished products (e.g., tablets, boluses, veterinary drenches),
  contract-manufactured goods, stability samples, validation lots, and cleaning
  validation samples using appropriate analytical techniques.
  
• Performing water analysis and environmental monitoring
  according to relevant procedures and schedules.
  
• Inspecting incoming materials such as foils, labels, bulk
  finished goods, and injectables.
  
• Operating, calibrating, and maintaining laboratory
  equipment in accordance with calibration and maintenance protocols.
  
• Adhering to all relevant Standard Operating Procedures
  (SOPs), pharmacopoeias, specifications, regulatory guidelines, and industry
  standards.
  
• Maintaining laboratory logbooks, notebooks, and
  associated documentation in compliance with Good Laboratory Practices (GLP).
  
• Supporting the QC testing schedule to help achieve a
  customer service level of >95%.
  
• Ensuring all QC records are accurately maintained and
  properly filed.
  
• Liaising with team leaders, supervisors, and production
  staff to ensure timely reporting and resolution of results.
  
• Providing prompt feedback and escalating any
  discrepancies, deviations, or non-conformances as required.
  
• Coordinating the dispatch of samples for external
  analysis when necessary.
  
• Managing relationships with external suppliers/vendors
  for QC-related consumables.
  
• Participating in internal laboratory rota tasks and
  contributing to general housekeeping and hygiene within the lab.
  
• Upholding laboratory safety standards and identifying
  areas for improvement.
  
• Performing additional responsibilities as assigned by the
  QC Team Leader, Supervisor, or Manager.
  

Education & Experience:

• Bachelor’s degree (Level 8 or equivalent) in a
  chemistry-based discipline.
  
• Experience working in a pharmaceutical Quality Control
  laboratory operating under cGLP standards.
  
• Familiarity with regulatory guidelines including EU GMP
  and US FDA standards (experience preferred but not essential).
  

Skills & Competencies:

• Strong knowledge of analytical techniques including HPLC,
  IR, UV, dissolution, and physical testing.
  
• Ability to build effective working relationships and
  collaborate within cross-functional teams.
  
• Excellent verbal and written communication skills.
  
• Maintains high ethical standards; escalates issues
  appropriately when necessary.
  
• Demonstrates flexibility and a willingness to learn and
  develop technical expertise.
  
• Highly organised, methodical, and systematic in approach
  to work.
  
• Positive, proactive, and energised by responsibility and
  accountability.
  
• Able to prioritise tasks effectively, distinguishing
  between urgent and non-urgent matters.
  
• Takes initiative, seeks clarification when needed, and
  accepts direction constructively.
  
• Contributes to a supportive, team-oriented environment.
  
• Strong computer literacy, particularly in Microsoft
  Office (Excel, Word, Outlook, etc.).