CQ Engineer (Pharma)

ORKA LIFESCIENCE PARTNERS PTE. LTD.

Singapore

On-site

SGD 60,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Work that Matters
Career Development
Professional Environment
Impactful Learning and Mentoring

Job summary

ORKA LIFESCIENCE PARTNERS PTE. LTD. is seeking a CQ Engineer to deliver commissioning and qualification services for equipment across life sciences facilities in Singapore.

You will draft URS, IQ/OQ protocols, review IOQ, perform CQ activities, and support vendor calibration and maintenance, ensuring compliance with cGMP and 21 CFR Part 11.

Qualifications

  • Hold Bachelor’s degree in Life Sciences, Engineering or related field.
  • Have worked for at least 2 years in pharmaceutical, medical device or related environment.
  • Have experience supporting or performing equipment CQ activities.
  • Understand computerised system requirements in the pharmaceutical industry (e.g., 21 CFR Part 11, Annex 11).
  • Preferably with experience in using VLMS like Kneat or Valgenesis.

Responsibilities

  • Deliver CQ services to support introduction, upgrade or decommissioning of manufacturing, manufacturing support and laboratory equipment in the Life Sciences (pharmaceutical / medical device) clients.
  • Draft equipment qualification deliverables such as URS, risk assessment, data integrity related assessment, CQ (IQ/OQ) protocols, specifications and RTM.
  • Review equipment vendor's IOQ documents.
  • Execute and document qualification activities.
  • Monitor and support equipment vendor in conducting equipment CQ, calibration and maintenance.

Skills

CQ activities experience
cGMP knowledge
21 CFR Part 11 familiarity
VLMS (Kneat/Valgenesis)

Education

Bachelor’s degree in Life Sciences, Engineering or related field

Tools

Kneat
Valgenesis

Job description

The CQ Engineer delivers commissioning and qualification services for equipment such as temperature controlled equipment / temperature controlled unit, warehouse, laboratory equipment (e.g., TOC analyzer, micro plate reader, MALDI-TOF, HPLC, osmometer), manufacturing support equipment (e.g., weighing balance, pH meter, weighing balance, CEDEX, ViCell, Solo VPE), HVAC, utilities (e.g., WFI, compressed air) and process equipment. The Engineer ensures that all systems are installed, tested, and qualified in compliance with cGMP, regulatory requirements, and project-specific standards.

Key Responsibilities:
  • Deliver CQ services to support introduction, upgrade or decommissioning of manufacturing, manufacturing support and laboratory equipment in the Life Sciences (pharmaceutical / medical device) clients.
  • Draft equipment qualification deliverables such as URS, risk assessment, data integrity related assessment, CQ (IQ/OQ) protocols, specifications and RTM.
  • Review equipment vendor's IOQ documents.
  • Execute and document qualification activities.
  • Monitor and support equipment vendor in conducting equipment CQ, calibration and maintenance.
  • Draft, revise and review SOPs, forms and related operational and maintenance documents.
Requirements:
  • Hold Bachelor’s degree in Life Sciences, Engineering or related field.
  • Have worked for at least 2 years in pharmaceutical, medical device or related environment.
  • Have experience supporting or performing equipment CQ activities.
  • Understand computerised system requirements in the pharmaceutical industry (e.g., 21 CFR Part 11, Annex 11).
  • Preferably with experience in using VLMS like Kneat or Valgenesis.
Why Join ORKA:
  • Work that Matters:Support clients bringing innovative and life saving solutions to the population.
  • Career Development:Build a consulting career in a professional consulting company with Life Sciences focus.
  • Professional Environment:Work with similar professionals possessingIntelligence, Resourcefulness, Loyalty and Teamworkcharacteristics.
  • Impactful Learning and Mentoring:Develop yourself in an environment that heavily foster learning attitude and benefit from access to training materials, references, mentors and management with wide range of regulated industry experiences.
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