Senior Commissioning

CAI is looking for an individual with a range of experience in the areas of commissioning, qualification, and validation to join our team in Singapore. Experience in the pharmaceutical, medical device or biotechnology industries is required.

**About CAI**:
CAI is established in 1996, it has grown year over year to more than 800 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.

Meeting a Higher Standard

Our approach is simple; we put the client’s interests first, we do not stop until it is right, and we will do whatever it takes to get there.

As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally:
We act with integrity

We serve each other

We serve society

We work for our future.

We strongly believe that one person’s success is everyone’s success; we work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially.

**Requirements include**:
Position Description:
We are now seeking a Senior CQV Engineer to join our growing operations in Singapore. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. He/She is responsible for protocol writing and execution, field verification, and development of summary reports at the client site.

The role of a Senior CQV Engineer in CAI is to:
Develop documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.

Responsible for protocol writing and execution (field verification), and development of summary reports at client sites. Other responsibilities include planning / coordinating work and directing small teams in document development and / or execution.

Position Requirements:
BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience

5 - 12 years’ experience performing commissioning and / or qualification activities in an FDA regulated industry. Ideally, you will already have experience in facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, generation & execution, etc.

Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.

Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues

High attention to detail

Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines

Ability to work independently, while quickly building and nurturing a project team

Managing the C&Q documentation and execution lifecycle from SLIA generation through to OQ completion.

Support onsite and offsite activities, such as: FATs, SATs, IOQ and PQ Executions and System Walkdowns

Experience in planning / directing C&Q activities

Proficient in life science manufacturing processes in areas such as biotech, aseptic processing, aseptic fill/finish, OSD, Gene Therapy or equivalent experience.

Familiarity with Baseline Guide 5 (Second Edition) a plus

Other Requirements:
Expertise in Microsoft Word and Excel

Excellent oral and written English are required.

Able to travel domestically if required

Able to work in Australia without sponsorship

In return for your skills and knowledge, CAI offers a wide range of benefits including:
Highly Competitive Salary

Continuing education (internal and external)

Opportunities to work on cutting edge projects in a highly evolving field

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