OverviewCAI is looking for individuals with a range of experience in the areas of commissioning, qualification, and validation to join our team in Australia.
Experience in the pharmaceutical, medical device or biotechnology industries is required.About CAICAI is a 100% employee-owned company established in 1996, with nearly 700 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.Our approachOur 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: we act with integrity, we serve each other, we serve society, and we work for our future.
With employee ownership, 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.CAI agents (employees) will be exposed to cutting edge technologies in the advanced medicine space.
You will have an opportunity to work with recognized subject matter experts allowing you to be a key player in bringing lifesaving therapies to market, including COVID-19 vaccines and therapies.
We invest in your future and commit to hands-on certifications as well as skilled training.
Our collaborative culture ensures that our customers benefit from exemplary work across our entire range of professional services.Position DescriptionWe are now seeking a Senior CQV Engineer to join our growing operations in Australia.
The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation.
These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site.
The role includes developing documentation for the commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment, as well as planning/coordinating work and directing small teams in document development and/or execution.ResponsibilitiesDevelop 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.Plan, coordinate work, and direct small teams in document development and/or execution.Support onsite and offsite activities, such as FATs, SATs, IOQ and PQ Executions and System Walkdowns.Experience in planning/directing C&Q; activities.Manage the C&Q; documentation and execution lifecycle from SLIA generation through to OQ completion.Position RequirementsBS 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.
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 Life Sciences clients.Excellent technical problem-solving and troubleshooting skills, with a 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.Experience in documenting and executing C&Q; activities from start to finish.Proficient in life science manufacturing processes such as biotech, aseptic processing, aseptic fill/finish, OSD, Gene Therapy or equivalent experience.Familiarity with Baseline Guide 5 (Second Edition) is a plus.Other RequirementsExpertise 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.BenefitsHighly competitive salary.Continuing education (internal and external).
Opportunities to work on cutting-edge projects in a highly evolving field.
#LI-JW1Equal OpportunityWe are an equal opportunity employer; we are proud to employ veterans and promote diversity and inclusion in our workplace.
Diversity is a strength for our global company.
We pledge that CAI will be operated in a way that is fair and equitable to all – our employees, our customers, and the broader society.This job description is not all-inclusive and you may be asked to do other duties.
CAI will also consider qualified applicants with criminal histories in a manner consistent with the Fair Chance Act (FCA) / Fair Chance Ordinance (FCO).
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📌 Senior Pharmaceutical Commissioning Qualification Validation Engineer
🏢 Cai
📍 Melbourne