Senior Pharmaceutical Commissioning Qualification Validation Engineer
vor 4 Wochen
Brisbane, Australia / Australia / Full Time
CAI 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 CAI:CAI is a 100% employee-owned company established in 1996, it has grown year over year to 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.Meeting a Higher StandardOur 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 integrityWe serve each otherWe serve societyWe 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. That is how we have grown exponentially.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 COVID19 Vaccines and therapies. As part of our company culture, we invest in YOUR future, and commit to hands on certifications as well as professional training. Our collaborative culture ensures that our customers benefit from exemplary work across our entire range of professional services.Requirements include:Position Description:We 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 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 experience5 – 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 issuesHigh attention to detailAbility to multi-task and take initiative to accomplish assigned tasks accurately by established deadlinesAbility to work independently, while quickly building and nurturing a project teamManaging 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 WalkdownsExperience in planning / directing C&Q activitiesProficient 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 plusOther Requirements:Expertise in Microsoft Word and ExcelExcellent oral and written English are required.Able to travel domestically if requiredAble to work in Australia without sponsorshipIn return for your skills and knowledge, CAI offers a wide range of benefits including:Highly Competitive SalaryContinuing education (internal and external)Opportunities to work on cutting edge projects in a highly evolving field(Varies by Country, Below is a General Overview)100% Employee Owned24 Days PTO/5 Sick days per year + Additional Holidays depending on CountryMedical / Dental / Vision (In accordance with each countries’ applicable regulations)Professional Development (Approximately $5,000 paid career-related, continuing education)ESOP/401k – 15% Company ContributionCompany Paid Long-Term DisabilityCompany Paid Life InsuranceCompany Paid Parental Leave (In accordance with each countries’ applicable regulations)
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Brisbane City, Österreich Cagents VollzeitSenior Pharmaceutical Commissioning Qualification Validation Engineer - Australia Brisbane, Australia / Australia / Full Time CAI 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...
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Brisbane City, Österreich Cagents VollzeitSenior Pharmaceutical Commissioning Qualification Validation Engineer - Australia Brisbane, Australia / Australia / Full Time CAI 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...
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