Work Schedule10 hr shift/daysEnvironmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degrees, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.
), Will work with hazardous/toxic materialsJob DescriptionAbout us:As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale.
Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer.
We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.Location/Division Specific InformationThe role sits within the Upstream (USP) team at our Brisbane site which is focused on the manufacture of biopharmaceutical products in compliance with international quality requirements set by TGA, FDA, EMEA, ICH, and other regulatory bodies.About the Role:The USP Team Lead will join an existing team and manage a team of 4 direct reports.
The Brisbane site of Thermo Fisher Scientific produces various products for clinical trials and commercial use.
There are many different processing steps for each product due to the diverse range of customers.
The Team Leader must be able to assess the impact of situations on product quality, yield, and compliance with EH&S and cGMP.What You'll Do:Key Responsibilities:Foster and develop a hard-working team through effective coaching and leadershipEnsure growth and development of the USP team with a focus on building talent depthDeliver sustained improvement in the site key performance indicators of Right the First Time and On Time DeliveryDeputise for the USP Supervisor when they cannot be present as well as demonstrate leadership and accountabilityContribute to the direction of site operations and ensure the use of new and innovative processing techniques, such as Perfusion technology, Bioreactor technology, and advanced harvesting methods like single-use centrifugation.Communicate effectively in a variety of communication settings; provide timely and helpful information to others across the organization; encourage others to contribute ideas and opinionsPossess a high level of independence along with a recognised sound and consistent approach when facing technical or personnel problemsIndependently organize and complete USP unit operations following the relevant production protocols and planning schedules in a clean room environment under cGMP conditionsIdentify and overcome practical problems, proposes possible solution and communicates to the responsible personSupport USP and facility functions by maintaining production suite, supplies, equipment, logbooks, and data.
Also responsible for closing out batch record and material reconciliation following site SOPs and policiesReview, revise, and author manufacturing batch records, SOPs, and logbooks.
Collaborate with the Quality Department to review and approve completed batch recordsAdhere to Patheon cGMP Quality Management System and the Patheon EH&S requirements.
Be the lead investigator for minor and major deviation reportsBe fully trained on all USP unit operations and equipment as well as maintain up to date training matrixTrain colleagues on unfamiliar unit operations or equipment, including approving on-the-job trainingsPropose and implement corrective and preventive actions and drive the on-time closure of deviation reports and change controlsImplement lean (OE) initiatives and continuous improvements with minimal directionCommunicate with suppliers about issues of a technical natureKeys to Success:Education:Tertiary education in science or engineering based field (i.e.
biopharmaceuticals manufacture, biotechnology, process technology)Skills and Experience:At least 3 years of relevant industry work experience within the bio (pharmaceutical) fieldsVery good knowledge and experience working within cGMP environmentSpecific knowledge and experience in relevant quality systemsDemonstrated strong leadership skills to influence and build effective teamsExcellent planning and organizational skillsSpecific knowledge of relevant bioprocess unit operationsStrong organisational, scheduling and planning skills.Ability to work unsupervised.Good communication, flexibility, reliability and assertiveness.Responsible and proactive.Due to involvement in the timely execution of manufacturing processes, interpersonal and organisational skills and flexibility in working hours are required.Benefits:Join our team and take advantage of these great benefits!
Apply now to learn more about the full range of benefits we offer.Health & Wellbeing:Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues.Flexibility:Balance your work and personal life with flexible arrangements.Extra Leave:Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.Charitable Giving & Volunteering:Make an impact with paid volunteer time to support non-profit organizations that matter to you.Learning & Development:Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender EqualityOur Mission is to enable our customers to make the world healthier, cleaner and safer.
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