Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance or compliance, your contribution will directly impact patients.
What You Will Achieve
You will be a member of Pfizer's dedicated and highly effective laboratory technical services team. You will be responsible for validation of laboratory instrumentation and systems. Your methodological approach will help us ensure compliance of our quality systems with company standards and government regulatory requirements. Your
problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct analysis to resolve validation exceptions. Your documentation skills will guide the writing, review and approval of for validation documents and technical reports related to equipment and systems.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues.
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
- Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
- Assists with development of validation protocols and assist with execution of validation protocols.
- Participate in exception investigations to identify root causes and define corrective and/or preventative actions.
- Adhere to all company and Good Manufacturing Practices {also cGMP} procedures, along with safety regulations within the plant and participates in developments of validation programs as needed to remain current with cGMPs and industry.
- Work effectively as a member of the Laboratory Technical Services (LTS) as well as directly with Business Area /Coordinators and SMEs within Quality to support Good Manufacturing Practices {also cGMP}.
- Report to the Laboratory Technical Services Manager, the Validation Associate will assure that laboratory equipment and systems are validated in accordance with {Current} Good Manufacturing Practices (GxP) principles, regulatory requirements, and company policies and standards.
- Work on summarization of data into concise reports that is reviewed by and approved by system owners and quality management.
- Work in a team environment to meet all team objectives and communicate progress on scheduled projects.
Qualifications
Must-Have
- Bachelor's Degree (Science or Engineering discipline)
- Excellent attention to detail and working knowledge of Food and Drug Administration Regulations/Guidance, and Good Manufacturing Practices
- Excellent organizational skills, and ability to handle changing deadlines
- Strong communication with written and verbal skills
- Working knowledge of Microsoft Office, especially Excel for evaluation of data
- Working knowledge of equipment qualification and calibration specifically for laboratory equipment
Nice-to-Have
- Technical writing experience
- Pharmaceutical Industry with laboratory equipment validation experience
Work Location Assignment: On Premise
At Pfizer we care about our colleagues' wellbeing and offer a range of great benefits for them, including:
- Paid parental leave
- Access to Health & Wellness apps
- Career Growth Experiences program
- Recognition & rewards program
- Paid volunteer days
- Life Insurance Benefits
- Pfizer Learning Academy access to top content providers
- Access to flu vaccines & skin checks
- Options to purchase additional leave
- Salary packaging & novated lease options
*Benefits listed may vary depending on your position and location and may be subject to change.
Pfizer Australia and New Zealand's diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity & Inclusion (DE&I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.
If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.
Quality Assurance and Control
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What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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