About the role

Aplyr's Quick Take

This role is primarily focused on quality assurance tasks within a pharmaceutical setting, including drafting documents, executing change assessments, and participating in audits. It's an individual contributor position that requires collaboration with various internal teams to ensure compliance with regulatory standards.

Good fit

Ideal candidates will have a background in science or engineering, preferably with some experience in a cGMP environment. Those who thrive in dynamic settings and possess strong communication skills will do well here.

Worth noting

The job emphasizes a collaborative work environment and continuous improvement initiatives, which could appeal to those looking for a proactive role. However, the spec is vague on day-to-day responsibilities beyond general QA tasks.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

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.

What You'll Do:

Drafting article code forms (site specification documents for materials)
Executing change notification impact assessments; draft and approve change notification change controls
Assist in activities within the quality agreement system
Assist in regulatory and client audits from readiness activities through to engagement
Building and maintaining effective working relationships with key internal stakeholders from other teams and departments that foster a collaborative work environment
Participate in implementing continuous improvement (PPI) initiatives that realise cost savings and drive efficiency
Updating SOP’s and other documents to meet current regulatory and corporate standards
Ownership of quality records including but not limited to deviations, CAPAs, Audit findings etc. as required
Participate in global projects and initiatives related to the remit of the Materials Management Team, as required

Education

Tertiary education in science or engineering-based field (i.e. biopharmaceutical manufacture, biotechnology, process technology) or relevant experience in the pharmaceutical industry.
Experience in a cGMP environment is highly desired but not essential.

Experience

Experience in a cGMP environment is highly desired but not essential.

Knowledge, Skills, Abilities

Good knowledge of cGMP
Desire to work in a highly dynamic, frequently changing environment with a wide variety of people and perspectives
Flexible and adaptable attitude
Strong written, verbal and interpersonal communication skills
Strong collaborative skills with the ability to build rapport with internal and external stakeholders

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 Equality

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 125,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Aplyr's read

Thermo Fisher Scientific is a powerhouse in biotechnology, attracting professionals passionate about advancing scientific research and innovation across diverse roles and regions.
Synthesized from recent postings & public sources

What's promising

•Thermo Fisher is a leader in the biotech industry, offering stability and growth potential.
•The company invests heavily in R&D, fostering innovation and cutting-edge solutions.
•Global presence provides diverse career opportunities across multiple regions and disciplines.

What to watch

•High pressure and fast-paced environment may not suit everyone.
•Complex organizational structure can lead to communication challenges.
•Frequent acquisitions may result in uncertainty and change for employees.

Why Thermo Fisher

•Thermo Fisher's broad product portfolio spans laboratory equipment to clinical diagnostics.
•The company plays a crucial role in global scientific advancements and healthcare solutions.
•Strong focus on sustainability and corporate responsibility sets it apart in the industry.

Aplyr’s read is generated by AI from public sources. Was it useful?

About Thermo Fisher

Thermo Fisher

thermofisher.com

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Thermo Fisher Scientific is a global leader in serving science, providing a range of products and services to help researchers and scientists in laboratories and clinical settings.