Home Australia Manufacturing Supervisor, Drug Product - Day Shift

Home Australia Manufacturing Supervisor, Drug Product - Day Shift

Manufacturing Supervisor, Drug Product - Day Shift

Full time at a Laimoon Verified Company in Australia
Posted on April 23, 2024

Job details

Manufacturing Supervisor, Drug Product - Day Shift page is loaded Manufacturing Supervisor, Drug Product - Day Shift Apply locations Melbourne - Australia Drug Manufacturing time type Full time posted on Posted Today job requisition id R15047 *We are excited to announce that we are expanding our team and have multiple positions available for this role - join us in shaping the future!* The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.

Moderna is committed to enhancing Australia's biotech landscape through a long-term partnership that focuses on strengthening pandemic resilience. Our Melbourne-based large-scale mRNA vaccine manufacturing facility will be a cornerstone in Australia's ability to respond to future health threats efficiently. This collaboration not only brings cutting-edge medical technology to the forefront but also emphasizes job creation and local talent development. We're inviting visionary professionals to be part of this transformative journey, making a tangible impact on global health security.

As a day-shift Manufacturing Supervisor at Moderna, you will play a central role in our mission to produce safe, effective mRNA vaccines. This position requires a balance of scientific understanding, operational leadership, people skills, and digital acumen. Your main responsibilities include managing production timelines, ensuring cGMP compliance, and overseeing health and safety regulations. With your expertise in mRNA technology and production processes, you will inspire a team, maintain meticulous attention to detail, and drive operational excellence in a dynamic environment.

Here's What You'll Do: Within 3 Months, You Will… Familiarize with Moderna's safety procedures and local HSE laws, ensuring strict adherence.

Begin developing batch records, SOPs, and training materials for commercial programs.

Work autonomously within GMP, SOPs, and manufacturing documentation.

Initiate incident and HSE event investigations.

Start managing the training and development of the manufacturing team, including fostering a collaborative relationship with the Night Shift team.

Within 6 Months, You Will… Collaborate with QA for timely disposition of commercial batches.

Investigate and open deviations, establishing corrective actions.

Monitor and manage team performance, including regular one-on-ones and addressing non-performance.

Coordinate with Supply Chain for inventory management and process orders.

Address equipment, process, and digital issues rapidly and effectively.

Within 12 Months, You Will… Be recognized as a mentor and trainer, elevating team capabilities.

Ensure efficient resource utilization for mRNA medicine manufacturing.

Implement KPI-based performance monitoring and corrective actions.

Lead and participate in projects aimed at continuous improvement.

Drive alignment of team goals with Moderna's corporate and commercial objectives.

Here's What You'll Bring to the Table: Typically, 5-7+ years of experience in a GMP manufacturing environment

A Bachelor's Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field preferred

Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company preferably in GMP

Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these values in the workplace

Ability to collaborate fluidly with peers, supervisors and cross-functional support groups required

Exceptional written, oral communication, and organizational skills required

Skills in project management, including planning, execution, monitoring, and closing projects

Aseptic experience, Visual Inspection and PFS knowledge

Experience with chromatography and tangential flow filtration would be an asset

Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines

Knowledge of environmental monitoring practices in a cleanroom or controlled manufacturing environment

Specific expertise in mRNA technology, vaccine production and equipment - beyond a general scientific understanding

Understanding/Detailed knowledge of regulatory requirements specific to mRNA drug products and vaccine production

Expertise in quality control measures and assurance processes specific to pharmaceutical manufacturing

Knowledge of validation processes for manufacturing equipment and processes

Ability to analyze production data and generate reports for management

Specific methodologies for continuous improvement, such as Lean, Six Sigma, or others.

Experience in leading Kaizen events or other process optimization initiatives

Experience in coordinating with supply chain for raw materials and inventory management.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work. We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

Quality healthcare and insurance benefits Lifestyle Spending Accounts to create your own pathway to well-being Free premium access to fitness, nutrition, and mindfulness classes Family planning and adoption benefits Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown Educational resources Savings and investments Location-specific perks and extras! The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. 

By living our mission, values, and mindsets every day, our people  are the driving force behind our scientific progress and our culture.  Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We're focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at ****** . (EEO/AAP Employer) 

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At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA). This novel drug platform builds on the discovery that modified mRNA can direct the body's cellular machinery to produce nearly any protein of interest, from native proteins to antibodies and other entirely novel protein constructs that can have therapeutic activity inside and outside of cells.

We have a clear mission to propel the field of mRNA science forward and deliver new medicines to patients and a unique vision for how to achieve this mission.

Our Mission: To deliver on the promise of transformative messenger RNA (mRNA) science to bring new medicines to patients.

Our Vision: To unlock the potential of mRNA by establishing an ecosystem of teams and partners that will work together to develop the broadest possible array of drugs, across diverse therapeutic areas and routes of administration, for serious diseases that are not treatable today.

Third Party Staffing Agencies M oderna does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Moderna from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Moderna and do not obligate Moderna to pay fees if we hire from those resumes.

Reasonable Accommodation Notice Moderna will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.Applicants with disabilities may be entitled to reasonable accommodation under the terms of the Americans with Disabilities Act and certain state or local laws. Please inform the company's personnel representative by calling 617-460-9346 or emailing ****** if you need assistance completing any forms or to otherwise participate in the application process.Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.

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