Product Development Associate, China

Swisse Wellness; City of Melbourne; Hybrid; AUD 90,000 - 120,000; Full time

Benefits offered by this job

Flexible work arrangements

Bonuses

Health benefits

Wellness programs

Flexible annual leave

Job summary

Swisse Wellness in Melbourne is seeking a Product Development Associate to turn innovation concepts into viable products for the China CBEC portfolio. You will collaborate with Marketing, Science, Quality, Regulatory, Sourcing and manufacturing teams to support development from concept to commercialisation.

The role requires post-graduate qualifications in Pharmaceutical Science or Formulation Science, at least 3 years in the supplements or pharmaceutical sector, and experience with tablet,

Qualifications

• Bachelor-level qualification in Pharmaceutical Science or related field.
• Minimum 3 years in complementary medicines, supplements, pharmaceutical or FMCG with manufacturing exposure.
• Experience developing tablet, capsule, powder, liquid, softgel and nutraceutical formulations.
• Experience in TGA, FDA and China GB regulatory environments.

Responsibilities

• Own and lead product development activities across a portfolio of CBEC NPD/EPD projects from concept to commercialisation.
• Translate concepts into viable products by coordinating formulation, feasibility, scale-up and launch activities.
• Support sourcing and procurement to onboard manufacturing partners and drive optimisation.
• Collaborate with Marketing, Science, Regulatory and Commercial teams on consumer-led opportunities.
• Work with Quality and Manufacturing to investigate challenges and provide technical recommendations.
• Coordinate product trials, scale-up activities and manufacturing validation for successful commercialisation.
• Interpret stability data to identify trends and inform lifecycle management.

Skills

Tablet formulation

Capsule formulation

Formulation development

Stability data analysis

Technical documentation

Cross-functional collaboration

Travel availability

Education

Pharmaceutical Science

Formulation Science

Job description

If you are looking for a fantastic team and a challenging, fast, and dynamic work environment, you are at the right place!

On our journey to making a positive difference across the world, you will work with passionate people in an innovative and collaborative organisation as we inspire wellness through#PurposeLedCareers

We are dedicated to our customers, community and environment and are looking for similar-minded talent to join us! As an equal opportunity employer, we care deeply about creating an inclusive workplace where our team members feel valued, respected, and empowered.

Our total rewards package offering includes additional annual leave, bonuses, wellness programs, health benefits, flexible and remote working arrangements, and performance awards - not to mention various social and recreational activities, all of which are regional specific.

With over 3,400 team members working across the globe, our vision is focused on premium nutrition and lifetime wellness, backed by science. We have 3 business segments - Baby, Adult and Pet Nutrition and Care - supporting whole - family health and happiness across 7 international brands.

What this means for you

The variety of work creates unlimited opportunities to excel across a breadth of disciplines; you will be presented with a wealth of new pathways and opportunities to explore throughout your career. Working with us will be more than just a job; we guarantee a life-changing experience as you step into an environment that moves quickly and presents new challenges daily.

Your role within the team

As a Product Development Associate, you will turn innovation concepts into commercially viable products across the China CBEC portfolio. Partnering with Marketing, Science, Quality, Regulatory, Sourcing and manufacturing teams, you will support product development from concept and feasibility through to commercialisation and ongoing optimisation. You will also contribute to product quality, compliance and operational excellence through formulation development, manufacturing trials, stability monitoring, technical investigations and continuous improvement.

Key responsibilities include:

• Own and lead product development activities across a portfolio of China CBEC NPD and EPD projects, ensuring delivery from concept through to commercialisation.
• Translate product concepts into commercially viable products by partnering with internal stakeholders and external manufacturing partners to progress formulation, feasibility, scale-up and launch activities.
• Support Sourcing and Procurement teams to identify, onboard and brief new manufacturing partners, while driving continuous improvement and optimisation across existing product portfolios.
• Collaborate with Marketing, Science, Regulatory and Commercial teams to identify consumer-led opportunities and develop innovative concepts for the NPD pipeline.
• Partner with Quality and Manufacturing teams to investigate product, formulation and process-related challenges, providing technical analysis, recommendations and risk-based solutions that support decision-making and product performance.
• Coordinate product trials, scale-up activities and manufacturing validation to support successful commercialisation and ongoing product improvement.
• Interpret technical and stability data, identify trends, and provide insights and recommendations that support product quality, compliance and lifecycle management.
• Develop and maintain technical documentation, specifications and project records to support governance, compliance and Stage Gate requirements.

Desired Skills & Experience

To set you up for success in this role, you will bring:

• Tertiary qualifications in Pharmaceutical Science, Formulation Science or a related Applied Science.
• At least 3 years’ experience in the complementary medicines, supplements, pharmaceutical or FMCG industry, with exposure to a manufacturing environment.
• Experience developing tablet, capsule, powder, liquid, softgel and nutraceutical formulations.
• Experience supporting product development projects from concept through to commercial launch, including feasibility assessments, formulation development, raw material selection, trial coordination, specification review, technical documentation and product lifecycle management.
• Experience working in a TGA and GMP manufacturing environment, with an understanding of product scale-up processes, pilot trials, pre-commercialisation activities and technology transfer requirements.
• Sound knowledge of complementary medicines regulatory environments, requirements and industry standards, including TGA, FDA and China GB regulations.
• Ability to review and interpret technical documentation, including Certificates of Analysis (CoAs), raw material specifications, manufacturing documentation, validation reports and stability studies.
• Proficiency in interpreting stability data, identifying trends, and translating findings into actionable insights and recommendations that support product quality, risk management and evidence-based decision-making throughout the product lifecycle.
• Availability to travel locally and interstate to support business needs as required.

H&H Group believes in the benefits of a diverse & inclusive workplace & aims to reflect the varied cultures within which we exist. We are committed to providing a working environment that is free from discrimination & harassment,creating a safe and inclusive environment for all.

We encourage applications from people of all ages, nationalities, religions, racial and gender identities,sexual orientations, abilities and cultures, & our hiring decisions will be based on business needs, position requirements, & the qualifications and experience of individuals. If you require support or assistance during the application process, please notify us at the time of application and we will be sure to enable reasonable adjustments where suitable.