Manufacturing Scientist (Pharmaceutical Manufacturing)

Evolve Scientific; Rutherford; Vor Ort; AUD 55.000 - 83.000; Vollzeit

Benefits dieser Stelle

Free on-site parking

Collaborative team environment

Exposure to global veterinary pharma

Zusammenfassung

Evolve Scientific is seeking a Manufacturing Scientist to join the Rutherford facility on an initial 4-month contract. You will support process validation, cleaning validation and media fill activities ensuring GMP compliance, while authoring and reviewing validation protocols and reports.

Working within a documentation-focused team, you will coordinate sample collection, liaise with Production and Quality, and contribute to continuous improvement in a regulated manufacturing environment.

Qualifikationen

• Bachelor's Degree in Science, Chemical Engineering, Industrial Engineering or related discipline.
• Experience in pharmaceutical/biopharmaceutical or cosmetics manufacturing environments.
• Direct validation experience in a regulated GMP environment.
• Experience authoring validation protocols and validation reports.
• Strong data analysis and technical documentation skills.
• Experience reviewing batch documentation and manufacturing records.
• Understanding of pharmaceutical quality systems and GMP requirements.

Aufgaben

• Author and review process validation protocols and reports.
• Support process validation, cleaning validation and media fill activities.
• Analyse validation data and prepare technical reports.
• Review batch and manufacturing documentation.
• Ensure validation protocols are executed in accordance with requirements.
• Coordinate sample collection and validation activities.
• Liaise with Production teams regarding validation planning and execution.
• Liaise with Quality teams to support GMP compliance and document approval.
• Support new product introduction activities.
• Assist with validation-related deviations, investigations and CAPAs.
• Support process improvement initiatives and manufacturing operations as required.

Kenntnisse

Data analysis

Documentation

Validation

GMP knowledge

Stakeholder engagement

Autonomy

Prioritization

Ausbildung

Bachelor's Degree in Science/Engineering

Tools

Minitab

SAP

ETS

Viva document control

Jobbeschreibung

About the Company & Role:

Join a Leading Veterinary Pharmaceutical Company who specialise in the development and manufacturing of veterinary medicines. This is your chance to be part of a team committed to excellence and innovation. An exciting opportunity is available for a Manufacturing Scientis t to join their Rutherford manufacturing facility on an initial 4-month contract. Working within the Validation team, you will support process validation, cleaning validation and media fill activities while ensuring compliance with GMP requirements.

This is a documentation-focused role suited to candidates with experience authoring validation protocols and reports, analysing validation data, reviewing batch documentation and collaborating with Quality and Production teams within a regulated manufacturing environment.

Duties:

• Author and review process validation protocols and reports
• Support process validation, cleaning validation and media fill activities
• Analyse validation data and prepare technical reports
• Review batch and manufacturing documentation
• Ensure validation protocols are executed in accordance with requirements
• Coordinate sample collection and validation activities
• Liaise with Production teams regarding validation planning and execution
• Liaise with Quality teams to support GMP compliance and document approval
• Support new product introduction activities
• Assist with validation-related deviations, investigations and CAPAs
• Support process improvement initiatives and manufacturing operations as required

Skills & Experience:

• Bachelor's Degree in Science, Chemical Engineering, Industrial Engineering or a related discipline
• Experience within pharmaceutical, biopharmaceutical, consumer healthcare or cosmetics manufacturing environments
• Direct validation experience within a regulated GMP environment
• Experience authoring validation protocols and validation reports
• Strong data analysis and technical documentation skills
• Experience reviewing batch documentation and manufacturing records
• Understanding of pharmaceutical quality systems and GMP requirements
• Experience with Minitab, SAP, ETS, Viva document control systems - highly regarded
• Experience with synthetic chemical manufacturing processes - highly regarded
• Strong communication and stakeholder engagement skills
• Ability to work autonomously and manage multiple priorities

Culture & Benefits:

• Free on-site parking for your convenience
• Be part of a collaborative and experienced technical team
• Work closely with Validation, Production and Quality professionals
• Gain exposure to a globally recognised veterinary pharmaceutical manufacturer
• Supportive team environment with strong technical leadership

A police check and pre-employment medical (including drug and alcohol screening) are required prior to commencement. These will be organised by the company.

For any questions about the role, contact Mairead on +61 ***********.