IPQC (In Process Quality Control) / Quality Assurance

Lavida Pharmaceuticals; Sydney; Presencial; AUD 70.000 - 95.000; Jornada completa

Descripción de la vacante

Lavida Pharmaceuticals in Eastern Creek Sydney is seeking an IPQC (In Process Quality Control) / Quality Assurance professional to lead day-to-day QC activities across pharmaceutical production. You will ensure product quality metrics through process controls, accurate documentation and defect prevention.

You will perform in-process testing on dosage forms, support manufacturing processes, train staff on QC procedures, ensure GMP compliance, and help deliver on-time product releases while

Formación

• A Bachelor of Science, Quality Assurance or related field.
• Experience in chemical analysis.
• Working hours starting from 6:30am every weekday and experience with quality documentation and product review.
• Strong understanding of quality control methodologies, mechanical systems and regulatory compliance in the pharmaceutical industry.
• Advanced knowledge of Excel or other spreadsheet software is preferred.
• Strong understanding of GMP requirements and pharmaceutical quality processes.
• Clear and concise communication skills.
• Excellent attention to detail and written communication skills.
• Commercial awareness and the ability to apply technical knowledge in a practical manner.
• A collaborative approach and willingness to support colleagues as required.
• Effective time management and organizational skills.
• A professional approach, confidence and the ability to work effectively under pressure.

Responsabilidades

• Perform in-process quality control testing and inspections at various stages of manufacturing for all dosage forms, including solid oral dosage forms.
• Conduct physical testing of raw materials, intermediates and finished products in accordance with approved standard operating procedures and compendial methods.
• Participate in the design and validation of manufacturing processes and equipment to ensure suitability for pharmaceutical production.
• Document and record testing procedures, results and observations accurately in compliance with regulatory guidelines and GMP requirements.
• Analyze and interpret test results and promptly report deviations or non-conformances to the appropriate personnel.
• Investigate out-of-specification and out-of-trend results, conduct root cause analysis and contribute to corrective and preventive actions.
• Provide technical support and training to production personnel on quality control procedures.
• Support production and business goals by helping ensure quality standards and committed product delivery dates are achieved.

Conocimientos

Chemical analysis

Quality control

Regulatory compliance

Excel

Written communication

Educación

Bachelor of Science, QA or related field

Descripción del empleo

IPQC (In Process Quality Control) / Quality Assurance

Join Lavida Pharmaceuticals Eastern Creek Sydney facility as an IPQC (In Process Quality Control) / Quality Assurance professional responsible for leading day-to-day quality control activities in pharmaceutical production. You will help ensure production quality metrics are achieved through effective process controls, employee training, accurate documentation and defect prevention across a range of dosage forms.

Key responsibilities

Perform in-process quality control testing and inspections at various stages of manufacturing for all dosage forms, including solid oral dosage forms.

Conduct physical testing of raw materials, intermediates and finished products in accordance with approved standard operating procedures and compendial methods.

Participate in the design and validation of manufacturing processes and equipment to ensure suitability for pharmaceutical production.

Document and record testing procedures, results and observations accurately in compliance with regulatory guidelines and GMP requirements.

Analyze and interpret test results and promptly report deviations or non-conformances to the appropriate personnel.

Investigate out-of-specification and out-of-trend results, conduct root cause analysis and contribute to corrective and preventive actions.

Provide technical support and training to production personnel on quality control procedures.

Support production and business goals by helping ensure quality standards and committed product delivery dates are achieved.

Maintain compliance with GMP requirements relating to the safety and hygiene of materials, products, goods and production processes.

Adhere to safety requirements and maintain a clean and organised work environment.

Fulfil other duties as required by management and other department personnel.

What we're looking for

A Bachelor of Science, Quality Assurance or a related field.

Experience in chemical analysis.

Working hours starting from 6:30am every weekday and experience with quality documentation and product review.

Strong understanding of quality control methodologies, mechanical systems and regulatory compliance in the pharmaceutical industry.

Advanced knowledge of Excel or other spreadsheet software is preferred.

Strong understanding of GMP requirements and pharmaceutical quality processes.

Clear and concise communication skills, with the ability to adapt communication style to different audiences.

Excellent attention to detail and written communication skills.

Commercial awareness and the ability to apply technical knowledge in a practical manner.

A collaborative approach and willingness to support colleagues as required.

Effective time management and organizational skills, with the ability to meet schedules and deadlines.

A professional approach, confidence and the ability to work effectively under pressure.