1,829 Sun Pharmaceutical Industries jobs in India

• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory standards.
• Review and approve batch production and control records.
• Conduct internal audits and inspections of manufacturing processes and facilities.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints.
• Develop, implement, and manage Corrective and Preventive Actions (CAPA).
• Participate in change control management activities.
• Validate processes, equipment, and analytical methods.
• Review and approve Standard Operating Procedures (SOPs) and other quality-related documents.
• Provide quality training to manufacturing personnel.
• Monitor key quality indicators and generate quality reports.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
• Thorough understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
• Experience with quality management systems (QMS).
• Proficiency in reviewing batch records and investigating deviations.
• Strong analytical and problem-solving skills.
• Excellent documentation and technical writing skills.
• Attention to detail and a commitment to accuracy.
• Good communication and interpersonal skills.
• Familiarity with validation processes is a plus.

Pharmaceutical Manufacturing Operator / Line Setter

• South East Melbourne
• Permanent role
• Afternoon and Night Shift

Seeking motivated Line Setters with minimum 2-3 years’ experience, preferably in pharmaceutical or food industry for afternoon and night shift. Do not miss an opportunity to be part of a growing, innovative Australian owned Pharmaceutical company based in South East Melbourne!

Key Responsibilities:

• Ensure that the line runs efficiently and productively; coordinate tasks so that the line runs as continuously as possible
• Troubleshoot and adjust equipment during the run to achieve optimum output and minimal down time minimise wastage
• Set up filling and packing equipment and strip down, wash and reassemble filling equipment to produce a quality product as efficiently as possible
• Monitor the quality of product throughout the filling run and make appropriate adjustments to maintain quality and compliance
• Be able to operate and maintain equipment safely and change parts in a clean and orderly manner
• Ensure that all work is done according to the highest standards of Good Manufacturing Practice (GMP)
• Carry out required tasks in SAP and other systems; complete all relevant documentation and reporting
• Participate in required training, including SOPs, GMP, OH&S and 5S

Key Requirements:

• Written and oral communication skills
• High mechanical aptitude
• Troubleshooting and problem solving skills
• Advanced GMP and sound understanding of OHS
• Proactive, self-motivated and ability to work unsupervised
• Proven machine operating experience in either food manufacturing or pharmaceutical

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IMPORTANT: It is a requirement of all our jobs that you have a PR or AU/NZ Citizenship. A work visa is not sufficient as all our jobs are permanent. Please do not apply if you do not meet these requirements.

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Night Shift Manager | Pharmaceutical Manufacturing Industry

• $80-90k (negotiable subject to experience)
• Supervising up to 25 employees
• Monday to Friday 10pm to 6am

Would you love to work for a growing family owned pharmaceutical business in Melbourne's South East suburbs?

We are looking for someone who loves working Night Shift with a proactive attitude, attention to detail, ability to motivate & organise people effectively, time management skills and have a strong work ethic to supervise the manufacture and packaging of products in compliance with the Australian Code of Good Manufacturing Practice.

Key Job Requirements:

• A minimum 3 years supervision/manufacturing experience within a GMP facility
• Engineering background and sound IT skills desired

Apply now!

IMPORTANT: It is a requirement of all our jobs that you have a PR or AU/NZ Citizenship. A work visa is not sufficient as all our jobs are permanent. Please do not apply if you do not meet these requirements.

Apply Now

• Design, develop, and optimize chemical processes for pharmaceutical manufacturing.
• Create and maintain Process Flow Diagrams (PFDs) and Piping & Instrumentation Diagrams (P&IDs).
• Perform mass and energy balance calculations for chemical processes.
• Conduct Process Hazard Analyses (PHAs) and implement safety measures.
• Troubleshoot process deviations and implement corrective actions.
• Ensure processes comply with GMP, FDA, and other regulatory requirements.
• Lead process validation activities and documentation.
• Identify opportunities for process automation and technology implementation.
• Collaborate with R&D and production teams for process scale-up and technology transfer.
• Monitor process performance and implement continuous improvement initiatives.

• Master's or Bachelor's degree in Chemical Engineering.
• Minimum of 7 years of experience in chemical process engineering, preferably within the pharmaceutical industry.
• In-depth knowledge of chemical engineering principles and unit operations.
• Experience with GMP, FDA regulations, and validation procedures.
• Proficiency in process simulation software (e.g., Aspen Plus).
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills.
• Ability to work effectively in a manufacturing environment.