53 Pharmaceutical Production jobs in India

Night Shift Production Manager - Pharmaceutical Manufacturing - South Eastern Suburbs

Night Shift Production Manager - Pharmaceutical Manufacturing - South Eastern Suburbs

• $80,000-$90,000 (negotiable subject to experience) + 30% shift loading + 9.5% Super
• Supervising up to 25 employees
• Monday to Friday - 10 pm to 6 am

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

Apply now!

(As we are currently receiving a high number of applications, only shortlisted applicants will be contacted)

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

Production Supervisor - Pharmaceutical

Seeking: Production Supervisor - Pharmaceutical

Location: South Eastern Suburbs

Industry: Pharmaceutical

Experience level: 5 - 8 years

Shift time: 7am - 3pm

Objective:

To provide supervision and quality control for all production lines in designated area. Must have the willingness and capability of communicating to the line operators the need for the strictest compliance with the code of GMP and, the Safety, Health and Environmental requirements of the company.

Day-to-day responsibilities:

• Be a role model to all employees by maintaining the highest standard of compliance with the companies GMP and Safety, Health and Environmental policies and procedures.• Direct process line supervision.

• Assist in employee training reviews and where required, in the development and delivery of the training.

• Labour allocation to be commensurate with production requirements, any excess labour to be returned to the site labour coordinator or appropriate area shift manager.

• Assist with employee performance reviews; report any employee skill or attitude deficiencies that may have a negative impact on your production program.

• Provide objective feedback to the area manager regarding subordinate compliance with GMP and OHS training. Specifically gaps in understanding and practical application. Do not permit any employee to continue to work if they are in breach of Personal Hygiene & Gowning Requirements.

• Communicate updates of SOP’s and other quality/safety specific documentation changes when required.

• Report any discrepancies between theoretical and practical application of work instructions to the area manager, participate in SOP upgrades if required.

• Conducts QC checks when required by EJS through all lines for designated area.

• Focus on line start-ups for all lines in designated area.

• Direct communication with line crews about what they are to be observant of in relation to quality and safety.

• Liaise with setters, always working as a team to ensure production lines run efficiently.

• Liaise with component marshals for line changeovers to ensure reconciliations and returns occur promptly and in real time.

• Ensure that the half hourly labour rotation is adhered to.

• Ensure that you have provided suitable manual handling direction to the line operators and ensure that manual handling equipment is used where reasonable available to minimise any risk of injury.

• Report to your manager any manual handling activities that present risk of injury.

Key requirements:

• 5 - 8 years of experience in a similar Production Supervisory role within Pharmaceutical or Food Manufacturing.
• Degree Qualification in business, science, engineering is ideal but not mandatory.
• Experience with GMP, HSE and quality control in a TGA environment highly advantageous
• Must have PR or AU / NZ Citizenship

If you meet the above requirements, we would love to hear from you, please apply directly to this ad or email your resume to:

(Please note, only shortlisted candidates will be contacted)

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

Seeking: Afternoon Shift Production Supervisor for the Pharmaceutical Manufacturing Industry

Seeking: Production Supervisor for the Pharmaceutical Manufacturing Industry

Location: South Eastern Suburbs

Industry: Pharmaceutical

Experience level: 5 - 8 years

Shift time: 2:10pm to 10:10pm (Monday to Friday)

Annual Salary: $75K - $80K + Super

Workforce: 30 - 40 people in Specific Department (Company has 400+ employees all up)

Objective:

To provide supervision and quality control for all production lines in designated area. Must have the willingness and capability of communicating to the line operators the need for the strictest compliance with the code of GMP and, the Safety, Health and Environmental requirements of the company.

Day-to-day responsibilities:

• Be a role model to all employees by maintaining the highest standard of compliance with the companies GMP and Safety, Health and Environmental policies and procedures.

• Direct process line supervision.

• Assist in employee training reviews and where required, in the development and delivery of the training.

• Labour allocation to be commensurate with production requirements, any excess labour to be returned to the site labour coordinator or appropriate area shift manager.

• Assist with employee performance reviews; report any employee skill or attitude deficiencies that may have a negative impact on your production program.

• Provide objective feedback to the area manager regarding subordinate compliance with GMP and OHS training. Specifically gaps in understanding and practical application. Do not permit any employee to continue to work if they are in breach of Personal Hygiene & Gowning Requirements.

• Communicate updates of SOP’s and other quality/safety specific documentation changes when required.

• Report any discrepancies between theoretical and practical application of work instructions to the area manager, participate in SOP upgrades if required.

• Conducts QC checks when required by EJS through all lines for designated area.

• Focus on line start-ups for all lines in designated area.

• Direct communication with line crews about what they are to be observant of in relation to quality and safety.

• Liaise with setters, always working as a team to ensure production lines run efficiently.

• Liaise with component marshals for line changeovers to ensure reconciliations and returns occur promptly and in real time.

• Ensure that the half hourly labour rotation is adhered to.

• Ensure that you have provided suitable manual handling direction to the line operators and ensure that manual handling equipment is used where reasonable available to minimise any risk of injury.

• Report to your manager any manual handling activities that present risk of injury.

Key requirements:

5 - 8 years of experience in a similar Production Supervisory role within Pharmaceutical or Food Manufacturing.Degree Qualification in business, science, engineering is ideal but not mandatory.

Experience with GMP, HSE and quality control in a TGA environment highly advantageousMust have PR or AU / NZ Citizenship

If you meet the above requirements, we would love to hear from you, please apply directly to this ad or email your resume to:

(Please note, only shortlisted candidates will be contacted)

Employer questionsYour application will include the following questions:

Which of the following statements best describes your right to work in Australia?Which of the following statements best describes your Covid-19 vaccination status?

How many years' experience do you have as a Pharmaceutical Manufacturing Production Supervisor?Which of the following forklift licences do you have?

Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?What's your expected annual base salary?

How much notice are you required to give your current employer?Are you willing to undergo a pre-employment medical check?

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 and pharmaceutical manufacturing processes to improve yield, efficiency, and quality.
• Lead the scale-up of laboratory processes to commercial manufacturing, ensuring robust and reproducible results.
• Develop and implement process validation strategies and protocols in compliance with regulatory requirements (e.g., FDA, EMA).
• Troubleshoot and resolve complex process-related issues, identifying root causes and implementing effective corrective actions.
• Collaborate with R&D, Quality Assurance, and Production teams to ensure seamless integration of new processes and technologies.
• Develop Standard Operating Procedures (SOPs) and batch records for manufacturing processes.
• Conduct process hazard analyses (PHAs) and implement safety measures to ensure a safe working environment.
• Utilize process simulation software and data analysis tools to model and predict process performance.
• Stay current with industry trends, new technologies, and regulatory changes in pharmaceutical manufacturing.
• Mentor and guide junior engineers, fostering a culture of continuous improvement and technical excellence.
• Manage process improvement projects, including defining scope, objectives, and timelines.
• Prepare technical reports, documentation, and presentations for internal stakeholders and regulatory submissions.
• Ensure compliance with all GMP, safety, and environmental regulations.
• Evaluate and recommend new equipment and technologies to enhance manufacturing capabilities.
• Optimize existing processes for cost reduction and waste minimization.

• Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a closely related field.
• Minimum of 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
• Strong understanding of GMP, FDA, and other relevant regulatory guidelines.
• Proven experience in process design, scale-up, optimization, and validation.
• Proficiency in process simulation software (e.g., Aspen Plus, CHEMCAD) and statistical analysis tools.
• Excellent analytical, problem-solving, and project management skills.
• Demonstrated ability to lead projects and mentor junior team members.
• Strong communication and interpersonal skills, essential for remote collaboration.
• Experience with process analytical technology (PAT) is a plus.
• Knowledge of sterile manufacturing processes is advantageous.
• Ability to work independently and manage multiple priorities effectively in a remote setting.

• Design, develop, and implement new chemical processes or improve existing ones for pharmaceutical manufacturing.
• Conduct feasibility studies, pilot plant trials, and scale-up operations for chemical processes.
• Optimize process parameters to enhance yield, purity, safety, and reduce costs.
• Troubleshoot process-related issues and implement corrective actions to maintain product quality and operational efficiency.
• Develop and maintain process documentation, including P&IDs, operating procedures, and batch records.
• Ensure compliance with all relevant regulatory requirements, including GMP, FDA, and environmental standards.
• Collaborate with R&D, production, quality control, and maintenance teams to achieve project goals.
• Perform process hazard analyses (PHAs) and implement necessary safety measures.
• Evaluate and recommend new equipment and technologies for process improvement.
• Provide technical support and training to plant operations personnel.

• Bachelor's or Master's degree in Chemical Engineering or a related discipline.
• Minimum of 5-8 years of experience in process engineering, preferably within the pharmaceutical or fine chemical industry.
• Proven experience in process design, scale-up, optimization, and troubleshooting.
• Strong understanding of chemical reaction engineering, thermodynamics, fluid mechanics, and separation processes.
• Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements for pharmaceutical production.
• Experience with process simulation software (e.g., Aspen Plus, HYSYS) is highly desirable.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong communication and interpersonal skills, with the ability to work effectively in a multidisciplinary team.
• Proficiency in technical documentation and report writing.
• Commitment to safety, quality, and continuous improvement.

• Lead the design, optimization, and validation of pharmaceutical manufacturing processes.
• Ensure compliance with cGMP and other relevant regulatory requirements.
• Troubleshoot and resolve process-related issues to maintain operational efficiency.
• Drive continuous improvement initiatives to enhance product quality and reduce costs.
• Collaborate with R&D, QA, and Operations teams on process development and scale-up.
• Manage process transfer projects and implement new manufacturing technologies.
• Mentor and guide junior process engineers.

• Bachelor's or Master's degree in Chemical Engineering or a related field.
• Minimum 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
• Proven expertise in process validation, scale-up, and optimization.
• Strong knowledge of cGMP regulations and pharmaceutical manufacturing standards.
• Proficiency in process simulation software and statistical analysis tools (SPC, DoE).
• Excellent leadership, communication, and project management skills.
• Experience with Lean manufacturing principles 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

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

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