36 Pharmaceutical Production jobs in India
Pharmaceutical Production Executives
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Updated knowledge in pharmaceutical manufacturing technologies with experience in production planning, exposure to WHO-GMP norms, documentation skills and people management skills will be essential.
To follow and implement the systems, procedures, and practices for packaging operations and execution of production packing plan.
Organize regular Preventive maintenance of packing machines, able to perform troubleshooting during product packing operation to reduce downtime
Preparation of SOPs, Preparation, and Review of Art Work, Review of Packing specification, and various GMP documents.
Carry out in-process checks, online documentation as per the respective SOP and Batch records
Reporting and investigation of the Deviation, Market complaints or any Noncompliance in the Production area.
Execution of Production packing Plan, monitoring of shop floor activity, Instant shop-floor planning, Meeting all the delivery schedules as committed in the Business Plan.
**Job Types**: Full-time, Regular / Permanent, Fresher
**Salary**: ₹15,000.00 - ₹30,000.00 per month
**Benefits**:
- Health insurance
- Leave encashment
- Paid time off
- Provident Fund
Schedule:
- Day shift
- Monday to Friday
- Weekend availability
- Weekend only
Supplemental pay types:
- Performance bonus
- Shift allowance
- Yearly bonus
Ability to commute/relocate:
- Hosur, Tamil Nadu: Reliably commute or planning to relocate before starting work (required)
**Speak with the employer**
+91
- Health insurance
Production / Systems Planner | FMCG / Pharmaceutical Manufacturing Industry
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Production / Systems Planner | FMCG / Pharmaceutical Manufacturing Industry
- Generous salary package
- South Eastern suburbs
- Pharmaceutical Manufacturing industry
The role:
We have an exciting opportunity for a hands-on Production Planner to plan and execute production activities and help implement and improve current systems on site. You will be proactive, have a positive attitude and be flexible to support internal team and external stakeholders, including supply chain, purchasing and production.
The successful candidates will have:
- Proven experience as a Production Planner or similar role - FMCG/pharmaceutical/food background highly desired
- Understanding of short-shelf life and sterile products
- Excellent analytical, organisational and planning skills
- Ability to drive and apply continuous process improvement strategies
- Excellent communication and interpersonal skills.
- Intermediate to advanced computer skills
- Strong experience with ERP/MRP/SAP or similar systems
- Tertiary qualifications in Operations, Supply Chain or a related business discipline desired
Don’t miss out on a great opportunity to join a growing business! APPLY NOW!
For more information email or call 0407 300 881 for a confidential discussion.
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 Production Manager - Pharmaceutical Manufacturing - South Eastern Suburbs
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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
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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
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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
Pharmaceutical Manufacturing Operator / Line Setter
Posted today
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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
Senior IT Manager in Pharmaceutical Manufacturing
Posted today
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Job Description
Job Title:
Digital Infrastructure Specialist in Pharmaceutical Manufacturing
We are looking for a skilled Digital Infrastructure Specialist to lead our IT operations and ensure seamless integration of technology with manufacturing processes.
This role requires a strong background in server management, networking, and information security. The ideal candidate will have experience in designing and implementing robust infrastructure systems that support various internal functions within the manufacturing facility.
The successful candidate will oversee the installation, configuration, and management of servers, ensuring optimal performance for reliable operations. They will also manage active and passive networking components, including switches, routers, firewalls, and cable systems.
In addition to technical skills, the candidate must have a good understanding of pharmaceutical processes and their importance on product quality and safety. They will ensure all IT systems comply with industry regulations and standards, particularly those relevant to GxP standards.
Maintaining good documentation practices for IT infrastructure, applications, configurations, and procedures is crucial for this role. The candidate should be able to ensure information security measures, including cybersecurity protocols and privacy security standards to protect sensitive data.
Collaboration with cross-functional teams and headquarters departments is essential for resolving systems issues, improving processes, and implementing new projects.
The ideal candidate should have experience in diagnosing and resolving technical issues related to IT systems, providing timely support to minimize downtime. They should also be able to perform root cause analysis for specified issues.
Data backup of all critical systems and knowledge of online backup systems like Veeam and Acronics are essential skills for this role.
Familiarity with major audits like US FDA, MHRA, TGA, and relevant guidelines and compliance standards is desirable. Knowledge of cGAMP and compliance requirements like 21 CFR Part 11 and EU-Annexure 11 is also an advantage.
This role requires strong analytical and problem-solving skills, as well as the ability to assess system gaps and implement corrective actions. Experience in L1 system upgrades and L2 integration, such as DAS/Historian, is also beneficial.
Knowledge of quality management systems, change controls, incidents, and deviations handling, RA & CAPA is a must. Awareness of Industry 4.0 strategies and smart manufacturing initiatives will be an advantage.
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Night Shift Manager | Pharmaceutical Manufacturing Industry
Posted today
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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
Production Formulator – Pharmaceutical Contract Manufacturer
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Production Formulator – Pharmaceutical Contract Manufacturer
- Opportunity to grow in a stable, Australian owned and operated company as a Production Formulator.
- South Eastern suburb location
This Large Scaled Manufacturing Facility has a lot to boast about, working with the most astute talent in the pharmaceutical space it consists of an R&D department, state of the art manufacturing plant, warehousing and logistic solutions along with a workforce of 250 people to ensure clients requirements are met on-time and to their strict requirement guidelines.
In order to be successful for one of these amazing opportunities you must be able to demonstrate:
- Solid experience as a formulator
- Experience working in GMP / HACCP / TGA regulated environments in either Food FMCG or Pharma
- Must be available day and afternoon shift
- Excellent written, mathematic and communication skills
- High level of attention to detail
If you are interested in this exciting opportunity and want to join a company that will support your development and growth, submit your resume now.
This position has been filled, but openings for this type of position come up very frequently. We highly recommend to Register Your Interest below so that you will be the first to know when the next position opens up.
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.
Register Interest
Reliability Engineer | Pharmaceutical Manufacturing Industry | South East
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Reliability Engineer | Pharmaceutical Manufacturing Industry | South East
- South East Melbourne
- Day Shift
- A great opportunity to work with the maintenance department
- Work with great management, supervisors and a rewarding company
- Opportunities for learning and progression
- Full Job Description and Recruitment Information Pack available to shortlisted candidates
We are seeking a skilled Mechanical Reliability Engineer to join a leading Pharmaceutical Manufacturing company based in the South East of Melbourne. You will have:
- A have a solution focused mindset
- A positive attitude
- A love of learning (having exposure to more advanced reliability techniques is nice to have)
- A drive for the responsibility of having production run at its optimal through detailed analysis of equipment and technical expertise.
Responsibilities include; but not limited to:
- Collaborating with Production, Engineering, Maintenance & Quality teams to identify ongoing issues and aim to improve overall equipment productivity, reliability and production continuity
- Dig deep into issues to find the root cause the problem across the areas of, safety, quality, productivity, people and continuous improvement
- Understand the goal of the department and team to contribute your skills and knowledge for it’s plans such as cost reduction, innovation and ensuring full GMP compliance
- Providing leadership and support to project outcomes and implementation
About you:
- You will be a tertiary qualified in Mechanical Engineering with an exceptional mechanical and electrical aptitude with proven experience working within a FMCG, or manufacturing environment (Experience working in Food or Pharmaceutical industry would be an advantage)
- You will be proactive, self-motivated, possess excellent communication skills and have the capability to work within a diverse, multi-functional environment and have the ability to effectively manage both internal and external stakeholders.
Don't miss out on a great opportunity to join an expanding Australian owned business!
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