Cipla is a leading global pharmaceutical company headquartered in India, known for its strong focus on respiratory, anti-retroviral, and chronic disease treatments. Founded in 1935, the company has grown into a trusted name in over 80 countries, supplying affordable and high-quality medicines to millions of patients worldwide.
Cipla’s impact is especially significant in improving access to life-saving drugs in developing markets while maintaining a strong presence in regulated regions like Europe and North America. With a workforce spanning research, manufacturing, and commercial operations, Cipla continues to expand, creating consistent job opportunities across multiple disciplines.
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Current Vacancies at Cipla
Lead National Accounts – Remote
Major Tasks:
Manage specific customer relationships
Deliver perspective and strategy around proposals and opportunities (future-looking and pipeline) for assigned accounts
Support the sales administration and operational needs of the customer
Increase the depth of sales with accounts.
Assess market needs, review objectives, develop actions plans for achieving sales targets.
Deliver product proposals and effectively position company against competitors to “win” at the customer
Present the company story and strategy during customer introductions and ongoing engagements to continuously strengthen the company’s position within the customer.
Evaluate existing and future portfolio against assigned customer base and direct company to align customer interests to available products
Maintain customer forecasts and support demand planning function.
Qualifications:
10+ years of total sales experience, preferred last 5 years with direct pharmaceutical experience with an emphasis on key account management; generics sales experience a plus
Good analytical skills
Good people management skills to coordinate with multiple teams and get the work done in time
Strong interpersonal skills to develop relationships with customers
QC Chemist III – MDI
Major Tasks:
Conduct routine testing or other analysis in a specific group or department setting.
Conduct advanced testing and/or critical testing, as required.
Operate specialized equipment or conduct specialized skill testing
Working knowledge of raw materials testing and release
Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP
Lead investigation activities.
Ensure compliance to all data integrity and cGMP practices, procedures, and expectations.
Ensure compliance with all good documentation practices.
Other duties and responsibilities as assigned by the Head of the Department or Section Head
Qualifications:
- Bachelor’s degree (BS or BA), physical sciences preferred
- Proficiently speak English as a first or second language
- Proficiently communicate and understand (read and write) scientific work in English
- Have excellent organization, learning and teaching skills required to work in teams
- Ability to understand and analyse complex data sets.
- Working knowledge of Microsoft Office programs and other scientific based software.
- Experience in Inhalation products (MDI) is a plus
Manufacturing Operator I – MDI 2nd Shift
Major Tasks:
- Dispensing raw material and primary packing materials as per work order.
- Ensure the proper planning and execution of batches.
- Monitoring cleaning and sanitation of production area and machinery as per respective SOP during batch to batch and product to product changeover.
- Daily monitoring and recording of production materials and production lines.
- Conducting process checks and recording in batch manufacturing record.
- Controlling machine operations with minimum rejections and maximum outputs while maintaining quality standards within the standard norms.
- Operating equipment and performing necessary maintenance on machinery.
- Safeguard equipment for smooth functioning with co-ordination of engineering for preventive maintenance and calibration.
- Manufacturing and filling of products as per Batch Manufacturing Records and SOP.
- Maintaining inventory of machine parts, tools and accessories.
- Working individually and in collaboration with others as part of a team.
- Coordinating with other departments like packaging, engineering, QA and QC for better planning and execution
Qualifications:
Maintaining 100% cGMP and SOP Compliance during complete operation hours.
Complying with all company policies and procedures.
Reporting all issues that arise to the department head or reporting manager.
Performing daily maintenance on equipment and machinery.
Completing all documentation in a timely manner, ensuring their integrity, accuracy and completeness.
Maintaining discipline in department.
May be required to assist in the training of other employees in the department.
Flexible to work extended hours to achieve the manufacturing schedule when needed.
Packaging Operator I – 2nd Shift
Major Tasks:
Understanding basics of mechanical machinery and principles of control systems.
Operating pharmaceutical packaging equipment with minimum rejection and maximum output, maintaining quality standard within standard norms.
Cleaning machines and areas as per batch-to-batch and product-to-product changeovers.
Performing operations and preventative maintenance of machines.
Identifying and assisting in the corrective actions of packaging-related issues.
Correcting status labelling at all stages of the packing line with a signature.
Ensuring that appropriate equipment calibrations are performed and records are maintained.
Ensuring line clearance before initiating packaging activities in each area.
Wearing appropriate PPE as stated in the SOP before initiating the process.
Working individually and in collaboration with others as part of a team.
Executing procedures to complete tasks in a safe and efficient manner.
Completing documents on time, ensuring accuracy and completeness.
Adhering to all cGMPs, compliance/regulatory mandates and quality requirements.
Qualifications:
A high school diploma or equivalent is required.
An accredited college certificate or university degree is preferred.
Minimum of one (1) year experience in packaging operations preferred.
Proficient in the English language (speaking/reading/writing) to understand work instructions and document results.
Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment is highly preferred.
Basic understanding of mechanical machinery and the operating principles of control systems.
Ability to follow both verbal and written instructions.
Demonstrated ability to work in both independent and team environments.
Good knowledge of health & safety procedures, including OSHA.
Strong mathematical and organisational skills.
Machine Operator – Manufacturing 2nd Shift
Major Tasks:
Dispensing raw material and primary packing materials as per work order.
Ensure the proper planning and execution of batches.
Monitoring cleaning and sanitation of production area and machinery as per respective SOP during batch to batch and product to product changeover.
Daily monitoring and recording of production materials and production lines.
Conducting process checks and recording in batch manufacturing record.
Controlling machine operations with minimum rejections and maximum outputs while maintaining quality standards within the standard norms.
Operating equipment and performing necessary maintenance on machinery.
Safeguard equipment for smooth functioning with co-ordination of engineering for preventive maintenance and calibration.
Identifying and assisting in any corrective actions.
Manufacturing and filling of products as per Batch Manufacturing Records and SOP.
Maintaining inventory of machine parts, tools and accessories.
Working individually and in collaboration with others as part of a team.
Coordinating with other departments like packaging, engineering, QA and QC for better planning and execution.
Sampling as per schedule and in coordination with QA and QC.
Check and ensure status labels at all stages of manufacturing and filling.
Qualifications:
- High school diploma or equivalent is required.
- Accredited college certificate or university degree is preferred.
- Minimum one (1) year of manufacturing experience with MDI or aerosol products required.
- Proficient in the English language (Speaking/Reading/Writing) to understand work instructions and document results.
- Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred.
- Basic understanding of mechanical machinery and the operating principles of control systems.
- Ability to follow both verbal and written instructions.
- Demonstrated ability to work in both independent and team environments.
- Good knowledge of Health & Safety procedures, including OSHA.
- Strong mathematical and organizational skills.
Officer – EHS
Major Tasks:
Prevent incidences across Unit to ensure employees and stakeholder¢â¢s safety
Assess and Improve emergency preparedness across Unit to reduce impact of Incidences to human and property
Execution of the planned Activity, promotional Activity and improvement and Statutory compliance
Qualifications:
Science graduate in chemistry/ Diploma or Degree with Diploma in Advance industrial safety
2 years of safety experience in Pharma or chemical industries
How to Apply for Cipla Vacancies
Step 1: Visit the Official Careers Portal
Go to Cipla’s official careers page and search for open roles by location, department, or experience level.
Step 2: Create a Candidate Profile
Register with your email, upload your CV, and complete your professional details. Ensure your profile reflects measurable achievements, not just responsibilities.
Step 3: Filter Relevant Jobs
Use keywords like “graduate”, “entry-level”, or specific roles such as “quality control” to find suitable openings.
Step 4: Submit Your Application
Apply directly through the portal. Tailor your CV and cover letter to match the job description, especially key skills and compliance requirements.
Step 5: Assessment and Interview
Shortlisted candidates may go through:
- Aptitude or technical assessments
- Virtual or in-person interviews
- HR screening for cultural fit
Pro Tips:
Cipla places strong emphasis on regulatory standards. Expect interview questions around GMP, quality control, and ethical practices, especially in technical roles.
Cipla remains one of the most stable and opportunity-rich pharmaceutical companies globally. Whether you are a fresh graduate or an experienced professional, there are multiple entry points into the organisation. The key is not just applying, but applying strategically, aligning your profile with what the company actively needs.
If approached correctly, Cipla vacancies are not just job openings, they are long-term career pathways in a globally respected organisation.
