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Cipla is one of the most respected pharmaceutical companies not just in India but across more than 170 countries. Our portfolio includes 2000 products in 65 therapeutic categories with one quality standard globally. Cipla turnover in FY13 was 1.5 billion USD.
Cipla Careers Opportunities for Graduate 2025, Cipla Graduate Freshers in various domain such as HealthCare’s, Finance, Logistics, Engineering, Technology, HR, Finance, Legal, Operation, Business
Cipla Limited is an Indian multinational pharmaceutical company headquartered in Mumbai. Cipla primarily focuses on developing medication to treat respiratory disease, cardiovascular disease, arthritis, diabetes, depression, paediatric and various other medical conditions.
Cipla, a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines invites online applications from eligible Graduate (B.Pharm or B.E) and Diploma (Mechanical/electrical) holders for Walk-In Interview on 22nd Jan 2025 at Goa location
We’re Hiring! Here’s your opportunity to work at Cipla’s state-of-the-art manufacturing facility at Sikkim. Refer to the walk-in interview details below. For those unable to attend, kindly send your application to [email protected].
Cipla Careers Opportunities for Graduates 2025
Team Member – CDT -India
Compile dossier in accordance with regulatory strategy, manage deficiencies, evaluate products and submit tenders to ensure adherence to regulatory requirement for various regulated/international markets within agreed timelines
I. Review documents and compile and handover quality dossier as per enforcement of/updates in regulatory guidelines for various regulated/ international market, so as to minimize deficiencies from the health authority
II. Evaluate and compile quality deficiency response to all regions to meet the targeted timelines of the health authorities/customers.
III. Assess and submit product evaluation and tender documents to regional teams for DRF conversion and product commercialization
IV. Adopt and disseminate information on new regulatory guidelines through ongoing training and interaction with regional teams to minimize deficiencies
Qualification:
Graduate/Post Graduate in Pharmacy or Life Sciences
Relevant Work Experience
5 years in the field of Regulatory Affairs/Quality Assurance
Competencies/Skills
Collaborate to Succeed
Innovate to Excel
Perform with Accountability
Lead with Empathy
Act with Agility
Strong Domain Knowledge
People Management
For more details to apply, Click here!
Pilot Plant Supervisor, Maintenance and Engineering -US
Performing daily maintenance and monitoring of equipment to ensure a high level of reliability.
Participate in designing, implementing, and monitoring, of continuous improvement in the facility.
Assist with installation and commissioning of new equipment.
Evaluate and repair a wide variety of machinery and equipment using acquired knowledge, skills and experience, company supplied tools, some fabrication of parts and new and/or used but serviceable repair parts.
Raise the change controls whenever required changes are to be made in facility and equipment.
Prepare for operation, maintenance and engineering procedures of all equipment.
Fill the deviation report for CAPAs and change controls as per company procedures.
Prepare & implement procedure as per Current Good Manufacturing Practices (cGMP) guidelines by Quality Assurance (QA).
Check and monitor for cleanliness, maintenance, upkeep of the facility, premise and equipment.
Maintain concurrent entries of all operations/activities.
Assist with any carpentry activities to include building walls/rooms with minimal guidance, installing repairs and finish drywall to completion, priming/painting new and existing walls, ceilings, doors, etc. throughout the site internally and externally.
Install and troubleshoot facility electrical systems.
Qualification:
High school diploma required with minimum of three (3) years experience in mechanical maintenance and electrical work in a pharmaceutical or industrial setting.
Bachelors degree, Advanced vocational training or education in pharmaceutical engineering, industrial engineering or related field of study from an accredited college/university is preferred.
Minimum of five (5) years experience in quality assurance in a cGMP pharmaceutical manufacturing operation environment.
For more details to apply, Click here!
Pilot Plant Manufacturing Operator
This job is a multifunctional role. The primary nature of this job is to serve as a Machine Operator. As a secondary requirement, this position will be expected to provide support to other operational functions including but not limited to Warehouse Operations and Facilities Operations.
Job Description:
The Machine Operator performs all functions relating to the production of MDI products; consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP). Incumbents in this position are responsible for the safe and efficient execution of their job duties, while ensuring product compliance to established standards.
Job Responsibilities:
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, filling and packing of products as per Batch Manufacturing and Packing Records and SOP.
Maintaining inventory of machine parts, tools and accessories.
Qualifications:
High school diploma or equivalent is required.
Accredited college certificate or university degree is preferred.
Minimum one (1) year of manufacturing and packing 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.