Posted by Overview
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, Shell 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 11th Jan 2025 at Bengaluru location
We’re Hiring! Here’s your opportunity to work at Cipla’s state-of-the-art manufacturing facility at Bengaluru
Cipla Careers Opportunities for Entry Level Graduates 25
Junior Team Member – Statistician
Job Description:
I. Life Cycle Management – Annual Product Quality Review
II. Implementation of New Statistical concepts
III. Root Cause Analysis for Investigations
IV. DOE concepts during Equipment Qualification
Qualification:
Fresher Good Communication Skills in English as well as Hindi, well versed with data analysis and statistical applications, troubleshooting during process.
Software applications required: MINITAB & MS office, SAS, R-Language
Competencies/Skills
Relevant Work Experience
Perform with Accountability
People Management
Lead with Empathy
Collaborate to Succeed
Strong Domain Knowledge
Innovate to Excel
Job Location : Bangalore
For more details to apply, Click here!
Junior Team Member – QA
Job Description:
I. Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
II. Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
III. Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
IV. Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
V. Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
VI. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
VII. Prepare final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements
Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines
Qualification:
B. Pharma/ M.Sc
2 years of experience in quality assurance department
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!
Junior Officer – Production
Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets
Job Description:
I. Execute production activities in a shift by managing available resources to achieve production target
II. Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
III. Prepare manufacturing records and update online documentation to meet production and cGMP requirements
IV. Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment
V. Execute production activities in a shift by managing available resources to achieve production target
Qualification:
Bachelor in Pharmacy
2 years of experience in pharmaceutical manufacturing
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!
Junior Officer – Engineering
Job Description:
Execute the maintenance activities in the plant & ensure the minimum breakdown with maximum efficiency by following safety & GMP Standards
I. Give inputs for preparing & adhere to unique planner for planned preventive maintenance & instrument calibrations for effective maintenance and adherence to standards.
II. Handle breakdown maintenance to avoid recurrence and maintain continuous process operations
III. Use new technologies initiated by Management while adhering to CAPEX and OPEX targets to improve Machine/system performance
IV. Follow HSE safety standards to maintain high level of Safety during maintenance so as to avoid major breakdown and report accidents/ incidences
V. Perform Material and Spare management and issue Consumables, spares , materials , log books etc. in order to avoid delays due to unavailability of materials
Qualification:
Graduate Engineer / Diploma In Engineering
2 years of experience in Pharma / API industry (Maintenance and Projects)
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!
Medical representative – US
As a Sales Representative based in Rabat , you will be responsible for promoting Cipla Maroc products to healthcare professionals. You will play a key role in expanding sales and achieving business objectives in your assigned territory, while maintaining strong relationships with physicians, pharmacists and other key partners.
Job Responsibilities:
Promote Cipla products to healthcare professionals (doctors, pharmacists, etc.).
Ensure the achievement of sales and growth objectives in the assigned geographic area.
Building strong, lasting relationships with healthcare professionals to ensure loyalty to Cipla products.
Plan and organize regular visits to provide information on products and the latest therapeutic innovations.
Actively participate in conferences, workshops and events to promote Cipla products.
Analyze the market and competitive activities to optimize the business strategy.
Respect the ethical and legal standards of the pharmaceutical industry in all interactions with healthcare professionals.
Qualifications
Excellent personal leadership skills and autonomy in achieving objectives.
Proactivity, ability to solve problems and adapt to a constantly changing environment.
Exceptional communication skills and ability to build lasting relationships with healthcare professionals.
An ability to work in a team and collaborate with other departments, such as marketing and medical, to ensure excellence in the execution of strategies.
A degree in life sciences, pharmacy, or a relevant medical field is a major asset.
Fluency in French and Arabic; English is a plus, both spoken and written.
For more details to apply, Click here!
QA Analyst I – US
The purpose of the QA Analyst position is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs).
The Quality Assurance (QA) Analyst position is an individual contributor role and a member of the InvaGen Pharmaceuticals Quality Team. The position reports to the Quality Assurance Manager and maybe matrixed to other functional leaders within the Quality or other departments.
QUALIFICATIONS
Minimum high school diploma.
Advanced vocational training or education in pharmaceutical manufacturing, industrial management or related field of study from an accredited college/university.is preferred.
Minimum of three (3) years’ experience in a quality assurance in a GMP pharmaceutical manufacturing operation and work environment.
Experience in MDI or parentals preferred.