Cipla Ltd Recruitment 2023. Cipla Ltd Notification full details below.Intrested and eligible candidates can Send Apply Online.Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms.
Vacancy details:
- Post Name: Junior Officer/Junior Operator – Production/Junior Officer – PackingFormulation ADL – Analyst
- Qualification: M. Sc. (Analytical Chemistry) / M. Pharm/Bachelor in Pharmacy/Diploma in Pharmacy / Mechanical Engineering
- Experienced:2 years of experience in quality assurance department
Job Description: Greeting From Cipla Ltd !!!!
Important Details :
- Location: India -Goa/Maharashtra – Vikhroli
- Post of date:28/01/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Roles and Responsibilities:
Division
IPD
Department
Formulation ADL
Job Purpose
Execute the core method development activities and conduct analysis of routine as well as stability samples to finalize specifications and ensure timely delivery of product to unit.
Key Accountabilities (1/6)
- Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators
- Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation
- Document and interpret the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms
- Provide support to units or CFTs for transfer of analytical methods and techniques by visiting and demonstrating them with the relevant analysis to ensure successful and timely transfer of products
- Maintain proper safety, GLP, and GMP environment in the work place to minimize accidents and incidents
- Review the analytical requirements and recommend corrections in specifications by coordinating with units and CFTs to ensure smooth operations
Education Qualification
M. Sc. (Analytical Chemistry) / M. Pharm
Relevant Work Experience
- 2-4 years of experience in pharmaceutical organisation with knowledge of handling instruments like HPLC, GC, Dissolution tester and DPI related instruments
- Knowledge of current guidelines like ICH, EMEA, WHO
Department
Employment Type
Job Purpose
Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets
Accountabilities
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
Department
Employment Type
Job Purpose
Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift
Accountabilities
I. Operate the equipment efficiently without error and deviation as per SOP to meet shift targets
II. Provide suggestions for optimization of processes to manufacture quality product
III. Execute and update online documentation to meet cGMP requirements
IV. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations
Education Qualification
Diploma in Pharmacy / Mechanical Engineering
Relevant Work Experience
2 years of experience in a manufacturing organisation preferably in pharmaceutical industry
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