Cipla Released Job Openings On 04/03/2022.Cipla Limited is an Indian multinational pharmaceutical company, headquartered in Mumbai, India.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Cipla Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.Â
Vacancy Details:
Cipla Recruiting  Graduate/Post Graduate /B. Pharma/ M.Sc with 1-5 years of Experience for Team Member – CDT/Site Head – Safety/Devices scale up & validation expert/Director and Head Supply Chain – Cipla Therapeutics /Team Member – QA/Junior Team Member – QA/Team Member – Primary Packaging Development/Lead – Microbiology/Team Member – Formulation Tech Transfer Position.
Important Details :
- Location: Mumbai/Vikhroli/ Goa/Sikkim – Rangpo
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application:04/03/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : Sun Pharma Walk In On 07th & 8th March 2022 – Unable To Attend Mail Resume Â
Job Description/Skills Required
Team Member – QAÂ
Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines
Accountabilities
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
VIII. Collect, compile and review raw data and finalise the same for timely submission of MHRA, UK interim update document to corporate as per agency requirement by tracking interim updates at a site level, for risk based inspection planning
IX. Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
X. Execute on time and errorless submissions by reviewing product license, all certificates for product registration and tender , staff approvals and other applications to adhere to legal requirements
XI. Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction
Lead – Microbiology
- Communication Skills (clarity of thought, comprehension)
- Likely potential for growth
- Job / Product / Technical Knowledge / Pharma domain knowledge
- Presentation & Interpersonal skills (If applicable)
- Managerial or People Management skills
- Safety awareness (If applicable)
- Relevance of Previous Experience
- Comprehension, Analytical & Problem solving abilities
- Productivity & Result Orientation (If applicable)
- Attitude
- Qualification fitment
- Sales drive (If applicable)
- Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)
Team Member – Primary Packaging Development
Design and propose sustainable, robust, cost effective packaging system and aesthetically appealing primary packaging components by understanding barrier requirements for new product formulations which offer product protection throughout their shelf-life and in order to the product in appropriate condition to the ultimate consumer
Accountabilities
- Analyse Innovator pack characterization and recommend appropriate packaging for new product formulation in order to provide a sustainable, robust and cost-effective packaging system
- Primary Packaging & Device development
- Robustness protocol design, development, execution and reporting
- Device design history file /Design Controls
Therapy Manager
Job Purpose
Achieve the tertiary and secondary business of the division in the respective territory and therapy by managing relationships with the key stake holders viz. doctors & chemists and by creating prescriptions by marketing the company’s brands and providing superior customer service thereby achieving the company’s overall Business targets for the division in India
Accountabilities
I. Achieve the Sales targets by brand marketing against the plan for the year
II. Monitor business details thereby planning the sales achievement
III. Maintain the Basic Working standards for daily operations
IV. Develop and continuously enhance In-clinic Effectiveness for driving better results and increasing prescriptions
V. Manage customer relationship for continued engagement of Key support customers
Site Head – SafetyÂ
- Communication Skills (clarity of thought, comprehension)
- Likely potential for growth
- Job / Product / Technical Knowledge / Pharma domain knowledge
- Presentation & Interpersonal skills (If applicable)
- Managerial or People Management skills
- Safety awareness (If applicable)
- Relevance of Previous Experience
- Comprehension, Analytical & Problem solving abilities
- Productivity & Result Orientation (If applicable)
- Attitude
- Qualification fitment
- Sales drive (If applicable)
- Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)
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