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, and various other medical conditions.
Overview:
Cipla is hiring eligible and interested applicants for the post of Junior Team Member – QC at their Sikkim, India location.
To complete details for this job are as follows.
Role and Responsibilities:
- Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis
- Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body
- Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements
- Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit
- Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed
Education Qualification
- M.Sc. / B. Pharma
Relevant Work Experience
- 2 years of experience in QC department of a pharmaceutical organization
Competencies/Skills
- Collaborate to Succeed
- Innovate to Excel
- Perform with Accountability
- Lead with Empathy
- Act with Agility
- Strong Domain Knowledge
- People Management
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Team Member – Project Management
Job Purpose
Plan, monitor and execute IPD projects within budget and time to secure the launches as per the business need
Accountabilities
I. Drive successful product approval by developing product development strategy and a detailed work plan to ensure successful project delivery within the laid down parameters of time and cost
II. Mitigate risks proactively by monitoring project progress against identified risks, tracking deliverables, reviewing milestones and providing feedback and information to the Project team to ensure timely execution
III. Drive effective project communication to ensure sound decision by doing cross functional project team meeting and sharing consistent information across stakeholders
IV. Build relationship with Business team, portfolio and external customer by sharing project progress, doing project review meetings for achieving targeted deliverables
V. Ensure continuous improvement of internal processes and project execution by monitoring progress for smooth functioning of the projects
Education Qualification
B. Pharm/M. Pharm/ MSc preferably PMP certified
Relevant Work Experience
2-5 years in the field of product development and/ or project management in Pharmaceutical industry
Competencies/Skills
Job Location
Vikhroli
Junior Team Member – QC
Division
Department
Employment Type
Job Purpose
Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirements
Accountabilities
I. Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis
II. Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body
III. Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements
IV. Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit
V. Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed
Education Qualification
M.Sc. / B. Pharma
Relevant Work Experience
2 years of experience in QC department of a pharmaceutical organization
Competencies/Skills
Job Location
Rangpo
