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.
Junior Team Member – QC
About the job
Division
Quality
Department
Quality
Employment Type
Permanent
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
Collaborate to Succeed
Innovate to Excel
Perform with Accountability
Lead with Empathy
Act with Agility
Strong Domain Knowledge
People Management
Job Location
Rangpo
Shift Hours
Section Head – QA
About the job
Division
Quality
Department
Quality
Employment Type
Permanent
Job Purpose
Drive compliance of unit as per Quality management system and regulatory expectation while seeking continuous improvement in cGMP to ensure
Accountabilities
I. Establish system for appropriate investigations of various non-conformances of quality management systems, to determine root cause and implementation of CAPA, as per cGMP requirements
II. Design plan for compilation, review and on-time closure of QMS documents in order to meet compliance with respective quality systems
III. Control the system to analyse QMS documents for completeness and accuracy in line with cGMP requirements
IV. Seek opportunities of continual improvements in QMS by review of regulatory updates through simplification of SOPs / procedures to ensure adherence to cGMP requirements
V. Plan regulatory compliance of audit observations by monitoring and supervising of compliance till its closure to meet regulatory compliance
VI. Direct and supervise communication to provide feedback to internal and external customers on queries related to QMS documents/ deficiency as per standard procedures and technical agreements
VII. Develoaid them in performing their job roles better and contributing to achieving team goals
Education Qualification
B. Pharm. / M. Pharm. / M. Sc
Relevant Work Experience
8-12 years for B. Pharm or 6-8 years for M. Pharma / M. Sc.
Competencies/Skills
Collaborate to Succeed
Innovate to Excel
Perform with Accountability
Lead with Empathy
Act with Agility
Strong Domain Knowledge
People Management
Job Location
Rangpo
Shift Hours
Junior Team Member – QC
About the job
Department
Quality
Employment Type
Permanent
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
Collaborate to Succeed
Innovate to Excel
Perform with Accountability
Lead with Empathy
Act with Agility
Strong Domain Knowledge
People Management
Job Location
Rangpo
Shift Hours