Apotex is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines (both generic and innovative pharmaceuticals) for patients around the world. We are the 7th largest generic pharmaceutical company globally with more than 12,000 employees and estimated sales of approximately $3 billion. Our fully integrated operation is comprised of four lines of business: Global Generics; Apobiologix; Global Active Pharmaceutical Ingredients (API); and ApoPharma (Innovative Products). With our worldwide manufacturing sites, Apotex can produce up to 24 billion dosages per year. We produce 300 medicines in 4,000 dosages and formats that are exported to 115 countries. Apotex will spend $2 billion over the next 10 years on research and development.
Post : Technical Writer-Documentation COE
Job Summary
Responsible for creating and/or making formatting changes and edits to draft documents based on supporting documentation from Business Units (ie. Technical Transfer packages; Technical Operations Reports, Validation Reports) for Apotex.
Responsible for creating and/or making formatting changes and edits to draft documents based on supporting documentation from Business Units (ie. Technical Transfer packages; Technical Operations Reports, Validation Reports) for Apotex.
Job Responsibilities
• To be self-disciplined & maintain the same discipline in the production documentation department.
• Creating and/or making formatting changes and edits to draft documents based on supporting documentation from Business Units (ie. Technical Transfer packages; Technical Operations Reports, Validation Reports).
• Migration of MPPDs into new MMaR templates.
• Make a list of changes in word document.
• Complete projects with strict deadlines under minimal supervision and prioritize workload to deliver business needs.
• Manage own workload and completion of assigned MMaR within established cycle time commitments.
• Liaise with TO TWS and other internal customers to monitor efficiency and effectiveness in meeting targets for documentation changes.
• Perform all work in compliance with current SODs and GMPs.
• Ensure compliance with current Standard Operating Procedures and Work Instructions related to Document Specialist activities and report errors and inconsistencies associated with approved procedures to the Team leader.
• Develop and maintain effective working relationships with internal and external customers.
• Works as a member of a team to achieve all outcomes.
• Performs all work in support of our Corporate Values ; Demonstrates strong and visible support of our values.
• Performs all work in accordance with all established regulatory and compliance and safety requirements.
• All other duties as assigned.
• To be self-disciplined & maintain the same discipline in the production documentation department.
• Creating and/or making formatting changes and edits to draft documents based on supporting documentation from Business Units (ie. Technical Transfer packages; Technical Operations Reports, Validation Reports).
• Migration of MPPDs into new MMaR templates.
• Make a list of changes in word document.
• Complete projects with strict deadlines under minimal supervision and prioritize workload to deliver business needs.
• Manage own workload and completion of assigned MMaR within established cycle time commitments.
• Liaise with TO TWS and other internal customers to monitor efficiency and effectiveness in meeting targets for documentation changes.
• Perform all work in compliance with current SODs and GMPs.
• Ensure compliance with current Standard Operating Procedures and Work Instructions related to Document Specialist activities and report errors and inconsistencies associated with approved procedures to the Team leader.
• Develop and maintain effective working relationships with internal and external customers.
• Works as a member of a team to achieve all outcomes.
• Performs all work in support of our Corporate Values ; Demonstrates strong and visible support of our values.
• Performs all work in accordance with all established regulatory and compliance and safety requirements.
• All other duties as assigned.
Candidate Profile
• Graduate degree in Pharmacy from a recognized college
• Desired candidate will have 0-1 years of experience
• Should be proficient in MS office tools
• Should have excellent verbal & written communication skills
• Experience of working on online modules / software would be an added advantage
• Graduate degree in Pharmacy from a recognized college
• Desired candidate will have 0-1 years of experience
• Should be proficient in MS office tools
• Should have excellent verbal & written communication skills
• Experience of working on online modules / software would be an added advantage
Additional Information
Experience : 0-1 years
Qualification : B.Pharm
Location : Mumbai
Industry Type : Pharma
Functional Area : Technical Writer
End Date : 31st May, 2018
Experience : 0-1 years
Qualification : B.Pharm
Location : Mumbai
Industry Type : Pharma
Functional Area : Technical Writer
End Date : 31st May, 2018
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