2.0 - 4.0 years

2 - 3 Lacs

Ahmedabad

Remote

Role: Technical Specification Writer Location: WFH / Sanand Third-party: Ashkom Media INDIA Pvt Ltd 1) Keeping multiple manufacturing processes specs up to date in current dynamic situations whenever changes are impacted by changes in Compendia, Suppliers, market promotions, New Launches, etc. 2) Create, Maintain, and Revise Process specifications & standards, such as Formula cards, making instructions, multiple Raw material specifications, and Approved Supplier lists including supporting preparing reports as justifications for various healthcare products. 3) Reaching out to multiple people in different countries on different products to clarify their doubts on approval seeking and concurrences and gain approvals and end-to-end tracking and coordination till closure 4) Gain approvals through the change management system by providing Justifications using the GTRAQ system 5) Mastery of Enovia - current Enova system & new DI system 6) Prepare TS track sheets & summarize weekly meetings about new specifications, standards, and GTRAQ records. 7) Make process validation protocols based on minimum data available 8) Review the compendia changes vs. actual P&G RMS and update the RMS accordingly to meet the compendia 9) Auditing the Brand wellness reviews and identifying the Issues & keeping track of the closures 10) Support other contractors on their training, and review standards. 11) Support Product Quality Assessment /Expansion Checks for Process 12) Must be professional in English Warm Regards, ______________________________________ "Your Manpower Managers" Varun Shrivas TA | HR ASHKOM MEDIA INDIA PVT. LTD. Mobile : +91-6262600059 / 8989271488 Website: www.ashkom.com

Posted 2 months ago

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Technical Writer Ashkom

2.0 - 4.0 years

2 - 3 Lacs

Ahmedabad

Remote

Role: Technical Specification Writer Location: WFH / Sanand Third-party: Ashkom Media INDIA Pvt Ltd 1) Keeping multiple manufacturing processes specs up to date in current dynamic situations whenever changes are impacted by changes in Compendia, Suppliers, market promotions, New Launches, etc. 2) Create, Maintain, and Revise Process specifications & standards, such as Formula cards, making instructions, multiple Raw material specifications, and Approved Supplier lists including supporting preparing reports as justifications for various healthcare products. 3) Reaching out to multiple people in different countries on different products to clarify their doubts on approval seeking and concurrences and gain approvals and end-to-end tracking and coordination till closure 4) Gain approvals through the change management system by providing Justifications using the GTRAQ system 5) Mastery of Enovia - current Enova system & new DI system 6) Prepare TS track sheets & summarize weekly meetings about new specifications, standards, and GTRAQ records. 7) Make process validation protocols based on minimum data available 8) Review the compendia changes vs. actual P&G RMS and update the RMS accordingly to meet the compendia 9) Auditing the Brand wellness reviews and identifying the Issues & keeping track of the closures 10) Support other contractors on their training, and review standards. 11) Support Product Quality Assessment /Expansion Checks for Process 12) Must be professional in English Role & responsibilities Preferred candidate profile Perks and benefits

Posted 2 months ago

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