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Manufacturing Chemist - Transdermal

3.00 to 8.00 Years   Ahmedabad   31 Jan, 2023
Cadila Healthcare Ltd
Job LocationAhmedabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

    Key 1. Preparation of Commercial product / stability batches / exhibit batches / process validation batches / engineering batches , Oversight and Investigation report, action and closure , CAPA plans and closure, Protocols & reports, Internal Quality Audit / Regulatory Quality Audit Compliance and closure. Responsible for Change control, Standard Operating Procedure, Planned Modification, Master Batch manufacturing record and Master Batch Packaging record.2. Responsible for training activity of staff members, technicians and contract workers of Transdermal as a chemist.3. To assist the senior for planning and execution of batch manufacturing, packing and controlling the functions related of Transdermal department Manufacturing & Packing activity.4.Responsible for overall production activities, of the manufacturing and packing area on daily basis in achieving total production requirements in quantity, quality with cGMP requirement.5. Work allocation to the operators and production supervisor as per production planning.6. Optimization of the resources like men, materials and machines in manufacturing and packing area.7. Training the men-power to meet the organizational goals and achieve GMP compliance.8. To co-ordinate with quality assurance (QA) department for release of batch, cleaning & process validation.9. To co-ordinate with engineering department for machine maintenance and preventive maintenance and calibration schedule.10.To co-ordinate with warehouse department for issuance of materials to achieve schedule plan. Designation and monitoring of storage conditions for materials and products.11.Monitoring & control of manufacturing environmental and plant hygiene.12.To co-ordinate with F & D / Tech off for execution of engineering/trial/exhibit batches.13.Preparation and review of risk assessment, process validation protocol whenever is required.14.Review, updation & execution of MBMR / MBPR/ SOP /Qualification Protocol whenever is required.15.Review of Master Formula & Master Product Specification which is received from F & D whenever is required.16.Responsible for raising the purchase requirement for procurement of change parts of machine and miscellaneous items as when required.17.To co-ordinate with purchase department for status of purchase order and delivery of consignment from supplier as when required.18.To prepare the daily report and monthly report of department on regular basis.19.Shall be participating in Internal Quality Audit.20.Responsible for ensuring market complaints, failures deviations are investigated and corrective and preventive actions are implemented as per set timeline.21.To adhere with EHS requirements and compliance the observation related to EHS.22.Escalation of any issue to be inform to immediate supervisor /reporting authority.23.Responsible for supervise and monitor the cleaning activity as per respective SOP.Requirements:Qualification : B.Pharma/M.PharmaTotal Years of Experience : 3 - 8 YearsExperience in Zydus : Min. One Year,

Keyskills :
chemistrygmpcosmeticsquality control

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