Hospira is the world's leading provider of injectable drugs and infusion technologies. Through our broad, integrated portfolio, we are uniquely positioned to Advance Wellness™ by improving patient and caregiver safety while reducing healthcare costs. Through our offering of high-quality, lower-cost generic medications, we continue to help reduce the overall costs of healthcare — to improve both the affordability of care for patients and the financial strength of the global healthcare system.
B.Pharm, M.Pharm,BSC,MSC Jobs in Hospira
Hospira is the world's leading provider of injectable drugs and infusion technologies. Through our broad, integrated portfolio, we are uniquely positioned to Advance Wellness™ by improving patient and caregiver safety while reducing healthcare costs.
Through our offering of high-quality, lower-cost generic medications, we continue to help reduce the overall costs of healthcare — to improve both the affordability of care for patients and the financial strength of the global healthcare system.
Post: Executive
Job Description
Responsibilities
Execute project and routine validations and compile results
* Execute validation of manufacturing equipment, QC instruments, facilities, utilities, computer system, cleaning and sterilization process in accordance with regulatory requirements, cGMPs, corporate policies and procedures and as per schedule
* Calibration of KAYE Validators and Accessories
* Coordinate and plan validation activities with Manufacturing, QC, Microbiology and Projects
* Compile validation documents and results
* Ensure revalidations are performed within the established intervals
Technical Skills
* Understanding of pharmaceutical manufacturing, packaging, quality assurance, and quality control operations
* Knowledge of validation principles and practices related to the following areas: manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and IT systems
* Conversant with design & working principles of key equipment used in sterile manufacturing –autoclave, tunnel, lyophilizers, homogenisers, isolators, filter integrity testing devices
* Well versed with aseptic process simulation – design, execution and review of media fill runs
* Experience in plant and QC lab operations
* Good document review skills, with ability to identify issues and recommend actions
Skills/Experience Education/Certification: minor-latin; mso-ansi-language:EN-GB; mso-fareast-language:EN-US; mso-bidi-language: AR-SA">M.Pharm/M.S (Pharmacy)/ B. Pharm
minor-latin; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:
AR-SA">2+ years Experience in validation function of sterile dosage form facility
Additional Information:
Qualification: B.Pharm, M.Pharm
Location: Chennai, Tamil Nadu
Functional Area: Other
Employment Type: Full Time
Job Type: Regular
End Date: 10th September, 2015
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