Safe Parenterals Pvt. Ltd - Job Vacancy for Experienced in Production / Micro -Parenterals @ Narasaraopet, Guntur Dist. - PHARMA WISDOM

Pharma, Life Science, Healthcare, Engineering Job Updates

Recent Updates

Monday, 2 November 2020

Safe Parenterals Pvt. Ltd - Job Vacancy for Experienced in Production / Micro -Parenterals @ Narasaraopet, Guntur Dist.

 

Job Vacancy for Experienced in Production / Micro -Parenterals @Narasaraopet, Guntur Dist.         

Greetings of the Safe Parenterals Pvt. Ltd., (A Pranaya Group) Jobs...!!!

We have an Urgent requirement for the following departments    

Department: Microbiology  (Injectable Experience)

Position: Incharge        

Experience -5-7 years

Openings: 01                   

Location: Safe Parental, Narasaraopet, Guntur Dist.

Qualification: B.Pharm and M.Pharm-Pharmacy

Job Description: NOTE: Please Mention in Subject as "Microbiology Incharge"

·       Microbial Analysis of Water and Finish Product and Raw Material.

·       Sterility Testing For Finish Product and Raw Material

·       Swab and Bioburden test.

·       Staining Method.

·       Culture Maintain and Culture Preservation.

·       Growth Promoting Test.

·       Autoclave Operation

·       Daily Temperature Monitoring of Incubator.

·       Participate in Media fill Validation Process.

·       Environmental Monitoring, and Water Sampling

·       Media Preparation.

·       Media fill

·       BET of Water and Finish Product of Sample.

·       Trend Analysis of PW and WFI and EM

·       Regulatory knowledge & guidelines – GLP, Schedule M, ICH, WHO TRS etc

 Please share interested profiles to hr.corporate@pranayagroup.com  and samhitha.hr@pranayagroup.com

Department: Production (Injectable Experience)

Position: Incharge        

Experience -12-15 years

Openings: 01                   

Location: Safe Parental, Narasaraopet, Guntur Dist.

Qualification: B.Pharm and M.Pharm-Pharmacy

Job Description: NOTE: Please Mention in Subject as "Production Incharge”

Job Description:

·       Ensuring the execution of validation activity of Formulation, Filling & Material Preparation Area/equipment’s dedicated with co-ordination with QA or internal and external agencies as per validation schedule.

·       Responsible for review of SOP’s, validation protocols, extended documents/reports preventive maintenance schedule, log books, calibration schedules and regulatory guidelines.

·       To ensure the cleaning, operation, documentation & maintenance of all dispensing, formulation, filling, solution & material preparation area as per production planning.

·       To evaluate and monitor the training need of the immediate subordinates and arrange for the on job training for the staff.

·       To ensure GMP compliance as per the applicable National and International rules and guidelines such as Schedule M and WHO.

·       Coordination with other departments, R & D and other manufacturing sites for technology transfer of production process.

·       Coordination with Warehouse/QA/QC/RA/HR/Administration/Accounts and Maintenance departments for the smoother functioning of manufacturing activities.

·       Planning & Execution of medial fill activity as per schedule.

·       To manage & coordinate the supply chain of products being manufactured at site.

·       To create an organization culture where people believe in building process capability by building functional capability (Functional capability to serve process objective).

·       Responsible for handling incident & deviation, their root cause evaluation & effective CAPA compliance w.r.t. minimize the re-occurrence of same type of incident.

·       Responsible to ensure the online documentation as cGMP along with routine log book management of production activity & equipment.

·       Development of Subject Matter Expert (SME) for better production activity.

·       To prepare and or review the assessments associated to the software or GXP equipment’s.

·       To prepare and or review the DIM associated to the Software or GXP equipment’s.

 Competencies

·       Must understand Aseptic Behavior – (aseptic handling, aseptic working & aseptic cleaning).

·       Must understand Sterile Operations, Scientific practices & process criticalities of Injectable manufacturing.

·       Analytical approach – Good in trend analysis, data evaluation & process calculations.

·       Adequate, Timely & Quality deliverance/ Output within stipulated timeframe.

·       Regulatory knowledge & guidelines – Schedule M, ICH, WHO TRS, ISO.

·       Thorough understanding of PQS & its compliances with risk based approach and patient safety.

Please share interested profiles to hr.corporate@pranayagroup.com  and samhitha.hr@pranayagroup.com

Regards,
Samhitha K


Join for Regular Job Updates in What's App  & Telegram
Thank You for Visiting
More Updates Visit daily @ www.pharmawisdom.co.in
Reach us on social media:

https://www.facebook.com/PharmaUdyog/https://www.linkedin.com/in/pharmaudyoghttps://twitter.com/PharmaUdyogg?s=09

1 comment: