Friday, October 8, 2021

Safe Parenterals Ltd – Urgent Requirements for B.Pharm, M.Pharm, M.Sc, B.Sc, ITI, Diploma Candidates – Production / QA / AQA / IPQA

 Safe Parenterals Limited is the first pharmaceutical industry in Narasaraopet which is having 20 years of experience in Pharmaceuticals.

Greetings from Pranaya Group

We have an Urgent requirement in SAFE PARENTAL at Narasaraopet, Guntur Dist. for the following departments

  • Preference will be given to those who can Join immediately and are nearby of Narasaraopet or willing to really relocate to Narasaraopet

Department: Production (Injectable Experience)

  • Position : Filling operators                     
  • Experience : 2 to 5 Years (Injectable Experience)
  • Openings : 10
  • Location : Safe Parental, Narasaraopet, Guntur Dist.
  • Qualification: M Pharma / B Pharma, B.Sc / M.Sc, ITI / Diploma

Job Description:

  1. Operation & Cleaning of Vial Filling and Stoppering Machine.
  2. Responsible for filtration of different products.
  3. Maintaining good housekeeping in their work area.
  4. Online documentation of all the activities in log books.
  5. Operation of Equipment during periodic qualification stage.
  6. Compliance to Standard Operating Procedures during the operation and cleaning of the equipment.
  7. Co-ordination with Engineering department during preventive maintenance and machine break downs.
  8. Reporting all the deviations to the immediate supervisor.
  9. Responsible for smooth operation of the machine and giving the desired output in the scheduled timelines with defined cGMP standards.
  10. Maintain discipline and motivate the workforce for better productivity and cGMP compliance.

Department: QA / AQA / IPQA (Injectable Experience)

  • Position : Executives / Senior Executives
  • Experience : Executives (2-5 Yrs.) / Senior Executives (6-9 Yrs.)
  • Openings : 10
  • Location : Safe Parental, Narasaraopet, Guntur Dist.
  • Qualification : M Pharma / B Pharma,

Job Description:

AQA: Review of RAW data and reports of raw materials, packaging materials, in process finished product, submissions of batches /equipment/instrument calibration and stability studies. Participate in Regulatory Audits and various customer audits. Review preliminary investigation for OOS, stability OOT in QC.

QA: Hands on experience on TMS Nichelon software. Conduct induction, orientation for New joinees. Conduct and facilitate Generic Training Program, Refresher sessions, SOP trainings. Prepare Power Point Presentations.

IPQA : Having experience in Manufacturing activities, Media Fill, Cleaning Validation, Finished Product Sampling, Process Validation, Bulk Sampling, Line Clearance, Production Line Monitoring

Interested Candidates, please share us your updated resume/profile (with Photo) along with CTC Letter to