Thursday, September 2, 2021

Admiron life Sciences Pvt Ltd urgent requirement in QA AQA development Apply Now

 Greetings from Pranaya Group

We have an Urgent requirement in Admiron Life Sciences at 

Parawada, Visakhapatnam. for the following departments

Department : AQA (Bulk Drugs /API Experience)

Experience : 4 - 6 years in review of QC Documentation

Qualification : M.Sc. / B Pharmacy (Male candidates)

• Monitoring of Quality Control related activities. 

• Review of audit trials for Laboratory Instruments. 

• Review of Laboratory Instruments qualification and calibrations.

• Review and Monitoring of Calibrations, Preventive maintenance 

schedules, working standards management. 

• Review & Monitoring of analyst qualifications and schedules, Backup and 

restoration of analytical data. 

• Review of finished product analysis results and its raw data, Certificate of 

analysis before dispatching the material, BPCRs and equipment cleaning 


• Review of stability data and schedules, packing and labelling records.

• Should have Knowledge on OOS /OOT /CAPA / Risk Assessment

• Knowledge in Empower and Open lab Software

• Knowledge in other software related to UV and IR instruments

Department : QA (Bulk Drugs /API Experience)

Experience : 8-10 year in review of QA Compliances and Document’s

Qualification : M.Sc. / B Pharmacy (Male candidates)

• Preparation of internal audit & employee training schedules and timely 


• Handling of errata and non-conformance. 

• Preparation of annual product quality reviews & continued process 


• Handling CAPA, SMF, QM, MRM & vendor qualification activities. 

• Handling Deviations, Customer complaints, return goods and recalls, line

clearance, Change control. 

• Preparation of SOPs and other quality related documents.

• Monitoring document traceability.

• Issue and receiving of batch production records and cleaning records. 

• Review, distribution and retrieval of all controlled documents. 

Department : QA-Validation (Bulk Drugs /API Experience)

Experience : 4-6 years’ experience in review of Validation Document

Qualification : M.Sc. Organic / Analytical Chemistry (Male candidates)

• Verification of Compliance against the Production SOPs.

• Must Have through knowledge in Process Validations, drying 

validations, cleaning validation.

• Review of Production online documentation

• Must be a good IPQA reviewer

• Must be aware of all QMS documents review.

Department : QA-Liaison (Bulk Drugs /API Experience)

Experience : 4-6 years’ experience in handling Liasioning activities

Qualification : M.Sc. / B Pharmacy (Male candidates)

• Apply the test license

• Apply the manufacturing license

• Apply the Methanol, Ethanol License

• Knowledge in CDCSO portal

• Should have awareness on all Liasioning activities

Interested candidates can send their resumes