Openings in Zydus for Validation/QMS/AQA/IPQA/Production and ARD/FRD in Abryl Pharma

Openings in Zydus for Validation/QMS/AQA/IPQA/Production and ARD/FRD in Abryl Pharma

 Zydus logo

About the Company 

The company originated in the year 1952, with the headquarters located in Ahmadabad Gujarat. The company have revenue of 119.05 billion turn over. Zydus is a generic leading pharma company in India. Company is impacting 24000 people living across 4 continents. The firm ranks 4th Indian pharmaceuticals in India. 


Firm distributed over the locations in India like Gujarat, Maharashtra, Himachal Pradesh and Sikkim, without side countries like USA, France, Spain, Latin America and Brazil. Zydus have portfolios in New molecular entity's, Biologic s and Vaccines. 

About the Job 


Opportunities in Quality Assurance / USP/DSP - Production Department of Zydus Biologics, Biotech Park, Ahmedabad

  

Senior Executive/Assistant Manager (Candidate must have 4 to 8 years exp.)

Quality Assurance (M.Sc Biotech/B.Pharm/M.Pharm ):

1. Validation: Code QA1

Must have experience in Equipment Qualifications (Autoclave, Tunnel etc), Process validations, Cleaning Validation, Utility Qualifications, HVAC, Water System, Protocol preparation and its compilations. Should be responsible for Media fill activities, protocol & BMR preparation 

2.  QMS: Code QA2

Must have experience in QMS related activities like Failure investigation, Quality events handling and investigations, change control, APQR, OOS/OOT trending etc.

3. Analytical QA: Code QA3

Must have experience in review of Analytical Reports, Stability Protocols and data sheets, Investigation, Review and disposition of OOS, OOT, OOG & OOE results, handling of Incidents, Deviations, and Change Controls in the Laboratory along with review of all types of Qualification documents. Review and approval of all Lab Standard Operating Procedures.

4. QA Oversight manufacturing (IPQA): Code QA4

Must have experience in QA Oversight (IPQA) related activities for Drug substance manufacturing along with handling of process validations, cleaning validations OOS, change control, deviation, investigation, CAPA and QMS activities. 

 

Dy. Manager/Associate Manager (Candidate must have 9 to 12 years exp.)

1. USP & DSP – Production (M.Sc Biotech / Btech Biotech / B.E Biotech)

USP Production (Code P1) Must have experience in Aseptic handling of mammalian cell culture, Media/feed preparation and its filtration, Readiness of bioreactor and associated vessels (CIP, FIT, PHT, SIP), Operation of bioreactor, Readiness and operation of centrifuge, Clarification of cells, Manufacturing of monoclonal antibodies/ bio therapeutic protein

DSP Production (Code P2) Must have experience in downstream purification process for recombinant products, TFF system, chromatography system, depth filtration procedures, CIP/SIP of the equipment.


For all above positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential. 

Candidate from Biotech, Vaccine & Injectable Pharma plants will be preferable who have knowledge of process equipment’s like as Autoclaves, Bio-reactors, fermenters, Lyophilizes etc.


Preference will be given to those who matches with above mentioned requirement and submit their CVs based on the mentioned code no. along with current and expected CTC to [email protected] by on or before 20th Dec'2022.

For FR&D / AR&D - Abryl Pharma 

We have an open positions for F&D (6-12 years), RA (5-12 years), ARD. (10-14 years). Interested candidates can share updated resume at below email I'd.

[email protected]

[email protected]