Zydus Lifesciences Pvt. Ltd Walk-in 13th April 2025 for Executive / Senior Executive / Assistant Manager-Production and QA,QC (Drug Substance)

Zydus Lifesciences Pvt. Ltd Walk-in Interview .Zydus Lifesciences Pvt. Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.. 

Vacancy details:

• Department: Executive / Senior Executive / Assistant Manager-Production and Quality Departments (Drug Substance)
• Experience:  5 – 12 Years
• Qualification: M.Sc. / B. Tech / B.E / M. Tech in Biotechnology/ Biochemistry/Microbiology

Important Details :

• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Walk-In Interviews in Pune on 13th April 2025 (Sunday) for Production and Quality Departments (Drug Substance) of Zydus Biologics

Date: 13th April 2025 (Sunday)

Time: 8:00 AM to 5:00 PM

Venue: Hotel Radisson Blu, 136/1 Hinjewadi Phase 1 Rd, behind Mahindra International School, Phase 1, Hinjawadi Rajiv Gandhi Infotech Park, Hinjawadi, Pune, Pimpri-Chinchwad, Maharashtra 411057. Contact Number: 020-69528000

Job Profiles: 

1. Drug Substance Production:

USP Production: Experience in the fermentation department with a minimum of 2 years of experience of working in mammalian culture. The person should have handled SS bioreactor/fermenter having a capacity of 500 L or more.

DSP Production: Experience in the purification department with a minimum of 2 years of experience in working on mammalian culture products. The person should have handled the chromatography system (capacity: Minimum 600-L/h or more), Column (Capacity: 600 mm or more diameter), and Automated TFF system.

QMS Production: Risk assessment, Root cause analysis for deviations, OOT, OOS, and QMS document via Trackwise. Reviewing cGMP and equipment qualification.

2. Quality Assurance:

IPQA: Hands on experience in QA Oversight activities of drug substance manufacturing/ warehouse and shop floor activities.

QMS: The Job requires knowledge of handling/review of deviation, change control, CAPA, OOS, OOT, Lab incident etc / QMS role/along with IPQA and qualification knowledge.

3. Quality Control:

Protein Lab: Technical expertise in protein analytics (Quantitative & Qualitative).

Bioassays: In-vitro testing (Cell based & ELISA) for protein therapeutics and monoclonal antibodies.

RMPM: Sampling and Analysis of RM and PM. Exposure in wet analysis and Instrument based techniques i.e.  HPLC, GC, KF, UV, IR, etc.

Additional Requirements for All Positions

Candidates must have experience with regulatory documentation and cGMP/GLP standards. Preference will be given to candidates knowledgeable in Biosimilar product manufacturing operations.

Note:

1. Employees will work in shifts based on allocation. Shift deployment for male candidates will be A/B/C.
2. Interested candidates may attend a walk-in interview with their CV, salary slips, and all relevant original documents.