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11 Zentiva Jobs

ESO QA Specialist

2-5 years

Ankleshwar

1 vacancy

ESO QA Specialist

Zentiva

posted 21hr ago

Job Description

MISSION STATEMENT
To ensure the quality lifecycle management for dedicated, subcontracted, product portfolio. Qualified auditor.
MAIN ACCOUNTABILITIES AND DUTIES
Operational skills
Operational quality management of a dedicated product portfolio which includes:
  • Quality management of deviation and complaint records and their related CAPAs
  • Assessment and management of change controls
  • Edition of QA Agreements with Zentiva third parties and subcontractors
  • Collection and evaluation of PQRs and stability data
  • Compliance evaluation of Third Parties and products
  • Maintenance of product database
  • Collection and review of CoA/CoC
  • QA support of product launches and transfers
  • GMP, GDP, MDR, HACCP, Food Supplements and Cosmetics regulations and legislations
Auditing
  • Prepare audit and audit plans
  • Conduct and participate to external audits
  • Evaluation of audit reports
  • Participate to internal audits and inspections
KPI monitoring and reporting
Other tasks may be performed under the direction of the Manager within the agreed type and scope of work.
REQUIRED QUALIFICATIONS, EXPERIENCE & SKILLS
  • University degree in Pharmacy, Chemistry, Biology, or relevant Life Science
  • Minimum of 5 years in a similar role or equivalent experiences in a GMP related environment
  • Thorough knowledge of GMP requirements as well as knowledge of ICH and pharmaceutical regulatory requirements
  • Management of subcontractors is an advantage
  • Proven track record of project management skills
  • Strong communication skills and negotiation strength
  • Proactive attitude
  • Problem solving skills
  • Hands-on attitude, flexible and open minded
  • Collaborative and team-spirited
  • Knowledge of IT tools
  • Language - English: Advanced level

Employment Type: Full Time, Permanent

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Prepare for QA Specialist roles with real interview advice

Top Zentiva QA Specialist Interview Questions

Q1. How to start method development of unknown compound by HPLC for RS ?
Q2. Force degradation and mass balance what to do if mass balance not achieved?
Q3. How to reduce peak tailings and improve resolution?
View all 7 questions

What people at Zentiva are saying

What Zentiva employees are saying about work life

based on 135 employees
60%
83%
67%
97%
Flexible timing
Monday to Saturday
No travel
Day Shift
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Zentiva Benefits

Free Transport
Job Training
Health Insurance
Free Food
Team Outings
Cafeteria +6 more
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