Qualification/Validation Specialist

Posted 2 Days Ago
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Chennai, Tamil Nadu
Hybrid
Senior level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
The Qualification/Validation Specialist is responsible for performing qualification and validation activities for pharmaceutical lab equipment, conducting periodic reviews and audits, managing project qualification deliverables, and ensuring compliance with regulatory and quality standards such as GxP and 21 CFR.
Summary Generated by Built In

Role Summary:

  • Responsible to perform qualification and validation activities of all Pharmaceutical laboratory equipment's.
  • Responsible to perform System audit trail and user management periodic review
  • Must have experience in equipment/instrument qualification/validation 7-12 years in pharmaceuticals industry


ROLE RESPONSIBILITIES & SKILL SETS

  • Must be familiar in IQ/OQ/PQ execution and developing qualification protocols of Analytical equipment/instruments
  • Should be familiar in identifying qualification deliverables as per AIQ.
  • Should be familiar in DI/ERES concepts
  • Should possess in depth knowledge on Periodic review concepts and requirements.
  • Should have working knowledge on laboratory equipment like Chromatography systems (HPLC, GC, UPLC etc), MS, Titrators, Balances, Autoclave, stability chambers, lyophilizes etc.
  • Must possess good knowledge in Enterprise software like Empower, chromeleon etc
  • Responsible to co-ordinate with vendors for qualification/commissioning
  • Responsible for designing calibration, and preventive maintenance schedules based on equipment complexity.
  • Responsible to maintain Equipment qualification related documents for Audit purpose.
  • Should able to perform periodic Audit trail and user management review for computerized and Non-computerized systems.
  • Must possess through Knowledge on GxP concepts
  • Must be familiar in Handling of Deviations/ Incident, Change controls and Investigations etc in Trackwise system.
  • Should possess In depth knowledge in 21CFR part 11 compliance and requirement
  • Knowledge on analytical equipment calibration and maintenance will be an added advantage.
  • Must be familiar on regulatory requirement like 21 CFR, annexure 11 etc.. and GAMP concepts.
  • Should possess good negotiation skills.
  • Possessing knowledge in Asset manager would be added advantage.


Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Engineering
#LI-PFE

Top Skills

Iq,Oq,Pq

What the Team is Saying

Daniel
Anna
Esteban
The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Employees engage in a combination of remote and on-site work.

Typical time on-site: Not Specified
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