Executive – Equipment Qualification (Validation)

Job Description
Jubilant Generics Limited is looking for an experienced Executive – Equipment Qualification (Validation) for its pharmaceutical manufacturing operations in Roorkee, Uttarakhand.

The ideal candidate should have 4–6 years of relevant experience in pharmaceutical equipment qualification and validation, preferably with exposure to a regulated pharmaceutical company and OSD (Oral Solid Dosage) manufacturing environment.

The role will involve preparation, execution and review of qualification and validation documentation for facilities, equipment and utilities, along with compliance activities such as Change Control, Deviation, CAPA and investigations.

Jubilant Generics has a pharmaceutical manufacturing facility in Roorkee, and publicly available information confirms the site’s exposure to equipment qualification, calibration and pharmaceutical regulatory requirements.

Key Responsibilities
Equipment Qualification & Validation
Prepare, execute and review URS, SAT, IQ, OQ and PQ documents for new facilities and equipment.
Prepare and execute qualification protocols for pharmaceutical equipment and systems.
Support qualification of new equipment, facilities, systems and utilities.
Perform qualification activities for newly installed or modified equipment and systems.
Ensure qualification activities are completed according to approved protocols and timelines.
Review qualification results and prepare appropriate reports and supporting documentation.
Requalification Activities
Prepare and execute requalification protocols for critical equipment and utilities.
Handle requalification activities for systems such as:HVAC
Water Systems
Compressed Air
Other pharmaceutical utilities
Maintain records of completed qualification and requalification activities.
Compliance & Quality Systems
Ensure compliance with Change Control, Deviation, CAPA and Investigation procedures.
Support investigations related to equipment qualification and validation activities.
Ensure appropriate documentation is maintained for audit and inspection requirements.
Coordinate with Quality Assurance, Engineering, Production and other relevant departments.
Facility & Equipment Qualification
Qualify facilities, systems and equipment associated with new installations and modifications.
Review technical documents and qualification requirements.
Coordinate with Engineering and other technical teams during installation and qualification.
Support inspection readiness by maintaining complete and traceable qualification records.
SOP & Risk Assessment
Prepare and review Standard Operating Procedures (SOPs) related to qualification and validation activities.
Prepare and review risk assessments for equipment, facilities and systems.
Identify potential risks associated with qualification activities and support appropriate controls.

Desired Candidate Profile
Experience: 4–6 years in pharmaceutical Validation / Equipment Qualification.
Experience in a regulated pharmaceutical company is required/preferred.
Exposure to OSD (Oral Solid Dosage) manufacturing will be preferred.
Practical experience with URS, SAT, IQ, OQ and PQ documentation and execution.
Experience with qualification/requalification of HVAC, Water Systems and Compressed Air systems.
Good understanding of Change Control, Deviation, CAPA and Investigation processes.
Experience in SOP preparation/review and risk assessment.
Strong documentation and compliance skills.
Good communication and cross-functional coordination abilities.

Key Skills
Equipment Qualification, Pharmaceutical Validation, URS, SAT, IQ, OQ, PQ, Requalification, HVAC Qualification, Water System Qualification, Compressed Air Qualification, OSD, Change Control, Deviation, CAPA, Investigation, SOP, Risk Assessment, GMP, Pharmaceutical Compliance.

How to Apply
Interested and eligible candidates can share their updated resume at:

Email: niketa.chauhan1@jubl.com

Job Location: Roorkee, Uttarakhand