Job Description:

EXECUTIVE VALIDATION (PROCESS EQUIPMENT )

The main activities will be as below:

– Writing Validation documents including User Requirement Specifications, RA, DQ, IQ, OQ
protocols for various Process equipment used in Pharmaceutical and Biopharmaceutical Industry.
– Interactions with client and vendors/ contractors
– In office client-vendor co-ordination for validation activities execution as per GMP
– Execution of Validation Protocols at site and Validation document compilation.
– Maintaining Quality documentation & safety at site.

Candidate Profile:

– The candidate should be familiar with the above job description.
– Should be conversant with Schedule M, ISPE guidelines, cGMP. Shall aware of GAMP5, ASME BPE,
ASTM etc.
– Should be well versed in written & spoken English




– Strong interpersonal Skill.
Qualification:
– BE / B Tech (Chemical / Mechanical)

Requirements:

Degree/Diploma in Electrical/ Mechanical/Instrumentation/Chemical engineering with
min. 5+ years of experience in the pharma industry with a wide range of exposure including handling
projects, qualification, maintenance and troubleshooting

Experience: 3 to 6 Years in Commissioning, Qualification and Validation of Process Equipment and
other utilities in Pharma

Job location:

Pune, but will need to travel extensively anywhere In India & Abroad

Job Scope:

– Full time

📌 Exec. Validation (Pune)
🏢 Biopharmax
📍 Pune