Innoxel Lifesciences has announced exciting career opportunities for pharmaceutical professionals across multiple departments. This hiring drive is ideal for candidates with experience in sterile USFDA-approved facilities and looking to grow in a dynamic pharma environment.
The company is inviting applications for roles in Quality Control, Quality Assurance, Engineering, Validation, Warehouse, Microbiology, and Project Management. Candidates with relevant qualifications and experience are encouraged to apply.
Available Job Roles
Quality Control (QC)
- Role: Analysts
- Work Area: Analytical Method Validation, RM/PM
Sterile / Liquid Oral Manufacturing
- Roles: Operators & Supervisors
- Work Area: SKID Operation, Autoclave, Vial Washing, Tunnel, Manufacturing, Filling
QC Microbiology
- Role: Microbiologists (EM & Analysts)
Quality Assurance (QA)
- Role: Sr. Officers / Executive
- Work Area: Qualification & Validation, QMS, Validation, IPQA, Compliance
Warehouse
- Role: Warehouse Officer
Validation
- Role: Sr. Officer / Executive
Engineering
- Roles: Technicians / Officers / Executive
- Work Area: Plant Maintenance, Process Maintenance, HVAC, Utility, QMS
Project Management (PM)
- Role: Project Management Professional
Required Qualifications
Candidates must meet the following educational criteria based on the role:
- B.Sc / M.Sc / B.Pharm / M.Pharm
- B.Sc / M.Sc (Microbiology)
- ITI / Diploma (for Operators & Technicians)
- B.E / Diploma (for Engineering roles)
- B.Com (for Warehouse role)
- M.Pharm with relevant injectable experience (for PM role)
Experience Required
- Quality Control: 1โ10 years
- Manufacturing / Microbiology: 1โ8 years
- Quality Assurance: 4โ8 years
- Warehouse: 3โ8 years
- Validation: 3โ7 years
- Engineering: 2โ8 years
- Project Management: 2โ8 years
Preference will be given to candidates with Sterile USFDA experience.
Roles and Responsibilities
Depending on the department, selected candidates will be responsible for:
- Performing analytical testing and validation activities
- Handling sterile manufacturing processes and equipment
- Ensuring compliance with GMP and regulatory standards
- Conducting microbiological analysis and environmental monitoring
- Managing documentation and quality systems
- Supporting engineering maintenance and utilities
- Executing validation protocols and reports
- Coordinating project timelines and execution
Salary and Benefits
- Expected Salary Range: โน2.5 LPA โ โน12 LPA (based on role and experience)
- Additional Benefits:
- Growth opportunities in USFDA-approved facility
- Learning and development programs
- Professional work environment
- Exposure to advanced pharmaceutical processes
Job Location
- India (Pharmaceutical manufacturing facility โ exact location shared by employer)
How to Apply
Interested candidates can apply by sending their updated CV to the following email addresses:
- hr1@innoxells.com
- vikrant.datta@innoxells.com
- kaveri.kansara@innoxells.com
- vishal.joshi@innoxells.com
Make sure to mention the applied position in the subject line for faster processing.
