Otsuka Pharmaceutical India Private Limited Walk In Interview 2025.Otsuka Pharmaceutical India Private Limited Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue.
Vacancy details:
- Department : QA- Equipment Qualification & Validation/Quality Control -Microbiology
- Qualification: B.Pharma in Any Specialization, DMS/M.Sc(Science) in Biotechnology, Chemistry, M.Pharma in Pharmacy/B.Sc in Microbiology/MS/M.Sc(Science) in Microbiology
- Experienced: -0-8 years
Important Details :
- Location: Ahmedabad( Moraiya )
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
Job Description: Greeting from Otsuka Pharmaceutical India Private Limited!!!
Role & responsibilities
Validation & Qualification of Equipment
Experience in Autoclave, Terminal, Sterilizer, Mixing Vessel, Tunnel Qualification, washing machine and filling machine.
HVAC Qualifications
Validation and qualification protocol and report.
To ensure material issuance for validations activities & keep Section Manager updated.
To ensure implementation of validation, qualification activities & inform to Section Manager
for any deviation from written procedure.
Equipment Qualification Steam Heat Sterilizer, Terminal sterilizer,
Preferred candidate profile:-
- Result orientated
- Communication skills
- Presentation skills
- Analytical skills
- Lateral coordination
* Candidate can share their resume at anee.silas@otsukapharma.in
Role & responsibilities
We are looking for a highly motivated and detail-oriented QC Microbiology Fresher to join our Quality Control team. As a QC Microbiology Fresher, you will be responsible for performing various microbiological testing, ensuring that products meet regulatory standards and maintaining the microbiology lab’s cleanliness and safety protocols. The role offers a great opportunity for growth and learning in the pharmaceutical/biotech industry.
- Microbial Testing: Conduct sterility testing, endotoxin testing, and bioburden testing.
- Sample Handling:
Collect and handle microbiological samples (raw materials, in-process materials, and finished products). Maintain accurate records of sample analysis. - Media Preparation:
Prepare and sterilize microbiological media, solutions, and reagents as per the standard operating procedures (SOPs). - Lab Equipment Maintenance:
Operate, maintain, and calibrate laboratory equipment, including autoclaves, incubators, and microscopes. Ensure equipment is functioning properly and troubleshoot as necessary. - Documentation and Reporting:
Document test results accurately and ensure that they are in compliance with company standards and regulatory requirements.
Assist in preparing microbiological reports and quality control documentation.
- Compliance:
Follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) in all lab operations. Ensure compliance with environmental health and safety guidelines within the lab. - Quality Assurance Support:
Assist in the preparation for audits by regulatory bodies (e.g., FDA, WHO). Participate in internal and external quality control audits.
Preferred candidate profile
- Strong attention to detail and accuracy.
- Good communication and interpersonal skills.
- Ability to work effectively both independently and as part of a team.
- Full-time position.
- Opportunity for career growth and advancement within the QC department.
Interested candidates can share their CV on Anee.Silas@otsukapharma.in
ABAC
