Otsuka Pharmaceutical India Private Limited (OPI) a fully-owned subsidiary of Japanese company, Otsuka Pharmaceutical Factory, Inc. (OPF), Japan.OPI has its roots in Japan and has flourished with its branches across India and in 60+countries of the world. It has state-of-the-art manufacturing units, maintaining world-class standards and Otsukas quality culture.
Candidates from parenteral or Injectable would only be preferred.
Interested candidate can share their resume at anee.silas@otsukapharma.in
Role:
Quality Assurance – OtherIndustry Type:
Pharmaceutical & Life SciencesDepartment:
Quality AssuranceEmployment Type:
Full Time, PermanentRole Category:
Quality Assurance – Other
Job description
Role & responsibilities
- Responsible for Analytical Method Validation and Method Development activity.
- Responsible for F&D sample analysis.
- Responsible for Good Lab Practices (GLP) Activities and its complies.
- Responsible for Calibration of lab instruments.
- Responsible for Preparation and review of Validation Protocols/Reports and Analytical Reports including data.
- Responsible for Departmental SOP Preparation/Review and its compliance.
- Responsible for Procurement of analytical and Lab requirements.
Preferred candidate profile
- Key technical skills:
- Key behavioral attributes:
- Lateral coordination
- Team working
- Policy compliance
- Task completion orientation
Role:
Quality Assurance – OtherIndustry Type:
Pharmaceutical & Life SciencesDepartment:
Quality AssuranceEmployment Type:
Full Time, PermanentRole Category:
Quality Assurance – Other
Education:
B.Sc in Chemistry, B.Pharma in Pharmacy
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