Milan Laboratories (India) Pvt. Ltd. is one of the leading Pharmaceutical Manufacturer and Exporter from India. An ISO 9001:2015 and WHO-cGMP certified company, is a Govt. Recognized Star Export House and a winner of various awards for Quality Excellence and Outstanding Export Performance.
- Vacancy details:
- Department: QA Officer / Senior Officer
- Experience:2 – 4 years
- Qualification: B.Pharm / M.Pharm – QA
Greetings From Milan Laboratories Ltd … !!
Important Details :
- Location:Panvel
- Post of date:29/07/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Job description
Position: QA – Officer/Sr. Officer (Documentation)
Job Location: Kamothe, Panvel
Qualification: B.Pharm / M.Pharm – QA
Experience: 2 to 4 years in Pharma QA (Compulsory)
Role & responsibilities:
1. Preparation and issuance of BMR and BPR in Caliber BRM.
2. Issuance of APR and OPR in Caliber BRM.
3. To investigate NCR, Deviations and complaints.
4. Preparation of Excipient Risk Assessment Report.
Interested candidates can share their resume at talentpool@milanlabs.com / 8828829932.
- Department: Officer/Sr. Officer – Process Validations
- Experience:2 – 4 years
- Qualification: B.Pharm
Job description
Company Name: Milan Laboratories (India) Pvt. Ltd.
Dosages forms, OSD, Semi Solids and Penicillin OSD
Job Location: Kamothe, Panvel
Position: Production Officer/Sr. Officer – Process Validations (Documentation)
Experience: 2 to 4 years in Production – Process Validations (Documentation) Mandatory
Qualification: B. Pharmacy
Job description:
Validation Planning and Execution:
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- Develop and implement process validation protocols (IQ, OQ, PQ) for new and existing production processes.
- Coordinate and execute validation activities including process simulations, equipment qualification, and system validation.
Documentation and Reporting:
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- Prepare and maintain comprehensive validation documentation including validation plans, protocols, reports, and standard operating procedures (SOPs).
- Ensure all documentation meets regulatory and quality standards (FDA, EMA, GMP).
Compliance and Quality Assurance:
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- Ensure all validation activities comply with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other regulatory requirements.
- Conduct risk assessments and develop mitigation strategies for process-related risks.
Process Improvement:
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- Analyze validation data to identify trends and areas for improvement in manufacturing processes.
- Collaborate with cross-functional teams (R&D, QA, Production) to implement process improvements and optimize production efficiency.
Training and Support:
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- Provide training and support to production staff on validated processes and equipment.
- Assist in troubleshooting process deviations and non-conformances related to validated processes.
Regulatory Audits and Inspections:
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- Participate in regulatory audits and inspections, providing validation documentation and supporting information as needed.
- Address audit findings related to process validation and implement corrective actions.
Interested candidates can share their resumes
- Email ID: talentpool@milanlabs.com
- WhatsApp number – 8828829932
