Array ( [0] => pharmaceutical-quality-assurance [1] => thane ) Pharmaceutical Quality Assurance Jobs in Thane,Pharmaceutical Quality Assurance Job Vacancies in Thane Maharashtra

Pharmaceutical Quality Assurance Job Vacancies in Thane

FDA Approved/Deputy QA Manager/Veterinary Pharmaceutical Company/Palghar East

Double HR Consultancy

  • 2 - 8 yrs
  • 6.5 Lac/Yr
  • Palghar Thane
FDA Approved QA-quality Assurance
Urgent OpeningQuality Assurance/QADeputy QA Managerin Veterinary Pharma CompanyLocation: Palghar EastSalary: Rs. 5 LPA to Rs. 6.5 LPAExperience: 2 yrs to 8 yearsImmediate Joining shall be preferred
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QA/ Quality Assistant Manager Assurance/pharmaceutical Company/dombivli East/

Double HR Consultancy

  • 6 - 7 yrs
  • 9.0 Lac/Yr
  • Dombivli Thane
QA-quality Assurance Assistant Manager
Quality Assurance/Assistant ManagerEducation: M.Sc/B ScExperience: 6 to 7 YearsJob Location: Dombivli East MIDC
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FDA Approved/quality Assurance) Pharmaceutical/dombivli East

Double HR Consultancy

  • 2 - 5 yrs
  • 4.0 Lac/Yr
  • Dombivli Thane
Quality Assurance Executive
FDA Approval is required1. Responsible for Preparation and review of master documents of QA department and review of all master documents and formats of respective departments other than QA.2. Responsible for review of technical documents such as Technology Transfer, MPCR, BPCR, Specification and Standard test procedure, stability data, etc.3. Responsible for preparation of training schedule and provide training on QA-related topics, guidelines, regulatory and cGMP requirements to all concerned employees.4. Responsible for preparation and review and updation of Drug master file and handling of regulatory queries.5. To evaluate quality and stability of finished APIs.6. Responsible for organizing and execution of internal audit program, review of observations, follow ups and closures.7. To investigate Out of Specification cases8. Responsible for review of MSDS and approval9. Responsible for preparation of annual product quality review.10. Responsible for providing effective CAPA procedures, tracking completion and implementation of the same.11. Responsible for validation activities as per validation master plan.12. Responsible to investigate customer complaints and provide responses to customers regarding complaints.
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Assistant QA Manager / Wada Factory,Pharmaceutical,Palghar

Double HR Consultancy

  • 5 - 8 yrs
  • 6.0 Lac/Yr
  • Wada Thane
Assistant QA Manager Quality Assurance Pharmaceutical
Urgent OpeningAssistant QA Manager(Pharmaceutical Company)Location: Wada Factory, Palghar, Maharashtra Qualifications: B.Sc/M.Sc/ B. Pharm Experience: 58 years in QA (with minimum 3 years supervising IPQA).Experience in a WHO-GMP-approved facility preferred.Reporting to: QA Head / Director, oversee and strengthen the Quality Assurance function, ensuring the IPQA team performs effectively in production areas, deviations are addressed, yields are reconciled, and QMS compliance is maintained across all departments.Key Responsibilities1. Oversight of IPQA Team2. Yield & Reconciliation3. QMS & Documentation4. Training & DisciplineKey Skills RequiredStrong knowledge of WHO-GMP guidelines and IPQA oversight.Ability to lead and monitor a team.Problem-solving and a strict enforcement mindset.Strong documentation and audit readiness.
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QA Senior Executive/Quality Assurance/Pharmaceutical/Dombivli Thane MH

Double HR Consultancy

  • 6 - 8 yrs
  • 5.5 Lac/Yr
  • Dombivli Thane
QA Senior Executive Quality Assurance Pharmaceutical
1. Responsible for Preparation and review of master documents of QA department and review of all master documents and formats of respective departments other than QA.2. Responsible for review of technical documents such as Technology Transfer, MPCR, BPCR, Specification and Standard test procedure, stability data, etc.3. Responsible for preparation of training schedule and provide training on QA-related topics, guidelines, regulatory and cGMP requirements to all concerned employees.4. To evaluate Quality and stability of finished APIs.5. Responsible for organizing and execution of internal audit program, review of observations, follow ups and closures.6. To investigate & approve Deviations, Out of Specification7. Responsible for preparation, review of MSDS and approval8. Responsible for preparation, review & approval of annual product quality review.9. Responsible for providing effective CAPA procedures, tracking completion and implementation of the same.10. Responsible for validation activities as per validation master plan.11. Responsible to investigate & approve customer complaints and provide responses to customers regarding complaints.12. Ensure handling, effectiveness and continuous improvement of the QMS System.13. Initiates Follow-Up Audit activities in order to verify Audits and record the implementation and effectiveness of the Corrections & Corrective Actions
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