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Job Description

1) Procurement of Raw Material / Packing Material / Machinery /Stationers etc.

2) To monitor daily stock level closely and to maintain co-ordination with plant and production persons on daily basis.

3) To float inquiries, make comparative sheet of available quotations and to place an order.

4) To monitor book stock and physical stock of material.

5) To develop new vendor in case of new product and alternate vendor in case of existing product

. 6) To enter purchase order in the system

7) To verify Goods Receipts Notes as per Purchase Order

8) Follow up for timely delivery and pending orders.

9) To give declaration to insurance company fortnightly for the material lying in transit.

10) Correspondence of complaint, rejection and return of material.

11) Preparation of reports for top management on monthly basis.

12) Preparation of reports for ISO audit on yearly basis.

13) To allot payment priorities to account dept.

14) Miscellaneous administrative work.

Industry

Pharma/BioTech/Clinical Research

Functional Area

Purchase / Supply Chain

Number of Vacancy

3

Education

Professional Degree, Other Bachelor Degree


About Purvanchal Business Solution

1. To establish the quality system
a. Establish the quality management system to describe how the firm complies
CGMPs and operates to maintain a state of control
b. Keep current with good industry practices, and applicable to the mission of your operation.
2. To audit compliance to the quality system
a. Audit for compliance to policies and procedures: on paper vs. practice
b. Report on the performance of the quality system, including trends, that help
decision making for targeted actions
3. To establish procedures and specifications
a. Ensure that procedures and specifications are appropriate and followed
b. Ensure that the procedures and specifications of firms under contract are also appropriate and followed, i.e., maintain control and take responsibility for third-party services providers (contract manufacturers, contract laboratories, etc.)
4. To establish manufacturing controls
a. Ensure that appropriate manufacturing in-process controls are implemented
b. Ensure in-process controls are performed during manufacturing operations and results are satisfactory
5. To perform laboratory tests or examinations
a. Perform laboratory testing of components, containers, in-process materials, packaging materials and drug product using validated methods against scientifically-derived, fit-for-purpose specifications
b. Approve or reject drug products manufactured, processed, packed, or held under contract by another company, i.e., final product release is not delegated to a contractor
c. Perform retests or reexamine approved components, drug product containers and closures after long storage or exposure to adverse conditions
6. To review and approve or reject all things CGMP
a. Review and approve/reject any document that gives work instructions and set requirements such as procedures, protocols, test methods, and specifications—including changes to these documents
b. Review and approve/reject reprocessing and rework proced

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