Gland Pharma Released Job Openings On 26/07/2022.A holistic objective of dispensing health through a portfolio of injectable products across various therapeutic segments and delivery systems, has helped us expand to seven manufacturing facilities in India, with a capacity of approximately 750 million units. Â
Vacancy Details:
Gland Pharma Recruiting B.Pharma,M.Pharma,M.Sc Candidates with 03-07 years experience for QA / QC Executive Position.Complete Details for the QA / QC Executive as follows.
Important Details :
- Location :Visakhapatnam
- No of Vacancies:01
- Details of Salary:NA
- Opening date for online Application: 26/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : Pharmacovigilance & Clinical Research 50 FRESHER Openings At Clininfotech(whatsapp Resume)Â
Job Description/Skills Required
1. Understand the scope of the project, feasibility check and also gap analysis to develop appropriate process requirements.
2. Preparation of budget based on the scope of the project and Gland responsibilities
3. Preparation of project plan and time line of the project.
4. Procurements of API / RM /PM / Consumables and its follow up with purchase and QC for receipt, sampling, testing and approvals.
5. Preparation of BPCRs, Protocols and reports.
6. Co ordination with client responsible project leader for various activities of the project to ensure timely execution of the activities.
i. Clarity of the various technical issues (if any) for material specifications, analysis, manufacturing, documents etc
ii. To make required documents available from the client to complete the activities as per the agreed time line
iii. Other requirements like documents for custom clearance, license, permits, standards, impurities, columns and equipment’s etc. as applicable to
projects which also based on the responsibilities.
7. Ensure all the Gland project team is available for all project meetings as per the agreed meeting schedule.
8. Responding to the client queries in timely manner in co ordination with other internal departments or team members.
9. Ensure that, all the required documents are reviewed and controlled by relevant cross functional teams and are made available as per the project time line.
10. Conducting the pre SB batches meeting with internal team to ensure there is effective technology transfer (no deviations and quality issues).
11. Follow up with internal department and also with client (if applicable) to close deviations, change controls, incidents of the project (if any).
12. Ensure that manufactured SB batches are optically inspected and packed for stability initiation within the stipulated time line.
13. Ensure that, all the required documents for dossier compilation are provided to Gland DRA in timely manner ( as per the agreed time line) so that, the Gland DRA can review and provide the documents to client DRA for dossier filing . Update the stability data to client.
14. Co ordinate and be as team member for addressing the deficiency through the product final approval.
15. Ensure that, all the project documents are handed over to plant QA after the product is approved for commercialization.
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