SkillSet\: clinical development, education, lounge, good clinical practice, clinical. Hello, There is an urgent opening in CRO \- Quantys Clinical Pvt Ltd as Volunteer Recruiter Officer at Gandhidham Location \(CRO Unit\). No bar for education, qualification and salary. Only we prefer the minimum experience of 3\-6 years in CRO. Candidates need to find volunteers for Clinical Trails on human Bodies Interview Venue \: Quantys Clinical Pvt Ltd \(CRO\) Plot no. 668 671,672New Area Kandla Special Economic ZoneGandhidham. Kutch, Gujarat\-370230 Regards Priti Singhvi 022\-42383063,Industry \: Pharma / BiotechFunctional Area \: Recruitment,General / Other SoftwareJob Location \: Kandla, Gandhidham

GenNext Human Resource Management \- Kandla, Gujarat \- Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data.

SkillSet: retirement benefits, vision insurance, loa, story structure, employee assistance programs . Hello, There is an opening with Rusan Pharma Ltd as Approved Chemist - Production (R&D Center). Candidates can apply only if there are interested to relocate in Kandla Location. (Gandidham) METHOD OF ANALYSIS Raw Material Testing. Tablet Dissolution Ultra Violet - Visible Spectroscopy Tablet Disintegration Test Water by Karl - Fisher Method Assay & RS by HPLC F.T.I.R GAS Chromatography Regard Interview Venue Navin Saxena Research & Technology Pvt Ltd (NSRT) Plot no. 667 669,670 Sector- II, New Area Kandla Special Economic Zone Gandhidham. Kutch, Gujarat-370230 Priti Singhvi 022- 42383063 Desired Candidate Profile Perks and Benefits

SkillSet: professional liability, hplc, r, technology transfer, schedule. Opening for Manager - Production (API) with Rusan Pharma Ltd (RD Center) Location: Kandla, Gandhidham (Gujarat) Exp: 5+ Years of Exp from RD API Background Profile: Manager Production in R D Candidate can apply only if wants to relocate at Gandhidham Location. Education: Masters or PhD qualification in Organic Chemistry Job Description: Development, Technology transfer and production operation in API. Expertiseinbuildingteambystreamliningmanufacturingoperationsusingprocedurestofacilitaterobustqualitymanagementsystemswithprocessoptimizationandcontrolrespectingquality,safety and process norms. Route scouting, synthesis and scale-up of small organic molecules/intermediate Plans and schedule synthesis campaigns to support large scale demands Responsible audit - the lab documentation in the PRD lab Innovates solutions to synthetic/scale-up issues (chemical, physical, preparative, application specific and analy

Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibration activities & review of certificates of analysis. 15. Anal

Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibration activities & review of certificates of analysis. 15. Anal

Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibration activities & review of certificates of analysis. 15. Anal

Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibration activities & review of certificates of analysis. 15. Anal

Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibration activities & review of certificates of analysis. 15. Anal

Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibration activities & review of certificates of analysis. 15. Anal

SkillSet: banking, sales, customer service, mis, accounts. Roles and Responsibilities 1. To review deviation & CCP in trackwise. 2. Preparation, checking, approval of SOP s of QA Department. 3. CCP approval. 4. Issuance & control of documents as and when required. 5. Follow up for compliance & closure of CAPA. 6. Failure investigation & root cause analysis. 7. OOS extended investigation & closure. 8. Checking & approval of TMD and BPR. 9. To review and ensure that all related log books, analytical records and electronic data are maintained & updated at the time of activity. 10. To review/ ensure all related log books and records of HPLC/GC, analytical dockets and to ensure timely upgradation. 11. To ensure the completion of daily activities/ targets. 12. To maintain inward register of experiments and to ensure timely removal of left over samples from laboratory. 13. Ensure timely submission and compliance of all related documents to QA. 14. Ensure & timely plan for outside calibrat

SkillSet: banking, sales, customer service, mis, accounts. Roles and Responsibilities Analysis of in process, finished product and stability samples by instrument HPLC/ GC To Check Calibration status in All Q.C Instrument. Chemical Testing. Operating the Laboratory instruments as per the Standard operating procedure. Monitoring of sophisticated instrument analysis (HPLC) Skill: He should be familiar with HPLC, GC Should have exposure in Formulation Plant.

1. Analysis of in process, finished product and stability samples by instrument HPLC/ GC 2. Calibration status All Q.C Instrument 3. Operating the Laboratory instruments as per the Standard operating procedure 4. Exposure of Formulation Plant The original job offer can be found in Kit Job: www.kitjob.in/job/20797762/officer-senior-officer-qc-pharma-formulation-osd-gujarat-ku919-kandla/

Rusan Pharma Ltd \- Kandla, Gujarat \- Hello, There is an opening with Rusan Pharma Ltd as Approved Chemist \- Production \(R&D; Center\). Candidates can apply only if there are interested to relocate in Kandla Location. \(Gandidham\) METHOD OF ANALYSIS Raw Material Testing. Tablet Dissolution Ultra Violet \- Visible Spectroscopy Tablet Disintegration Test Water by Karl \- Fisher Method Assay & RS by HPLC F.T.I.R GAS Chromatography Regard Interview Venue Navin Saxena Research & Technology Pvt Ltd \(NSRT\) Plot no. 667.

Hello, There is an opening with Rusan Pharma Ltd as Approved Chemist - Production (R&D; Center). Candidates can apply only if there are interested to relocate in Kandla Location. (Gandidham) METHOD OF ANALYSIS Raw Material Testing. Tablet Dissolution Ultra Violet - Visible Spectroscopy Tablet Disintegration Test Water by Karl - Fisher Method Assay & RS by HPLC F.T.I.R GAS Chromatography Regard Interview Venue Navin Saxena Research & Technology Pvt Ltd (NSRT) Plot no. 667 669,670 Sector- II, New Area Kandla Special Economic Zone Gandhidham. Kutch, Gujarat-370230 Priti Singhvi 022- 42383063 Desired Candidate Profile Perks and Benefits The original job offer can be found in Kit Job: www.kitjob.in/job/20543617/vw-957-approved-chemist-production-with-rusan-pharma-ltd-gandhidham-kandla/

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