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1.0 - 5.0 years
3 - 4 Lacs
Navi Mumbai
Work from Office
Exp. in ARD/AMD of minimum -1 to 5 years Exp. in pharmaceutical formulation of Tablet and capsules Exp. in semi-regulated - ROW
Posted 1 week ago
1.0 - 6.0 years
4 - 6 Lacs
Navi Mumbai
Work from Office
Exp. in ARD/AMD of minimum -7 to 10 years Exp. in pharmaceutical formulation of Tablet and capsules Exp. in regulated market-EU & US Validation,Development,Scientist Required Candidate profile Job Opening at Taloja(Panvel)Location-ARD(Regulated market) send resume to sunil@flamingopharma.com Current CTC & In Hand:- Expected CTC & In Hand:- Notice Period:-
Posted 2 weeks ago
3.0 - 8.0 years
3 - 6 Lacs
Bharuch, Ankleshwar
Work from Office
Review the Lab validation Protocol and Report of CRD Review of Process Development report for DMF filing. Required Candidate profile Lead the DQA department to implement CGMP rules and regulations in Research & Development.
Posted 3 weeks ago
0 - 5 years
2 - 7 Lacs
Pune, Navi Mumbai
Work from Office
Urgent Job Opening - Multiple Quality Assurance, Quality Control, Clinical Research , Regulatory Affairs, Medical Record Summerization , Medical Claims , Medical Officer, Medical Billing , Pharmacist, ADL, ARD, FRD, CDM, Production, R&D Required Candidate profile - Pharmaceuticals , Healthcare , Life Sciences , IT B.Sc , M.Sc - Analytical , Organic , Chemistry, Microbiology , Botany, Zoology, Bio technology B-Pharmacy , M-Pharmacy , BDS , BHMS , BAMS
Posted 2 months ago
3 - 8 years
2 - 7 Lacs
Nalagarh
Work from Office
Vacancy in Multiple Roles Sterile FRD & ARD Production Manager Operator (Production)-NASAL / Tablet/ Lotion Quality Control (AMV/ QMS/ Finish/ Stability/GLB/RM) Engineering (Electrical/Mechanical/ Utility/Water/CIVIL/ ETP) Logistic Receptionist PPIC
Posted 2 months ago
2 - 7 years
1 - 6 Lacs
Bengaluru, Bangalore Rural
Work from Office
Candidates should be from formulation background 2+ Years of experience required
Posted 2 months ago
5 - 10 years
0 - 0 Lacs
Mohali
Work from Office
1) Experience in preparing and reviewing of Method Development Report. 2) Knowledge of ICH Guidelines. 3) Strategic planning and performing Validation studies, Solubility Studies, Impurity and Standard Qualification. 4) Exposure of working on HPLC, LCMS, GC, UV and other equipment. 5) Ability to perform an analysis of related substances, assays and purity by using HPLC, IC. 6) Ability to perform analysis of residual solvents by using gas Chromatography. 7) Preparation and Review of development and validation/ method transfers/ protocols and reports based on R&D qualifications or monographs. 8) Ability to work in a team and contribute towards collective goals.
Posted 3 months ago
0 - 4 years
2 - 5 Lacs
Pune, Navi Mumbai
Work from Office
Below mentioned are the details Designation : Quality Assurance , Quality Control , R&D , CDM , CRA , Pharmacist Salary : 1.8 to 5 L Experience : 0 to 4 years Gender : Male /Female Job Location : Pune , Mumbai , Navi Mumbai , Mahad , Goa
Posted 3 months ago
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