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9 Ard Jobs

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10.0 - 20.0 years

10 - 20 Lacs

Panvel

Work from Office

Exp. in ARD/AMD of minimum -15 to 20 years Lead the development and validation of analytical methods Prepare and review technical documentation Drive analytical strategy in global or cross-functional project teams

Posted 5 days ago

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1.0 - 5.0 years

0 Lacs

maharashtra

On-site

As an Associate in the Life Sciences (AR&D) Services - SDTM Programming team at Accenture, you will play a crucial role in supporting the world's leading biopharma companies in bringing their vision to life. Your responsibilities will include Program mapping of eCRF and external data into SDTM standards using SAS/ETL tools as applicable. Accenture is a global professional services company known for its expertise in digital, cloud, and security services. With a workforce of 699,000 professionals across more than 120 countries, we deliver cutting-edge solutions to clients in over 40 industries. At Accenture, we believe in embracing change to create value and shared success for our clients, employees, shareholders, partners, and communities. In this role, you will be aligned with our Life Sciences R&D vertical, which offers services ranging from research laboratories and clinical trials support to regulatory services and patient solutions. You will be part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, where you will work towards improving outcomes by focusing on the patient experience. To excel in this role, you are expected to have a minimum of 1-3 years of experience and possess a degree in Any Graduation, BE, or BTech. Your primary responsibilities will involve solving routine problems based on general guidelines, with most interactions happening within your team and under direct supervision. You will receive detailed instructions for all tasks, and your decisions will have a direct impact on your work with close supervision. Please note that this role may require you to work in rotational shifts to meet the demands of the project. If you are looking to be part of a dynamic team that values innovation and collaboration, this role at Accenture might be the perfect fit for you.,

Posted 6 days ago

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0.0 - 4.0 years

1 - 6 Lacs

Pune, Mumbai (All Areas)

Work from Office

Urgent Job Opening Quality Assurance, Quality Control, Clinical Research , Regulatory Affairs, Medical Record Summarization , Medical Claims , Medical Officer, Medical Billing , Pharmacist, ADL, ARD, FRD, CDM, Production, R&D , Lab Technician

Posted 2 weeks ago

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5.0 - 10.0 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 2 weeks ago

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0.0 - 4.0 years

2 - 6 Lacs

Pune, Solapur

Work from Office

Urgent Job Opening Quality Assurance, Quality Control, Clinical Research , Regulatory Affairs, Medical Record Summarization , Medical Claims , Medical Officer, Medical Billing , Pharmacist, ADL, ARD, FRD, CDM, Production, R&D , Lab Technician

Posted 3 weeks ago

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0.0 - 4.0 years

2 - 5 Lacs

Navi Mumbai, Pune

Work from Office

Urgent Job Opening Quality Assurance, Quality Control, Clinical Research , Regulatory Affairs, Medical Record Summarization , Medical Claims , Medical Officer, Medical Billing , Pharmacist, ADL, ARD, FRD, CDM, Production, R&D , Lab Technician

Posted 1 month ago

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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 month ago

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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 months ago

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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 2 months ago

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