14 Ard Jobs

As a Project Manager at Sai Life Sciences, a leading Contract Research, Development, and Manufacturing Organization (CRDMO), you will play a crucial role in overseeing the successful delivery of projects within the API-CRDMO department based in Hyderabad. Your responsibilities will include: - Ensuring timely kick-off of awarded projects and preparing comprehensive Gantt charts for project delivery schedules. - Managing end-to-end project management activities, including maintaining schedules and project budgets. - Coordinating regularly with Cross-Functional Teams (CFT) such as PR&D, AR&D, PE, QA, QC, and Production through meetings to address project-related issues. - Updating and maintaini...

Job Description Summary: Leads and supports establishing and maintaining the GxP management system of the ARD Line Units at site level, serves as a contact point between local QA and the local ARD Line Units for general inquiries, represents the ARD in GxP-related committees and networks. Lead and manage all compliance/project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD strategies and goals. Responsibilities include, but are not limited to: Oversee and lead all activities of assigned teams /projects to meet customer needs. Work according to appropriate standards for quality, ethics, health, safety, environment, protection and i...

Exp. in ARD/AMD of minimum -20 to 30 years Lead the development and validation of analytical methods Prepare and review technical documentation Drive analytical strategy in global or cross-functional project teams

Job description Position: ARD Officer/ Sr. Officer, Wet, GC, HPLC (API) Note: Candidate should be working in Pharma API industry In ARD Department in Wet, GC and HPLC section. Interested one can share updated resume on anuverma@sauravchemicals.com or WhatsApp/ call at 9875994190/9988339860 Role & responsibilities Position: ARD Officer Wet lab (API Plant)- No. of positions :10 Role & responsibilities Perform routine analytical tests and analyses on incoming raw materials, intermediates, and finished products using various wet chemistry techniques and instrumentation. Maintain accurate records of all testing procedures, results, and observations in accordance with Good Laboratory Practices (GL...

You should have a minimum of 3 years of experience in an international Enterprise-level customer-facing role, preferably in Enterprise Support or as a Technical Consultant. Your role will require proven troubleshooting and problem-solving skills. During the interview stages, we would appreciate some brief examples, especially those related to Python. Fluency in English at an excellent level is a must, along with experience in working with Enterprise customers. You should feel confident in delivering presentations to larger audiences. Experience in Enterprise infrastructure solution architecture is essential. It is important to have a good understanding of OAuth2.0, OpenID Connect, and SAML s...

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

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, emp...

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

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.

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

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

Exp. in ARD/AMD of minimum -1 to 5 years Exp. in pharmaceutical formulation of Tablet and capsules Exp. in semi-regulated - ROW

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:-

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.