Analyst with experience Pharma Lab The candidate must have hands of experience in handling XRD &amp; PSD instrument, Material Characterization and analysis techniquesDevelop and optimize reaction protocols and synthesis techniques. Analyze experimental data, interpret results and draw conclusion. Documentation and repor

A Masters Graduate with hands of experience in Micro dept, able to perform individually.Media Preparation, incubation conditions, storage, assessment with expiry date along with consumption and accountability. Supervise and conduct research on various microbiological activities on a regular basis.Maintain knowledge on various research methods and perform all manual operatio

Job description Analyst with experience Pharma Lab The candidate must have hands of experience in handling XRD instrument, LCMS Material Characterization and analysis techniquesDevelop and optimize reaction protocols and synthesis techniques. Analyze experimental data, interpret results and draw conclus

An Efficient QA Officer should ensure all processes follow guidelines of QMS, and also ensure documentation conforms to company policy and GMP's requirements. Key Job Responsibilities:Review and approval of Finished Products, Validations protocols and reports Stability samples, Raw Materials and Water Samples.Review &amp; Approval of SOP’s QMS elements like change

An Efficient QA Officer should ensure all processes follow guidelines of QMS, and also ensure documentation conforms to company policy and GMP's requirements.Key&nbsp;&nbsp;Job Responsibilities:&nbsp; <ul><li>Responsible for review of all type of documents related to Thermal, Calibration, HVAC, Compressed air, Pure steam, PLC and QA and records of calibration and qualificat

MSC -Chemistry /M- Pharmacy / B- Pharmacy is must.Expert in Chromatographic analysis, especially in XRD, LCMS/ HPLC / GCExperience on method development and validation by LCMS / XRD / HPLC /GCResponsible to ensure the compliance of procedures as per cGMP and GLPResponsible for preparation of project evaluation reportsResponsible for sample tra

An Efficient QA Officer should ensure all processes follow guidelines of QMS, and also ensure documentation conforms to company policy and GMP's requirements.Key&nbsp;&nbsp;Job Responsibilities:&nbsp;<ul><li>Responsible for effective execution of Training.&nbsp;</li><li>Ensuring effective control of documents through issuance, review, retrieval and archival system co

A Diagnostic sales representative is responsible for advertising, marketing and distributing a specific pharmaceutical product to relevant medical establishments. They meet with doctors and hospital teams and make presentations to persuade potential clients to use their Services , and medical equipment, to a variety of customers including general practitioners (GPs), hospital doctors

Ideal Candidate having experience in Analytical Research Lab and hands on various chromatography analysis like LCMS, GC, HPLC, XRD. Job ResponsibilitiesResponsible for method development activities related to HPLC,GC and wet analysisperform the regular analysis of HPLC and GC and stability analysis.Ensure all lab safety and GLP practices are maintained in t

Umed Pharma Lab Pvt. Ltd. is established in June 2011 with a vision of providing multi-disciplinary
services ( Validation & Calibration of Equipment's, analytical services as well as highly specialized testing services using modern technologies) to meet the regulatory affairs for emerging Pharmaceuticals and Biological industries.

Experience CSV Engineer for Pharma Testing Lab <ul><li> Conception, planning and performing of Computer Systems Validation (CSV) in the regulated environment (Pharma, Medical Devices, Biotech)</li><li>Implementation of qualification / validation activities within projects of new and existing computer systems according to our client requirements</li><li>Co-ordinating / Assign project task to the team members</li><li>Co-ordinate with customer to complete projects intime.</li><li>Monitor and Implement projects related to Drug Safety and Regulatory affairs.</li><li>Review and Approve validation deliverables and system changes as defined in procedures as Technical Owner</li><li>Experience in Drug Safety and Regulatory Affairs domain including applications involving knowledge of both front end and back end</li><li>Relevant Department instruments to be calibrated as scheduled.</li><li>Preparation, review &amp; execute the protocols which are mentioned in department SOP’S.</li><li>Strong verbal and written communication skills</li></ul> &nbsp;

Not relevant field experience Resumes, so unable to hire

<ul><li> Ø Conception, planning and performing of Computer Systems Validation (CSV) in the regulated environment (Pharma, Medical Devices, Biotech)</li><li>Implementation of qualification / validation activities within projects of new and existing computer systems according to our client requirements</li><li>Co-ordinating / Assign project task to the team members</li><li>Co-ordinate with customer to complete projects intime.</li><li>Monitor and Implement projects related to Drug Safety and Regulatory affairs.</li><li>Review and Approve validation deliverables and system changes as defined in procedures as Technical Owner</li><li>Experience in Drug Safety and Regulatory Affairs domain including applications involving knowledge of both front end and back end</li><li>Relevant Department instruments to be calibrated as scheduled.</li><li>Preparation, review &amp; execute the protocols which are mentioned in department SOP’S.</li><li>Strong verbal and written communication skills</li><li> </li></ul> &nbsp;

not relevant field resumes so unable to select them 

wanted Team Lead with more than 3 years of Experience in Analytical Lab, Qualification: MSC -Chemistry /M- Pharmacy / B- Pharmacy is must. 1.&nbsp;Testing of samples on&nbsp;GC-TCD &amp; FID, GC-MS, LC-MS &amp; ICP-MS and instruments&nbsp;responsibility.2.&nbsp;Calibration of analytical instruments as per the calibration schedule.3.&nbsp;Analytical method developments, Method verifications and Method validations.4. Preparation&nbsp;and review of&nbsp;all&nbsp;SOP's,&nbsp;protocols,&nbsp;documents,&nbsp;environmental&nbsp;monitoring data in&nbsp;Quality&nbsp;control&nbsp;department.&nbsp;5.&nbsp;Initiating and investigation of change controls, Deviation, Laboratory incidents, OOS and OOC.6.&nbsp;Preparation&nbsp;and&nbsp;reviewing&nbsp;of&nbsp;reports &amp; COA’s and&nbsp;technical&nbsp;data.7. Audit Compliance support.8.Ensure Good Laboratory Practice (GLP) and good documentation practice (GDP) as per the regulatory requirement.&nbsp;&nbsp;

MSC -Chemistry /M- Pharmacy / B- Pharmacy is must.1.&nbsp;Testing of samples on&nbsp;GC-TCD &amp; FID, GC-MS, LC-MS &amp; ICP-MS and instruments&nbsp;responsibility.2.&nbsp;Calibration of analytical instruments as per the calibration schedule.3.&nbsp;Analytical method developments, Method verifications and Method validations.4. Preparation&nbsp;and review of&nbsp;all&nbsp;SOP's,&nbsp;protocols,&nbsp;documents,&nbsp;environmental&nbsp;monitoring data in&nbsp;Quality&nbsp;control&nbsp;department.&nbsp;5.&nbsp;Initiating and investigation of change controls, Deviation, Laboratory incidents, OOS and OOC.6.&nbsp;Preparation&nbsp;and&nbsp;reviewing&nbsp;of&nbsp;reports &amp; COA’s and&nbsp;technical&nbsp;data.7. Audit Compliance support.8.Ensure Good Laboratory Practice (GLP) and Good documentation practice (GDP) as per the regulatory requirement.&nbsp;&nbsp;

Umed Pharma Lab Pvt Ltd based in Hyderabad, Accredited with NABL &amp; ISO 17025:2017, Umed is equipped with international standards modern Laboratory facility and Skilled staff, providing services like Routine &amp; Specialized Analytical and Molecular services to API, Pharma, Chemical, Biotech &amp; Food Industry. The ideal candidate from Analytical Research Lab background as Business development Executive, experience in B2B Sales. Responsibilities: <ul><li>Experience in selling Analytical Research Lab services to Pharma &amp; Biotech Industry.</li><li>Business Development strategies to ensure long term success</li><li>Well versed with the activities of Analytical Laboratory Services</li><li>Develop new relationships in an effort to grow business and help company expand</li><li>Maintain existing line of business</li><li>Identify New Clients from Pharma Industry and Retain the Existing one</li><li>Promote positive relationships with major customers to understand their needs</li></ul> Qualifications<ul><li>Bachelor's degree or equivalent experience</li><li>1-3 years' pharma industry related business development experience</li><li>Strong communication and interpersonal skills</li><li>Proven knowledge and execution of successful development strategies</li><li>Focused and goal-oriented</li></ul>

UMED PHARMA LAB PRIVATE LIMITED

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Quality Assurance Manager

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Automation Engineer

Automation Engineer

Analytical Lab Scientist

Asst Manager - QC

Business Development Executive