• 541
  • Active Jobs Found
    (Last Updated: Jan 29, 2023)
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Chemist/ Sr. Chemist - Quality Control

Lee Pharma Limited

Full time
  • 1+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Qualification & Experience MSc / BSc With 1 to 5 Yrs Experience in QC activities in API  

  • Quality control
  • clinical research
  • pharmacovigilance

Scientist III- Microbiology

US Pharmacopeia

Full time
  • 3+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 3+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Responsibilities Demonstrates strong skills and expertise in laboratory methods in Microbiology. The tests including but not limited to Identification, Enumeration, pathogenic tests, Sterility test, Bacterial endotoxin test, Antibiotic assays. Reviews, and evaluates test protocols and scientific literature and actively engages in the overall project and ensures own work is aligned with overarching goals. Independently executes all testing / analysis, and records experimental data, ensuring clear and accurate transcription of results and calculations. Records experimental data, ensuring clear and accurate transcription of results and calculations and prepares reports. Independently plans and executes experiments for project tasks assigned. Derives interpretation and conclusion of results. Plans daily work, records and review results and documents to ensure correctness and to fulfill targets on time. Completes assigned work with quality and in a timely manner. Assists the group leader in implementing laboratory procedures and systems. Coordinates with other team members as per requirement. Prepares protocols and reports including calculations and conclusions. Prepares presentations and documents related to projects and various scientific discussions as delegated. Performs peer review of data as needed. Follows QMS practices. Recommends improvements to systems and all other supporting activities. Assists supervisor in planning, evaluating, and implementing lab procedures and systems. Takes part in audits as per delegation. Adheres, follows, and ensures aspects related to USP Mission and Core Values. Follows and ensures aspects related to safety, ethics, and legal compliance. Performs in-charge duties for the allocated lab/equipment/inventory/supporting activities and takes responsibility for the timely completion of the tasks assigned. Demonstrates a strong desire to continue learning, grow personal capability and willingness to learn and contribute in the relevant and other areas of Biologics. Performs other duties as assigned.  

  • Quality control
  • clinical research
  • pharmacovigilance

Assistant Manager - Regulatory Affairs

Bharat Serums And Vaccines Limited

Full time
  • 6+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 6+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Responsibilities Preparation and reviewing of CTD and ACTD dossier. Co-ordination with Plant and R&D to collect inputs required for Regulatory Submission. Co-ordination with plant for Regulatory compliances. Timely achievement of monthly plan & timely query response. Gap Analysis/ Updating Master data. Review of Change Controls, Stability Protocol, Clinical Trial Protocols & Artworks. Get feedback from all the countries for respective variation, and there timely submission. Renewals. Master data Updating. Follow ups with plant for documentation regularly and review meeting. Tracking and reviewing of document requirements of upcoming new filing in ROW and Emerging markets.   Qualification & Experience M Pharma / MSc Biotech 6-8 years of relevant experience eCTD, CTD, Validation, ICH requirements, EMA Filings, WHO Prequalification, MCC South Africa for Biological and Biotech products Has exposure to in-licensed dossier filing and out licensing  

  • pharma
  • clinical research
  • pharmacovigilance

Medical Writer - Remote

Xogene

Full time
  • 1+ years
  • Not Disclosed
  • Pune, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • Pune, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Responsibilities Performing clinical trial posting activities for drug, device, and biologic clinical trials Performing clinical and non-clinical document redaction to remove confidential information Authoring plain language summaries Reviewing documents and content as part of a quality check process Managing timelines and communicating with internal team and/or stakeholders to ensure compliance Tracking status of all active clinical trials and recording clinical trial disclosure activities and compliance Supporting administrative aspects of maintaining US and international clinical trial registry and results database website postings Acting as point of contact for inquiries   Qualification & Experience Bachelor Degree in a health or life science related discipline; Masters degree preferred 1+ year(s) medical writing and/or medical data entry experience Demonstrated knowledge of drug development or clinical science Strong knowledge-base of the evolving clinical trials disclosure regulatory environment Excellent organizational and time management skills Strong analytical skills and communication skills (both written and verbal) Strong computer skills with Microsoft Word, Excel, PowerPoint and Adobe (or any other PDF-related program) Experience with Clinicaltrials.gov and / or EudraCT is a plus (but not required) Attention to detail Intercultural understanding with a global perspective  

  • pharma
  • clinical research
  • pharmacovigilance

Physician Assistant

Caritas Hospital

Full time
  • 1+ years
  • Not Disclosed
  • Kottayam, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • Kottayam, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Qualification & Experience B.sc Physician Assistant Minimum 1 year experience in hospital  

  • mbbs
  • MD
  • Operations

Anaesthetist & Gastroenterologist

Narayana Health

Full time
  • 0-1 years
  • Not Disclosed
  • Ahmedabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 0-1 years
  • Not Disclosed
  • Ahmedabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Qualification & Experience Anaesthetist: MBBS + MD or DA or DNB 0 to 3 years of experience Gastroenterologist: MBBS + MD or DM or DNB 1 to 4 years of experience  

  • mbbs
  • MD
  • Operations

Microbiologist

Westfort Hitech Hospital Road

Full time
  • 1+ years
  • Not Disclosed
  • Thrissur, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • Thrissur, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Qualification & Experience M.sc in Microbiology Minimum 1 year in a reputed hospital labroratory/ medical lab  

  • Quality control
  • clinical research
  • Operations

Clinical Research Associate- Remote

Worldwide Clinical Trials

Full time
  • 1+ years
  • Not Disclosed
  • New Delhi, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • New Delhi, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Responsibilities Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data Actively participate in study team and investigator meetings Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)   Qualification & Experience Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and one year experience with clinical research (e.g. study coordinator, CTA, etc.) Ability to meet the travel requirements of the job  

  • pharma
  • clinical research
  • pharmacovigilance

Sr. Research Scientist

Jubilant Biosys Limited

Full time
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Responsibilities Planning and implementation of novel approaches to drug discovery and development independently or in collaboration. Driving SAR for novel chemical series in at least 2 disease areas in conjunction with his / her Reporting Manager. Deploy modern methods of medicinal chemistry, parallel chemistry and Analytical methods in discussions with the Function Head or Reporting Manager. Ensures that all project members are practicing SOPs and EHS guidelines. Manages the drug designing and synthesis efforts in projects and is partially accountable for the success of these projects to his / her Reporting Manager. Optimal utilization of resources in the specific project team through monitoring, measuring and reporting on scientific issues, opportunities and developmental plans and achievements within agreed formats & timescales. Ensure adherence to the various policies & processes in his / her project team in conjunction with his / her Reporting Manager. Manages and drives the project through interdepartmental coordination and communications.   Qualification & Experience Ph.D (Organic Chemistry/ Medicinal Chemistry/ Pharmaceutical Chemistry) + Post-doctoral experience Experience in a drug discovery industry or Post-doc experience from a reputed institute (2-6 years). Ability to manage processes of maturing a target candidate from Hit finding to LO using different techniques and skills like triaging high throughput screening hits, rational drug design, chemical tools and structure based design. Should have peer reviewed publications and presentations in areas related to drug discovery.  

  • Quality control
  • clinical research
  • Operations

Officer - Senior Executive (Production)

Aspiro pharma

Full time
  • 3+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 19, 2023
  • End Date: Mar 19, 2023
  • 3+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 19, 2023
  • End Date: Mar 19, 2023

Qualification & Experience B.pharma / M.pharma / M.sc chemistry 3 to 10 years of experience Having Injectable Experience of Shop floor Supervising activities like Aseptic Filling. Autoclave Operations, Compounding Operation, Vial Washing, Lyophilizer Operations, Production Compliance(QMS), BMR BPR Protocols Review and Preparation, CCF Investigations, Change Controls, CAPA, Investigations.  

  • pharma
  • Quality control
  • pharmacovigilance
  • product management

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