• 541
  • Active Jobs Found
    (Last Updated: Jan 29, 2023)
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  • 2+ years
  • Not Disclosed
  • Ahmedabad, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 2+ years
  • Not Disclosed
  • Ahmedabad, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Pharmazone, Ahmedabad hiring for Pharmacovigilance department.   Experience Minimum 2 years into ICSR case processing (Drug cases only)  

  • pharma
  • pharmacovigilance
  • Drug Safety

Quality Assurance - Officer/Executive

Emcure Pharmaceuticals Limited

Full time
  • 2+ years
  • Not Disclosed
  • Ahmedabad, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 2+ years
  • Not Disclosed
  • Ahmedabad, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities To prepare and review annual product quality review data. Initiate, review and verify the QMS documents such as change control, deviation, CAPA, laboratory and production failures investigation, LIR, market complaints, product recall, etc., and its tracking. To prepare, review, and approve the trend of QMS activity (change control, deviation CAPA, self-inspection, OOC, and LIR. Participates in vendor qualification and Service provider activity, Nitrosamine impurity evaluation, and review. Coordinate training program and external laboratory audits (vendor audit), self-inspection program. Issuance and retrieval of GMP documents of QA and cross-functional department, review document control system. To provide the necessary support during regulatory and customer Audits   Qualifiication & Experience B.Pharma in Any Specialization/M.Pharma in Any Specialization 2 to 8 years of experience  

  • pharma
  • Quality control
  • pharmacovigilance
  • 2+ years
  • Not Disclosed
  • Gurugram, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 2+ years
  • Not Disclosed
  • Gurugram, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities Develops, drives and finalizes new products approvals in India and for all products in neighboring markets, in line with local regulatory requirements and business plans. Ensures submission in a timely manner and follow up to obtain earliest approvals for new products approvals in India and for neighboring markets. During the assessment of the registration files, ensures adequate follow-up with regulatory agencies and addresses quickly agencies’ requests on quality clinical and non-clinical information. Coordinates actions effectively and proactively with HQ and local support groups and in order to support products launches in due time and avoid business loss. MAINTANENCE OF EXISTING PRODUCTS Ensures timely submission and follow up of both labeling and quality-related variations to the marketing authorizations, in cooperation with the key stakeholders Ex., worldwide product labeling, CMC, RAI, HQ and regional regulatory support team. Ensures timely submission and follow up of quality-related variations (CMC) to the marketing authorizations, in cooperation with the key stakeholders to the Health Agency laboratory. Manages renewal process in liaison with CMC, RAI, HQ and regional regulatory support team ensuring that renewal files are prepared, submitted and approved in due time. Efficient regulatory input for packaging and label components to ensure timely implementation of artwork efforts. Responsible for implementing local regulatory procedures in a timely manner, in close synergy with HQ /regional groups. Trains appropriate personnel on regulatory procedures. Plans and tracks all regulatory actions to document and ensure full compliance with relevant legislation and with internal procedures Pro-actively shares intelligence on competitive products, generics, as well as on emerging regulations Responsible for supporting competitive intelligence   Qualification Education - Bachelor degree in Biological Sciences - eg BioMedical, Biochemistry, Pharmaceutical Science, Biotechnology etc. Working knowledge of Indian regulatory mechanism Detail oriented, meticulous and organized Basic IT knowledge  

  • Quality control
  • clinical research
  • pharmacovigilance

Sr Clin Process Associate

IQVIA

Full time
  • 2+ years
  • Not Disclosed
  • Thane, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 2+ years
  • Not Disclosed
  • Thane, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities Developing VBA macro based excel templates to create the dashboards. Advanced level Excel knowledge Creating calculated fields and conditional formatting in Pivot tables. Creating Dynamic range in Excel. BASIC, INTERMEDIATE, ADVANCE Level Excel VBA knowledge Creating the excel templates to collate the multiple source data. Excellent in data modelling. Basic/Advanced level of knowledge on creating Spotfire dashboards. Conditional Formatting. Basic and advanced level of Knowledge on POWER Queries, Power Pivots etc. Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and maintain effective project/ site communications Create and maintain relevant project documents Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information Participate in document management (creation, review, maintenance, storage, as applicable) Coordinate and collaborate with various project stake holders. Review, evaluate and recommend modifications to designated processes Participate in (study) team meetings and implement action items Collaborate with the project lead/team members in creation/review of study documents Setting quality standards and reviewing deliverables to the same for process tasks. Act as SME/mentor/buddy for new joiners and support with system/process trainings. May be assigned role of systems expert - guiding teams on using of systems, creating guidance documents, updating relevant trainings and any new updates available in the systems. Relaying the trainings to the team and be available to address the queries for the teams.   Qualification & Experience Bachelor's Degree life sciences or related field Typically requires Minimum 2-5 years of relevant experience. Requires knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education.  

  • Quality control
  • clinical research
  • pharmacovigilance
  • 9+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 9+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities Management of allocated personnel: Allocation of projects in conjunction with Group Management, as appropriate. Performance reviews, as required. Administer training and development of personnel, as required. Group management for allocated projects To oversee and guide with planning and management of study timelines and resources. To manage progress against schedules and report to management. To perform project management reviews across all functions for a study as appropriate. Management of CRFs and all related tasks. To contribute to the efficient running of the Clinical Data Management department as part of the Clinical Data Management leadership team. To pro-actively keep abreast of current data management developments and systems. To mentor data management staff To assist in the creation and review of in-house SOPs. To research and provide input into in-house strategies and systems. To produce a clear breakdown of bookable time for invoicing and ensure the same for direct reports. To perform other reasonable tasks as requested by management. Ensure launch, delivery, and completion of all Data Management procedures according to contractual agreement and relevant SOPs, guidelines, and regulations. Be willing to travel both domestically and internationally as necessary. To undertake other ad hoc tasks as required.   Qualification & Experience Qualified to an appropriate standard, preferably to degree level in a life sciences subject. Extensive knowledge of at least 2 Clinical Data Management systems such as Oracle Clinical, Medidata Rave, Inform. 9+ years of core CDM experience Ability to effectively lead project teams across multiple locations. Excellent project management skills. Thorough knowledge of ICH Guidelines and GCP including regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing. Excellent leadership/management skills.  

  • Quality control
  • clinical research
  • pharmacovigilance

Executive Quality Assurance

Novartis

Full time
  • 5+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 5+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities Ensure and coordinate that QA activities are being done as per laid down procedure. To ensure that Production adheres to GMP standards, procedures, and systems in all respects of manufacturing including storage. Monitoring of product quality, in-process control, and manufacturing environment. Ensure effective implementation of the Quality system and procedure as per cGMP requirement at shop floor, warehouse, and engineering along with documentation. Investigation of the complaint, deviation, and OOS to ensure appropriate root cause analysis and CAPA plan. Review all BMR, and BPR for their correctness and retention until destruction. Review of quality records in a periodical basis and review of analytical data in COA. Issuance of BMR, BPR, Cleaning checklists, Logbook, and Labels as per requirement. Sampling of FG control samples, stability samples and other samples as per requirement along with related documentation. Responsible for alarm review and trending as and when required. Training of new employees, system practices and procedure to develop competency. Review and approval of executed batch manufacturing, packaging documents & other quality documents. Handling of material on shop floor through approval for MRN, LRN, and MRQN. Submission of In-process analysis report from QC to production after review. Handling of non-conformance. Online stage wise BMR/BPR review. Handling of SAP & track wise activity as per Quality Assurance procedure. Approval of line clearance during product changes over/ Batch change over. To ensure the Environment, Health and Safety related activities are completed. To report near miss and incidences as observed as per EHS requirement. To ensure data integrity compliances at the site and while performing activities.     Qualification & Experience M. Pharm/B. Pharm. from reputed institute with more than 5 years of experience in a pharmaceutical company. Having good interpersonal skills and stakeholder management. Experience in Shop floor activities, QMS, Audit & Other GMP activities, Engineering services, Quality decision making, Knowledge of production systems, IT Applications & tools, TQM and related industry GxP standards and processes.

  • pharma
  • Quality control
  • pharmacovigilance

Emergency Care Physicians

VR Revankar Hospital

Full time
  • 1+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 1+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities Assessing patients who enter the emergency room immediately and overseeing emergency recovery. Conducting follow-up visits to monitor the patient’s condition. Requesting the appropriate medical tests and based on them, following a treatment plan. Developing effective patient care plans. Referring patients to appropriate specialists. Ensuring that patients are stable before transferring them to the proper department for further evaluation. Providing instructions for discharge and any relevant paperwork. Maintaining patients' medical records. Coordinating with different ER departments to ensure patients receive the necessary treatment.   Qualification & Experience Bachelor’s degree in medicine from an accredited institution. 1 – 3 years experience In-depth knowledge of current medical treatments and procedures. Great attention to detail with excellent analytical skills.  

  • mbbs
  • MD
  • Operations
  • 4+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 4+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Qualification & Experience Bachelors/Masters in Pharmacy OR Bachelors/ Masters in any of Life  Relevant years of experience (4-7 yrs) in Regulatory Affairs-CMC, should be willing to work in EU Shifts (12:00 – 9.00 PM) Understand the regulatory framework for EU/US and RoW Liaise closely with cross-functional team members. Experience of handling RIM tools - Veeva Vault specifically. Knowledge and authoring skills for CTD – M1 and M3. Excellent communication skills.  

  • Quality control
  • clinical research
  • pharmacovigilance

Packaging Development - R&D

Sun Pharmaceutical Industries Ltd.

Full time
  • 5+ years
  • Not Disclosed
  • Vadodara, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 5+ years
  • Not Disclosed
  • Vadodara, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Responsibilities Characterization of RLD pack samples Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement Identification of new packaging material & new vendor development for packaging material Mold development for primary packaging material & secondary packaging material & its validation. Support to Regulatory team on ANDA’s/NDA’s filling for regulated market Coordination with NPI & planning team for launch of ANDA’s/NDA’s Preparation & revision of packaging material specification   Preparation & review of MPC & FMEA Preparation & review of Development Study protocol & report & execute the study. Coordination with Cross functional team like FDD/RA/Plant/PPIC/Marketing/BD/PMO for completion of task Participating in FAT of machines Handling of Medical Devices, injectables and characterization. Preparation of Packaging documentation like Pack Style, Justification Report etc. as per Product/Regulatory requirements   Qualification & Experience Qualification : B.sc / B.Pharm / M.Pharm with PG Dip in Packaging Development Experience : 5 – 10 years as a Packaging Scientist in Pharmaceutical Co.  

  • pharma
  • Quality control
  • pharmacovigilance

Stuff Nurse / Nurse Incharge

Meitra Hospital

Full time
  • 1+ years
  • Not Disclosed
  • Kasaragod, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023
  • 1+ years
  • Not Disclosed
  • Kasaragod, India
  • Post Date: Jan 27, 2023
  • End Date: Mar 27, 2023

Qualification & Experience GNM/ BSc Nursing With valid Kerala Nursing Council Registration 1 year and above experience    

  • Quality control
  • clinical research
  • Operations

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