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Clinical research courses

  • Pfizer Require Chem Analytical Scientist | Ph.D, M.Pharm, MSc Apply

    Single use systems or other process materials used during pharmaceutical or biopharmaceutical manufacturing, e.g. filter systems, tubing, connectors, storage bags, seals, and membranes.
  • Work as GMPE Manager at Pfizer - Ph.D, Pharm.D, M.Pharm Apply

    Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.

    Post : GMPE Manager

  • Work as Investigator Contracts Lead at Pfizer
    This also includes managing the Per-Subject Cost PSC process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or pCRO and collaborating with other lines to plan site contracting timelines through start-up.
  • Pfizer Hiring Safety Surveillance Associate
    Experience in pharmacovigilance, in clinical care, or in clinical or scientific research is an advantage but not a requirement. Demonstrated computer literacy, particularly in the use and management of relational databases.
  • Pfizer Require Senior Safety Surveillance Associate
    Liaise with key partners, including Pfizer Country Organizations, Clinical Development, License Partners, and other stakeholders regarding safety data collection and data reconciliation.
  • Walk in Interviews for Freshers D.Pharm in Manufacturing at Pfizer
    Operate production equipment such as injectable machines, sterile machines, parenteral machines, formulation machines, filling machines, capping machines, compounding machines, washing machines, sealing machines and packing machines.
  • Pfizer Hiring Safety Surveillance Sr. Associate

    Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.  

    Post : Sr. Associate - Safety Surveillance

  • Job Openings for Fresher D.Pharm in Production Department at Pfizer

    Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.

    Fresher Job Openings Production Operators (Injectables)

  • Work as Reg CMC Associate at Pfizer
    Bachelor or Master degree Biotechnology, Pharmacy, Science or Ph. D Biotechnology, Biological Sciences or equivalent. Minimum 3-5 Years of experience in Pharmaceutical Industry with major experience in Regulatory Sciences group handling new submissions and, or LCM submission to global health authorities especially USFDA, EMA and other EU authorities.
  • Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.

    Post : Associate I – Regulatory Conformance

    Job Description 
    Job Summary
    • Committed to quality in compliance and conformance
    • Accountable for maintaining the HA status in corporate change and dossier management system for the allocated Regions / Markets
    • Manages the day to day work by self with periodic supervision by the Lead/Designee

    Job Description
    • Committed to quality and excellence in compliance and conformance
    • With the reasonable understanding of regional regulations, would perform the evaluation of the notifications assigned.
    • Accountable for maintaining the HA status in corporate change and dossier management system for the allocated Regions / Markets
    • Contributes independently and manages own time to meet the timelines.
    • Work in collaboration with GRA colleagues to ensure the gaps are identified and escalated on time.
    • Independently Perform accurate updates in system for most of the cases and consult with TL/Designee for clarification of any discrepancies in complex cases, before updating the system.
    • Makes informed decisions on straight cases within guidelines and policies
    • Support for updates in system for License withdrawals
    • Operate in line with internal SOPs and policies
    • Adhere to standard turnaround timelines
    • Escalate any potential compliance issues to management
    • Support periodic and ad-hoc system reports to estimate metrics
    • Contribute to local and regional regulatory initiatives promoting a culture aligned with Pfizer values
    • Assist in ensuring internal regulatory processes and procedures are well documented
    • Assist in remediation activities
    • Support the teams in ADHOC activities
    • Shares the learning time to time with the team colleagues

    Technical Skills
    • Theorotical Knowledge on Regulatory Affairs / Compliance
    • Experienced in Regulatory / Quality Assurance/ Production or any other functions in Pharmaceutical or related industries
    • Diligence and attention to detail
    • Good communication skills
    • Understanding stakeholder needs

    Candidate Profile
    Standards, Processes and Policies - General standards, processes and policies of Pfizer Behavioural/Any other Skills – An assertive, results oriented, positive “can do” attitude, and Time management skills. 
    Preferred Qualification – Master’s / Bachelor’s degree or equivalent i.e. degree in Chemistry, Pharmacy, or a related life sciences. Preferred Year Of Experience - 2 to 4 years of experience  Type of Experience – Any relevant experience in Pharmaceutical or relevant industry. Experience in Regulatory or Quality or Compliance roles is preferrable.

    Additional Information
    Experience : 2 to 4 years
    Qualification : Master’s / Bachelor’s degree or equivalent
    Location : Chennai
    Industry Type : Pharma / Healthcare / Clinical research
    Functional Area : Regulatory
    End Date : 20th August 2024

    Apply Online

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