Vacancy for Regulatory Affairs Analyst at Dr. Reddy's Laboratories

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Dr. Reddy's Laboratories is an emerging global pharmaceutical company with proven research capabilities. The company is vertically integrated with a presence across the pharmaceutical value chain. It produces finished dosage forms, active pharmaceutical ingredients and biotechnology products and markets them globally, with focus on India, US, Europe and Russia.

Post : Regulatory Affairs Analyst

Job Description
• Knowledge of the regulatory guidance available with FDA, ICH, EMA, with expertise in ANVISA, other regulatory agencies for APIs and fair understanding of the drug products approval cycle.
• Search & review the regulatory assessment reports (RLD / SBOA/EPAR/other literature evidences) available in regulatory websites or public domain and share the inputs with HPT for fixing the limits for impurities or defining the control strategy based on the maximum daily dosage.
•  Must have sufficient chemistry knowledge to evaluate the synthetic schemes and aid in selection of appropriate regulatory starting materials for these complex APIs and define regulatory requirements for the selected starting materials in consultation with their managers.
• Participate in the technical discussions with the HPT for defining & finalizing the specifications for starting materials/intermediates/drug substance.
• Ensure GTI evaluation is carried out and necessary control strategies are put in place based on purge study, purge factors and/or routine or non-routine testing of the PGIs at appropriate stages.
• Responsible for communicating the global & region specific regulatory requirements to HPT for a global development.
• Review the documents received from CFTs and ensure quality of the technical reports and DMF.
• Responsible for responding to the regulatory deficiencies with adequate data and within stipulated timeline. 
• Co-ordinate with GMO teams Plant documentation needed for DMF preparation/deficiency responses/customer support. 
• Stay well-informed of the regulatory procedures and the changing regulatory requirements. Must be aware of QbD principles, ICH guidelines to ensure their applications during product development and preparation of DMF submissions.
• Share the learning from regulatory deficiencies and updated regulatory guidelines with CFTs periodically during the daily meeting to integrate the requirements.
• Provide customer support by arranging technical packages, open part DMFs, and addressing customer queries in timely manner. 
• Must have basic computer knowledge eg.MS-office, Chem Draw, etc.
• Maintain records to comply with regulatory requirements. Update and maintain paper/electronic document archival systems.

Candidate Profile
Basic understanding of API global regulatory affairs & proficiency in Brazil/ANVISA requirements;

Additional Information
Experience : 2 to 5 Years
Qualification : M.Pharm / M.Sc
Location : Bachupally, Hyderabad, Telangana, India
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th August, 2020.

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