
Manager-Development Quality Assurance
21 hours ago
Role & responsibilities
* Prepare and Review SOPs and Guideline for DQA.
* Formulate Documentation Process for the Key divisions of SRD
and ARD.
* Review documents with respect to drug substance such as
protocols, SOPs, test methods, data COAs and report through
collaborate with CRD, ARD, and QC scientists.
* Successfully manage and complete all Audits that come up from
time to time and conduct periodic internal audits and ensure
compliance as per regulatory requirements
* Review process development documents including KSM/KRM
identification, specification proposal, analytical method
development and validation reports, stability protocols& reports
and safety studies.
* Handle Vendor Qualifications for KSM/KRM, Solvents etc.
* Ensure Regulatory compliance as per USFDA and other such
regulatory bodies.
* Impart training to all employees on SOPs/Safety. Support on
Onboarding on new employees joining the organization
* Responsible for assessing the impact, review and closure of
change control requests and deviations.
* Responsible for CAPA implementations, verifications of and
effectiveness.
Preferred candidate profile
* Mainly Preferred API Synthesis R&D Experience not formulation & Analytical
• Bachelors or Masters degree in Pharmaceutical Sciences,
Chemistry, Chemical Engineering, or related field.
• Minimum 5-8 years of experience in Quality Assurance, with
at least 3 years in a managerial or leadership role in the
pharmaceutical industry, specifically with API products.
• In-depth knowledge of GMP, ICH guidelines, FDA, EMA
regulations, and quality systems.
• Proven experience in conducting internal and external
audits, and leading regulatory inspections.
• Strong understanding of the API development and
manufacturing process.
• Ability to manage cross-functional teams and interact with
senior management.
• Experience in CAPA, deviation investigations, root cause
analysis, and risk management.
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