Job Information
Glenmark Pharmaceuticals Inc., USA Associate Director-Analytical Method Validation & Transfer in Monroe, North Carolina
Associate Director-Analytical Method Validation & Transfer
Department: Analytical Research-Formulations
Location: Monroe, NC
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POSITION SUMMARY
The Associate Director AMV is the analytical method validation lead & works with the Head Analytical Research (Formulations)/Head Global Analytical Validations based in India. The AMV lead at Monroe will liaison with injection development teams in India and oversee successful method validation at Monroe site. The Associate Director is responsible to provide analytical support for ANDA filings and regulatory deficiency response. The position also supports analytical method validation lifecycle management.
Project Coordinator Duties and Responsibilities:
Lead and manage the team carrying out the analytical validation for all methods of API, Excipients and Finished products.
Approve validation protocols, reports, SOPs related to validation and method change justifications.
Lead and manage invitro studies at site as per requirements.
Lead and manage the analytical method technology transfer of API, Excipients and Finished products to QC (Both in house and from third party CTLs).
Coordinate and collaborate with QC during Exhibit batch analysis and stability analysis.
Collaborate with Analytical R&D, QA, Manufacturing, Tech Transfer, and Regulatory Affairs.
Provide technical guidance during investigations, OOS/OOT, and CAPA implementation.
Submission of analytical documents to Regulatory affairs for filing purpose.
Respond to regulatory queries, FDA deficiencies, and observations related to analytical methods.
Lead and manage the life cycle management for analytical methods for API and Finished Products.
Coordinate with CMOs for analytical work and help them to do troubleshooting.
Act as a subject matter expert (SME) for analytical validation during regulatory inspections and audits.
Expected to support Pillar, Argentina and Osasco Brazil for analytical validation related activities
JOB RESPONSIBILITIES
Responsibilities
Manage the AMV team at Monroe to achieve the ANDA filings as per the project GRID
Collaborate with RA and Global PM teams to plan and execute experiments, provide justification/write-up for regulatory queries related to ANDA filing
Collaborate with CMO/CTL for successful execution analytical activities in support of ANDAs
Collaborate with quality team at Monroe for successful execution of ANDAs
Any other activities as assigned
KNOWLEDGE, SKILLS AND ABILITIES
Education
Minimum MS/Ph D in Pharmaceutical Sciences, Analytical Chemistry, or equivalent
Experience
18 + years in the Pharmaceutical Industry
Knowledge and Skills (Functional / Technical)
Chromatography
Wet chemistry
Injectable products in general
In Vitro studies
US FDA guidance related to analytical development, validation, specifications and
Knowledge of instrumentation like HPLC, GC, Malvern PSD, Zetasizer, UHPLC etc.
Sameness Studies
Leadership / Managerial Attributes
Able to manage a team of 4-6 direct reports
Able to deal with multiple locations
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