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Azurity Pharmaceuticals
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Director, Technical Operations

Director, Technical Operations

Azurity Pharmaceuticals

15 - 20 years

25 - 30 Lacs

Hyderabad

Posted:23 hours ago| Platform:

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Skills Required

Supply chain Neurology Manager Quality Assurance Cardiovascular Pharma Analytical Packaging Life sciences GMP Endocrinology

Work Mode

Work from Office

Job Type

Full Time

Job Description

Brief team/department description:

Technical Operations is responsible for management and oversight of technical process strategy, CMO and CDMO management, and execution of product deliverables in alignment with Azurity policies, Azurity clients and in accordance with company objectives. The position leads staff and / or contractors and collaborates cross-functionally to achieve project milestones in support of process scale-ups and process validation, technical transfers, implementation of lifecycle post approval changes, and investigation / closure of deviations / OOS for commercial products.

Principle Responsibilities:

Manage the planning and execution of manufacturing along with associated qualification and validation activities as they relate to both development and commercial products.

In cooperation with contract facilities, manage the review, approval, and execution of controlled documentation concerning late-stage development, qualification, validation, and commercial manufacturing activities as needed.
Direct tasks associated with late stage product / process development (as applicable), product transfers, equipment qualifications, and validation activities to ensure alignment with company policies and objectives.
Support and / or lead product launch and commercialization efforts.
Ensure that appropriate policies, SOPs and documentation are in place to support validation practices according to regulatory requirements and applicable industry guidance documents.
Support Management Review and Compliance related activities as needed. Assist in preparing metrics and compiling summaries to effectively communicate status and recommendations to Senior Management.
Support Due Diligence activities to support company objectives including product development, technical transfer, commercial manufacturing, and/or commercial launch.
Collaborate closely with cross-functional team members from functions including Supply Chain, Product Development, Quality Assurance, and Regulatory Affairs.

Qualifications and Education Requirements

Bachelor s degree in Life Sciences (Master s Degree preferred), or related field.
Minimum 15 years of experience in biopharmaceutical / pharmaceutical GMP environment or related industry.
Expertise in cGMPs, ICH and Validation related requirements and guidances
In-depth experience in performing technical transfer of multiple dosage forms (solid oral, liquid oral, injectables, etc.)
Experienced in multiple validation disciplines including manufacturing process validation of multiple dosage forms, cleaning validation, packaging validation, analytical methods validation, terminal sterilization validation, hold time studies, shipping studies, equipment / utilities qualification, and facilities validation
Ability to work in a strategic, tactical, and hands-on level.
Candidate must be proficient in Microsoft Word, Excel, and Powerpoint.
Experienced in participating in regulatory agency inspections.

By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

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Director, Technical Operations