Manager, Technical Operations at Azurity Pharmaceuticals - India

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

16 Dec, 25

Salary

0.0

Posted On

17 Sep, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Technical Operations, GMP, Validation, Product Development, Quality Assurance, Regulatory Affairs, Manufacturing, Process Validation, Technical Transfer, Documentation, Project Management, Cross-Functional Collaboration, Metrics Preparation, Compliance, Change Control, CAPA, Investigations

Industry

Pharmaceutical Manufacturing

Description

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. 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, develop and/or review, approval of controlled documentation concerning late-stage development, qualification, validation, and commercial manufacturing activities as needed, and support execution of those activities. Mange and support 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. Responsible for daily management of commercial manufacturing projects including technical review and approval of applicable change controls, CAPAs, deviations, and investigations. 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 of 8 years of experience in biopharmaceutical/pharmaceutical GMP environment or related industry. Thorough knowledge of cGMPs, ICH and Validation related requirements and guidances Experienced 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.

Responsibilities

Manage the planning and execution of manufacturing and associated qualification and validation activities for development and commercial products. Collaborate cross-functionally to achieve project milestones and ensure compliance with regulatory requirements.