Associate Director Quality Assurance, Data Integrity OfficerAssociate Director Quality Assurance, Data Integrity Officer 3 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. About Glenmark

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Glenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark Generics Limited has a fast growing and robust US generics business. The subsidiary also markets APIs to regulated and semi-regulated countries. About Glenmark

Glenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark Generics Limited has a fast growing and robust US generics business. The subsidiary also markets APIs to regulated and semi-regulated countries.

Glenmark employs nearly 10,000 people in over 80 countries and with its twelve manufacturing facilities in four countries, five R&D centers and Front-ends in US, EU, India, Brazil and other markets worldwide, Glenmark is well placed on the road of growth and is exceedingly well prepared to take the competition head-on.

Position Summary

The Associate Director - Data Integrity Officer (“DIO”) is responsible for ensuring the accuracy and reliability of cGMP data and data supporting regulatory submissions. Generally, this requires implementing, as appropriate, and overseeing systems and processes to ensure complete, consistent, enduring, and accessible data is attributable, legible, contemporaneously recorded, original or a true copy, and accurate.

The associate Director – Data Integrity Office (DIO) will implement procedures, training and oversight aligned with corporate policies and global regulations to ensure the integrity of data generated to support manufacturing and testing processes. This role is responsible for all site DI Plan(s) and will collaborate across functions and sites to ensure full compliance are maintained.

Additionally, the DIO will serve as an active member of the site Quality Leadership Team and the Global Corporate DI Network and will implement DI practices and procedures to meet regulatory requirements. Coordinate routine DI Surveillance, weekly DI awareness topics, and monthly reporting to the site leadership team. Collaborate with cross functional teams for continuous improvement of processes to facilitate right first-time documentation.

Overall Job Responsibilities

Provide oversight for governance, management, and coordination of activities related to risk assessment, utilizing Quality Risk Management (QRM) principles, such as Failure Mode Effects Analysis (FMEA) Oversee remediation plans, retrospective assessments, and responses to regulatory audit findings related to data integrity Conduct audits and gap assessments based on regulatory requirements and industry guidance as updated and issued from time to time Facilitate risk assessments for new and existing equipment and systems and provide strategic direction for remediation. Develop, own, and update procedures as necessary to ensure clear direction and understanding of data integrity principles and requirements. Leads data integrity training to ensure awareness and compliance to data integrity regulatory and program requirements. Support the change control and deviation management processes with respect to potential data integrity impact and ensure appropriate implementation actions are carried out to maintain compliance. Serve as the point person during client and regulatory inspections for DI. Confirm new and existing equipment and instruments are appropriately validated, when appropriate, to protect data and ensure activities can be audited and reviewed at appropriate intervals Oversee the selection, validation, and implementation of software used for the generation of cGMP data Conduct audits and gap assessments based on regulatory requirements and industry guidance as updated and issued from time to time Oversee the selection, validation, and implementation of software used for the generation of cGMP data Assess training program and materials for adequacy to educate employees on expectations related to data integrity and conduct or oversee training, as appropriate Comply with applicable regulations and guidance, including, but not limited to, 21 CFR Parts 11, 210, and 211, and FDA data integrity guidance

Education

KNOWLEDGE, SKILLS AND ABILITIES:

Bachelor’s degree or higher in Chemistry, Biotechnology, Life Sciences, Engineering or related working experiences.

Experience

7 years in a regulated industry OR 5 years with related technical knowledge including data integrity related to computer systems / data related to manufacturing equipment, QC instruments, and support equipment/systems. Experience with quality control data, chromatographic systems, laboratory instruments, manufacturing equipment and quality management systems preferred. Prior management experience preferred. Knowledge of and experience with Data Integrity, Quality, Quality Control, Computerized Systems, Good Manufacturing Practice, Good Documentation Practice, Good Laboratory Practice, and other aspects of cGMP environments Demonstrated leadership experience over personnel, systems, and processes Experience working for a multi-national/multicultural organization is a plus

Knowledge & Skills

Excellent knowledge Data Integrity, Quality Control, Computerized Systems Relations, Performance Management, and Learning and Development Demonstrated ability to influence management and collaborate with others Strong problem-solving skills; developing creative solutions to meet objectives Demonstrated experience in prioritizing multiple projects / tasks at the same time, with successful results Experience with pre-submission audits Experience with FDA data integrity

Leadership/Managerial Attributes

Collaborative mind-set Management experience Clear and transparent communication style Good judgment and problem solving ability & is capable of understanding the impact of decision making on both Glenmark and their customers. Seniority level Seniority levelDirector Employment type Employment typeFull-time Job function Job functionStrategy/Planning and Information Technology IndustriesPharmaceutical Manufacturing Referrals increase your chances of interviewing at Glenmark Pharmaceuticals by 2x Sign in to set job alerts for “Associate Director Quality Assurance” roles.Assurance Manager, Quality Management - IS Assurance Charlotte, NC $100,000.00-$150,000.00 2 weeks ago Nuclear Program Quality Assurance Manager We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

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