Global Blockchain Talent
Overview
Career Opportunities with Glenmark Pharmaceuticals Inc.
A great place to work.
Current job opportunities are posted here as they become available. Subscribe to our RSS feeds to receive instant updates as new positions become available.
Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules – both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets APIs to regulated and semi-regulated countries.
Glenmark Pharmaceuticals Ltd. employs over 10,000 people in more than 60 countries, including twelve manufacturing facilities, five R&D centers, and front-ends in the US, EU, India, and Brazil. Currently, Glenmark is in a phase of immense growth both in the U.S. and abroad, and is well-positioned to successfully emerge as a leading integrated research–based pharmaceutical company.
Position Summary
Under the direction of the Senior Manager, Quality Compliance, the Quality Compliance Specialist is responsible for managing the investigation and resolution of Quality Systems notifications including, but not limited to: Complaints, Field Alerts and Recalls, Vendor and Contract Lab Qualifications, Internal and External Audits. This individual works closely with cross-functional teams at the site and abroad. This individual will routinely report on system and business process performance; proactively identifying, providing guidance and implementing process and system improvements to resolve complex issues in a timely manner. This position will also provide site representation for regulatory surveillance program.
Responsibilities
Provide support in resource planning, allocation and manage within approved budgets while building best in class quality processes and systems at site.
Ensure that complaints are logged, triaged, investigated, and resolved according to established deadlines, company and regulatory requirements.
Coordinate the reviews of relevant records (e.g. batch records, quality control data, quality investigations, etc.).
Track quality system metrics related to complaints and create detailed trend analysis reports. Prepare formal reports for complaint closing.
Ensure that site is in compliance with CGMPs in respect to internal/external regulations and procedures.
Provide support in evaluation of implementation for Global Policies and Procedures.
Evaluate and assist in the implementation of new changes for the site.
Support implementation of projects that improve site Quality and/or efficiency.
Keep track of certified auditors for internal audit and external audit (vendor/CTL).
Maintain records for audit reports pertaining to vendors and CTL at site along with schedule.
Participate in regulatory surveillance program and work with CFT members for necessary changes to prevent observations at the site.
Provide support in handling Field Alerts and Product Recalls as required for marketed products.
Approve creation or modification of Materials and Vendors.
Create or modify Quality view data such as shelf life and Quality Info Record (QIR) based on Vendors qualification status.
Support audits/inspection processes, including government, regulatory, Corporate or vendor audits and audit readiness activities.
Support internal and external/regulatory audits/inspections when required.
Stakeholder
Ensure site is in compliant with CGMPs and internal/external regulations and procedures.
Provide guidance and work with stakeholders from various departments to process complaints, internal and external audit CAPA and follow-up with external parties (Vendor/CTL) for audit closure.
Provide required support in Annual Product Review.
Establish, revise, review and continuously improve procedures for applicable Quality Systems.
Establish Key Performance Indicators (KPIs) for functional area and ensure systems are operating within target.
Education Bachelor of Science (BS) / Bachelor of Arts (BA) in Science, Engineering, Pharmaceutical Sciences, or equivalent
Experience Minimum 3 years in Quality Assurance in the pharmaceutical, biopharmaceutical, or medical device industry, or a combination of education and experience.
Knowledge and Skills Knowledge and Skills : Strong understanding of current GMPs and related regulatory health authority guidance (FDA regulations, ICH guidelines, etc.) as they relate to the pharmaceutical industry.
Must be proactive, results-oriented with a strong attention to detail and strong time management skills.
Ability to manage multiple projects simultaneously, meet deadlines, and handle an ever-changing, fast-paced critical work environment.
Ability to analyze details and perform structured decision-making on a daily basis.
Excellent verbal and written communication/documentation skills. Must be able to read, write, and speak English.
Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
Intermediate Excel and/or Minitab skills are required including, but not limited to: spreadsheet manipulation, charting, and analysis tools.
Ability to work independently, or within a team structure, and on multiple projects, with flexibility to adapt to changing priorities is required.
Self-starter with the ability to work independently with minimum supervision and use good judgment, or as a contributing member of a team.
#J-18808-Ljbffr
A great place to work.
Current job opportunities are posted here as they become available. Subscribe to our RSS feeds to receive instant updates as new positions become available.
Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules – both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets APIs to regulated and semi-regulated countries.
Glenmark Pharmaceuticals Ltd. employs over 10,000 people in more than 60 countries, including twelve manufacturing facilities, five R&D centers, and front-ends in the US, EU, India, and Brazil. Currently, Glenmark is in a phase of immense growth both in the U.S. and abroad, and is well-positioned to successfully emerge as a leading integrated research–based pharmaceutical company.
Position Summary
Under the direction of the Senior Manager, Quality Compliance, the Quality Compliance Specialist is responsible for managing the investigation and resolution of Quality Systems notifications including, but not limited to: Complaints, Field Alerts and Recalls, Vendor and Contract Lab Qualifications, Internal and External Audits. This individual works closely with cross-functional teams at the site and abroad. This individual will routinely report on system and business process performance; proactively identifying, providing guidance and implementing process and system improvements to resolve complex issues in a timely manner. This position will also provide site representation for regulatory surveillance program.
Responsibilities
Provide support in resource planning, allocation and manage within approved budgets while building best in class quality processes and systems at site.
Ensure that complaints are logged, triaged, investigated, and resolved according to established deadlines, company and regulatory requirements.
Coordinate the reviews of relevant records (e.g. batch records, quality control data, quality investigations, etc.).
Track quality system metrics related to complaints and create detailed trend analysis reports. Prepare formal reports for complaint closing.
Ensure that site is in compliance with CGMPs in respect to internal/external regulations and procedures.
Provide support in evaluation of implementation for Global Policies and Procedures.
Evaluate and assist in the implementation of new changes for the site.
Support implementation of projects that improve site Quality and/or efficiency.
Keep track of certified auditors for internal audit and external audit (vendor/CTL).
Maintain records for audit reports pertaining to vendors and CTL at site along with schedule.
Participate in regulatory surveillance program and work with CFT members for necessary changes to prevent observations at the site.
Provide support in handling Field Alerts and Product Recalls as required for marketed products.
Approve creation or modification of Materials and Vendors.
Create or modify Quality view data such as shelf life and Quality Info Record (QIR) based on Vendors qualification status.
Support audits/inspection processes, including government, regulatory, Corporate or vendor audits and audit readiness activities.
Support internal and external/regulatory audits/inspections when required.
Stakeholder
Ensure site is in compliant with CGMPs and internal/external regulations and procedures.
Provide guidance and work with stakeholders from various departments to process complaints, internal and external audit CAPA and follow-up with external parties (Vendor/CTL) for audit closure.
Provide required support in Annual Product Review.
Establish, revise, review and continuously improve procedures for applicable Quality Systems.
Establish Key Performance Indicators (KPIs) for functional area and ensure systems are operating within target.
Education Bachelor of Science (BS) / Bachelor of Arts (BA) in Science, Engineering, Pharmaceutical Sciences, or equivalent
Experience Minimum 3 years in Quality Assurance in the pharmaceutical, biopharmaceutical, or medical device industry, or a combination of education and experience.
Knowledge and Skills Knowledge and Skills : Strong understanding of current GMPs and related regulatory health authority guidance (FDA regulations, ICH guidelines, etc.) as they relate to the pharmaceutical industry.
Must be proactive, results-oriented with a strong attention to detail and strong time management skills.
Ability to manage multiple projects simultaneously, meet deadlines, and handle an ever-changing, fast-paced critical work environment.
Ability to analyze details and perform structured decision-making on a daily basis.
Excellent verbal and written communication/documentation skills. Must be able to read, write, and speak English.
Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
Intermediate Excel and/or Minitab skills are required including, but not limited to: spreadsheet manipulation, charting, and analysis tools.
Ability to work independently, or within a team structure, and on multiple projects, with flexibility to adapt to changing priorities is required.
Self-starter with the ability to work independently with minimum supervision and use good judgment, or as a contributing member of a team.
#J-18808-Ljbffr