AQA Associate I MDI

About the role

This position requires a strong analytical chemistry/lab background and experience. The job duties for this position include but are not limited to the following:

Responsibilities

• Reviewing and confirming the compliance related to raw materials, inprocess and finished product analytical documents.
• Making sure that laboratory personnel follow current Good Laboratory Practices (cGLP) during routine operations to ensure adherence to procedures.
• Verifying the completeness of laboratory chemicals/reagents, standards against standard operating procedures (SOPs).
• Reviewing laboratory audit trials during data review against standard operating procedures (SOPs).
• Coordinating with the Analytical Laboratory Teams to arrange required documents for cross-functional teams.
• Maintaining all incoming documents with proper tracking, recording, storage, and archiving.
• Identifying gaps within the system during routine monitoring and informing the supervisor of necessary improvements.
• Participating in reviewing data related to laboratory investigations and incidents and ensuring proper compliance.
• Performing other departmental and cross-functional projects and assignments given by the manager/supervisor.

Requirements

• Possess a minimum bachelor’s degree in chemistry, Pharmaceutical Sciences, or related field of study from an accredited institution. Master’s degree in the above and/or related fields of study as noted above preferred.
• A minimum of 1-3 years in analytical (preferably in analytical quality assurance).
• Proficient in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.
• Knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP), etc.

Technical Knowledge and Computer Systems Skills

• Understanding of laboratory equipment operation, qualification, and calibrations which includes their software audit trial reviews. E.g. pH meter, conductivity meter, analytical balance, UV-Vis spectrophotometer, IR Spectrophotometer, etc.
• Effective interpersonal relationship skills and the ability to work in a team environment.
• Experience in Inhalation products (MDI) is a plus.
• Ability to work in a fast-paced, dynamic environment within a manufacturing operation setting.

Education and Experience

The position requires a strong analytical chemistry/lab background and experience. The job duties for this position include but are not limited to the following:

Professional and Behavioral Competencies

• Proficiently speak English as a first or second language and ability to read, write and communicate effectively the same.
• Self-starter and demonstrates initiative to seek additional training or direction as needed.
• Willing and able to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday.
• Knowledge of good manufacturing practices and good documentation practices preferred.
• Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously.
• Excellent organizational skills with the ability to focus on details.

Work Schedule and Other Position Information

• General shift but must be willing and able to work any assigned first or second shift. Work schedule may be Monday to Friday, Tuesday to Saturday, or some combination thereof based on business needs.
• Must be willing to work some weekends based on business needs as required by management.
• Relocation negotiable.
• No remote work available.
• This role works in cGMP laboratory or manufacturing environment, where personal protective equipment (PPEs) is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc.
• The role may be assigned on a work-shift basis where required (Day, Evening, Night). Weekend or Holiday work may be requested or required based on business needs.

GLOBAL COMPANY

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.

EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.