AQA QA Associate II

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 current Good Laboratory Practices (cGLP) are followed by laboratory personnel during routine operations to ensure adherence to procedures.
• Ensuring compliance with protocols and reports of method validations, verifications, comparison reports, and other study reports.
• Preparing and reviewing laboratory investigation (OOS/OOT/Deviation) reports and ensuring compliance.
• Verifying the completeness of laboratory chemicals/reagents, standards against standard operating procedures (SOPs).
• Assessing and implementing Pharmacopoeia changes whenever there are new editions, supplements, amendments, or other changes in the Pharmacopoeia.
• 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.
• Reviewing and identifying gaps within the system during routine monitoring and informing the supervisor of necessary improvements.
• Participating actively in the review of 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 from an accredited institution. A master’s degree in the above and/or related fields preferred.
• A minimum of 4-8 years in analytical (preferably in analytical quality assurance for at least 3 years).
• Proficient in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.
• Strong 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), USP monograph requirements.

Technical Knowledge and Computer Systems Skills

• Understanding of laboratory equipment operation, qualification, and calibrations, including their software audit trial reviews. Examples include HPLC, UV Vis Spectrophotometer, GC, Potentiometer, pH meter, Stability chambers, etc.
• Strong knowledge on USP monograph requirements, FDA & ICH guidance requirements, etc.
• Effective interpersonal relationship skills and the ability to work in a team environment.
• Experience in Inhalation products (DPI) is a plus.
• Ability to work in a fast-paced, dynamic environment within a manufacturing operation setting.

Professional and Behavioral Competencies

• Proficiently speak English as a first or second language and ability to read, write, and communicate effectively in English.
• 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, Tuesday to Saturday, or some combination thereof based on business needs.
• 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 a 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.

Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)

About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.