Manufacturing Supervisor

Company & Job Information

In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. We articulated our 2022 winning aspiration to double the number of patients we serve and hence, double the impact we create as a global pharmaceutical company.

Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division. We at Cipla are inspired by our purpose of 'Caring for Life' and strive to extend this philosophy to our associates and their families. We are looking for talented individuals to grow their careers while growing our business.

Job Purpose

The purpose of this role is to assist in managing manufacturing operators and functions at our manufacturing site, InvaGen.

Job Responsibilities

Plan, organize and oversee all activities related to the manufacturing of tablets and capsules to include delivery, in-process, and finished product samples in a defined schedule.

Provide daily supervision and support to the operators in regarding day-to-day production activities such as trouble shooting and other work tasks.

Manage performance and train assigned employees using Company systems, procedures, policies, practices, and other tools to meet established performance standards, productivity targets, and overall business requirements.

Review and compile the documents generated during production like batch manufacturing records and validation protocols. Initiate and review written procedures such as standard operating procedures (SOPs), operating instructions, cleaning procedures, safety procedures, and other work procedures as needed.

Ensure compliance with safety, quality, productivity, and established job performance standards. Effective implementation of current good manufacturing practices (cGMP) and safety practices.

Coordinate with departments such as Quality Assurance (QA), Quality Control (QC), Research & Development (R&D), Maintenance & Engineering, Supply Chain and Warehousing, Human Resources, and other internal functional partners to ensure the completion of work and achieving production targets and objectives.

Work with Integrated Product Development (IPD)/R&D on the execution of bio-batches (abbreviated new drug applications - ANDA) and validation batches.

Perform any other work or job assignments as allocated and required by management.

Job Requirements & Preferred Skills

Minimum High School Diploma or GED / foreign equivalent is required.

Bachelor’s degree in Pharmaceutical Engineering or related field of study from an accredited college/university preferred. Minimum three (3) years direct work experience in pharmaceutical manufacturing as an Operator or Supervisor preferred. Understanding of granulation, compression, coating, and encapsulation machines.

Capable of conducting troubleshooting, investigations and root cause identification and analysis. Capable of handling and participating in compliance and regulatory audits at the local and federal levels. Must be proficient in computer skills and software applications such as Microsoft Office tools.

Experience using SAP business system and applications is a plus. Knowledge of statistical packages is a plus.

Able to effectively lead and manage teams of diverse cultures and backgrounds. Able to prioritize, plan and work under tight schedules and deadlines.

Must possess strong documentation and writing skills, and able to apply relevant scientific principles and practices.

Must communicate effectively across all levels, both orally and written with a proficient command of the English language. Preference for bi-lingual Spanish language proficiency (translation and interpretation).

Must be able to work under general supervision and able to work independently and in a team environment. Must be able to exercise appropriate decision-making and professional judgment on matters of significance.

Physical Requirements

Must be willing and able to work any assigned shift and manufacturing unit (Central Islip and Hauppauge) as required. Must be willing to start work early or stay late past scheduled work hours based on business needs, if required.

Must be willing to work weekends based on business need and as required by management.

Ability to wear appropriate PPE is required.

Individual may be required to wear respiratory devices that include but are not limited to: Air Purifying Respirators (APR) which include half-face and full-face negative pressure respirators, hooded powered air purifying respirators, or Supplied Air Respirators (SAR), which include hooded or full face supplied air respirators.

Location

Hauppauge, NY

Job Category

Full-time

Cipla’s Commitment to Equal Employment Opportunity

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.