DPI Manufacturing Supervisor

Job Title

DPI Manufacturing Supervisor

Organization Name

InvaGen Pharmaceuticals, Inc.

Location

Hauppauge, NY location

Employment Type

Full Time

Salary Range

(Base/salary)

$ 70k - $ 80k

Benefits

In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits.

Work Hours/ Shift/ Remote

Must be willing and able to work any assigned shift ranging from first, second, or third shift. Work schedule may be Monday to Friday, Tuesday to Saturday, or some combination thereof based on business needs.

Responsibilities/ Accountabilities

• 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.

• Review and compile the documents generated during the production of tablets and capsules such as batch manufacturing records and validation protocols.

• Ensure and compliance with safety, quality, productivity, and performance expectations and execution of manufacturing operations.

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

• 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 with respective to the completion of quality work and achieving the production schedules and performance objectives.

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

• Effective implementation of current good manufacturing practices (cGMP) and safety practices in the operations and manufacturing of products.

• Initiate and review written procedures such as standard operating procedures (SOPs), operating instructions, cleaning procedures, safety procedures, and other work procedures as needed.

• 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.

• Participate in safety related programs and or safety teams as needed.

• Enforce and follow safety regulations and ensure the working area is clean.

• Adhere to CIPLA's Safety, Health, and Environmental policies.

• Must be able to work under general supervision and able to work independently and in a team environment.

• Must be able to exercise appropriate professional judgment on matters of significance.

• Must be willing to work in a pharmaceutical manufacturing setting.

• Other duties assigned as required by Manufacturing Management.

Education Qualifications

• Master's or Bachelor's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university required.

Experience

• One (1) to three (3) years of direct work experience in pharmaceutical manufacturing. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.

Skills/ Competencies

• 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 technical writing skills and be able to apply relevant scientific principles and practices.

• Must communicate clearly and concisely across levels, both orally and in written.

• Strong command over written and verbal English is required.

• Preference for bi-lingual Spanish language proficiency (reading, writing, and speaking).

About Cipla

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. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. 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. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.

InvaGen Pharmaceuticals, Inc.

InvaGen Pharmaceuticals is a Cipla subsidiary 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. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States.

Equal Opportunity Employer

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter.

About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.