QA Inspector II - DPI
Company: Cipla USA
Location: Hauppauge
Posted on: May 21, 2025
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Job Description:
Job TitleQA Inspector IIOrganization NameInvaGen Pharmaceuticals, Inc.Location7 Oser Ave, Hauppauge, NY 11788Employment Type(Hourly/ Full Time)Full Time a" Hourly/Non-ExemptSalary Range(Base/ Hourly)$20 - $29 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 a" medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) a" 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 benefitsShift2nd Shift a" 3:00 PM a" 11:00 PMResponsibilities/ AccountabilitiesThe QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing or packaging in compliance with established specifications.
Perform in-process testing (e.g.,
weight, thickness, hardness, disintegration, friability, etc.) as
per manufacturing batch record instructions.Perform room and
equipment checks (where applicable) prior to each stage of
manufacturing process as guided through written procedures.Perform
AQL, Blend sampling, In-process Sampling, and inspections as
required.Prepare in-process and finished product samples (where
applicable) for QC lab, following detailed documentation procedures
and delivering them to QC lab.Maintenance of standard weights and
perform daily verification of balances which includes physically
carrying ability of 100 kg (25 Kg x 4 Noas) weights for multiple
balances.Ensure the proper isolation of rejected material generated
during batch process and accountability in the batch record.Monitor
facility and product environmental operating conditions.Review of
engineering records (temperature and humidity data calibration and
PM records, Pest control records and contractor related
functions).Review of online batch records in terms of completeness
of signatures, entries, and actual reconciliation / yields prior to
initiation of next processing step.Verification of functionality of
all the equipment and associated controls during the batch
run.Perform applicable testing and prepare reports for customer
complaints.Identify and report any non-conformances/discrepancies
to management if applicable.Other duties that management may assign
from time to time.Education Qualifications
Must have a minimum of a High School
Diploma or equivalent education credential (ex. GED)
required.Proficiently speak English as a first or second
languageProficiently communicate and understand (read and write)
scientific work in English.Have excellent organization, learning
and teaching skills required to work in teams.Working knowledge of
Microsoft Office programs and other scientific based
softwareExperience
Must have a minimum of three (3)
years of pharmaceutical QA experience. Skills/ Competencies
Knowledge of good manufacturing
practices and good documentation practices preferred.Ability to
read, write and communicate effectively.Self-motivated, with the
ability to work in fast-paced manufacturing environment and handle
multiple tasks simultaneously.Excellent organization skills with
strong attention to details skills.Strong fundamental mathematical
skills and knowledgePhysical Requirements
Work standing or walking unassisted
for 75% or greater of an 8-hour period.Unassisted lifting up-to 35
lbs., may be required.Able to wear appropriate personal protective
equipment at all times, when required.Other InformationThis role
works in a cGMP laboratory or manufacturing environment, where
personal protective equipment is required, which may include
uniforms, lab coats, safety glasses, respiratory protective
equipment, hearing protection, etc. Work with or around solvents,
powders, or other materials commonly found in a pharmaceutical
laboratory or manufacturing facility is required.The role may be
assigned on a work-shift basis, where required (Day, Evening,
Night). Weekend or Holiday work may be requested or required.No
remote work available & no relocation About CiplaCipla 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 Indiaas 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 aCaring for Lifea, Ciplaas 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 Ciplaas respiratory business in the United
States. Equal Opportunity EmployerRace, 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.
Keywords: Cipla USA, East Hartford , QA Inspector II - DPI, Other , Hauppauge, Connecticut
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