QA Inspector II - DPI

Merck & Co.; Hauppauge (NY); On-site; USD 33,062 - 42,705; Full time

Benefits offered by this job

401(k) savings plan

Health insurance

Paid time off (PTO)

Job summary

Merck & Co. is seeking a DPI QA Inspector II to ensure the quality standards during the manufacturing process in Hauppauge, NY. This full-time role includes responsibilities such as verifying raw materials, performing in-process checks, and conducting IPQA testing.

The ideal candidate will be a Science Graduate with 1-2 years of pharmaceutical experience. The position offers competitive hourly pay between $24 and $31 along with a comprehensive benefits package.

Qualifications

• A minimum of 1-2 years of pharmaceutical experience (DPI, MDI or Injectables) preferred.
• Preference will be given to candidates with experience in generic pharmaceutical manufacturing.

Responsibilities

• Verify raw materials during the dispensing process.
• Perform in-process checks during batch manufacturing and packaging.
• Collect in-process blend, finished product, validation samples for analysis.
• Maintain and clean sampling rods used for blend uniformity sampling.
• Perform IPQA testing on the manufacturing floor.

Skills

Knowledge of Good Manufacturing Practices

Ability to read, write and communicate effectively

Basic computer skills (Microsoft Word, Power and Excel)

Strong attention to detail

Strong fundamental mathematical skills

Education

Minimum Science Graduate

Job description

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.

Job Title

DPI QA Inspector II

Organization Name

InvaGen Pharmaceuticals, Inc.

Location

Unit 1 - 7 Oser Avenue, Hauppauge, NY 11788

Employment Type

Full Time

Shift

Third Shift: 11:00 PM - 7:30 AM (May vary based on business needs)

Salary Range (Base/salary)

$24/hr - $31/hr

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, employee discounts, and other benefits.

Responsibilities / Accountabilities

• Verification of raw materials during the dispensing process.
• Dispensing printed packaging materials to packaging.
• Perform in‑process checks during batch manufacturing and packaging, as per manufacturing & batch packaging record instructions.
• Collection of in‑process blend, finished product, validation samples for analysis, sample collection as per protocols. Specifically, to perform blend uniformity (BU) sampling.
• To clean and maintain the samplings rods/dies/sample boxes used for BU sampling.
• Perform IPQA testing on the manufacturing floor specifically LOD, Bulk Density, Tapped Density, Leak Test, Weight Variation test.
• Ensure cleaning of manufacturing and packaging equipment, area and provide line clearance.
• To perform posting of dispensed materials and samples into SAP system (ERP system) and to perform other transactions in SAP.
• Involve in investigation of Deviation, OOS, OOT, or any other non‑conformances.
• Ensure completion of individual training assigned and follow company policies, safety requirements, cGMP and SOP's.
• Review of online batch records, area/equipment logbooks, calibration/PMP records etc.
• Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record.
• Review of engineering records (temperature and humidity data, calibration reports and PMP records).
• To take daily Quality rounds at shop floor to ensure shop floor is maintained in state of compliance and per GMP requirement.
• Report, elevate to Manager quality assurance about daily shop floor activities and any discrepancy during batch manufacturing and packing.
• Other duties [additional support] that management may assign from time to time.

Education Qualifications / Experience

• Minimum Science Graduate
• A minimum of 1‑2 years of pharmaceutical experience (DPI, MDI or Injectables) preferred.
• Preference will be given to candidates with experience in generic pharmaceutical manufacturing.

Skills / Competencies

• Knowledge of Good Manufacturing Practices and 21 CFR Part 820.
• Ability to read, write and communicate effectively.
• Basic computer skills (Microsoft Word, Power and Excel).
• 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 knowledge.

Physical 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 Information

This 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. Remote work and relocation are not supported in this position.

Equal Opportunity Employer

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.