Inspector; QA Manufacturing - 3rd Shift (11:00PM - 7:30AM)

Contract Pharmacal Corp

Hauppauge (NY)

On-site

USD 28,000 - 36,000

Full time

3 hours ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Contract Pharmacal Corp. is seeking an Inspector, QA Manufacturing to ensure product quality across all manufacturing stages in accordance with current GMPs.

The role involves in-process monitoring, sample collection, and batch record review in a fast-paced production environment. The ideal candidate will have a High School diploma or GED and experience with GMP and good documentation practices, along with strong communication and organizational skills.

Qualifications

  • Must read, write, and communicate effectively.
  • Excellent organizational skills and attention to detail.
  • Able to work in a fast-paced manufacturing environment.

Responsibilities

  • Perform in-process monitoring of manufacturing operations.
  • Perform duties using good documentation practices.
  • Collect in-process and finished product samples as required.
  • Support collection of microbiological samples per procedure as required.
  • Review batch records and release for both Commercial and IP batch records.
  • Perform AQL sampling and inspections as required.
  • Identify and report any non-conformances to management.

Skills

Communication
Multitasking
Organizational skills

Education

High School diploma or GED

Job description

The Inspector, QA Manufacturing has the primary responsibility of ensuring product quality is maintained through all phases of manufacturing in accordance with current good manufacturing practices.

Description

Position Summary: The Inspector, QA Manufacturing has the primary responsibility of ensuring product quality is maintained through all phases of manufacturing in accordance with current good manufacturing practices.

Responsibilities
  • Perform in-process monitoring (e.g. weight, thickness, hardness, disintegration, friability, etc.) of all manufacturing operations
  • Perform duties using good documentation practices
  • Collect in-process and finished product samples as required
  • Support collection of microbiological samples per procedure as required
  • Perform room inspections/clearances as required
  • Perform Batch Record release of both Commercial and IP batch records
  • Perform AQL sampling and inspections as required
  • Identify and report any non-conformances/discrepancies to management if applicable
  • Review general SOPs are being met by production
  • Assist in employee training (initial and ongoing)
  • Support environmental monitoring activities (i.e. water sampling air sampling)
  • Provide additional QA technical support to Coating Department
  • Review batch record documentation
  • QMS form issuance as required to production
  • Daily scale weight verification
  • Maintain QA supplies
  • Review and approve weekly pest control logs
  • Sample transmittal to QC and Account Services
  • Review grounds logbook for Maintenance
  • Monthly audit of facility fire extinguishers
  • Other responsibilities as assigned by Senior Management
Requirements

Education and Experience

  • High School or GED diploma required
  • Knowledge of good manufacturing practices and good documentation practices preferred.
Skills, Knowledge And Abilities
  • Ability to read, write, and communicate effectively.
  • Self-motivated with the ability to work in fast-paced environment and handle multiple tasks simultaneously.
  • Excellent organizational skills with ability to focus on details.
Physical Demands
  • Required to reach with arms and use hands and fingers to handle or feel objects and tools
  • Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs and ladders
  • Must be able to lift and/or move up to 50 pounds
Work Environment
  • Work environment in production operations facilities include close proximity to heavy machinery with loud noises and pharmaceutical powders (dust).
  • Potential to move between production operations sites/areas to complete job functions.
  • Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion.
  • Work location are subject to change as needed to meet business requirements.
Supervisory Responsibilities
  • None
Personal Protective Equipment Or Attire Required For Position
  • Gowning as required by GMPs and/or SOPs
  • PPE as needed
Pay Range

$23.00 per hour

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Inspector; QA Manufacturing - 3rd Shift (11:00PM - 7:30AM)
Inspector; QA Manufacturing - 3rd Shift (11:00PM - 7:30AM)

Contract Pharmacal Corp. • Hauppauge (NY)

Hybrid
USD 28,000 - 36,000
QA Inspector Level I (3rd Shift)
QA Inspector Level I (3rd Shift)

Sharp Packaging Solutions, part of UDG Healthcare plc • Conshohocken

On-site
USD 45,000 - 60,000
QA Inspector Level I (3rd Shift)
QA Inspector Level I (3rd Shift)

Sharp Services • Conshohocken

On-site
USD 50,000 - 65,000
Quality Assurance Inspector
Quality Assurance Inspector

Pioneer Data • Carlisle

On-site
USD 40,000 - 60,000
Manufacturing Quality Inspector I
Manufacturing Quality Inspector I

ICU Medical • Austin (TX)

On-site
USD 30,000 - 44,000
QA Inspector I - 3rd Shift
QA Inspector I - 3rd Shift

Creative Solutions Services, LLC • Fall River (MA)

On-site
USD 52,000 - 66,000
QA Inspector II - 2nd Shift
QA Inspector II - 2nd Shift

Creative Solutions Services, LLC • Fall River (MA)

On-site
USD 65,000 - 93,000
QA Inspector (3pm-11:30pm)
QA Inspector (3pm-11:30pm)

American Regent, Inc. • Town of Brookhaven (NY)

On-site
USD <1,000
QA Inspector Level I (3rd Shift)
QA Inspector Level I (3rd Shift)

Sharp Clinical Services • Conshohocken

On-site
USD 42,000 - 54,000
Quality Assurance Inspector I
Quality Assurance Inspector I

PSG Global Solutions • Collegeville (PA)

On-site
USD 45,000 - 60,000