Hikma Pharmaceuticals · 1 week ago
QA Inspector, QA - 2nd Shift
Hikma Pharmaceuticals is committed to building a diverse and inclusive team and is seeking a talented and motivated QA Inspector for their 2nd shift. The QA Inspector will be responsible for monitoring in-process product quality, performing inspections and testing of components, and documenting results in accordance with cGMPs.
Health CareMedicalPharmaceutical
Responsibilities
Regular and predictable onsite attendance and punctuality
Performs in-coming tasks which include pallet checking, raw material sampling, review of test results, release of components, raw materials and production supplies
Contacts QA Coordinator or QA Supervisor for daily line assignments
Samples/Checks/Verifies Controlled Substances during in-coming monitoring and raw material sampling
Must pass frocking qualification for controlled areas and pass the respirator requirements for sampling raw materials
Samples using analytical instrumentation such as Analytical balances, glove boxes and compressed gases
Be able to push pallet(s) of raw material with the use of a pallet jack
Be able to lift 15-20 lbs
Maintains good housekeeping and safe working conditions
Accurately and clearly documents sampling/ inspection/test results in accordance to department and site SOPs
Performs other duties to support production or validation as determined by QA Supervisor
Participates in rotation for weekend coverage to support production. May work flexible hours and overtime on a short notice to support production
Qualification
Required
Associate's degree in science OR Bachelor's Degree with 0-2 years applicable laboratory, pharmaceutical manufacturing, or related experience
0-2-year applicable laboratory or pharmaceutical production experience (QA preferred)
Possesses proficient mathematical skills (addition, subtraction, multiplication, division, algebra, unit conversions, rounding significant figures, dividing polynomials, solving rational equations)
Familiar with cGMPs, EU, CFR and the USP
Demonstrates good attention to detail and accuracy
Good organizational skills and ability to multi-task and perform work in a timely manner
Demonstrates ability to work in a team environment with good communication skills and ability to communicate effectively with peers, department management and production personnel
Knowledge of computer systems at a level proficient to navigate input and/or reference computerized data
Must have sound judgment and demonstrate good analytical skills to assess risk to issues related to the manufacturing process
Must be able to pass the respirator requirements established for the Inspector position
Ability to stand/walk 85% of the shift to sample raw material and deliver to labs
Good manual dexterity to repetitively manipulate syringes to sample filled units for in-process monitoring
Good close visual acuity (eye exam required)
Noise levels on production lines may be moderate to high
Able to lift 15 lbs
Able to pull/push raw materials with use of a pallet jack
Preferred
Prior QA experience preferred
Company
Hikma Pharmaceuticals
Hikma focuses on a wide range of generic, branded generic and in licensed pharmaceutical products
H1B Sponsorship
Hikma Pharmaceuticals has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (16)
2024 (23)
2023 (22)
2022 (24)
2021 (28)
2020 (18)
Funding
Current Stage
Public CompanyTotal Funding
$250MKey Investors
International Finance Corporation
2025-07-15Post Ipo Debt· $250M
2005-11-04IPO
Recent News
2026-01-09
London Evening Standard
2025-12-16
2025-12-15
Company data provided by crunchbase