About the role

QA Inspector responsible for monitoring in-process product quality for pharmaceutical manufacturing. Ensuring compliance and executing quality assurance processes in a fast-paced production environment.

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
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.

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)
Able to lift 15 lbs.
Able to pull/push raw materials with use of a pallet jack.

Annual performance bonus, commission, and share potential
Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay
Hikma will match 100% of the first 6% of eligible pay that you contribute
A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date)
Additional days granted upon reaching work milestone anniversaries
3 personal days (prorated based on hire date)
11 company paid holidays
Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
Employee discount program
Wellbeing rewards program
Safety and Quality is a top organizational priority
Career advancement and growth opportunities
Tuition reimbursement
Paid maternity and parental leave