Job Posting for Quality Assurance Analyst II at Hikma Pharmaceuticals
OVERVIEW:
Conduct biochemical, chemical and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming raw materials to finished goods, and stability programs.
RESPONSIBILITES:
Conduct critical biochemical, chemical and physical analyses on raw materials, initial, in-process, final products, and stability programs. Work under minimum supervision.
Serve as Mentor to Quality Laboratory Associate (QLA) I positions. Provide training and work direction for QLA I positions as required.
Perform review of test data, which includes overall documentation practices. Perform release functions in LIMS or other computerized systems.
Use sophisticated laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biochemical and chemistry principles. Perform calibrations and maintenance as required.
Perform advanced biochemical and chemical assays requiring precise analytical skills and understanding of biochemical and chemistry principles.
Complete all testing, including special project / protocol testing in a timely and appropriate manner.
Maintain data integrity and ensure compliance with company SOPs and specifications, USP/Ph Eur, FDA, GDP and cGMP regulations.
Investigate deviations and write exception documents.
Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
Perform laboratory and manufacturing audits as required (cGMP, safety, housekeeping, etc.). Make necessary corrections as needed.
Responsible for maintaining laboratory housekeeping, cleanliness of laboratory equipment and work benches, and other general lab responsibilities as assigned by supervisor.
QUALIFICATIONS:
Proficient in wet and instrumental methods of analyses. Advanced laboratory skills, basic knowledge of statistical method. Strong technical problem solving skills. Ability to handle multiple tasks concurrently, and in a timely fashion. Computer literate. Must be able to communicate effectively with supervisors and peers. Must demonstrate effectiveness in ability to train others, empowerment, leadership, results orientation and task completion. Must be able to consistently demonstrate self-motivation and the ability to think independently. Maybe required to work flexible hours and overtime on short notice.
Education and/or Experience:
Bachelors Degree in Chemistry, or Biological Sciences with Analytical Chemistry or Laboratory coursework, with 2-5 years experience, or Masters Degree in Chemistry, or Biological Sciences, with 0-3 year’s experience.
What We Offer
Clean climate-controlled working environment
Annual performance bonus potential
401k employer match up to 6% of your contributions
23 vacation/personal days
11 paid Company holidays
Generous healthcare benefits
Employee discount program
Wellbeing rewards programs
Safety and Quality is a top organizational priority
Career advancement/growth opportunities
Tuition Reimbursement
Maternity and Parental Leave
*Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to a specific plan or program terms.
Job Type: Full-time
Pay: $75,000.00 per year
Schedule:
8 hour shift
Day shift
Ability to Relocate:
Cherry Hill, NJ 08003: Relocate before starting work (Required)
Work Location: In person
Salary.com Estimation for Quality Assurance Analyst II in Cherry Hill, NJ
$70,405 to $90,973
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