Chemist I in Bedford

Location: Bedford, Ohio

Job Type: Full-time

About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.

Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Chemist I. In this role, you will be responsible for performing functions of the Chemistry Laboratory and conducting chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming components and raw materials to finished goods and stability. The duties also include equipment maintenance, housekeeping and LIMS management.

Key Responsibilities:

• Regular and predictable onsite attendance and punctuality.
• Conduct critical chemical and physical analyses on incoming components, raw materials, initial, in-process, final products and stability, and samples collected from water for injection systems at Hikma manufacturing facilities, along with customer compliant and retain samples.
• Work under minimal supervision.
• Use sophisticated laboratory instrumentation (HPLC, GC, FTIR, AA, UV/Vis, etc.) and computer systems to collect and record data.
• Perform advanced assays requiring precise analytical skills and understanding of chemistry principles.
• Complete all testing, including special project/protocol testing in a timely and appropriate manner.
• Enter and approve data in LIMS.
• Execute validation studies in support of manufacturing processes and R&D projects including cleaning and process validation.
• Maintain data integrity and ensure compliance with company SOPs and specifications, USP, Ph.Eur., FDA, GLP, 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 housekeeping, safety and documentation audits monthly and maintain laboratory cleanliness and laboratory glassware maintenance as needed.
• Perform equipment maintenance and calibrations as required.

Qualifications:

We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

• Minimum: Bachelor’s degree in Chemistry or Biological Sciences with Analytical Chemistry or Laboratory coursework and 0-2 years’ experience.
• Ability to handle multiple tasks concurrently, and in a timely fashion.
• Computer literate.
• Must be detail oriented, conscientious and have high reading comprehension skills.
• Basic understanding of laboratory instrumentation.
• Must be able to communicate effectively with supervisors and peers.
• Must be able to accommodate a flexible work schedule (weekends, shift, etc.) which may be required for business needs.

Preferred Qualifications:

• Experience with HPLC and GC.

Compensation:

Hourly Rate: $26.00 per hour. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.

What We Offer:

• 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.

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.