Job Title: QC Chemist
Job Description

Responsible for performing day-to-day activities in the laboratory under prescribed procedures, including qualitative and quantitative analysis, solution preparation, calibration, qualification, and maintenance of laboratory instrumentation. Conducts environmental monitoring, assists with technical writing, and performs administrative tasks. Monitors study procedures to ensure data accuracy and report quality. Maintains a GMP/GLP Laboratory and evaluates the chemical and physical properties of various organic and inorganic substances.

ResponsibilitiesConduct analysis in compliance with cGMP requirements, compendia standards, and internal procedures.Maintain accurate records of analysis and perform documentation to company standards.Prepare test solutions, volumetric solutions, and samples used in analysis.Perform assigned sampling, physical, chemical tests, and assays on raw materials, active pharmaceutical ingredients, in-process, finished bulk, finished product, and stability products in an FDA-regulated lab environment.Use a variety of analytical instruments such as HPLC, GC, Dissolution, Malvern particle size analyzer, IR, Auto Titrator, UV Spectrophotometer, KF, Potentiometer, etc.Perform analysis with a practical understanding of the test procedure and instrument operation.Conduct laboratory investigations under the supervision of the laboratory manager.Perform maintenance and calibrations of laboratory instruments and equipment.Comply with all regulatory and in-house requirements, including safety, housekeeping, laboratory chemical waste, cGMP, cGLP, and documentation.Maintain required levels of training needed to perform GMP tasks.Prepare and/or review test procedures, SOPs, and protocols as assigned.Essential SkillsCurrent Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.Experience with dissolution, FT-IR, GC, UV-VIS, KF, TLC, and other analytical techniques.Proficiency in computer applications and programs related to laboratory applications such as HPLC, FTIR, TOC.Knowledge of sampling methods and quality control systems.Mathematics, including statistics.Sample preparation techniques.Spectroscopic techniques and chromatographic systems.Basic computer knowledge including MS Word, Excel, and Outlook.3-5 years of routine testing using HPL and Dissolution.Solid oral dosage with a focus on raw material and finished product.Experience with GC, FTIR, KF, UV VIS, and Pharma GMP.Additional Skills & QualificationsBachelor's or Master's degree in Pharmaceutical, Biological, Chemical Science, or related field.5-6 years of related laboratory work experience, with a minimum of 5 years as a QC Chemist in a GMP environment.Ability to work successfully in both a team/matrix environment and independently.Ability to work in a fast-paced environment, manage priorities, and maintain timelines for multiple projects.Ability to work safely in a chemical laboratory.Ability to perform basic calculations, read, write, communicate, and handle stress produced by time pressure and customer demands.Must be able to access all laboratory, manufacturing, and office areas.Must be able to wear required PPE for entering laboratory and processing areas.Specific vision requirements include reading written documents and using a computer.Must be able to sit or stand for prolonged periods and occasionally lift up to 25 lbs. with or without assistance.Work Environment

Laboratory setting with approximately 10 people. The role involves working with various analytical instruments and adhering to safety, regulatory, and laboratory standards. Requires wearing appropriate PPE and may involve prolonged periods of sitting or standing and occasional lifting.

Pay and Benefits

The pay range for this position is $30.00 - $40.00

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 specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Cranbury,NJ.

Application Deadline

This position will be accepting applications until Jan 24, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.