The Quality Control Chemist II:Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications.Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results.Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory.The Quality Control Chemist II reports into the Manager Quality Control or Team Leader Quality Control.RESPONSIBILITIES
Primary responsibilities of this role include the following:
Safety
Perform job functions in a safe manner consistent with site safe practices and regulatory (e.g. – OSHA) requirements
Participate in weekly/monthly safety training, identify potential safety hazards and cooperate with investigations of safety related incidents
Compliance
Conduct assigned tasks in compliance with cGXP requirements, current industry standards, compendia standards, FDA expectations and internal procedures
Assist with laboratory investigations to ensure they are conducted in a timely manner and are completed within established target completion dates
Maintain required level of training needed to perform a GMP task
Productivity
Perform routine sample analysis requiring general laboratory skills such as weighing, pipetting, titration, and basic operation of laboratory instrumentation
Comprehend and follow approved test methods accurately in the performance of sample analysis to ensure adherence to “Right-the First Time” philosophy
Perform analysis with a practical understanding of the test procedure and instrument operation
Use available software to control instrumentation, collect data, process and calculate results, and report results
Perform testing to evaluate physical characteristics of raw materials and finished products
Work under direction provided by supervisor
Calculate results and assess conformance with specifications
Notify manager immediately of nonconforming data or unexpected occurrences
Organize work schedule to complete assigned tasks efficiently and on schedule
Maintain accurate record of analysis and perform documentation to company standards
Prepare test solutions, reagents, and samples used in analysis
QUALIFICATIONS BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline1-3 years experience in a pharmaceutical QC laboratory environmentUnderstanding of cGXP requirements preferredOrganization, communication and interpersonal skillsPay and BenefitsThe pay range for this position is $65000.00 - $70000.00 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 TypeThis is a fully onsite position in Norwich,NY.Application DeadlineThis position will be accepting applications until Jan 31, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Full-time