Job DescriptionA global bio-pharmaceutical manufacturer is seeking a QC Scientist to join their Microbiology Quality Project Team. Individuals on this team will be performing testing and remediation activities for pharmaceutical products, APIs, and excipients. Test methods will include bioburden, endotoxin, and microbial enumeration. The Scientist will also be responsible for providing feedback on test methods, validation protocols, and procedures to management, and work in tandem with other associated departments aligned to the project.Responsibilities
Perform testing and remediation activities for pharmaceutical products, APIs, and excipients.
Conduct bioburden, endotoxin, and microbial enumeration tests.
Provide feedback on test methods, validation protocols, and procedures to management.
Collaborate with other associated departments aligned to the project.
Essential Skills
Experience with endotoxin testing (gel clot and kinetic on product) required
Minimum 2+ years of experience in a regulated pharmaceutical GMP lab.
Experience with method validation of endotoxin methods.
Bachelor's degree in biology, microbiology, or a life science field.
Additional Skills & Qualifications
Knowledge of GMP and SOP.
Experience in microbiology laboratory environments.
Familiarity with bioburden testing, BET, LAL, and bacteria testing.
Work EnvironmentThe role is primarily in a microbiology lab environment, with most time spent on the bench. The lab is located in a large sterile injectable manufacturing facility. Some time will also be spent in an office setting on a computerPay and BenefitsThe pay range for this position is $30.00 - $38.00/hr.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 TypeThis is a fully onsite position in Greenville,NC.Application DeadlineThis position is anticipated to close on Feb 7, 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 [email protected] (%[email protected]) for other accommodation options.