Job Title: Lab TechnicianJob DescriptionAs a Lab Technician, you will spend 75% of your time receiving and inspecting dried plasma and QC samples, performing document control, and maintaining records as required by GMP standards. You will conduct visual inspections of freeze-dried plasma, work within the BECS system, perform titer testing, and engage in hands-on pipetting, dilution, and reagent testing. This role involves repetitive tasks with some variety.Responsibilities
Perform inspection of raw materials and plasma isoagglutination tests.
Maintain laboratory reagent inventory and support laboratory scientists.
Conduct raw material inspections for blood products per established procedures for fresh frozen plasma, sterile water for injection, carbon dioxide, manufacturing labels, and more.
Perform isoagglutination tests for Type-A plasma titer screening according to established procedures.
Accurately record results on data forms, document the use of test reagents, equipment use/maintenance records, and laboratory environmental conditions.
Maintain good record-keeping practices as required by GMP.
Recognize problems or unusual results from inspection testing and results.
Track reagents and consumables for the Blood Products QC laboratory to ensure supplies are readily available.
Assist laboratory scientists in maintaining laboratory equipment per established procedures.
Perform other duties as assigned under the supervision of laboratory management.
Essential Skills
Associate degree or higher in a relevant field such as biochemistry or biology.
Experience with pipetting, dilution, and reagent preparation (can be from school).
Basic knowledge of safety in chemical, biological, or clinical laboratory settings.
Strong attention to detail and protocol.
Experience with Microsoft software – Outlook, Excel, Word.
Qualifications
Can be new sciences graduate or have 6 months of industry experience working in an FDA regulated environment.
GMP QC laboratory experience for the pharmaceutical, biotechnology, or medical devices industry is highly preferred.
Work EnvironmentThis position is onsite, involving 75% laboratory work and 25% desk work to complete basic paperwork. You will work alongside three other lab technicians and two clinical lab scientists. The individual in this role will gain experience working in a GMP lab, with opportunities to work alongside senior -level scientists and gain experience with GMP documentation. This is a 10-month contract with the possibility of converting to a full-time employee or extending the contract, depending on FDA approval in 2026. This role offers the chance to work with a new product for the military that will save lives on the battlefield. 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.