GMP Scientist II - (starting salary 58k)

　　SUMMARY

　　Responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working on collaboration with the Manager of GMP Operations and staff, provide hands on assistance for all day-to-day GMP production operations, including execution of production processes, documentation, as well as facility and equipment maintenance. Will support production efforts to deliver all products in a timely complaint, and fiscally responsible fashion by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for Manufacturing biological products.

　　70% setting up and running production

　　20% cleaning

　　10% documentation

　　SKILLS& QUALIFICATIONS

　　BS degree in a life science field, biochemistry, microbiology, or virology

　　GMP Experience (2-3 years) OR GLP Experience (3-4 years)

　　Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques and/ or fluid handling.

　　Experience with cells specifically with Mammalian or Eukaryotic.

　　This experience can be from school as long as it was hands on experience in labs

　　Understanding/exp. with cell culture, transfections, suspension cells, or adherent cells

　　Knowledge of GMP or bioprocessing

　　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.