Apply on
Original
Simplified
Manufacturing Scientist I (Urgently Hiring)
Job Description
As a GMP Scientist I, you will be responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Your role will involve hands-on assistance for all day-to-day GMP production operations, including execution of production processes, documentation, and maintenance of facility and equipment.
You will work closely with the Manager of GMP Operations and staff to deliver all products in a timely, compliant, and fiscally responsible manner. Your work will involve heavy solution preparation, assay management, and biology tissue culture-based work. You will also assist in process documentation review, revision, remediation, and process change controls. Your contribution will be crucial in cultivating and enacting the strategic direction of the GMP area, including determining schedule and project timelines. Additionally, maintaining materials inventory control to meet production goals will also be part of your responsibilities.
Required Skills:
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:
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] for other accommodation options.
Job Description
As a GMP Scientist I, you will be responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Your role will involve hands-on assistance for all day-to-day GMP production operations, including execution of production processes, documentation, and maintenance of facility and equipment.
You will work closely with the Manager of GMP Operations and staff to deliver all products in a timely, compliant, and fiscally responsible manner. Your work will involve heavy solution preparation, assay management, and biology tissue culture-based work. You will also assist in process documentation review, revision, remediation, and process change controls. Your contribution will be crucial in cultivating and enacting the strategic direction of the GMP area, including determining schedule and project timelines. Additionally, maintaining materials inventory control to meet production goals will also be part of your responsibilities.
Required Skills:
- BS degree in a life science field, biochemistry, microbiology, or virology
- Minimum 1+ years of experience in the scientific industry from a GMP or GLP setting
- Knowledge of GMP or bioprocessing
- Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques and/ or fluid handling.
- Experience with cells specifically with Mammalian or eukaryotic (experience can be from school as long as it was hands on experience in labs).
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
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] for other accommodation options.
Similar Jobs