- Experience working in GMP environment (2+ years)
- Experience working in a lab environment
- Biotech Certificate (minimum)
- Manual Cell Culture experience
- 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
Manufacturing Associate - Cambridge, United States - Actalent
Description
Please See Below for a Great Opportunity to start your career with one of the top Scientific companies in the Cambridge, MA area This Opportunity allows for a lot of growth and ability to work with Cell Culture Manufacturing practices
Description:
Manufacturing of cell therapy products.
Position Summary:
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements.
Day to Day Responsibilities
• Master core responsibilities of a Manufacturing Tech, Senior.
• Effectively write and investigate deviations in TrackWise.
• Able to train in the role of an On the Job Trainer and become a Qualified Trainer.
• Able to make culture decisions based on cell observations.
• Perform transactions in ERP system.
• In addition to being fully qualified in MACI or Epicel, cross train and qualify in at least one core competency e.g. 3T3, Media Prep, GP, TrackWise, Preactor, TeamShare, QT.
• Other duties as assigned.
Preferred Qualifications:
• Experience in small scale tissue culture processing.
• Experience working within a regulated environment that is frequently audited by internal and external Agencies, such as the FDA and ISO.
Skills:
GMP, cell culture, manufacturing, Bio Cert*
Additional Skills & Qualifications:
Basic Qualifications:
• Biotechnology certificate with 2-4+ years of experience working in a cGMP environment in the biotechnology or pharmaceutical industry or 6+ years of cGMP experience with GED or equivalent.
• Bachelor's or higher degree (Life Sciences or related field) or equivalent with 1-2+ years of experience working in a cGMP environment in the biotechnology or pharmaceutical industry.
• Excellent communication skills, written and verbal.
• Experience with Microsoft Office suite.
Experience Level:
Intermediate Level
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:
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 for other accommodation options.
By applying, you consent to your information being transmitted by beBee to the Employer, as data controller, through the Employer's data processor SonicJobs.
See SonicJobs Terms & Conditions at and Privacy Policy at and SonicJobs Privacy Policy at and Terms of Use at