Work for a well-regarded biotechnology company in Rensselaer, NY as a MSAT Specialist! This position is a one-year contract; with potential for extension or permanent hire. A great way to start your career!
What you need to know:
Starting Pay: $23 - $26/hour
Monday – Friday, 8 am – 4:30 pm
100% Onsite role
What you need to apply:
Nesco Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource, LLC) is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.
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What you need to know:
Starting Pay: $23 - $26/hour
Monday – Friday, 8 am – 4:30 pm
100% Onsite role
What you need to apply:
- Bachelor’s degree in a related field
- Related work or internship experience preferred!
- Strong Excel experience needed!
- Experience in a pharmaceutical/biologics cGMP environment or equivalent preferred
- Supporting the Drug Product Manufacturing Sciences and Technology (DP MSAT) departments through monitoring process performance, data trending, data analysis and/or laboratory testing.
- Providing support for the design and development of drug product processes and will be part of a team responsible for industrialization, troubleshooting and validation of drug product processes at manufacturing sites, both international and domestic.
- Performing verified data entry tasks into electronic systems in a timely and efficient manner.
- Tracking cycle time and metrics for data entry process.
- Supporting the implementation, expansion and continuous improvement of Regeneron's Application for Data Aggregation and reporting system.
- Managing quality system events pertaining to data integrity and data management such as investigations, CAPAs, Change Controls and general document approvals.
- Trending process performance to establish/improve process capability, uses data analytics and/or laboratory testing to develop metrics and ensures process is operating within intended process control strategy.
- Authoring policies, technical reports/protocols, change controls, etc. in support of cGMP activities.
- Supporting/leading efforts associated with the drug product Continued Process Verification (CPV), documentation and trending of In Process Control (IPC) initiative.
- Maintaining required training status on Regeneron specific work instructions and SOPs.
- Collaborating with cross-functional teams to define and execute drug product process development and technology transfer activities.
Nesco Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource, LLC) is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.