Biomanufacturing Operator 1

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Job description

**Biomanufacturing Operator I**

Direct Hire

$1000-$1500 sign on bonus

Relocation experience

Full Benefits (Medical, Dental, Eye and 401K)

**Position Summary**

The Biomanufacturing Operator will work daily within Company's labs performing tasks associated with Company's GMP services. The Biomanufacturing Operator is expected to become familiar with all Company products and to be able to perform most tasks associated with the purification of plasmid DNA.

**Essential Functions**

+ Segregation, line clearance and cleaning of GMP production areas

+ Plan and submit inventory requisitions

+ Plan and preparation of production events and process plan memos

+ Coordinate production events with buffer preparation operators?

+ Execute GMP?dispensing?projects: filtration, formulation, environmental monitoring, manual and semi-automated dispensing, and media fill and gowning qualification events; all special considerations associated

+ May include cross training on any of the items listed below

+ Upstream tasks include transformation, subculture, cell banking,?shake?flask growth and harvest, wave growth and harvest, fermentation, media fill events, final formulation, filtration and dispersion

+ Downstream tasks include project setup, lysis, anion exchange chromatography, and hydrophobic interaction chromatography (void and enrichment), thiophilic absorption chromatography,?defiltration,?small scale?processing and linearization

+ Completion of all documentation associated with GMP projects

+ Coordination and sample submission with Quality Control?

+ Equipment calibration and preventative maintenance

+ Assist in writing manufacturing summary reports after project completion

+ Maintain personnel training record

+ Assist with assembly and segregation of all consumables and equipment resources for GMP production runs

+ Participate and support in Company's internal audit program and provide requested information and respond to findings presented in the audit report

+ Communicate the status of operations, process issues, safety and maintenance issues to appropriate area of management

+ Follow Aldevron SOP's and adhere to regulatory expectations

+ Completion and maintenance of GMP Bill of Materials for GMP projects

+ Perform other duties as assigned

+ All employees are responsible for the general upkeep of work and shared spaces

+ Punctual and regular attendance is required of all employees

**Qualifications and Education**

BS in life science (biology, chemistry, biotechnology or related field)

New Graduates please apply

**Why Kelly** **®** **?**

Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

**About Kelly** **®**

At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. ()