Danaher Corporation Technician II (Formulation - GMP) - Weekend Overnights in Coralville, Iowa
IDT is the leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team.
IDT is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
During COVID-19 Shift Divisions this position would be assigned a Friday/Saturday/Sunday 7:00P-7:00A shift
The Technician II (Formulation - GMP) formulates custom oligonucleotides according to the customer’s specifications. This generally includes quantification, final packaging, and QC sampling of the products being made.
Job Specific Essential Functions:
Uses automated and manual lab equipment accurately; including limited maintenance and troubleshooting activities
Uses custom software packages to complete tasks and create final product
Utilizes stoichiometry to convert measurement units and creates custom solutions
Translates order requirements into a process to formulate oligos to the customer’s specifications
Quantifies and samples oligos for quality control tests
Assesses QC data accurately and makes pass/fail decisions for oligos
Maintains daily ship deadlines for all products
Maximizes automation for all processes
Incorporates new products and processes continuously
Adheres to safety regulations, lab SOPs, and contamination controls
Demonstrates behavior consistent with the Integrated DNA Technologies Core Values
Performs other duties as assigned
Position Specific Essential Functions:
Follows custom instructions outlined by Oligo Master Records or Manager Approved Process Flows
Keeps thorough records of specialized processes in the oligo process history
Organizes and handles customer owned materials as well as non-standard reagent formulations
Handles expensive oligos and reagents
Prepares standard and custom shipping paperwork and labels
Associate’s (2 year) degree or comparable combination of education and experience required.
Bachelor’s (4 year) degree preferred. Science related field (Biology, Chemistry, Etc.) preferred.
- Proficiency in a variety of PC software programs with strong working knowledge of Microsoft Office (and an emphasis on Excel) required
- Skill of accurately delivering proper volumes when hand pipetting required
Other Job Qualifications
Strong attention to detail
Uses aids and SOPs to make decisions about the proper production path per product
Ability to prioritize and organize workload to efficiently accomplish departmental goals
Ability to work in a team environment, remaining attentive to ideas, recognizing responsibilities, and actively participating with others to accomplish assignments and achieve desired goals.
Ability to manage time and works independently
Ability to communicate with peers and all levels of management
Ability to perform under stress when confronted with emergent, critical, unusual, or dangerous situations, or situation in which working speed and sustained attention are make-or-break aspects of the job.
Ability to perform a variety of duties, often changing from one task to another without loss of efficiency or composure.
Ability to maintain both a high standard of courtesy and cooperation in dealing with co-workers.
Ability to accept responsibility for the direction, control or planning of an activity.
Adaptability to situations requiring the precise attainment of set limits, tolerances or standards.
Ability to perform repetitive work or to perform continuously the same work, according to set procedures sequence or pace.
Exert 20-50 lbs. of force occasionally and/or 10-15 lbs. of force frequently
What We Offer:
Generous Paid Time Off Accruals
16 Hours PAID Volunteer Time Off
10 Paid Holidays
Up to eight (8) weeks of 100% paid parental leave to eligible U.S. associates
401(k) with Company Match
Medical, Dental, and Vision Insurance Options
Integrated DNA Technologies (IDT) conducts drug screens and background checks on applicants who accept employment offers.
When you join us, you’ll also be joining Danaher’s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.
If you’ve ever wondered what’s within you, there’s no better time to find out.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .
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