Sr. Quality Assurance Specialist

Posted 5 Days Ago
Be an Early Applicant
Boulder, CO
72K-90K Annually
3-5 Years Experience
Biotech
The Role
The Sr. Quality Assurance Specialist will maintain records for document handling and quality systems, prepare quality performance reports, assist in training development, and participate in audits. This role involves collaboration with manufacturing and support staff, ensuring adherence to defined protocols, while contributing to quality system functions.
Summary Generated by Built In

Integrated DNA Technologies (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 one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

This position is part of the Quality Assurance Team located in Boulder, Colorado and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things!

In this role, you will have the opportunity to:

  • Maintains records and processes for document handling, audit, process controls (NCR/Deviation/CAPA) and training – may participate in several aspects.
  • Interacts professionally and efficiently with manufacturing and support staff: administer/support the intra-department functionality of the QMS with departments throughout IDT. 
  • Prepares reports of quality system performance for internal departmental use, as well as management review. 
  • Assists in developing content for and delivering training on various quality systems functions such as NCR’s, deviations, document control, training system administration, and validation activities.
  • Participates in customer and third-party audits, serves as a member of internal audit teams, assists with the development and implementation of responses for customer, regulatory and certifying body audits.

The essential requirements of the job include:

  • Bachelor’s degree in life sciences (biology, chemistry, biochemistry, etc.) or related field or Advanced degree (Master's or PhD) in life science
  • 3+ years of experience in a manufacturing environment, especially life science or biotechnology industries
  • 3+ years of experience in a manufacturing operations, quality control, or quality assurance role
  • Demonstrated technical ability and accuracy to perform mathematical calculations and unit conversions
  • Experience working in a regulated environment, especially ISO 9001, ISO 13485

It would be a plus if you also possess previous experience in:

  • Familiarity with SAP, MasterControl, and Maintenance Connection
  • Experience working in a regulated laboratory environment in the biotech industry or academic environment
  • Quality Assurance experience in the manufacturing industry, especially biotechnology and next-generation sequencing (NGS)

The salary range for this role is $72,000 - $90,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

#LI-LCS

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at [email protected] to request accommodation.

The Company
HQ: Coralville, IA
1,749 Employees
On-site Workplace
Year Founded: 1987

What We Do

For over 35 years, IDT has been enabling genomics laboratories with an oligonucleotide manufacturing process unlike anyone else in the industry, with the most advanced synthesis, modification, purification, and quality control capabilities available.

Through our founder's dedication to innovation, the highest standards of quality, and deep genomics expertise, IDT has evolved from a leading oligo manufacturer to a genomics solutions provider supporting areas such as NGS, CRISPR, SynBio, and PCR. With these core efforts, IDT teams have been helping to drive science forward with increased quality, efficiencies, and unmatched customer service.

Today, technology is evolving faster than ever before. Scientists leading the transition from basic to translational research face new challenges with securing the custom solutions necessary to advance their research out of the lab and into the clinic. These emerging barriers have slowed down critical discoveries with potentially profound impacts on human and ecological health.

To help overcome these obstacles and push the boundaries of technology, we've expanded production facilities and capabilities to include GMP and cGMP manufacturing grades. These additions provide customers with a genomics solutions partner capable of supporting the entire research journey. Combined with a renewed collaborative agility, members of our organization and strategic partners are positioned to contribute to the greatest genomic breakthroughs of our time—guiding more effective vaccines, addressing world hunger and climate change, and driving new diagnostics and therapeutics for complex diseases. 

As we look to the future, our mission—accelerating the pace of genomics—honors our legacy and represents our commitment to the pursuit of new ideas to help us realize our shared vision of enabling researchers to rapidly move from the lab to life-changing advances. 

For more information, visit www.idtdna.com.

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