What are the responsibilities and job description for the Quality Control Analyst position at Watchmaker Genomics?
Position: Quality Control (QC) Analyst; Molecular Biology/Biochemistry
Position Type: Full-Time Employee
Location: Boulder, CO
Experience: 3 years laboratory experience (required) and 2 years Quality Control/Manufacturing/Quality Assurance experience (preferred)
Watchmaker Genomics is inviting applications for the full-time position of Quality Control Analyst.
The ideal candidate is an adept problem solver and a creative self-starter with excellent organizational skills. This position provides great opportunities for growth for candidates with a strong background in molecular biology and biochemistry. There are a variety of assays the QC Analyst will use to support the characterization of enzymes and reagents across our product portfolio. In addition to executing core QC processes, the individual will be increasingly responsible for the development and validation of new assays and implementation of new internal processes. This position reports to the QC Manager and will interface closely with many aspects of quality control, manufacturing, logistics, and research and development.
The successful candidate will thrive in a dynamic, fast-paced working environment and contribute directly to our company culture and success. The position provides an opportunity to gain valuable experience spanning many business facets to complement a strong technical background.
Responsibilities
Experience in biotech and a start-up environment are highly desirable. The following skills and experience are requirements for the position:
The base compensation for the Quality Control (QC) Analyst role starts at $50,000 - $60,000 bonus equity; actual pay will be adjusted based on skills and experience. Employees are eligible for Flexible Time Off, Holidays, employer covers 75% of base medical plan with buy-up options, employer paid dental, employer paid vision, employer paid $25,000 life/AD&D policy, paid parental leave, and a 401(k) retirement plan.
Application Requirements
To apply for the position, please submit the following in a PDF format on watchmakergenomics.com:
If selected to participate in the interview process, the names and contact information of three professional references who are able to assess your suitability for the position in terms of the specified requirements will be requested.
Watchmaker Genomics is committed to being an equal opportunity employer and creating a culturally diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics as protected by applicable law.
All applicants will be asked if currently eligible to work in the United States of America; and if now or in the future will require visa sponsorship to continue working in the United States.
This position may be subject to pre-employment checks, including driving history check, drug screening and a background check for any convictions directly related to its duties and responsibilities. All pre-employment checks will comply with all applicable federal, state, and local laws.
Position Type: Full-Time Employee
Location: Boulder, CO
Experience: 3 years laboratory experience (required) and 2 years Quality Control/Manufacturing/Quality Assurance experience (preferred)
Watchmaker Genomics is inviting applications for the full-time position of Quality Control Analyst.
The ideal candidate is an adept problem solver and a creative self-starter with excellent organizational skills. This position provides great opportunities for growth for candidates with a strong background in molecular biology and biochemistry. There are a variety of assays the QC Analyst will use to support the characterization of enzymes and reagents across our product portfolio. In addition to executing core QC processes, the individual will be increasingly responsible for the development and validation of new assays and implementation of new internal processes. This position reports to the QC Manager and will interface closely with many aspects of quality control, manufacturing, logistics, and research and development.
The successful candidate will thrive in a dynamic, fast-paced working environment and contribute directly to our company culture and success. The position provides an opportunity to gain valuable experience spanning many business facets to complement a strong technical background.
Responsibilities
- Execution, documentation, and analysis of routine QC processes
- Independent evaluation and interpretation of data from various assays
- Assay development and validation
- Participation in cross-functional teams to resolve product quality issues, corrective actions, investigations, and develop/implement in-process improvements
Experience in biotech and a start-up environment are highly desirable. The following skills and experience are requirements for the position:
- At least 3 years of relevant laboratory experience in biochemistry, molecular biology, or a related discipline.
- Creative and disciplined problem solving skills.
- Excellent organizational skills and superior attention to detail.
- The ability to multitask, work at a high standard, perform consistently under pressure along with pre-determined deadlines and work without supervision.
- Strong interpersonal skills and an ability to work as an effective member of a team.
- Excellent communication, personal task management skills and high levels of motivation and initiative.
- A creative and disciplined approach to problem-solving.
- Gel electrophoresis
- PCR, qPCR
- Next-generation sequencing (NGS)
- Enzyme activity assays
- Manufacturing in a controlled environment
- ISO 13485
- Quality Management Systems
- Good Laboratory Practice
- BS or MS in biotechnology, molecular biology, or related field
- 3 years experience (see above for details)
The base compensation for the Quality Control (QC) Analyst role starts at $50,000 - $60,000 bonus equity; actual pay will be adjusted based on skills and experience. Employees are eligible for Flexible Time Off, Holidays, employer covers 75% of base medical plan with buy-up options, employer paid dental, employer paid vision, employer paid $25,000 life/AD&D policy, paid parental leave, and a 401(k) retirement plan.
Application Requirements
To apply for the position, please submit the following in a PDF format on watchmakergenomics.com:
- Letter of motivation (upload where it says cover letter)
- Resume or Curriculum vitae, highlighting relevant qualifications and experience
If selected to participate in the interview process, the names and contact information of three professional references who are able to assess your suitability for the position in terms of the specified requirements will be requested.
Watchmaker Genomics is committed to being an equal opportunity employer and creating a culturally diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics as protected by applicable law.
All applicants will be asked if currently eligible to work in the United States of America; and if now or in the future will require visa sponsorship to continue working in the United States.
This position may be subject to pre-employment checks, including driving history check, drug screening and a background check for any convictions directly related to its duties and responsibilities. All pre-employment checks will comply with all applicable federal, state, and local laws.
Salary : $50,000 - $60,000