Position Code:  12-PD-022
Reports To: Manager of Equipment Services
Department:  Hardware

Description

• Transfer automation equipment & processes to production.
• Perform equipment support in production.
• Define equipment protocols to ensure production specifications are met.
• Manage outside equipment vendors with regard to PMs, uptime, repair, etc.
• Implement process, method & protocol changes as required by manufacturing.
• Create processes & procedures to ensure highest equipment uptime possible.

Responsibilities

• Programming & assay validation on liquid handling robotic systems from both Hamilton & Tecan.
• Volume verification using OD, gravimetric & fluorescent methods.
• Familiar with enzyme & reagent handling, properties and liquid handling compensation techniques.
• Low volume critical sample handling experience is highly desired.
• Troubleshooting automation equipment & assay issues.
• Interfacing with equipment vendors, lab technicians & engineers.
• Software programming for equipment interfaces / analysis

Qualifications

• High throughput wet lab experience in a controlled manufacturing environment.
• Demonstrated success in a lab which increased capacity by more than 2 fold.
• Demonstrated success with implementing protocol & equipment changes.
• CLIA experience is highly desired but not required.
• BS in related field.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-019
Reports To: Senior Manufacturing Manager
Department:  Operations

Description

As a member of the Operations group, the position will support Compete Genomics’ next generation processes for whole genome sequencing.  The successful candidate will operate sequencing instruments, manage data, troubleshoot, and maintain the operation in a 24/7/365 fashion using various proprietary and nonproprietary tools.

This in a “D” Shift position that requires working 12 hour shifts 3 or 4 days per week: Wednesday through Saturday/Sunday, 6PM till 6AM with a 1 hour lunch break.

Qualifications

• BS in Life Sciences (Biology, Chemistry, Biochemistry) or similar science related education.
• Molecular biology experience acquired from working with technologies such as PCR, sequencing, microarrays, and liquid handlers is preferred.
• Familiarity with processes used in molecular biology production environments, including use of SOPs and LIMS.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both lab notebook and electronic documentation.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-018
Reports To: Senior Manufacturing Manager
Department:  Operations

Description

As a member of the Operations group, the position will support Compete Genomics’ next generation processes for whole genome sequencing.  The successful candidate will operate sequencing instruments, manage data, troubleshoot, and maintain the operation in a 24/7/365 fashion using various proprietary and nonproprietary tools.

This in a “D” Shift position that requires working 12 hour shifts 3 or 4 days per week: Wednesday through Saturday/Sunday, 6PM till 6AM with a 1 hour lunch break.

Qualifications

• BS in Life Sciences (Biology, Chemistry, Biochemistry) or similar science related education.
• Molecular biology experience acquired from working with technologies such as PCR, sequencing, microarrays, and liquid handlers is preferred.
• Familiarity with processes used in molecular biology production environments, including use of SOPs and LIMS.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both lab notebook and electronic documentation.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. \

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-001
Reports To:  Senior Director, Lab Operations
Department:  Operations

Description

Complete Genomics is seeking a talented, driven, and accomplished leader to manage CGI’s sample prep and library construction operation.  This group is responsible for the complete process of transforming customer genomic DNA samples into DNA nanoballs (DNBs™) that are used in our Complete Genomics Analysis (CGA™) Platform.  This individual will be responsible for achieving quality, availability, and cost goals while scaling an operation to meet business objectives

Responsibilities

This individual will have the experience and a track record of performance in the responsibilities commensurate with a laboratory operations management role including, but not limited to:

Production:

• Ensure a safe work environment
• Manage multi-shift production team and ensure quality of day to day activities while meeting plan
• Develop, and maintain training programs for current and new employees.
• Develop and maintain equipment maintenance records and system suitability tests.
• Analyze applicable metrics to maintain quality and facilitate improvement

Continuous Improvement:

• Assist, and lead continuous improvement efforts to improve quality, increase capacity, and reduce cost.

Infrastructure:

• Document Control – Improve existing documentation for production and test  records within the company’s document control infrastructure
• LIMS / ERP - Establish requirements and phase implementation of LIMS/ ERP to scale with business needs
• Process Control – develop and maintain process monitoring program

Establish strong relationships with cross-functional interfaces:

• Quality – interface to ensure focus on continuous improvement
• Development – participate in management of critical relationships, ensure timely, effective implementation of appropriate improvements
• External Suppliers – participate in management of critical relationships
• Finance – interface to establish and monitor cost standards

Qualifications

• Proven management, interpersonal, communication, organizational, planning, and prioritization skills are required.  The position requires a demonstrated understanding of high throughput operations.
• The successful candidate will be a results oriented self-starter with exceptional quality of work, detail oriented, and ability to develop and execute in a dynamic environment.  The successful candidate will have a demonstrated history of continuous improvement within a production laboratory.
• An advanced degree in a relevant field is preferred with a proven track record of execution in a manufacturing or laboratory operation.
• A minimum of 7 years of industry related experience with 5 years of laboratory management experience is required.
• Experience in managing multiple shifts preferred.
• A strong background in molecular biology methods and laboratory management/ operations is required.
• Experience within a regulated (13485:2007, FDA Quality System Regulations and CMS CLIA/CAP) environments is highly desirable.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

 Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-011
Reports To: Samples Group Supervisor
Department:  Operations

Description

As a member of the Samples Group, the Molecular Biologist will play a key role in the quality control of incoming customer samples, as well as the initial steps in the transformation of these samples into DNA library sequencing substrates that are used in human genome sequencing operations.  This will include the processing of nucleic acid assays and manual as well as automated manipulation of DNA samples.  This individual’s main responsibilities will be to meet production goals associated with safety, quality, productivity, and cost.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 4 years of industry experience.
• Molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Experience with systems and processes used in laboratory production environments, including use of SOPs and LIMS.
• Experience in writing SOPs; executing validations; and implementing process monitoring are a plus
• Experience in operating high-end analytical instrumentation required.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both lab notebook and electronic documentation.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-010
Reports To: Samples Group Supervisor
Department:  Operations

Description

As a member of the Samples Group, the Molecular Biologist will play a key role in the quality control of incoming customer samples, as well as the initial steps in the transformation of these samples into DNA library sequencing substrates that are used in human genome sequencing operations.  This will include the processing of nucleic acid assays and manual as well as automated manipulation of DNA samples.  This individual’s main responsibilities will be to meet production goals associated with safety, quality, productivity, and cost.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 4 years of industry experience.
• Molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Experience with systems and processes used in laboratory production environments, including use of SOPs and LIMS.
• Experience in writing SOPs; executing validations; and implementing process monitoring are a plus
• Experience in operating high-end analytical instrumentation required.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both lab notebook and electronic documentation.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

 Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-017
Reports To:   Managing Senior Scientist
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the continuous improvement of novel library construction processes.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environments a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both written and electronic documentation.

Note:  This is a shift schedule position that will include weekend hours.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-016
Reports To:   Managing Senior Scientist
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the continuous improvement of novel library construction processes.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environments a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both written and electronic documentation.

Note:  This is a shift schedule position that will include weekend hours.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-015
Reports To:   Managing Senior Scientist
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the continuous improvement of novel library construction processes.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environments a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both written and electronic documentation.

Note:  This is a shift schedule position that will include weekend hours.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-014
Reports To:   Managing Senior Scientist
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the continuous improvement of novel library construction processes.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environments a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both written and electronic documentation.

Note:  This is a shift schedule position that will include weekend hours.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  11-PD-105
Reports To:   Managing Senior Scientist
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the continuous improvement of novel library construction processes.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environments a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both written and electronic documentation.

Note:  This is a shift schedule position that will include weekend hours.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-008
Reports To: Director, Purchasing
Department:  Operations

Description

Responsible for the distribution of reagent and consumables inventory in support of a high volume sequencing operation.  Responsible for execution, maintenance and continuous improvement of the cycle counting program.  Will also be available to back up Shipping and Receiving on an on-going basis.  Additional responsibilities include supporting material related activities as designated by the Purchasing Director.

Impact:

Failure to perform the essential functions of this job may lead to or result in; interruptions of the production schedule, inaccurate inventory balances, reduced efficiency of the Lab Operations, Purchasing, Operations Finance, and Accounts Payable groups.

Responsibilities

•  Perform cycle counts as required.  Maintain accuracy of consumable inventory counts. 
• Replenish consumable material kanbans in each lab.  Perform weekly stockroom counts of indirect & direct materials.
• Maintain stocks of personal protective supplies in each lab ante-room. 
• Facilitate the physical transfer of materials from various warehouse locations to end users as required.
• Act as back up for Shipping and Receiving.
• Sort and distribute company mail.
• Responsible for stocking all Safeway, Costco and Office City deliveries.
• Assist other members of the Supply Chain Group as required.
• Assist with projects as assigned by the Purchasing Director.

Qualifications

• High School diploma required.  Associate’s degree or higher preferred.
• Familiar with Microsoft Outlook, Excel, Word.
• Familiar with ERP/MRP software.
• Relevant experience in a manufacturing environment.
• Ability to read and interpret Certificates of Analysis.
• Ability to comprehend and convert between different physical units of measure.
• Possess a strong sense of customer service.
• Possess strong oral and written communication skills.
• Able to lift 50 pounds.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  12-PD-009
Reports To:  Director, Purchasing
Department:  Operations

Description

Manages key supplier performance to achieve continuous improvement in cost, delivery, quality and service.  Negotiates supplier contracts that drive accountability for high performance.  Responsible for processing purchase requisitions and related procurement activities in support of a high volume sequencing operation.  Monitors open purchase orders to ensure on-time delivery.  Resolves receiving and invoicing issues promptly.  Maintains accurate purchase order records in the ERP system and supporting authorization documents.  Supports related procurement activities as assigned by the Purchasing Director. 

Impact:

Failure to perform the essential functions of this job may lead to or result in: increased costs; interruptions of the production and development schedules; negatively impacting the Accounts Payable department workload; poor relationships with suppliers/internal customers.

Responsibilities

•  Supplier Management (Cost, Quality, Delivery & Service; Supplier Business Reviews)
• Identify and deliver on cost savings opportunities.
• Contracts (Strategy Development, Negotiation & Compliance Management)
• Prompt review of requisitions for compliance, then conversion to purchase orders.  Must efficiently and accurately verify proper authorization for all purchases.
• Prevent receiving and invoice discrepancies via careful alignment of purchase orders with supplier’s process.  Promptly resolve discrepancies as they occur.  Collaborate effectively with Accounts Payable, Receiving and Inventory Control colleagues.
• Negotiate best terms (price, delivery, and payment terms) with suppliers while maintaining efficient output of high volume of purchase orders.  Demand the best overall value for money being spent.
• Compliance to procurement policies & procedures.
• Clearly communicate requirements for goods and services to suppliers, both verbally and in writing.
• Maintain current and accurate purchase order data in the purchasing system (e.g.  delivery dates, pricing, change orders).
• Complete and maintain training requirements to support the primary responsibilities of the position and the back-up support for other related functions (e.g. Material Control, Planning).
• Deliver a high level of customer service within the company.

Qualifications

• Contract negotiations.  Able to develop a strategy with stakeholders, plan the negotiation and negotiate in a demanding yet professional manner.
• Working knowledge of ERP/MRP software.  Able to analyze MRP results and optimize planning parameters to maintain LEAN inventory levels while assuring product availability.
• Problem Solving.   Ability to quickly analyze problems, investigate and determine solutions.
• Organization.  Able to manage a wide variety of tasks, maintain and communicate task status to stakeholders.  Always notifies in advance when a risk of late delivery arises.
• Project Management.  Able to define goals and plans, then manage a project to completion.
• Microsoft Outlook, Excel, Powerpoint and Word.  Able to use these standard tools in a highly efficient manner.
• College degree required.
• 5 years of purchasing experience in a production environment in which the expected skill set above was used extensively.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

 Complete Genomics is proud to be an equal opportunity employer

Position:  12-PD-020

Reports to:  Biochip Production Manager

Dept:  Flow Slides

Description

The flow slides manufacturing technician is an enthusiastic, highly motivated person with great communication skills who can support the production of semiconductor-based flow slide device used in high-throughput genomic sequencing. The successful candidate will demonstrate the ability to perform a variety of production processes which include vacuum and wet processing, visual inspections, and mechanical assembly. The candidate must be willing to work in a dynamic environment in which production is ramping while processes are being improved.  In addition, the candidate should desire to work in a team setting where they will actively contribute to improving the production process.

Responsibilities

• Perform daily production processes including wet processing, chemical vapor deposition, resist coating, mechanical assembly, and visual inspections using high powered microscopes.
• Perform PM on processing equipment.  Support Engineering and Development on an “as needed” basis to perform basic tests and non-standard processing.

Qualifications

• Associates degree or equivalent
• 10 years’ experience in industry (semiconductor, telecom, or magnetic recording)
• Clean room manufacturing experience
• Experience using high-powered microscopes for visual inspections
• Good verbal and written communication skills
• Experience with data collection (familiarity with Excel, data entry, basic statistics, control limits, and SPC)
• Experience with MES (Manufacturing Execution System) or ERP (Enterprise Resource Planning) preferred but not required
• Knowledge of Lean Manufacturing best practices highly desirable but not required

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  11-PD-104
Reports To:   Managing Senior Scientist
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the continuous improvement of novel library construction processes.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environments a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both written and electronic documentation.

Note:  This is a shift schedule position that will include weekend hours.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  11-PD-100
Reports To:  Laboratory Supervisor
Department:  Operations

Description

Complete Genomics, Inc. in Mountain View, CA area has an immediate opening for California licensed Clinical Laboratory Scientist. Complete Genomics is the world’s leading whole human genome sequencing company. This is a unique opportunity to be at the leading edge of genome medicine. Please see our website for more information. www.completegenomics.com

Responsibilities

The successful candidate will be responsible for specimen processing, test performance, and data analysis. Experience with molecular diagnostics and sequencing technologies highly desired. This person will perform all aspects of whole genome sequencing using our proprietary technology and maintain accurate records of work performed. He/she will perform instrument calibration, maintenance, and will assist in training other CLS and laboratory assistants. Must comply with government regulations and Complete Genomics policies and procedures, and be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director. Must be able perform quality work within a dynamic environment  Must be cooperative, detail-oriented and have the ability and willingness to precisely follow complex operating procedures and strict regulations.

Qualifications

• ASCP certification in molecular genetics and/or current California license required
• Licensed in Clinical Molecular Genetic Scientist (full CLS or limited license CGMBS) or California-approved Medical Technologist (ASCP) with strong molecular background
• Specialist in Molecular (CGMBS) license highly desirable
• BS in Medical Technology, Biology, Chemistry, or related sciences
• 1+ year related experience required, 3+ years preferred
• Experience in laboratory accreditation and maintenance of standard operating procedures desirable

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  11-PD-99
Reports To:  Laboratory Supervisor
Department:  Operations

Description

Complete Genomics, Inc. in Mountain View, CA area has an immediate opening for California licensed Clinical Laboratory Scientist. Complete Genomics is the world’s leading whole human genome sequencing company. This is a unique opportunity to be at the leading edge of genome medicine. Please see our website for more information. www.completegenomics.com

Responsibilities

The successful candidate will be responsible for specimen processing, test performance, and data analysis. Experience with molecular diagnostics and sequencing technologies highly desired. This person will perform all aspects of whole genome sequencing using our proprietary technology and maintain accurate records of work performed. He/she will perform instrument calibration, maintenance, and will assist in training other CLS and laboratory assistants. Must comply with government regulations and Complete Genomics policies and procedures, and be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director. Must be able perform quality work within a dynamic environment  Must be cooperative, detail-oriented and have the ability and willingness to precisely follow complex operating procedures and strict regulations.

Qualifications

• ASCP certification in molecular genetics and/or current California license required
• Licensed in Clinical Molecular Genetic Scientist (full CLS or limited license CGMBS) or California-approved Medical Technologist (ASCP) with strong molecular background
• Specialist in Molecular (CGMBS) license highly desirable
• BS in Medical Technology, Biology, Chemistry, or related sciences
• 1+ year related experience required, 3+ years preferred
• Experience in laboratory accreditation and maintenance of standard operating procedures desirable

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  11-PD-097
Reports To:  Senior Quality Manager
Department:  Operations

Description

The Senior Quality Engineer/Associate is an enthusiastic, self-motivated person with great communication skills who can support the Quality Management System through management of the technology transfer program infrastructure as well as authoring of qualification and validation activities. The Senior Quality Engineer/Associate will demonstrate a high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The candidate will be comfortable in a rapidly evolving Biotech start-up environment assisting in the implementation of a value added QMS based on CLIA/CAP, ISO 15189:2007, ISO 13485:2003 and FDA QSR regulations.

Responsibilities

• Responsible for ensuring all requisite tasks are completed for a successful technology transfer from development to operations:
  • Creating, updating, reviewing, developing and executing standard operating procedures and supporting work instructions based in ISO 15189:2007, 13485:2007, FDA Quality System Regulations and CMS CLIA/CAP environments
  • Creating documentation including Manufacturing Process Instructions/Method Sheets, Bills of Material, Travelers, Instructions for Use/User Guides and Service Instructions
  • Preparing, managing, and assisting with execution of qualification, verification/validation protocols (e.g. IQ/OQ/PQ) in accordance with cGMP requirements
  • Direct and continuous involvement with development and operations to appropriate plan, facilitate and manage the technology transfer
• Supporting training of personnel in requirements of quality tools and techniques, QMS based on CLIA/CAP, ISO 13485/15189:2007, FDA 21 CFR 820 requirements
• Supporting supplier qualification and evaluations
• Supporting Change Control Board quality system/technology transfer representation
• Supporting Product Life Cycle/Development (PLC/NPD) quality inputs for design and phase reviews
• Any and all other undefined tasks, as directed by your supervisor.

 Qualifications

• Minimum, B.S./B.A. in Chemical Engineering, Molecular Biology, Chemistry or Life Science, Master’s preferred. 5+ years as a Quality/Process Engineer/Scientist or equivalent with part or all of it within a medical device or clinical laboratory environment
• Heavy experience with:
  • Creating user friendly technical documentation
  • Equipment and material qualifications
  • Process validation and biological assay validations
  • QC Method Development
  • Quality Planning
• Demonstrated knowledge of Risk Assessment tools, Quality Statistics, Reliability Engineering
• Experience in the Product Life Cycle/Development (PLC/NPD) process and able to add quality input for design and phase reviews
• Experience in medical device / Biotech start-up/fast growth company or similar working environment
• Working knowledge of cGMP’s
• An understanding of Biochemistry as it pertains to DNA sequencing is required at a level to be able to create procedural documentation
• ASQ certification will be viewed favorably
• Experience with Enterprise Resource software (ERP/MRP) a plus
• Experience in Clinical Laboratory regulated environments a plus
• A working knowledge of Six Sigma, Lean techniques and methodologies a plus

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer

Position Code:  11-PD-022
Reports To:  Sr. Director Lab Operations
Department:  Operations

Description

Complete Genomics is seeking a talented, driven, and accomplished leader to manage CGI’s sample prep and library construction operation.  This group is responsible for the complete process of transforming customer genomic DNA samples into DNA nanoballs (DNBs™) that are used in our Complete Genomics Analysis (CGA™) Platform.  This individual will be responsible for achieving quality, availability, and cost goals while scaling an operation to meet business objectives.  In addition, this individual will serve as the focal point for the transfer of new processing technology into the library operations team from internal R&D groups. 

Responsibilities

This individual will have the experience and a track record of performance in the responsibilities commensurate with a laboratory operations leadership role including, but not limited to:

1. Production
   1. Ensure a safe work environment
   2. Manage production team and ensure quality of day to day activities while meeting plan
   3. Establish, develop, and maintain training programs for current employees and new employees.
2. Technology Transfer
   1. Approve and assist in transitions of new technology into an operations environment from internal R&D groups.
   2. Approve, assist, and lead continuous improvement efforts to improve quality, increase capacity, and reduce cost.
3. Infrastructure
   1. Document Control – Improve existing documentation for production and test  records within the company’s document control infrastructure
   2. LIMS / MES - Establish requirements and phase implementation of improvements in LIMS/ MES to scale with business needs
   3. Process Control – establish and develop  process monitoring program and develop and maintain a process control infrastructure
4. Establish strong relationships with key interfaces –
   1. Quality – interface to ensure focus on continuous improvement
   2. Development – participate in management of critical relationships, ensure timely, effective implementation of appropriate improvements
   3. External Suppliers – participate in management of critical relationships
   4. Finance – interface to establish and monitor cost standards

Qualifications

• Proven management, interpersonal, communication, organizational, planning, and prioritization skills are required.  The position requires a deep understanding of high throughput operations.
• Abilities include establishing policies, establishing project plans, and meeting deadlines.
• The successful candidate will be a results oriented self-starter with exceptional quality of work, detail oriented, and ability to develop and execute in a dynamic environment. Additionally, the candidate will have a demonstrated history of successfully establishing, and continually improving well-defined and effective operational processes across all aspects of a production laboratory.
• A strong background in molecular biology methods and laboratory management/ operations I and a proven track record of maintaining a culture of continuous improvement  are required,
• An advanced degree in a relevant field is preferred with a proven track record of execution in a manufacturing or laboratory operation.
• A minimum of 10 years of industry related experience with 7 years of management experience is required; 
• Experience within a regulated environment (CLIA, IVD) is highly desirable.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer 

Position Code:  11-PD-023
Reports To:  Library Preparation Manager
Department:  Operations

Description

As a member of the Library Preparation group, the Molecular Biologist will play a key role in using production-scale molecular biology processes in the construction of sequencing substrates from customer DNA samples.  These processes will include the manipulation of nucleic acids using a variety of enzymatic methods to generate and QC sequencing substrates suitable for CGI’s high throughput sequencing platform.  This individual’s main responsibilities will be to meet production throughput and quality goals, though they will also contribute to the development, optimization and automation of novel library construction processes.

 Note: This is a shift schedule position that will include weekend hours.

Qualifications

• BS/MS in Life Sciences (Biology, Chemistry, Biochemistry) and at least 5 years of directly related experience.
• Extensive molecular biology expertise including PCR, genotyping, sequencing, or microarray analysis.
• Familiarity with systems and processes used in molecular biology production environments, including use of SOPs and LIMS.
• Familiarity with high throughput production environment a strong plus.
• Experience in operating high-end analytical instrumentation.  Liquid handling automation experience a plus.
• Excellent analytical and organizational skills, with great attention to detail and record keeping in both lab notebook and electronic documentation.

Apply for this position

Complete Genomics does not accept unsolicited agency resumes.  Please do not forward unsolicited agency resumes to our website, employees or Human Resources. 

Complete Genomics will not pay fees to any third party agency or firm and will not be responsible for any agency fees associated with unsolicited resumes. Unsolicited resumes received will be considered property of Complete Genomics and will be processed accordingly without fee.

Complete Genomics has the sole discretion to determine with whom we will enter into a contract.  If you wish to work with Complete Genomics, please contact the Human Resources department at careers@completegenomics.com.

Complete Genomics is proud to be an equal opportunity employer