Careers

Join Us.

Biomeme designs and manufactures precision portable instrumentation and test kits for DNA analysis and microbial detection in the field. We are a small but fast-growing company in this emerging tech space. Our products are being deployed in a variety of field settings throughout the world. However, much of our production today is focused on diagnostics to combat the SARS-Cov-2 Pandemic at the point of use. To do so, we need help and need it quick. Please take a look at the opportunities listed below and reach out now.

Here’s a look at some of the ways that we take care of our employees. 
– Health Insurance 
– HSA Matching 
– Commuter Benefits
– 401(k) Matching 
– Company Stock Options 
– Paid Time Off (PTO) 

Current Openings

Quality Engineer

To be considered for this position, please complete the following application: Quality Engineer

SUMMARY:

As a successful quality engineer, you will bring a proven track record of improving manufacturing quality through internal process improvement. Ideally, you have worked in corporate quality engineering in the medical device (or similarly regulated) field and are excited to bring strict quality regimentation to a business experiencing explosive growth. You have experience in quality control as it relates to mechanical, electrical and even biological (fluidic) components in a manufacturing environment.

In this fast-paced, startup environment a successful candidate will possess strong initiative and self-starting qualities with adaptability to any task. The candidate should fully understand that this position is not a “desk job” and that in the exciting times our business is experiencing there is no person here with a single duty. A QE may go from writing a work instruction to measuring components to designing solutions with the engineering team and further.  This position will report directly to the Head of Quality.

 

RESPONSIBILITIES:

– Develop inspection plans for custom components received for production

– Improve current measurement and inspection practices

– Assist in creating/updating work instructions for production processes

– Continually develop our QMS and assure compliance with regulatory requirements

– Work with engineering teams to develop tooling and new processes

– Manage/coordinate internal Material Review Board

– Root Cause Analysis on bad parts/bad assemblies

– Update DFEMAs and PFEMAs to align with advancements/updates to the thermocycler

– Manage the design package/Design History File for the thermocycler

 

QUALIFICATIONS:

– BS in Mechanical/Electrical/Biomedical Engineering

 

REQUIRED EXPERIENCE:

– 3-5 years’ minimum experience in a quality engineering role

– Corporate quality in a regulated environment (ISO:9001, AS9100D, ISO:13485, 21CFR820)

– Measurement methods/metrology

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law

Chief Financial Officer (CFO)

To be considered for this position, please complete the following application: Chief Financial Officer

 

SUMMARY:

Biomeme is an exciting medical diagnostic company that is experiencing extensive growth. We are looking to hire a CFO to lead the company from a financial perspective. You will work alongside the Founders and the rest of the executive team, taking ownership of all company fiscal matters. To do well in this role, you should have experience as a CFO or Finance Lead in the health care or related field and, importantly, have emerging growth company experience. Biomeme is a very hands-on company and you should be as comfortable developing board presentations as rolling up your sleeves and digging into the weekly invoices and bills.

 

RESPONSIBILITIES:

– Oversee the company’s fiscal activity, including budgeting, reporting, and auditing.

– Work to create corporate dashboards, financial reports, and budgets.

– Assure all corporate structure and tax documents are filed and monitor compliance with laws and regulations.

– Assist with high-level decisions about strategy.

– Help with recruiting new staff members when necessary.

– Supervise all finance personnel.

– Identify and address financial risks and opportunities for the company.

– Review financial reports for ways to reduce costs.

– Work well with the Founders and COO to develop the strategic plan.

 

REQUIREMENTS:

– Bachelor’s degree in a relevant discipline, masters degree or MBA.

– Experience in a senior management position.

– Strong financial and accounting background, including an understanding of profit and loss, balance sheet and cash flow management and general finance and budgeting.

– Experience with budget management, public accounting, and cash flow.

– Ability to understand new issues quickly and make wise decisions.

– Ability to inspire confidence and create trust.

– Ability to work under pressure, plan personal workload effectively and delegate.

– Ability to strategize and solve problems.

– Strong leadership and organizational skills.

– Excellent communication and people skills.

– Fluent in Microsoft Excel, with a strong experience in QuickBooks and/or other accounting software.  We are implemented Oracle NetSuite so experience there would be a plus.

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

 

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law

Device Test and Repair Technician

To be considered for this position, please complete the following application: Device Test and Repair Technician

SUMMARY:

In this position, you will be joining a team of technicians and engineers involved in the production of battery-operated, portable diagnostics. A Device Test & Repair Technician must be able to identify, repair, and test complex electro-mechanical faults.

Biomeme mobile instruments contain complex circuitry and sensitive optics. Must be comfortable using DMMs, oscilloscopes, and PC aided diagnostic software. Working knowledge of engineering theory, units, and terminology is a must.  The ability to debug analog and digital circuity at the system and component level is essential. 

Should be comfortable in a fast-paced production environment and demonstrate impeccable attention to detail. You will be directly involved with the engineering and manufacturing staff and thus have extremely good communication skills. 

 

RESPONSIBILITIES:

– Assemble small electronic and mechanical components and subassemblies into finished products.
– Join or secure parts in place using hand tools, power tools, adhesives, fixtures, and equipment.
– Perform on-line testing and visual inspection using magnifying devices,  measuring instruments, and computerized and electronic test equipment, to ensure parts and assemblies meet production specifications and standards.
– Perform tasks requiring fine motor skills and manual dexterity (ability to work with small parts).
– Follow verbal and written instructions carefully and consistently.
– Enter data into computer databases.
– Maintain a clean and organized work area.
– Perform repetitive tasks carefully and consistently.
– Possess corrected vision adequate to perform tasks.
– Work closely with others in a team environment.
– Communicate effectively with fellow team members.
– Work at the pace required to meet production goals.
– Read and follow verbal instructions in English
– Use basic numerical and mathematical skills.
– Maintain regular and reliable attendance.

 

REQUIREMENTS:

– 1-2 years electronics troubleshooting.
– 1-2 years of electronic printed circuit board test and repair.
– 1-2 years of electronic device assembly and/or testing.

 

PHYSICAL REQUIREMENTS:

– Comfortable lifting 10-50 pounds from ground and eye level.
– Good vision, and color vision.

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Tier 2 Help Desk Technician

To be considered for this position, please complete the following application: Tier 2 Help Desk Technician

JOB SUMMARY:

Biomeme is looking for a tier 2 help desk technician to improve and increase office productivity. Responsibilities will include windows desktop support, provisioning computers, continuously monitoring and improving IT systems. Great written and verbal communication skills are a must for the candidate to be successful.

 

RESPONSIBILITIES:

– Received assigned tickets from our dispatcher and manage them cradle-to-grave\Participate in daily round table discussions

– Participate in On-Call rotation

– Update and provide feedback on client documentation and SOPs

– Identify and recommend process improvement

 

QUALIFICATIONS:

– 4+ years of help desk experience

– Bachelor’s Degree in Computer Science, or related field (or adequate work experience)

– Experience with Office 365 management, and product lines

– Experience with Hyper-V or VMware virtualization

– Intermediate knowledge of server operating systems and services, AD, Group Policy, DHCP, and DNS

– Intermediate knowledge of VLANS, IP Addresses, and wireless

 

SKILLS:

– Superior communication (both verbal and written) and interpersonal skills with a strong desire to project a helpful and positive customer service attitude

– Excellent time accounting and schedule management

– Positive, easy-going attitude

– Natural aptitude for technology

– Detail-oriented and is comfortable in a process-driven work environment

– Demonstrates organizational skills such as the ability to multi-task, set priorities, and follow up in a timely manner

– Has experience with using a PSA, RMM, and Documentation tool such as Connectwise and ITGlue

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law

Industrial Engineer

To be considered for this position, please complete the following application: Industrial Engineer

WHO WE ARE:

Biomeme designs and manufactures precision portable instrumentation and test kits for DNA analysis and microbial detection in the field. We are a small but fast-growing company in this emerging tech space. Our products are being deployed in a variety of field settings throughout the world. However, much of our production today is focused on diagnostics to combat the Sars-Cov-2 pandemic at the point of need.

 

SUMMARY:

Responsible for improving the operational efficiency of our manufacturing operations. This will be done through the implementation of LEAN manufacturing principles.

 

RESPONSIBILITIES:

– Load and maintain manufacturing routings into our ERP system (Oracle)

– Document and determine room and facility layouts to maximize efficiencies

– Implement lean manufacturing principles across the manufacturing and engineering organizations

– Create engineered labor standards

– Perform time studys and cycle time analysis

– Workplace organization and visual management

– Method and process design and improvement

– Perform staffing design

– Perform data analysis & reporting

 

EDUCATION:

– B.S. in Mechanical Engineering, Biomedical Engineering, Industrial Engineering or related engineering degree.

 

PREFERRED EXPERIENCE:

– 3+ years experience in an industrial manufacturing environment

– Experienced in a regulated industry (Medical, Automotive, etc.)

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

 

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law

Automation Technician

To be considered for this position, please complete the following application: Automation Technician

WHO WE ARE:

Biomeme designs and manufactures precision portable instrumentation and test kits for DNA analysis and microbial detection in the field. We are a small but fast-growing company in this emerging tech space. Our products are being deployed in a variety of field settings throughout the world. However, much of our production today is focused on diagnostics to combat the Sars-Cov-2 pandemic at the point of need. 

 

SUMMARY:

Responsible for maintaining and improving the manufacturing equipment in Biomeme production areas. Implement and execute all tasks related to production equipment – including but not limited to electrical, mechanical, maintenance, cleaning, commissioning and improvement. Coordinate with production management and engineering to keep production running efficiently as possible.

All tools required for this position will be provided by Biomeme Inc.

 

AVAILABLE SHIFTS: 

– Monday – Thursday from 5:00 PM to 3:00 AM

– Friday – Sunday from 1:30 PM to 2:00 AM

 

RESPONSIBILITIES:

– Coordinate maintenance objectives with your immediate supervisor and engineering daily.

Routinely perform all necessary duties to ensure production is functioning at full efficiency.

Complete special projects as may be assigned and prioritized by the immediate supervisor.

Diagnose and perform maintenance/repair in a timely and professional manner.

Upkeep of the company maintenance log, where required.  Accurately document work performed on service request, including parts and/or vendor labor.

Coordinate with vendors for warranty or special maintenance requests.

Professional work ethic and appearance.

 

EDUCATION:

– Associates degree in automation and/or maintenance or equivalent experience

 

PREFERRED EXPERIENCE:

– Experience with the maintenance and implementation of PLC systems (Allen Bradley)

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law

Controls Engineer

To be considered for this position, please complete the following application: Controls Engineer

SUMMARY:

Biomeme designs and manufactures precision portable instrumentation and test kits for DNA analysis and microbial detection in the field. We are a small but fast-growing company in this emerging tech space. Our products are being deployed in a variety of field settings throughout the world. However, much of our production today is focused on diagnostics to combat the Sars-Cov-2 pandemic at the point of need.

We’re currently seeking a Controls Engineer to join a growing engineering team. The Controls Engineer will ensure that all controls equipment is designed, built, maintained, updated, working efficiently and programmed to specifications using approved engineering practices and meeting industry standards. They must possess a working knowledge of process development, machine design and control systems.

 

RESPONSIBILITIES:

– Responsible for technical support, designing, programming, and commissioning of PLC hardware and software on all types of equipment and machinery across the manufacturing network. Typically PLCs are Allen Bradley, but purchased equipment encompasses a variety of languages we need to maintain and implement.
– Ability to critically review, troubleshoot and improve equipment’s designs and manage risks.
– Promote adherence to good engineering practices throughout Engineering department.
– Collaborate with Leadership team, as needed to implement company wide improvements and initiatives.
– Maintain and improve electrical manufacturing documentation.
– Create PLC programs for new process equipment, upgrade for existing equipment.
– Create HMI screens for new process equipment and upgrade existing equipment.

 

KNOWLEDGE, SKILLS, and ABILITIES:

– Associates or Bachelor’s Degree in Software Engineering, Electrical or Mechanical Engineering or a related field
– 3+ years experience in Controls Engineering
– Self-starter who is well-organized, detail-oriented, creative and possesses excellent problem-solving skills.
– Strong time management skills; Must be able to handle multiple projects and important issues at one time.
– Proven ability to maintain and manage a dynamically changing schedule and balance overall workloads.
– Proficiency in Microsoft Office
– Experience PLC programming (Required: Allen Bradley).
– Experience in project management
– Electrical panel fabrication experience
– Optional: Machine Design, vision systems, Fanuc robots, and IDEC control systems

 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

 

Project Manager

To be considered for this position please complete the following application: Project Manager 

SUMMARY:
At Biomeme, Inc. we make a portable real-time PCR test that puts disease testing in the palm of your hand. Our development team, composed of engineers and biologists, are looking for a Project Manager to plan and organize development of the company’s next gen products. You will be working closely with the team to ensure that all project requirements, deadlines, and schedules are on track. Responsibilities include submitting project deliverables, preparing status reports, and establishing effective project communication plans as well as the proper execution of said plans. 

RESPONSIBILITIES:
– Coordinating with cross discipline team members including sales, engineering, and biology to make sure that all parties are on track with project requirements, deadlines, and schedules
– Meeting with project team members to identify and resolve issues
– Submitting project deliverables and ensuring that they adhere to quality standards
– Preparing status reports by gathering, analyzing and summarizing relevant information
– Establishing effective project communication plans and ensuring their execution
– Facilitating change requests to ensure that all parties are informed of the impacts on schedule and budget
– Coordinating the development of user manuals, training materials and other documents as needed to enable successful implementation and turnover of the process or system to the clients
– Identifying and developing new opportunities with clients
– Obtaining customer acceptance of project deliverables
– Managing customer satisfaction and expectations
– Conducting post project evaluation and identifying successful and unsuccessful project elements 

SKILLS:
– Ability to manage multiple small to medium-sized projects through to completion
– Great communication skills
– Strong understanding of formal project management methodologies
– Budget management experience 

As a Production Supervisor, you’ll bring a proven track record of hands-on
 
manufacturing setting – preferably relating to medical devices, GMP manufacturing,
 
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
 
 
As a Production Supervisor, you’ll b
ring a proven track record of hands-on
 
setting – preferably relating to medical devices, GMP manufacturing,
 
 
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
 
 
We are expanding rapidly in response to the global
 
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular
flexibility preferred.
 
organization of incoming raw goods and materials for biology
 
 
 
 
.

 

 

 

 

5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular

 

 

REQUIREMENTS:
– 5 years of experience in project management
– Bachelor’s or Master’s Degree in business or engineering

PREFERRED: 
– Project Management Professional (PMP) certification 
– Experience as a Project Manager in defense or government contracts
– Experience managing medical device products 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

 

 

Senior Assembly Technician

To be considered for this position please complete the following application: Senior Assembly Technician 

SUMMARY:
As a Senior Assembly Technician you will bring a proven track record of complex mechanical and electrical assembly to this position. Working in the Device Manufacturing department, you will be deeply involved in daily production of electromechanical instrumentation and next-generation prototype devices. Successful candidates will be able to guide and train other assembly operators, as well as function as a part of daily production to meet production goals. 

RESPONSIBILITIES:
– Assist in production assembly efforts as a member of the assembly team 
– Lead trainings with assembly operators on safe handling and assembling methods
– Assure work instructions are followed
– Notify the production and engineering teams of assembly difficulties caused by design or lack of tooling, fixturing, etc. 
– Participate in the quality control and assurance process of subcomponents used in assembly
– Work in cooperation with ERP/MRP software to keep track of open work orders

SKILLS:
– Experience in handling electronic components in an ESD safe manner
– Troubleshooting and debugging of electromechanical instruments
– Functional understanding of assembly drawing reading
– Ability to function with and without discrete work instructions 
– Ability to adhere to good documentation and manufacturing processes
– Ability to work alone as well as in an interdisciplinary and cross-functional team 

As a Production Supervisor, you’ll bring a proven track record of hands-on
experience participating in and organizing day-to-day production workflow in a
manufacturing setting – preferably relating to medical devices, GMP manufacturing,
and/or any regulated industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
efforts and assure that assembly technicians are effectively managed, trained, and
equipped to build product.
As a Production Supervisor, you’ll b
ring a proven track record of hands-on
exrience participating in and organizing day-to-day production workflow in a
setting – preferably relating to medical devices, GMP manufacturing,
and/or any regulated industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
efforts and assure that assembly technicians are effectively managed, trained, and
equipped to build product.
– Monday – Thursday, 7:00 AM – 5:30 PM 
– Monday – Thursday, 5:00 PM – 3:30 AM
– Friday – Sunday, 7:00 AM – 7:30 PM

Some occasional shift flexibility is required, regular flexibility is preferred. 
The Quality Assurance Analyst is responsible for maintenance and
organization of incoming raw goods and materials for biology
consumable manufacturing as well as quality control testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to the Quality Manager and assist in adherence to Biomee
quality system requirements.
We are expanding rapidly in response to the global pandemic
and are in search of experienced Production Supervisors for
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular
flexibility preferred.
Thuality Assurance Analyst is responsible for maintenance and
organization of incoming raw goods and materials for biology
consumable manufacturing as well as quality control testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to t assist in adherence to Biomeme
quality system requirements.

We are exp

anding rapidly in response to the global pandemic

and are in search of experienced Production Supervisors for
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular

flexibility preferred.

 

REQUIREMENTS:
– 5+ years of experience in assembly manufacturing
– Hands-on experience assembling small precision instrumentation
– Managerial or supervisory experience
– Familiarity with ISO 13485 quality and FDA compliance is preferred


Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

 

 

Assembly Technician

To be considered for this position please complete the following application: Assembly Technician 

SUMMARY:
For this position, you will be joining a team which builds portable PCR thermocyclers and under the Company’s Quality Management System. You will be involved in as many processes as your skills allow, and will gain experience in the mechanical and electrical technology implemented in a state of the art system. The candidate must be able to work independently towards a common goal shared by team members.
– Good attention to detail 
– Organizational skills
– Ability to follow detailed instructions (written or verbal)
– Ability to perform tasks without direction
– Punctuality
– Desire to learn
– Able to work as part of a team

 

RESPONSIBILITIES:
– Assembling hardware components for devices
– Performing quality control on all components and final products
– Following quality management system, filling out documentation of manufacturing work instructions and production specification lot history records and proper filing of those documents
– Participate in the quality control and assurance process of subcomponents used in assembly
– Work in cooperation with ERP/MRP software to keep track of open work orders

SKILLS:
– Experience in handling electronic components in an ESD safe manner
– Troubleshooting and debugging of electromechanical instruments
– Functional understanding of assembly drawing reading
– Ability to function with and without discrete work instructions
– Ability to adhere to good documentation and manufacturing processes
– Ability to work alone as well as in an interdisciplinary and cross-functional team

d industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation withl testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to t assist in adherence to Biomeme
quality system requirements.

 

anding rapidly in response to the global pandemic

 
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required,

.

 

 


Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

 

 

Quality Inspector

To be considered for this position please complete the following application: Quality Inspector

SUMMARY:

We are looking for a responsible Quality Inspector to check the quality of all incoming and outgoing material and products. You will be a firm advocate of quality in our business. 

The ideal candidate will possess a trained eye for detail and will be reliable and committed. In depth knowledge and comprehension of quality standards is essential. 

 

As a Production Supervisor, you’ll bring a proven track record of hands-on
experience participating in and organizing day-to-day production workflow in a
manufacturing setting – preferably relating to medical devices, GMP manufacturing,
and/or any regulated industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
efforts and assure that assembly technicians are effectively managed, trained, and
equipped to build product.
As a Production Supervisor, you’ll b
ring a proven track record of hands-on
experience participating in and organizing day-to-day production workflow in a
manufacturing setting – preferably relating to medical devices, GMP manufacturing,
and/or any regulated industry. You’ve worked in a deadline driven environment
producing a technical product with a sharp eye for quality while meeting business
output goals. The Production Supervisor will be in constant cooperation with upper
management, logistics, quality, and engineering teams to schedule production
efforts and assure that assembly technicians are effectively managed, trained, and
equipped to build product.
The Quality Assurance Analyst is responsible for maintenance and
organization of incoming raw goods and materials for biology
consumable manufacturing as well as quality control testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to the Quality Manager and assist in adherence to Biomeme
quality system requirements.
We are expanding rapidly in response to the global pandemic
and are in search of experienced Production Supervisors for
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular
flexibility preferred.
The Quality Assurance Analyst is responsible for maintenance and
organization of incoming raw goods and materials for biology
consumable manufacturing as well as quality control testing and
documentation for product in accordance with Biomeme SOPs and
MPIs as well as general regulatory guidelines. This position will report
directly to the Quality Manager and assist in adherence to Biomeme
quality system requirements.
We are expanding rapidly in response to the global pandemic
and are in search of experienced Production Supervisors for
three shifts; Monday-Thursday 7:00 AM-5:30 PM, Monday-
Thursday 5:00 PM-3:30 AM, and Friday-Sunday 7:00 AM-7:30
PM. Some occasional shift flexibility is required, regular
flexibility preferred.

RESPONSIBILITIES:

– Inspect incoming materials and verify requirements against dimensional drawings 

– Appropriately disposition materials based on inspection findings and acceptance criteria

– Complete inspection forms, file electronically, and ensure all ERP entries are accurate

– Prioritize workload to meet the demand of the manufacturing schedule

– Escalate nonconformities within the organization

– Lead/assist with company calibration event(s)

– Other duties and responsibilities as assigned 

 

REQUIREMENTS:

– Knowledge of general GD&T; ability to read and interpret parts and drawings  

– Ability to select the appropriate inspection instrument and measure to verify part dimensions are within acceptable limits

– Exercises sound judgement, is analytical in thought, and detail oriented 

– Comfortable working in a dynamic environment with many conflicting priorities

– Maintain an organized and clean workspace 

– Familiarity with principles of quality control

– Skilled at organizing and prioritizing assigned tasks to assure completion

– Can translate ideas on how to improve work tasks

– Strong verbal and written skills 

EDUCATION REQUIREMENTS: 

– Associate’s degree in engineering preferred but not required 

– CQI certification preferred but not required 

– Candidate must have a solid understanding and background in quality inspection within a highly regulated environment 

Due to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3)

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

 

 

Office Administrator

 To be considered for this position please complete the following application Office Administrator

SUMMARY:

We are seeking a motivated Office Administrator to join our growing Operations Team. The successful candidate will have experience communicating with customers, organizing office materials, scheduling and event coordination, and organizing and maintaining necessary documentation. A positive attitude and the ability to multi-task is key to succeeding in this role.  

RESPONSIBILITIES:

  • Organize and maintain paperwork
  • Assist in completing documentation (e.g. Credit Card Authorization Forms, Purchase Orders, etc.)
  • Assist the Operations department with filing and submitting reimbursement receipts
  • Manage office supply deliveries; maintain recurring deliveries
  • Prepare conference rooms for meetings and events
  • Answer the office phone and direct messages appropriately
  • Assist with employee on-boarding and off-boarding
  • Liaison with current employees, the Human Resources Manager, and outside benefits consultants to answer employee inquiries
  • Update open positions on the company website
  • Maintain the company’s applicant tracking system
  • Assist the Software department with placing and managing orders, and tracking inventory
  • Assist the Software department in setting up technology for new hires
  • Assist the Marketing department with implementing and organizing employee incentives and recognition programs
  • Design and implement an employee anniversary/birthday recognition program
  • Coordinate with building management to alleviate issues

 

SKILLS:

  • Ability to multi-task
  • Good written and verbal communication skills
  • Self-starter 
  • Strong organizational skills
  • Excellent problem-solving skills

 


REQUIREMENTS:

  • 2 + years of administrative experience

Lyophilization Manufacturing Technician

To be considered for this position please complete the following application: Manufacturing Technician 

JOB DESCRIPTION: 
The Manufacturing Technician proficiently performs a variety of complex tasks under general guidance of the Manufacturing Lead and in accordance with the manufacturing instructions following general regulatory and safety guidelines.

RESPONSIBILITIES: 
– Maintain and adhere to safe work habits and all applicable safety procedures and guidelines
– Proficient execution and knowledge of basic biochemical techniques and aseptic lab procedures
– Prepare solutions, aseptic filling and labeling of vials and tubes
– Assemble, disassemble and operates aseptic filling equipment and lyophilization equipment in controlled environments
– Assist in the formulation and dispensing of product per SOPs and MPIs
– Clean and/or sanitizes production areas and prepare equipment for production
– Complete and maintain documentation related to assigned work, including logbooks, batch records, etc.
– Adhere to verbal instructions and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation
– Identify, escalate and document events that deviate from normal operation; participate as needed in investigations
– Maintain compliance, cleanliness and orderliness of operational areas per appropriate SOPs
– Review and revise pertinent SOPs and production batch records as required
– Inspire and constantly strive to make Biomeme a great place to work and respected for the quality of its people and products and clients

REQUIREMENTS
– BA or BS degree in Biology, Chemistry, Biochemical Engineering or related field with 1+years of work experience
– Ability to weigh and measure raw materials and operate basic Benchtop instruments
– Able to follow written instructions. Seeks help with more complex and non-routine tasks
– Skilled at organizing and prioritizing assigned tasks to assure completion
– Can translate ideas on how to improve work tasks
– Strong verbal and written skills
– US Work eligibility

PREFERRED: 
– 2 + years of working experience, preferably in a manufacturing environment ideally in the pharmaceutical or medical device industry

 

DUE to ITAR compliance, this position requires candidates to be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3) 

Biomeme is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

Tweet Facebook in gplus

Biomeme's SARS-CoV-2 Test issued Emergency Use Authorization (EUA) by FDA

X