Senior process engineering technician job description

6K Inc. is a high-tech start-up focused on the sustainable production of advanced materials. The UniMelt® is our groundbreaking microwave plasma technology platform driving our two divisions: 6K Energy and 6K Additive. Our energy division focuses on the production of sustainable and domestically produced battery materials used in electric vehicles and grid storage while our additive division specializes in sustainably sourced, AM metal powder production and reclamation . Our technology is transforming engineered materials into revolutionary products that advance industries across additive manufacturing, renewable energy, aerospace, consumer electronics, and more. We are actively seeking team members who would bring a strong work ethic and personal integrity to our fast-paced dynamic environment and are looking for an opportunity to challenge the boundaries of traditional manufacturing.

6K is searching for an experienced Sr. Process Engineering Technician with strong experience working with vacuum-related and high-temperature equipment. The successful candidate will have strong electro-mechanical troubleshooting and maintenance skills in addition to demonstrated hands-on experience in broad areas of mechanics, electronics, and testing.

In this exciting and dynamic role, the successful person will work as part of a small research and development team providing support in the design, integration, and testing of various electronic, electrical, and electro-mechanical subsystems.

KEY RESPONSIBILITIES

As an integrated team member, this role is responsible for the production of advanced materials through operation, hardware implementation, and troubleshooting of our patented equipment. It is expected that the individual in this position will provide meaningful contributions and will gain exposure to advanced technology while providing hands-on assessments and revisions.

Further responsibilities include:

• Ownership of production operations of the assigned unit, adhering to and contributing to process development specifications;
• Lead activities that proactively maintain and maximize the unit uptime and output including support for plasma, electronic and mechanical systems;
• Engage in the continual system and process improvements with an eye toward cost reductions associated with material powder production and collection;
• Contribute to equipment prototype development and integration;
• Conduct process experiments, accurately recording and reporting data.

QUALIFICATIONS

• Associate’s Degree in engineering technology, mechanical or electrical engineering, or similar degree;
• 3+ years prior related experience in research or manufacturing environment; preferably in metals or chemical processing with 5S and Six Sigma background;
• Understanding of the utilization of human-machine interfaces (HMI) and automation as process monitoring tools; machine vision preferred
• Must have experience with vacuum chamber-related and high-temperature equipment;
• Experience in systematic troubleshooting and resolving technical-related issues;
• Ability to work independently and as part of a team in a collegial environment;
• Knowledge of metallurgical criteria is helpful;
• Previous experience with high voltage, microwave equipment, and electric devices is highly desirable but not required.

6K Inc, is an Equal Opportunity Employer.

IMPORTANT NOTE: THIS IS A 2ND SHIFT POSITION.

QuantumScape is on a mission to transform energy storage with solid-state lithium-metal battery technology. The company's next-generation batteries are designed to enable longer range, faster charging and enhanced safety in electric vehicles to support the transition away from legacy energy sources toward a lower carbon future.

QuantumScape is an energy storage technology company, located in San Jose, California, and we are working on a fundamental disruption in the field of energy storage. We seek to change the paradigm in energy storage by developing a completely new class of electrical energy storage device. We are backed by top VC firms and our groundbreaking technology is based on work done by researchers at Stanford University.
Do you want to make a major contribution to this part of the energy economy?

Join us on our mission as we transform energy storage to enable a more sustainable future. We are looking to add a Senior Cell Process Engineer, Senior Member of Technical Staff (SMTS) to our Cell Engineering and Process Development team. This individual will be responsible for developing tools and techniques at the cell assembly level to improve the manufacturability of our solid-state lithium-metal batteries. This work includes designing new processes for cell assembly and experimental validation of these new approaches. You must have experience working with electrochemical energy storage devices such as lithium-based batteries or similar technology.

Consideration will be given to qualified candidates from the battery, medical, semiconductor, consumer electronics, automotive, aerospace, or other fields with related technology and development models.

ROLE AND RESPONSIBILITIES

* Develop new cell assembly tools and techniques for manufacturing scale-up
* Refine and improve existing cell assembly tools and techniques for manufacturing scale-up
* Run experiments and use statistics to evaluate multiple different approaches and compare the effectiveness of each
* Collaborate with cell component design teams, equipment design teams, cell mechanical design teams, safety, quality, metrology, and production teams to execute your mission

SUCCESS FACTORS

* Embrace new challenges, learn new techniques, and surpass internal goals
* Curious, hands-on approach to problem-solving
* Shares a real passion for our mission and vision of a carbonless future
* Demonstrate flexibility and resourcefulness allowing smooth adaptation to a constantly evolving environment and work priorities
* Possesses a can-do spirit and is a collaborative leader and teammate
* Organized, meticulous, and has clear written and verbal communication skills

REQUIRED QUALIFICATIONS

* BS or higher degree in chemical engineering, materials science, mechanical engineering, or a similar concentration
* Minimum of 5 years experience with a Bachelor's degree, or a minimum of 3 years experience with a Master's degree
* Proven experience working on process development for manufacturing scale-up
* Competent in safe laboratory practices especially in handling powders, solvents, and chemicals
* Experience with DOE style experimentation and statistical analysis of data
* Familiarity with at least one scientific programming language, e.g. Python, R, Matlab, or JSL/JMP

PREFERRED KNOWLEDGE SKILLS AND ABILITIES

* Knowledge of lithium-ion battery science

PHYSICAL REQUIREMENTS

* Work is performed in a dry room, fume hood, lab area, or glovebox requiring the use of fine motor skills
* Sitting or standing for extended periods of time
* Reaching and twisting motions with hands
* Lifting up to 25 lbs.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive benefits and privileges of employment. Please contact us to request an accommodation.

**OVERVIEW**

We are seeking a highly motivated Senior Process Engineer to join the BioProcess Engineering (BPE) department, part of the Sanofi Global CMC Development organization. This role is accountable for rigorous and efficient transfer and implementation of cell culture processes across the Sanofi GMP manufacturing network according to the program timelines. This role will serve as a general/receiving lead for clinical transfers and sending lead for commercial transfers, with primary accountability to R&D and Industrial Affairs departments.

**KEY RESPONSIBILITIES**

+ Lead technical transfer activities, including facility fit, gap, and risk assessments, as well as provide technical support as Subject Matter Expert (SME) for implementation of cell culture processes at pilot and clinical scale.

+ Write and review technology transfer plans, process descriptions, control strategies, and campaign summary reports.

+ Perform Continued Process Verification (CPV) during campaign execution and organize review meetings with stakeholders to provide updates on process performance and deviations.

+ Act as the primary data steward for program development runs, scale-up pilot batches, and clinical manufacturing. Generate data visualizations for CPV, assessments, and root cause analysis.

+ Serve as Person-In Plant (PIP) for critical steps during manufacturing campaigns.

+ Act as SME for deviation investigations and CAPA planning to resolve complex process issues.

+ Lead evaluation and implementation of new process platforms and manufacturing technologies in collaboration with internal partners and external vendors.

+ Work collaboratively with members of other functional departments to streamline ways of working for tech transfer, CPV, and manufacturing operations.

+ In partnership with the global BPE team, maintain and update the knowledge base of equipment and operational specifications across the entire Sanofi manufacturing network, share best practices in tech transfer, and drive continuous improvement.

**BASIC QUALIFICATIONS**

+ Bachelor's degree in Chemical Engineering, Biochemistry, Biotechnology, or related discipline with minimum of 10 years industrial experience in GMP batch manufacturing, manufacturing readiness, or process development of biologics OR Master's degree with minimum of 8 years relevant experience OR Ph.D. with relevant experience.

+ Experience with a wide variety of cell culture techniques and products for use in recombinant protein production systems, with knowledge on scale-up, process transfer, and cGMP manufacturing operation.

+ Experience participating in large, cross-functional teams.

+ Excellent oral and written communication skills.

+ Experience working on multiple complex projects to aggressive timelines with the ability to adapt to rapid changes in project priorities.

**PREFERRED QUALIFICATIONS**

+ Experience in writing and revising protocols, procedures, and reports as necessary to support process scale-up, transfer, and implementation to cGMP manufacturing operations.

+ Working knowledge of cGMP manufacturing, quality, and regulatory requirements (FDA, EMA, ICH).

+ Experience in defining process control strategies and performing risk assessment following Quality by Design (QbD) principles.

+ Familiarity with statistical analysis techniques and packages (JMP).

+ Experience working with external partners and/or CDMOs.

**SPECIAL WORKING CONDITIONS**

+ Ability to gown and work in manufacturing areas.

+ Ability to work flexible hours.

**WORKING IN BIOPROCESS ENGINEERING**

Working in Bioprocess Engineering provides a unique growth opportunity for professional exposure to many facets of our global business. Successful programs regularly collaborate with multiple departments such as Operations, Development, Quality, Supply Chain, CMC, and Regulatory. This can be an ideal place for those looking for new and interesting challenges and experiences.

_At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce - and workplace - which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver. Join us and together we will build on our trusted legacy of breakthroughs for society._

_Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law._

_As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities._

_According to the CDC, an individual is considered to be "fully vaccinated" fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE._

\#GD-SA

\#LI-SA

PDN

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.