Evona Egy Gel Jobs in Usa

Spacecraft Manufacturing Engineer

Cape Canaveral, FL

Full-time | On-site

About the Organization

Evona is partnered with a VC-backed advanced space infrastructure company developing expandable habitat systems for lunar exploration, low Earth orbit, and future deep-space missions.

The team is building large, human-rated expandable structures that combine soft goods assemblies and metallic structures, enabling lightweight, high-volume space habitats for sustained human presence beyond Earth.

The Role

As a Spacecraft Manufacturing Engineer, you will define and implement the manufacturing processes, tooling, and build flows required to produce large expandable space habitat structures. You’ll work closely with engineering, quality, and test teams to translate complex designs into repeatable, flight-ready manufacturing processes.

Key Responsibilities

• Develop and document manufacturing processes for expandable habitat structures
• Translate engineering designs into certifiable build and assembly workflows
• Design and support specialized tooling, fixtures, and handling equipment
• Lead integration of soft goods and rigid structures
• Support manufacturing-related testing, qualification, and anomaly resolution
• Collaborate closely with Quality Assurance and Safety teams

Qualifications

• Bachelor’s or Master’s degree in Mechanical Engineering, Aerospace Engineering
• Strong background in aerospace or spacecraft manufacturing and integration
• Experience with flight-certified manufacturing processes and QA documentation
• Familiarity with NASA or similar human-spaceflight standards
• Hands-on, detail-oriented approach to building real hardware

Why This Role

• Work on groundbreaking lunar habitat hardware in a well-funded startup
• See direct impact of your work on flight-bound systems
• Join a small, mission-driven engineering team building the future of human spaceflight

Work Location: In person – Cape Canaveral, FL

At Asbury, we believe in making a meaningful difference every day. As a nationally recognized Great Place to Work®, we are guided by a mission of doing all the good we can. We are committed to innovation, integrity, and compassion in serving older adults and creating vibrant communities where residents and associates thrive. Joining our team means you’ll lead with purpose, have the autonomy to innovate, and be part of an organization that values people first.

For nearly a century, Asbury Methodist Village has set the standard for award-winning retirement living in Montgomery County, Maryland. Located in Gaithersburg, MD, our vibrant continuing care retirement community rises above the ordinary—offering exceptional well-being programs, high-quality health services, and an unparalleled lifestyle for older adults. Spanning 134 beautiful acres, our campus is a certified arboretum featuring a 17-acre wildlife preserve, creating a setting that radiates energy, camaraderie, and endless possibilities. Home to 1,150 friendly residents and supported by 720 dedicated associates, we foster a welcoming, mission-driven environment where people truly make a difference. With a 5-star reputation, our commitment to excellence is recognized and celebrated. Asbury Methodist Village is known for its rich cultural events, engaging clubs, and innovative, award-winning programs—including Kinnections Brain Health—designed to help seniors move better, feel better, connect more, and experience more

.
Full-time Opportuni

tyCompensation Range: $225,000- $250,00 annually plus annual incenti

ve
Asbury Communities is seeking an experienced and visionary Executive Director to lead and manage all aspects of Asbury Methodist Village. This role provides strategic direction, financial oversight, and operational leadership to ensure excellence in resident services, regulatory compliance, and community growth. The Executive Director serves as the campus leader with autonomy to implement and adjust strategies in alignment with Asbury’s mission and organizational goa

ls.
Key Responsibili

• tiesLead and oversee community operations, programs, and services to ensure high-quality resident experien
• ces.Develop and execute strategic and financial plans, managing an annual budget of 100 million doll
• ars.Drive performance in resident and associate satisfaction, census growth, and service innovat
• ion.Build partnerships with hospitals, physician networks, payors, and community organizations to strengthen integration and servi
• ces.Monitor team performance, provide coaching, and ensure alignment with Asbury’s strat
• egy.Create and manage leadership development pl
• ans.Ensure strong communication with residents, families, staff, and community stakehold
• ers.Organize and delegate duties effectively through departmental leaders
• hip.Represent Asbury Communities in professional associations and within the broader senior living indus
• try.Champion the Asbury brand on and off campus while supporting system-wide initiati

ves.
Qualificat

• ions:
  Extensive Executive Director experience in a medium to large Continuing Care Retirement Community (
• CCRC).Proven success coordinating a large associate base and with a focus on supporting older adults in new and innovative strat
• egies.Demonstrated ability to lead through influence, build consensus, and achieve results in a collaborative enviro
• nment.Experience managing relationships with state of Maryland and associated business par
• tners.Proactive engagement in corporate-level initiatives with a focus on future cons
• umers.Exceptional communication and interpersonal s
• kills.Business experience in senior living or retirement housing strongly pref

erred.
Depending upon the status of the position, Asbury offers generous benefits including medical, dental, and vision coverage; 401K with match; PTO and paid ho

lidays.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected

Company Description

Elite AI Technologies specializes in empowering industries through advanced artificial intelligence and innovative solutions. With a commitment to delivering excellence, the company continuously strives to enhance its products and services across diverse domains. Elite AI Technologies is dedicated to fostering a collaborative work environment where innovation thrives. As a growing leader in the AI sector, the company offers opportunities for creative and driven professionals to make a meaningful impact.

Our client is an FDA-registered 503B outsourcing facility dedicated to providing high-quality compounded sterile and non-sterile pharmaceutical products to hospitals, health systems, and healthcare providers nationwide. Our client's state-of-the-art facility operates under current Good Manufacturing Practices (cGMP) and is committed to patient safety, regulatory compliance, and operational excellence. We offer a collaborative work environment where every team member plays a vital role in delivering life-saving medications.

Job Summary

We are seeking a skilled QC Analyst to perform laboratory testing and analysis of raw materials, in-process samples, finished products, and environmental monitoring samples. The ideal candidate has hands-on experience with pharmaceutical analytical instrumentation, USP testing methods, and cGMP laboratory practices within a 503B or pharmaceutical manufacturing environment.

Key Responsibilities

• Perform potency, identity, and purity testing of raw materials, in-process samples, and finished products using HPLC, GC, UV-Vis spectrophotometry, and other analytical methods

• Conduct sterility testing per USP using membrane filtration and/or direct inoculation methods

• Perform Bacterial Endotoxin Testing (BET) using LAL methods (kinetic turbidimetric, chromogenic, or gel-clot)

• Execute particulate matter testing per USP / (light obscuration and microscopic methods)

• Conduct pH, osmolality, specific gravity, and other physicochemical tests

• Perform environmental monitoring including viable air sampling, surface sampling, and non-viable particulate counts

• Conduct water system testing (TOC, conductivity, microbial analysis) per USP

• Execute stability studies per ICH guidelines and company protocols

• Prepare reagents, standards, and media; maintain laboratory supply inventory

• Document all testing activities accurately in laboratory notebooks and LIMS per cGMP requirements

• Investigate out-of-specification (OOS) and out-of-trend (OOT) results per SOPs

• Maintain, calibrate, and qualify analytical instruments per established schedules

• Review and approve analytical data and certificates of analysis (COAs)

Required Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences, or related field

• Minimum 2-4 years of QC laboratory experience in a pharmaceutical, 503B, or cGMP-regulated laboratory

• Hands-on experience with HPLC, GC, UV-Vis, and dissolution testing equipment

• Proficiency in USP compendial testing methods

• Experience with sterility testing, endotoxin testing (BET/LAL), and environmental monitoring

• Strong understanding of cGMP laboratory documentation practices

• Excellent attention to detail, data integrity awareness, and analytical problem-solving skills

• Proficiency with LIMS and Empower or similar chromatography data systems

Preferred Qualifications

• Experience in a 503B outsourcing facility

• Knowledge of FDA 503B regulatory requirements and USP //

• Experience with method validation and method transfer

• Familiarity with ICH stability guidelines (Q1A-Q1E)

• Experience with Karl Fischer moisture analysis, FTIR, or ICP-OES

Physical Requirements

• Ability to work in a laboratory environment wearing required PPE (lab coat, gloves, safety glasses)

• Must be able to work in cleanroom environments when required for environmental monitoring

• Ability to stand for extended periods and perform precise manual tasks

• Must be able to lift up to 25 lbs (chemical containers, supplies)

Kodak is looking for Technicians to join our team in Kodak’s Advanced Materials and Chemicals Division in Rochester, NY.

Technicians work in a variety of roles, all of which are involved in manufacturing the highest-quality light-sensitive coated products in the world. Depending on qualifications and experience, technician candidates will be assigned a role in one of these areas.

Components Testing: Kodak’s legacy is the production of the finest coated film products in the world. This starts with testing all the components that go into our films and ensuring that they meet our tight standards. Technicians test our liquid components – from gel to sensitized emulsion layers – for chemical concentrations, particle size, density, viscosity, and light sensitivity, etc. Materials of unknown origin, such as dust, and components with unexpected results are also subjected to special testing to determine root cause and origin.

As a technician, you will likely:

• Work in both light and dark room conditions.

• Work 12-hour rotating shifts (days one week, nights the next).

• Work overnights.

• 2–5 years of employment experience

Required skills and experience for all technicians:

• Must be a detail-orientated team player.

• Must have the ability to be flexible between multiple positions, sometimes multi-tasking or moving within a shift.

• Must work effectively with minimal supervision.

• Ability to prioritize work to meet business needs.

• Ability to express oneself communicate clearly, both written and verbal, and comprehend a variety of work requests

• Willing to work overtime or adjust work schedule for business needs.

• Must be willing and able to lift and move objects up to 50 pounds.

• Must maintain a clean work area.

• Must maintain strict adherence to safety procedures and quality standards.

• Computer proficiency including navigating screens and data entry.

• Involvement in product quality and process improvement activities.

• Interaction with operators, engineers, and maintenance personnel.

Preferred additional skills and experience:

• Associate’s degree, technical certifications or equivalent

• At least 2 years of hands-on experience in a manufacturing environment.

• Understanding of film photography.

• Understanding of thin-film coating processes.

• Strong problem solving, data analysis, and computer abilities (Excel, Word, etc.).

• Knowledge of Outlook, One-LIMS, Felix, and the SAP system.

We recommend watching the following videos to learn more about the manufacturing process at Kodak.

A tour of our PET film base manufacturing plant.

How Does Kodak Make Film? (Kodak Factory Tour Part 1 of 3)  tour of our film sensitizing plant.

How Does Kodak Make Film? (Kodak Factory Tour Part 2 of 3) 

Located in Thousand Oaks, California, 20BLOC is a small privately held development-stage biopharmaceutical company, driven by a mission to create breakthrough protein-based drugs to save lives. Our lead product is an innovative solution to provide oxygen to tissues. Check us out at We are looking for a motivated and hands-on Quality Control (QC) Specialist to join our team.

How you will add value to 20BLOC

The Quality Control (QC) Specialist supports the day-to-day operation of the QC and analytical lab. The purpose is to ensure products meet testing requirements, and laboratory operation complies with regulatory requirements. This is an exciting opportunity to join an expanding start-up in a full-time position on site in Thousand Oaks, CA.

Key responsibilities

• Conduct assays under defined protocols to measure purity, potency, and stability using equipment and instruments supporting biotherapeutics.
• Execute compendial assays, ELISA, gel electrophoresis and chromatographic-based assays and qualification activities following protocols on in-process and final drug substance and drug product samples.
• Trouble-shoot and problem-solve with underlying knowledge of how the assays work when unexpected results appear.
• Write SOPs, analytical protocols and written reports in compliance to cGMP as needed.
• Perform the day-to-day operation of the QC lab and perform routine lab activities as need.
• Support the technology transfer of assays developed or qualified by CROs and outsourced parties.

Education

• Bachelor degree in analytical, biological, life sciences or related field.
• 3 to 5-year experience working in a laboratory with hands-on experience in analytical assays and qualification activities.

Experience

• Experience with Regulatory and GMP analytical chemistry.
• Hands-on experience with multiple protein analytical methods, both compendial and non-compendial, such as HPLC (SEC, AEX/CEX, HIC, RP, etc.) and additional product-specific methods such as ELISAs, electrophoretic methods (SDS-PAGE, icIEF), endotoxin, osmolality, pH and appearance preferred.
• Experience with LC/MS analyses, potency assay, PCR, western blot and MS-based methods a plus.

Skills & Competencies

• Working knowledge of and exposure to phase appropriate quality systems, including deviations, CAPA, change control, and document management systems.
• Excellent interpersonal, verbal and written communication skills and the ability to work in a cross functional collaborative work environment.
• Strong attention to detail and excellent organizational skills.

Please apply at – in subject line: Quality Control (QC) Specialist

This is a full-time, on-site position located in Thousand Oaks, California, and requires working on-site Monday through Friday. All applicants must be authorized to work in the United States. We are not sponsoring employment visas.

Compensation: The salary range for this position is $74,000.00. to $89,00.00 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.

20BLOC is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status, or other applicable legally protected characteristics.

We offer competitive compensation and benefits including health, dental, vision and life insurance, 401(k) and paid time off.

Production Manager - Specialty Chemicals Manufacturing

Overview

A leading manufacturer in the specialty chemicals and advanced polymers industry is seeking an experienced Production Manager to oversee daily operations at a high‑volume manufacturing facility. This organization produces materials such as resins, gel coats, and other thermoset polymers used across construction, marine, transportation, and industrial applications. The ideal candidate will bring strong leadership skills, a commitment to safety, and the ability to drive operational excellence in a complex chemical production environment.

Key Responsibilities

• Lead, coach, and develop production teams while fostering a culture of safety, accountability, and continuous improvement.
• Oversee daily plant operations to ensure production goals are met for safety, quality, throughput, and cost performance.
• Implement Lean manufacturing, Six Sigma, and other process‑improvement methodologies to optimize efficiency.
• Monitor production metrics to identify trends, troubleshoot issues, and drive data‑backed decision‑making.
• Collaborate closely with Maintenance, Engineering, Quality, and Supply Chain teams to resolve operational issues and support uninterrupted production flow.
• Ensure strict compliance with environmental, health, and safety (EHS) regulations common to chemical manufacturing environments.
• Manage scheduling, staffing, and workforce planning to align resources with production demands.

Qualifications

• Bachelor's degree in Engineering, Operations Management, Chemistry, or a related discipline (preferred).
• 5+ years of progressive leadership experience in manufacturing; experience in chemical, resin, polymers, or related processing industries strongly preferred.
• Demonstrated ability to lead teams, build culture, and achieve strong operational performance.
• Strong understanding of Lean, Six Sigma, or other continuous improvement frameworks.
• Excellent analytical, problem‑solving, and communication skills.
• Proven commitment to safety, product quality, and regulatory compliance.

Why This Role?

This is an opportunity to shape operations at a well‑established, innovation‑driven manufacturer within the specialty chemicals sector. The position offers a collaborative work environment, competitive benefits, and the ability to directly influence production efficiency, team development, and long‑term operational success.

Founded in 1984, Best Formulations LLC, a diversified nutraceutical and personal care company headquartered in City of Industry, California, is a contract manufacturer of thousands of branded SKUs, including high quality nutritional supplements. At the core of our ethos is a dedication to personal care, where every product is crafted with meticulous attention to detail and the highest standards of quality. Our longstanding expertise in contract manufacturing dietary supplements has uniquely positioned us as leaders in research, regulatory compliance, and quality assurance.

About the role:

We are seeking an experienced Quality Executive to lead our Quality Compliance and Quality Control functions within a dynamic lab environment. This role is pivotal in ensuring that all products meet regulatory standards, customer expectations, and internal quality benchmarks. The ideal candidate will champion a Quality by Design approach, fostering a culture of continuous improvement and operational excellence.

How will you contribute:

Quality Compliance:

• Ensure adherence to all relevant regulatory requirements (FDA, GMP, ISO, etc.) for nutraceutical manufacturing.
• Maintain and update quality systems, SOPs, and documentation to meet compliance standards.
• Oversee audits (internal, external, and customer) and manage corrective/preventive actions.

Quality Control:

• Lead and manage QC operations, including raw material, in-process, and finished product testing.
• Ensure robust analytical and microbiological testing processes are in place and validated.
• Collaborate with R&D and production teams to resolve quality issues promptly.

Strategic Leadership:

• Develop and implement a Quality by Design framework across all processes.
• Drive continuous improvement initiatives to enhance product quality and operational efficiency.
• Build and mentor a high-performing quality team.

Minimum Requirements/Qualifications:

• Bachelor’s or master’s degree in quality assurance, Chemistry, Pharmaceutical Sciences, or related field.
• Minimum 8+ years of experience in Quality roles within nutraceutical, pharmaceutical, or food manufacturing industries.
• Previous experience in dietary supplements manufacturing, specifically with soft gel dosage forms, is highly preferred.
• Strong knowledge of regulatory requirements (FDA, GMP, ISO standards) and other regulatory frameworks relevant to nutraceutical manufacturing.
• Proven experience in managing audits and compliance programs.
• Familiarity with analytical and microbiological testing methods.
• Excellent communication, interpersonal, and organizational skills.
• Certifications preferred: ASQ Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), Preventive Controls Qualified Individual (PCQI) or other relevant quality or regulatory certifications.

Work Environment:

• May involve exposure to allergens such as Soy, Wheat, Fish, Shellfish, Milk, Egg, Tree Nuts and Sesame.

More about us:

As a valued strategic partner, Best Formulations offers a comprehensive program of services, turnkey solutions, and client support that is unmatched in the industry. Our product development team can provide customized, proprietary formulations designed specifically to meet the needs of our customers and their method of distribution. Our vertically integrated manufacturing and packaging process allows us to schedule flexible production runs to respond quickly to shifting market demands. Every step of the way, we are committed to your growth and success!

"To develop and strengthen mutually beneficial relationships with our employees, customers, and business partners by providing the highest quality products and the Best customer service. Together We Grow!"

EEO Statement

Best Formulations is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Best Formulations will work with applicants to meet accommodation needs that are made known to Best Formulations in advance.

Medical Assistant

Location: Dubuque, IA – Onsite

Our client is seeking a Medical Assistant to join their orthopaedic clinic team in Dubuque, Iowa. This is an onsite position supporting physicians and patients in a fast-paced specialty medical office. Are you a Medical Assistant who thrives in a hands-on clinical environment? Do you enjoy supporting physicians while also building strong relationships with patients? Are you organized, detail-oriented, and passionate about delivering high-quality patient care? If yes, this may be the perfect Medical Assistant position for you. Keep scrolling to see what this company has to offer.

The Perks:

• Compensation: $18.00-$21.50/hour, based on experience
• 401k + Company Matching
• Health, Dental, and Vision Insurance Benefits
• Paid Time Off and Paid Holidays
• HSA, FSA

A Day in the Life of the Medical Assistant

In this role, you’ll be at the center of the patient experience, welcoming patients, assisting physicians with exams and minor procedures, and coordinating surgeries, MRIs, and testing. You’ll act as a key liaison between patients and providers, ensuring communication is clear, documentation is accurate, and every step of the orthopaedic workflow runs smoothly. Your work directly supports quality patient outcomes and an efficient, patient-focused clinic environment.

Responsibilities include:

• Welcome and room patients, collect vitals (including weight), verify medications, and document patient history in the EMR
• Record accurate, real-time documentation during patient visits
• Communicate clinic delays to registration staff to proactively manage wait times
• Schedule surgeries, radiology, MRIs, testing, and medication refills accurately and efficiently
• Coordinate all aspects of surgical cases, including H&P, PAT, COVID swabs, joint camp, notifications to reps and departments, and patient instructions
• Obtain insurance pre-certifications and verify insurance coverage
• Coordinate with the billing department to confirm payment arrangements and inform patients of financial obligations
• Complete and communicate detailed MRI orders, including CPT codes, authorization numbers, and scheduling details
• Remove dressings and sutures, redress wounds, and perform sterile preps
• Assist physicians with exams, minor office procedures, and cast applications
• Prepare and sterilize instruments and maintain exam and cast rooms
• Stock clinic rooms and order necessary supplies, including gel injections
• Monitor drug and supply expirations and dispose of outdated items appropriately
• Complete work releases, gym releases, handicap permits, and other documentation
• Provide patient education and serve as a physician-patient liaison
• Document all patient phone conversations in the EMR
• Maintain surgeons’ surgery schedules
• Follow HIPAA, OSHA, and compliance guidelines
• Participate in emergency response procedures when needed
• Support continuous quality improvement initiatives
• Assist in training new Medical Assistants

Requirements and Qualifications:

• High school diploma or equivalent required
• 1+ year of medical assistant experience, related experience, and/or training
• Medical Assistant certification is encouraged but not required
• Strong communication and interpersonal skills with the ability to handle sensitive information
• Proficient with computers, EMR systems, and standard office equipment
• Knowledge of medical terminology and patient scheduling systems
• Strong organizational skills and ability to prioritize in a fast-paced clinical environment
• Ability to stand and walk continuously throughout the workday
• Ability to frequently lift, push, or carry 25–50 lbs

About the Hiring Company:

Our client is a specialty orthopaedic practice committed to delivering high-quality, patient-centered care. Their team focuses on efficiency, professionalism, and compassionate service while maintaining strict compliance with HIPAA and OSHA standards. With a collaborative clinic environment and a strong commitment to continuous quality improvement, they take pride in supporting both their patients and their staff.

Come Join Our Clinical Team!

Start by filling out this 3-minute, mobile-friendly application here. We look forward to hearing from you!

THE COMPANY:

Formulated Solutions is redefining the Pharmaceutical and Self-Directed Consumer Healthcare CDMO experience through creativity and invention; delivering our world class Marketing Partners unmatched formulations, innovative packaging and cost effective, reliable supply.

Formulated Solutions is and shall always be a company of people with the knowledge and dedication to provide our Marketing Partners with a single source solution for delivering quality and innovative products to market. We shall embrace changes and new opportunities as a vehicle to continually develop and grow sustainable relationships. As a company we shall never accept anything less than a culture that fosters creativity, growth, and profitability for both our Partners and the company.

PRIMARY PURPOSE:

The Senior Commercial Process Engineer – Compounding/Blending (Formulating) is responsible for the development, continuous improvement, optimization, and technical support of manufacturing processes for pharmaceutical products, ensuring compliance with current Good Manufacturing Practices (cGMP). Key responsibilities include the hands-on leading technology of transfers, troubleshooting deviations, performing process validation, and collaborating with cross-functional teams to enhance product quality, efficiency, and safety throughout the product lifecycle. This role will be an integral member of the team that develops and brings new products to market, as well as drive process improvement for current products.

MAJOR DUTIES AND RESPONSIBILITIES:

Process Improvement & Optimization:

• Analyze commercial process monitoring data to identify trends, conduct technical investigations, and implement engineering solutions to improve yield, quality, and efficiency.

Technology Transfer:

• Directly lead or support the transfer of new products and processes from R&D or other sites to commercial manufacturing, including conducting gap analyses and risk assessments.

Validation & Documentation:

• Author and execute validation protocols for process validation, cleaning validation, and equipment qualification. Develop and maintain essential technical documentation, including user requirements, SOPs, and reports.

Troubleshooting & Deviation Management:

• Investigate technical issues, lead Root Cause Analyses, and support the implementation of corrective and preventative actions (CAPAs) for deviations.

Cross-Functional Collaboration:

• Work with Quality, Manufacturing, R&D, and Project Management teams to achieve project objectives and ensure successful process implementation.

Compliance & Regulatory Support:

• Ensure all manufacturing activities adhere to regulatory requirements and GMP standards. Participate in internal and external audits and inspections.

Equipment & Engineering Support:

• Define user requirements for new process equipment and participate in Factory/Site Acceptance Testing (FAT/SAT) and commissioning for new systems.

QUALIFICATION:

Engineering Expertise:

• A degree in chemical engineering, biomedical engineering, or a related field.
• Familiarity with compounding and processing liquids, creams, ointments, emulsions and aerosols.

Technical Skills:

• Proficient in statistical tools (e.g., JMP, Minitab) and data analysis, with strong technical writing and presentation skills.

Regulatory Knowledge:

• Thorough understanding of GMP and other relevant pharmaceutical manufacturing regulations.

Problem-Solving:

• Ability to conduct technical investigations and lead problem-solving initiatives to resolve complex manufacturing issues while operating within project completion deadlines.

Communication & Collaboration:

• Strong communication, interpersonal, and collaboration skills to work effectively in cross-functional teams.

Lean/Six Sigma:

• Familiarity with Lean or Six Sigma methodologies for driving continuous improvement.
• Black Belt Certification a plus

CRITICAL SKILLS AND ABILITIES:

• Demonstrated ability for independent work, thought, and analysis.
• Ability to coordinate with internal groups as needed to achieve desired goals and deliverables (Manufacturing, Engineering, Supply chain, QA, QC, R&D, Project Management, etc.).
• Exceptional time management and multi-tasking skills.
• Be able to explain technically complex theories to all levels of the organization effectively.
• Excellent written and verbal communication skills with expertise in good documentation practices.
• Ability to perform statistical analysis of data and interpretation of data.
• Must be capable of detailed record keeping and communicating results to others.
• Experience with pharmaceutical and consumer products related to creams, lotions, liquids, aerosols, nasal sprays, and/or gels is a plus.
• Cleaning validation experience is strongly preferred.
• Process validation experience is strongly preferred.

Education and/or Training

• Proficient with Microsoft Office 365, including Teams, Word, Excel, and PowerPoint.
• Minitab experience is preferred but not required.
• Lean Six Sigma Black Belt Preferred

Immediate need for a talented Quality Control Analyst I (Manufacturing/Quality). This is a 09 Months contract opportunity with long-term potential and is located in Swiftwater, PA , USA(Onsite). Please review the job description below and contact me ASAP if you are interested.

Job Diva ID: 26-07263

Pay Range: $ 20- $30 /hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Perform operations necessary for quality testing and plays a role in implementing new technology within quality control.
• At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods.
• Complete routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation.
• Aid in the development of test methods.
• Conduct data review and preliminary evaluation of results.
• Solve problems using limited predetermined options such as repeating the assay when parameters are not met to determine the cause, etc.
• Provide input to the technical composition of operating documentation.
• Work is closely supervised. Follows standard practices to obtain solutions.
• Contribute to the completion of routine technical tasks.
• Perform operations necessary for quality testing and plays a role in implementing new technology within quality control
• Failure to achieve results can normally be overcome without serious effect on schedules and programs.
• Contacts are primarily with immediate supervisor and other personnel in the section or group.

Key Requirements and Technology Experience:

• Key skills: - Perform routine testing as scheduled to support production, method validation as well as the stability program, and completing the required documentation.
• 0-3 years, entry position with lab experience, agarose gel work, pipetting, LIMS, excel, etc.
• Candidate will need to work well in a faced pace lan with critical thinking and group setting

Our client is a leading Pharmaceuticals industry , and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration

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Job Summary

Provides expert analytical support and data generation for daily chemistry testing activities related to raw materials, in- process and finish products. Perform all testing in a timely and accurate manner in accordance with approved GMP documents (test methods, Specifications, SOPs). Conducts investigations, drafts and executes protocols.

Essential Functions

• Inspects components, products and/or processes to ensure conformance with standards.
• Executes laboratory procedures for sample preparation.
• Independently performs materials analysis of substantial variety & complexity using ARx test methods, compendia methods, specifications.
• Ensure all analytical operations comply with cGMPs & ARx procedures and all laboratory experiments are properly documented in notebook and are in accord with regulatory requirements.
• Conducts method qualification, validation projects work from established documents using basic analytical techniques.
• Participates in the execution of validated test method transfer protocols; drafts & independently executes protocols.
• Recommends / initiates modifications of existing quality or production standards to achieve optimum quality with the equipment’s capability.
• Works independently to accomplish same and assists management in prioritization as needed.
• Conducts investigation of out-of-specification (OOS) or out-of-trend (OOT) results.
• Trains and/or mentors lower level chemists.
• Specializes and acts as lead expert in particular areas of quality control (e.g. methods, method development, statistical process control, etc.).
• Abide by the ARx Laboratory Chemical Hygiene Plan and other safety policies.Maintains a safe and clean work environment, notifying the supervisor of unsafe practices, conditions, or acts; takes on increasing responsibility for surfacing and implementing improved safety practices.
• Responsible for following all applicable waste handling procedures.

Additional Responsibilities

• Completes required paperwork / documentation accurately, neatly and in a timely manner.
• Effectively communicates with other associates, supervisors and various co-workers; relays information to the next shift (as needed); voluntarily assists other associates; communicates effectively to prevent problems from occurring.
• Interacts with and/or participates on cross-functional product development teams.
• Responsible for the proper disposal of hazardous waste into the proper labeled containers and drums.
• Make identifiable and substantial contributions to continuous improvement. Performs all duties consistent with established ARx guideline consistent with all regulatory requirements. Actively complies with and endorses Department and Company objectives.
• Performs other duties and responsibilities as assigned.

Job Specifications

• Requires a Bachelors (or higher) degree in Chemistry or closely related discipline (Analytical Chemistry preferred) plus a minimum of 5 years related experience.
• Knowledgeable and proficient in application of gas chromatography (headspace, high-pressure liquid & gel permeation), UV-VIS-FTIR spectroscopy, TOC, thermal and mechanical analysis (e.g. DMA, DSC, etc.); wet chemistry techniques desired.
• Mastery knowledge and understanding of scientific principles involved in the performance of analytical test methods.
• Ability to troubleshoot and perform basic maintenance to ensure optimum performance of instrumentation.
• Evidence of continuing education such as professional certification (i.e., ASQC) or college level courses related to the position.
• Ability to efficiently utilize time (coordinate several assignments concurrently).
• Ability to read and interpret documents such as test methods and procedure manuals.
• Knowledge of requirements for maintaining proper laboratory otebook documentation.
• Must have above average computer skills and knowledge; specifically in the operational use of analytical equipment have a computer interface.
• Ability to perform basic mathematical & statistical functions; capable of designing and drafting test method transfer protocols as well as executing same and writing related reports.
• Ability to apply basic statistical process control concepts such as control charting.
• Good communication skills (verbal and written).
• Excellent interpersonal skills.
• Requires common physical characteristics and abilities, such as above average agility and dexterity; physical exertion such as long periods of standing, recurring bending, crouching, stooping, stretching, reaching or similar activities should be expected.
• Work environment involves moderate risks or discomforts requiring special safety precautions, will be required to use personal protective equipment.

Job Title : Research Associate ( Associate Researcher )

Location : South San Francisco - 94080

Duration : 06 Months

Job Description :

• Direct, hands-on experience with adeno-associated viral nanoparticles
• Successful experience operating electrophoresis (CE, SDS-PAGE, alkaline gel, etc.), light scattering (DLS, MALS, etc.), UV/Vis spectrophotometry, or other technologies for protein/DNA-based product development.
• Experience operating PCR methods.
• Experience in analytical method development and assay transfer.

Experience operating chromatography methods (HPLC, etc.) and proficient understanding of chromatography software.

Ray Therapeutics mission is to restore vision to people with retinal degenerations. RayTx is using a novel bioengineered optogenetic protein optimized for human vision delivered by AAV to restore visual function in a mutation agnostic approach and without the need for light enhancing eyewear. The company is developing its lead candidate RTx-015 in retinitis pigmentosa, a degenerative retinal disease with significant unmet medical need as well as a pipeline to treat both rare and large market indications.

We are currently seeking an exceptional team member to join our team as a CMC Technical Development Specialist. This role will report to the Senior Director, CMC Analytics, and will have an active role supporting the general CMC department as well as our process, product management, and MSAT teams. The position requires hands on support for AAV analytical development, transfer, and qualification through validation support for our lead candidates from Pre-IND to BLA. The role is based in the Berkeley, CA office with a hybrid work from home/in office requirement and may require travel to our external vendors at in the United States. If the lab is where your curiosity comes alive and breakthroughs spark your excitement, this position may be right for you.

The job duties and responsibilities include but is not limited to the following:

• Collaborate with analytical development and process development teams to develop, qualify and/or validate AAV gene therapy assays.
• Develop analytical methods and support method optimization/characterization.
• Independently execute analytical assays including molecular biology assays, chemical/biochemical assays, and cell-based biological potency assays, for internal CMC commitments, process monitoring, release and stability.
• Develop protocols for analytical transfer, qualification and /or validation studies and execute associated wetlab work.
• Present aasay methodology and principles to external partners and support method transfers.
• Execute routine assays with high presicion and provide data summaries and reports in a timely manner.
• Document all raw data, method plans, and summarize conclusions.
• Author and review Test Methods, Reports, and Protocols.
• Work in the lab independently and in a collaborative environment with minimal guidance.
• Support CMC outside of analytical teams to move programs forward, e.g. shelf-life determination, upstream characterization etc.

Qualifications and Experience:

• BA/BS in Biochemistry, Biology, bioengineering or a related fields and at least 10 years of Biotech/pharmaceutical industry experienced required.
• Experienced in compendial methods, CE-SDS, gel electrophoresis, HPLC, DLS, ddPCR or qPCR, ELISA, and cell based potency assays.
• Hands on experience in AAV gene therapy analytical methods and testing required.
• Experience in precision pipetting and cell culture (handling, aseptic techniques, maintenance), plate-based imaging, ELISAs, luminescence and fluorescence detection techniques.
• Curiosity and good scientific knowledge and acumen.

Compensation Range and Benefits:

• For this role, the anticipated base salary range: $145,000 to $160,000, based on the candidate's professional experience level. The final salary offered for this position may take into account a number of factors including, but not limited to skills, education, and experience.
• Ray Therapeutics also offers annual performance-based bonus, annual equity awards and a comprehensive benefits package.

At Ray Therapeutics, we celebrate diversity and are committed to creating an inclusive environment for all employees; providing an environment of mutual respect where equal employment opportunities are available to all applicants and teammates without regard to race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law.

All employment is decided on the basis of qualifications, merit, and business need.

Search Firm Representatives Please Read Carefully

Ray Therapeutics does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Please, no phone calls or emails.

We are hiring a Junior Laboratory Technician

Biome Makers is a global agriculture technology company helping growers, agribusinesses, and CPG brands improve soil health, sustainability outcomes, and productivity through advanced soil microbiome analytics. With operations in over 56 countries, proprietary soil intelligence, and strong momentum across Latin America, Biome Makers is scaling rapidly to meet growing demand from agriculture and sustainability-driven organizations.

We are seeking a reliable Laboratory Technician to join our team in Davis, CA. This position supports daily laboratory operations and requires strong attention to detail, organization, and the ability to follow established protocols.

Schedule: Swing shift (after training period)

Location: Davis, CA

Responsibilities:

• Assist with processing and handling laboratory samples
• Follow laboratory SOPs and safety procedures
• Maintain a clean and organized workspace
• Support team members to ensure efficient workflow
• Wet lab sample processing, including manual and robot DNA isolation (potentially assist in library preparation and high-throughput sequencing machine operation)
• Accurately create, organize, and maintain laboratory data

Requirements:

• Reliable transportation to commute to the Davis lab
• Ability to work swing shift after the training period
• Strong attention to detail and organization
• Ability to follow written protocols and instructions
• Team-oriented with good communication skills

Qualifications:

• Previous laboratory or sample-handling experience
• Experience working in a fast-paced environment
• Interests in areas related to biology, biotechnology, biochemistry, or equivalent areas
• Experience with some lab techniques, including, but not limited to, pipetting, DNA isolation, PCR, and gel electrophoresis

We offer

• Unlimited Paid Time Off
• Healthcare Plans
• 401(k)
• Professional Development & Education Opportunities
• Cross-department Support

Biome Makers is an ecosystem. Our team specialises in soil science, agriculture, business, genetics, biotechnology, computer science, and much more. And we are located all over the world! We are a team with different nationalities: Spain, USA, Canada, France, Argentina, and many other countries. We are a team, focused on a final goal: To promote sustainable agriculture worldwide!

Afterall, soil is alive. It harbours an abundance of life forms that breathe, grow, work together, respond to their environment, and perform functions on a community level. Like soil, at Biome Makers, we grow, work together, and perform many functions to support each other and the mission towards soil recovery.

As part of our dedication to the diversity of our workforce, Biome Makers is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regards to race, colour, religion, sex, national origin, disability, or veteran status.

We'd love to hear from you!