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About You: You are an experienced Bachelor's or Master's level cell biologist and/or molecular biologist who enjoys collaborating across disciplines in order to solve complex problems. Experience with molecular cloning and transfection including designing DNA constructs, producing plasmids, and delivering to cells using transfection or electroporation.

YEAR

Molecular Matrix is pioneering innovative medical devices for tissue regeneration applications in multiple organ systems. We are seeking highly motivated, self-sufficient candidates who are interested in growing with our company in a fast-paced and exciting environment. About the role: Reporting to the Research & Development Lead, the Research Associate will use cell culture and molecular biology techniques to support the development of tissue engineering medical devices. The Research Associate works primarily in R&D to support advancements in bioprocessing, scaffolding, and large-scale tissue formation. About You: You are an experienced Bachelor's or Master's level cell biologist and/or molecular biologist who enjoys collaborating across disciplines in order to solve complex problems. You are good at communicating ideas, data, and bottle-necks to technical and non-technical audiences alike. You have knowledge or interest in tissue engineering and medical devices and are excited to bring your experience and enthusiasm to this nascent industry. You thrive in fast-paced environments. Responsibilities: <ul><li>Perform molecular cloning: PCR, restriction digest, DNA assembly</li><li>Perform gene expression assays using RT-PCR</li><li>Develop new cell lines by modifying growth factor signaling</li><li>Develop assays to screen, isolate, and validate cell lines</li><li>	Reagent preparation, aliquoting, inventory management</li><li>Collaborate with the preclinical team to support preclinical trials of novel technologies</li><li>	Contribute to various group efforts in research and development</li><li>Identify, suggest, purchase and operate supplies and equipment through established processes to support this role</li><li>Mentor junior members with technical skills, and experimental design</li></ul>Qualifications & Skills: <ul><li>Experienced in adherent mammalian cell culture</li><li>	Experience with molecular cloning and transfection including designing DNA constructs, producing plasmids, and delivering to cells using transfection or electroporation</li><li>Cell line development: able to screen, isolate, and validate targeted cell populations</li><li>Knowledge of basic cell biology with an ability to develop methods to manipulate</li></ul>We offer great benefits (health, vision, and dental insurance and a retirement plan) and challenging, impactful work. Join our growing team, work with smart and dedicated people, and help develop cutting-edge technologies that will positively impact the world. Job Type: Full-time Salary: From $64,480.00 per year Benefits: <ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Retirement plan</li><li>Vision insurance</li></ul>Schedule: <ul><li>8 hour shift</li><li>Weekend availability</li></ul>Ability to commute/relocate: <ul><li>Rancho Cordova, CA 95670: Reliably commute or planning to relocate before starting work (Required)</li></ul>Education: <ul><li>Bachelor's (Required)</li></ul>Experience: <ul><li>Mammalian cell culture: 2 years (Required)</li></ul>Work Location: In person

MOLECULAR MATRIX INC

Research Associate Cell Culture & Molecular Biology

Assay Development

Assays

Cell Biology

Cell Cultures

Cloning

Communication Skills

Experiment Design

Inventory Management

Medical Equipment

Mentoring

Molecular Biology

Polymerase Chain Reaction (PCR)

Pre-Clinical Trials

Problem Solving Skills

Process Development

Purchasing/Procurement

Research & Development (R&D)

Retirement Plan

Reverse Transcriptase PCR (RT-PCR)

Scaffolding

Tissue Engineering

ADAPTED_NOW

Total compensation considers multiple factors, including, but not limited to a candidate’s experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. + 2 years experience in retrospective data collection, patient interviewing, and interacting with a variety of patient populations in a variety of patient settings.

HOUR

We are so glad you are interested in joining Sutter Health! Organization: SHSO-Sutter Health System Office-Valley Position Overview: Collects, compiles and presents clinical data for assigned area, ensuring accuracy, timeliness and accessibility of information. Maintains clinical and/or research databases for identified programs/ specialty clinics. Collects data used for multiple purposes, which may include process improvement activities and clinical effectiveness/research studies. May prepare information for patient/family education and/ or participate in community outreach activities. Job Description : EDUCATION _Equivalent experience will be accepted in lieu of the required degree or diploma._ + Bachelor's: Science or health-related field or equivalent education/experience PREFERRED EXPERIENCE AS TYPICALLY ACQUIRED IN: + 2 years experience conducting clinical research. + 2 years experience in retrospective data collection, patient interviewing, and interacting with a variety of patient populations in a variety of patient settings. + 2 years experience ensuring compliance with research regulations. SKILLS AND KNOWLEDGE + Knowledge of Federal and State regulations and International Guidelines related to Good Clinical Practices in clinical research. + Ability to interpret a variety of data and instructions, furnished in written, oral, diagram, or schedule form. + Possess written and verbal communications skills to communicate with fellow team members, supervisors, patients, and other hospital personnel. + Well-developed time management and organizational skills, including the ability to prioritize assignments and work within standardized policies and procedures to achieve objectives and meet deadlines. + Knowledge of computer applications, such as Microsoft Office Suite (Word, Excel, Access, and PowerPoint). + Ability to prioritize assignments and work within standardized policies and procedures to achieve objectives and meet deadlines. Job Shift: Days Schedule: Full Time Shift Hours: 8 Days of the Week: Friday, Monday, Thursday, Tuesday, Wednesday Weekend Requirements: None Benefits: Yes Unions: No Position Status: Non-Exempt Weekly Hours: 40 Employee Status: Regular Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans. Pay Range is $37.68 to $56.52 / hour _The compensation range may vary based on the geographic location where the position is filled. Total compensation considers multiple factors, including, but not limited to a candidate’s experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. Base pay is only one component of Sutter Health’s comprehensive total rewards program. Eligible positions also include a comprehensive benefits package._

Masco Corporation (NYSE:MAS) is one of the world’s largest manufacturers of brand-name products for the home improvement and building product markets. Our home products include faucets, kitchen and bath cabinets, paints and stains, bath and shower units, spas, showering and plumbing specialties, windows, decorative hardware and decorative lighting products. We have market leading brands in architectural coatings (Behr®, KILZ®), windows (Milgard®, Griffin®, Premier®), plumbing (Delta®, Hansgrohe®, Axor®, Brizo®, Bristan®, BrassCraft®, Cobra®), cabinetry (KraftMaid®, Merillat®, Quality®, Cardell®), bathing (Delta®, Peerless®, Mirolin®, Huppe®), home hardware and other specialty products (Hot Springs Spas®, Brainerd®, Liberty Hardware®) and decorative lighting (Kichler®). For more information on the Masco family of brands, visit www.masco.com.
 
As a member of the Masco team, you will be joining a company that is a global leader in the design, manufacture and distribution of innovative, branded home improvement and building products. Our culture, which is strengthened by our commitment to diversity and inclusion, will challenge you to reach your full potential within a collaborative, forward-thinking environment. And, our many business units, expansive product lines and well-known leading brands offer you a variety of opportunities to pursue your career goals. We invite you to search our many career opportunities and learn more about Masco Corporation, an Equal Opportunity Employer.

Masco Corporation

Clinical Research Coordinator II, Advanced Diagnostics

Clinical Data

Clinical Data Collection

Clinical Information

Clinical Research

Data Collection

Establish Priorities

Federal Laws and Regulations

GCP (Good Clinical Practices)

Health Science

Hospital

Maintain Compliance

Medical Records

Microsoft Access Database

Microsoft Excel

Microsoft Office

Microsoft PowerPoint

Microsoft Word

Organizational Skills

Patient Education

Presentation/Verbal Skills

Process Improvement

Regulatory Compliance

Research Skills

State Laws and Regulations

Time Management

Writing Skills

Experienced RequiredBachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience . Work ConditionsMany roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings.

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.With our purified, high-precision investigational cell therapies we hope to not only replace patients' bloodand immune systems with healthy ones, but also restore their lives. We have built a state-of-the-art, 100,000-square-foot manufacturing facility in Sacramento, CA (7910 Metro Air Pkwy) to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies. The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. Physical Demands <ul><li>Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment. </li><li>Most roles must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed. </li></ul>Work Conditions<ul><li>Many roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings. Also, may be required to work scheduled overtime, weekends, or holidays based on business needs. </li></ul>Responsibilities Quality System Management: <ul><li>Oversee the management of quality systems including deviations, change controls, CAPAs, and document control. </li><li>Ensure that all deviations are investigated thoroughly and timely, identifying root causes and implementing effective corrective actions. </li><li>Review and approve change controls to ensure compliance with regulatory requirements and internal procedures. </li><li>Maintain and improve CAPA processes to ensure effective resolution of quality issues. </li></ul>Batch Disposition: <ul><li>Evaluate batch records and associated documentation to make informed batch release decisions. </li><li>Collaborate with manufacturing and quality control teams to ensure all products meet regulatory and quality standards before release. </li><li>Monitor and document any quality issues related to batch production and implement corrective measures as necessary. </li></ul>Document Management: <ul><li>Maintain the document management system to ensure all quality-related documents are accurate, current, and compliant with regulatory standards. </li><li>Conduct regular reviews of quality documentation to ensure adherence to established protocols and procedures. </li></ul>Regulatory Compliance: <ul><li>Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality assurance. </li><li>Assist in preparing for internal and external audits, ensuring that all quality systems and documentation are audit-ready. </li></ul>Training and Support: <ul><li>Provide training and guidance to staff on quality systems, processes, and compliance requirements. </li><li>Serve as a point of contact for quality-related inquiries and issues, fostering a culture of quality within the organization. </li></ul>Continuous Improvement: <ul><li>Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes. </li><li>Identify areas for improvement within quality operations and suggest appropriate solutions. </li><li>Track completion of quality records and maintain metrics. </li><li>Perform other duties as requested by supervisor/manager to support Quality </li><li>Work collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products. </li></ul>General Requirements<ul><li>Communicate effectively with team members and contribute to a positive and collaborative work environment </li><li>Actively participate in group and project teamwork; project and process improvements </li><li>Strong organizational skills and the ability to manage multiple tasks concurrently </li><li>Willingness to learn and adapt in a fast-paced, dynamic environment </li><li>Adhere to cGMP policies and procedures, including documentation activities </li><li>Able to wear appropriate personal protective equipment </li><li>Willingness to work overtime as required </li></ul>Experienced Required<ul><li>Bachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience </li><li>Understanding of FDA regulations, GMP compliance, and quality system processes </li><li>Experience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferred </li><li>Able to meet project and testing timelines </li><li>Detail-oriented with a commitment to data integrity and accuracy, and an ability to identify problems with data management </li><li>Able to work collaboratively to respond to changing priorities and challenges </li><li>Ability to work both independently and collaboratively with a multi-disciplinary team in a fast-paced and regulated environment </li><li>Prior experience doing internal audits and document control management </li></ul> $75,000 - $90,000 a year The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations. Who we are We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them. We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility. We innovate on a path that hasn't been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren't afraid to ask "why not" and challenge the status quo. We maintain a start-up culture of camaraderie and leadership by example, regardless of title. We're proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers. Notice to staffing firms Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Weekend Research Jobs in West Sacramento, CA

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Weekend Research Jobs in West Sacramento, CA

Research Associate Cell Culture & Molecular Biology MOLECULAR MATRIX INC

Clinical Research Coordinator II, Advanced Diagnostics Masco Corporation

Specialist, Quality Assurance - Weekend Shift (Friday-Monday) Orca Bio

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