UNKNOWN

ADAPTED_NOW

HOUR

BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology.

Advance your career with Mindlance! We have been connecting talented IT professionals with world-class companies since 1999. Mindlance is here to help you to find the perfect fit with just the right company. Currently, we are seeking an Operational Analyst for an exciting career growth opportunity. Make your next big career move with the kind of position that will allow you to be genuinely passionate about the work you do! Our recruiters will work closely with you to help you get the edge over the competition. Let Mindlance advocate for you – apply today! “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”  Job Title: Medical Laboratory ScientistJob Category: HealthcareIndustry: Healthcare - Health Services Job Location: West Hills ,CA (Only Local candidates)Zip Code: 91304Pay Range*: $30.00 TO $40.00 Top 3/5 Skills: laboratory's procedures for specimen handling and processing, test analyses  Job Responsibilities <ol><li>Performs repetitive and simple analyses, under the guidance by applying techniques of medical technology.</li><li>Performs simple routines, such as preparing solutions and sterilizing equipment for testing.</li><li>Completes records for tests performed.</li><li>Recognizes equipment malfunctions and notifies supervisor immediately.</li><li>Insures that all quality control criteria are met.</li></ol> Job Requirements 1 year Clinical experience (high complexity testing) preferred. Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology. National and State licensure as required.ASCP EligibleForeign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States educated candidates must provide a detailed original transcript. 1 to 3 years work experienceBS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990. Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States educated candidates must provide a detailed original transcript. A successful candidate should possess or be eligible for national certification as an MT / MLT from a recognized organization (ASCP or AMT). Current state CLS license - Required in the state of CA

Mindlance

Medical Laboratory Scientist

Analysis Skills

Biology

Chemistry

Clinical Laboratory

Code of Federal Regulations

Healthcare

Laboratory

Operational Audit

Quality Control

Sterilization

Test Equipment

cb_wl_jobs_master

FULL_TIME

FEED

OTHER

WHAT AWAITS YOU.The student intern will obtain exposure to the development and maintenance of various automation systems, databases, IT-tools in the Emission lab. Knowledge of various databases and programming languages (Access, SQL, C-#, Javascript, PHP, Perl etc.).

WHAT AWAITS YOU.<ul><li>The student intern will obtain exposure to the development and maintenance of various automation systems, databases, IT-tools in the Emission lab</li><li>Further development of several tools / systems used in emissions testing</li><li>Data collecting, transferring, converting, automated verification, report creation, and analysis</li></ul>WHAT YOU SHOULD BRING.<ul><li>Currently enrolled in a bachelor or master's degree program at an accredited college or university</li><li>Possess a minimum cumulative GPA of 3.0 (not just in major)</li><li>Have completed at least 60 college credits or be at least a rising Junior</li><li>Field of study: Computer Science</li><li>Must attach a copy of college unofficial transcript</li><li>Ability to work full-time (36.25 hours/week)</li><li>Prior BMW Group experience (applicable to international J1 students only)</li><li>Knowledge of various databases and programming languages (Access, SQL, C-#, Javascript, PHP, Perl etc.)</li><li>Excellent time-management skills; ability to prioritize and handle multiple tasks simultaneously</li><li>Ability to manage sensitive and confidential information</li><li>Excellent organizational and planning skills</li><li>Self-motivated, adaptable to a dynamic environment</li><li>Able to work both independently and as part of a team</li><li>Strong analytical capabilities</li></ul>WHAT YOU CAN LOOK FORWARD TO.<ul><li>Medical Insurance</li><li>Paid Time Off in addition to Company paid holidays where eligible</li><li>Hybrid work environment</li><li>Intern Vehicle Lease Program</li></ul>This is a full-time internship position for our Fall Rotation, from September 21, 2026 through March 19, 2027 in Oxnard, CA.The hourly rate for Undergraduate students is $29.90 The hourly rate for Graduate students is $36.80The selected student's academic level will be used to determine the final pay rate. This statement is in accordance with state and local pay disclosure requirements. Even more so than the generous compensation and benefits, the culture and values of Shared Services make it the ultimate working environment. These values are Responsibility, Appreciation, Transparency, Trust, and Openness. We allow these values to guide the way we conduct ourselves and our business.BMW in the United States is an equal opportunity employer. It is the policy of BMW Group in the United States to provide equal employment opportunity (EEO) to all qualified persons regardless of age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

<img alt=" " height="1" src="https://ars2.equest.com/?response_id=c9624dc254fbbc358a9a8e474e198be6&view" width="1"/>

BMW Of North America LLC.

Intern, Computer Science Emissions Lab

equestftpin

Fusion Academy

Math and Science Teacher

Algebra

Anatomy

Astronomy

Calculus

Communication Skills

Corporate Policies

Dental Insurance

Employee Assistance Plan

Geometry

Interpersonal Skills

Life Insurance

Marine Biology

Mathematics

Mentoring

Organizational Skills

Physics

Physiology

Problem Solving Skills

Psychiatry and Mental Health

Record Keeping

State Laws and Regulations

Statistics

Training/Teaching

Trigonometry

Vision Plan

Zoology

[AW]-iCims

Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc. Preferred Qualifications:Bachelors Degree in Engineering, Chemistry, Biochemistry, Pharmaceutics, Materials Science, or related discipline with at least 2+ years of relevant laboratory work experience.

This role in Pivotal Drug Product Technologies will be to provide support of drug product formulation and process development of biologics. The candidate will work closely with a team of engineers and scientists responsible for the technical aspects of the client's drug product commercialization and lifecycle management. Responsibilities:
<ul><li>Participate in the planning, design, execution, and documentation of studies related to drug product formulation and process development in support of commercialization and life cycle management of biologics.</li><li>Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.).</li><li>Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc.</li><li>Data analysis and documentation/review in electronic notebooks.</li><li>Author, review, and data verify technical documents such as protocols, reports, regulatory documents, etc.</li><li>Clearly and consistently communicate data in progress reports and presentations.</li><li>Participate in cross-functional teams in a fast-paced environment to progress product development.</li><li>Adhere to all training, compliance, and safety guidance.</li><li>Support lab operations and inspections as required of all lab-based staff.</li><li>Work primarily onsite with remote work as appropriate to role and tasks.</li><li>Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.).</li><li>Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc.</li><li>Data analysis and documentation/review in electronic notebooks.</li></ul>Basic Qualifications:<ul><li>Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience</li></ul>Preferred Qualifications:<ul><li>Bachelors Degree in Engineering, Chemistry, Biochemistry, Pharmaceutics, Materials Science, or related discipline with at least 2+ years of relevant laboratory work experience. Or Masters degree without any experience.</li><li>Understanding of physical/chemical stability of proteins.</li><li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with procedures and policies.</li><li>Proficient computer skills, including Microsoft Office, PowerPoint, Word, and Excel.</li><li>Self-motivation, adaptability and a positive attitude.</li><li>Critical thinking, problem solving, and independent research skills.</li><li>Good organizational skills with strong attention to detail.</li><li>Excellent oral and written communication skills.</li></ul>

The Steely Group

Scientist Senior Associate

Biochemistry

Biological Processes

Computer Skills

Cross-Functional

Data Analysis

Detail Oriented

Documentation

Drug Products

High Performance Liquid Chromatography (HPLC)

Laboratory Operations

Material Science

Microsoft Excel

Microsoft Office

Microsoft PowerPoint

Microsoft Word

Multitasking

Operational Support

Osmolarity

Performance Analysis

Performance Testing

Pharmaceutics

Physical Chemistry

Pivotal CRM

Presentation/Verbal Skills

Process Development

Product Development

Product Lifecycle Management

Product Support

Product Testing

Product/Service Launch

Progress Reports

Regulatory Reports

Research Skills

Safety Compliance

Team Player

Technical Writing

Work From Home

Writing Skills

HaleyMarketing

401K

Employee Referral Program

Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed.

Our Client, a Medical Research company, is looking for a Medical Laboratory Scientist for their West Hills CA location.   Responsibilities:<ul><li>Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result</li><li>Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens</li><li>Analyze specimens using approved testing procedures (see department SOPs).</li><li>Review and release test results.</li><li>Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective guidelines.</li><li>Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed</li><li>Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.</li><li>Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor.</li><li>Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.</li><li>Follow department's procedure in reporting STATS or Critical results to clients.</li><li>If applicable, answer questions from customers or other lab personnel.</li><li>Maintain complete records of all testing performed on-site.</li><li>Maintain general appearance of the department.</li><li>Make sure reagents/test kits have received dates, expiration dates, and if applicable opened dates.</li><li>Review/train on new procedures.</li><li>Attend monthly department and any additional training/educational meetings.</li><li>Participate in all applicable safety training sessions.</li><li>Know the location and contents of the safety manual.</li><li>Know the location/use of all applicable safety equipment.</li><li>If needed, participate in government or regulatory agency inspections.</li><li>Perform other duties as directed by supervisor.</li></ul>   Requirements:<ul><li>Required Knowledge:</li><li>A solid understanding of basic laboratory testing is required for this position.</li><li>The successful candidate must possess good computer skills and be able to adapt to working in multiple computer systems.</li><li>Must have knowledge of QC and QA as well as knowledge of all areas of the laboratory.</li><li>Education:</li><li>BS in Medical Technology preferred or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493.</li><li>1433 published in March 14, 1990. Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation).</li><li>United States educated candidates must provide a detailed original transcript.</li><li>A successful candidate should possess or be eligible for national certification as an MT / MLT from a recognized organization (ASCP or AMT).</li><li>Work Experience:</li><li>1 year Clinical experience (high complexity testing) preferred.</li><li>Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology.</li><li>National and State licensure as required.</li><li>Special Requirements:</li><li>Must have the ability to establish work priorities and handle several procedures simultaneously.</li><li>Must interact with other departments.</li><li>Contact with clients may be required, good customer service skills are important.</li><li>Must protect patient confidentiality at all times.</li></ul>   Why Should You Apply?<ul><li>Health Benefits</li><li>Referral Program</li><li>Excellent growth and advancement opportunities</li></ul>   ICONMA is an Equal Opportunity Employer. All qualified applicants will receive considerationfor employment without regard to any status protected by applicable law.

ICONMA&nbsp;is a global information consulting management firm providing Professional Staffing Services and Project-Based Solutions for organizations in a broad range of industries.
<ul class="ic_list">
<li>Corporate Headquarters in Troy, Michigan; 20+ locations worldwide.</li>
<li>Certified Woman-Owned Business Enterprise (WBE); certified by Women&rsquo;s Business Enterprise National Council, National Women Business Owners Corporation (NWBOC); and California Public Utilities Commission (CPUC).</li>
<li>Founded in 2000</li>
<li>2000+ Employees</li>
</ul>
The company was founded on the principle that success is derived from delivering high quality service and resources in the most responsive, flexible, and innovative way. ICONMA invests in people and resources with a single goal: To provide our customers with the highest quality service in the most responsive manner. Through its network of offices, ICONMA provides the resources to help clients maintain their competitive advantage.

Iconma

Clinical Medicine

Computer Systems

Corrective Action

Document Management

Establish Priorities

Government Regulations

HIPAA (Health Insurance Portability and Accountability Act)

Health Plan

Identify Issues

Laboratory Techniques

Laboratory Testing

Medical Records

Medical Research

OSHA

Patient Confidentiality

Performance Management

Quality Assurance

Resolve Customer Issues

Safety Equipment

Safety Training

Sample/Specimen Processing

Specimen Analysis

Standard Operating Procedures (SOP)

Technical Leadership

Testing

This group performs assays for small molecule and peptide analysis using LC-MS/MS, ELISA assays using MSD and Spectrmax readers and Immunogenicity assays that are Anti-drug antibody and Neutralizing Antibody assays using MSD, Spectramax, Envision and Vicell type readers. You will work closely with the global Pharmacokinetics and Drug Metabolism  Bioanalytical Sciences (PKDM BA) team, collaborating with colleagues across sites in California and Germany, as well as with software vendors and internal subject matter experts.

We are seeking a highly motivated and detail oriented individual with strong We are seeking a highly motivated and detail oriented individual (e.g. Analyst) with strong expertise in life sciences and Laboratory Information Management Systems (LIMS) to support the modernization of our global Bioanalytical Sciences LIMS/ELN ecosystem. 
This group performs assays for small molecule and peptide analysis using LC-MS/MS, ELISA assays using MSD and Spectrmax readers and Immunogenicity assays that are Anti-drug antibody and Neutralizing Antibody assays using MSD, Spectramax, Envision and Vicell type readers. This contract role offers the opportunity to contribute to a major digital transformation initiative within a world class scientific organization. 
You will work closely with the global Pharmacokinetics and Drug Metabolism  Bioanalytical Sciences (PKDM BA) team, collaborating with colleagues across sites in California and Germany, as well as with software vendors and internal subject matter experts. Your work will directly shape the implementation of our new LabVantage LIMS/ELN platform and help harmonize data and workflows across our global bioanalytical community. Key Responsibilities:<ul><li>Partner with PKDM-BA and Research Informatics SMEs to understand workflows, map business processes, and define system requirements for experimental data and metadata management.</li></ul>Master Data Integration<ul><li>Lead the integration of assay and study metadata, reagent and equipment information, and experimental raw data/results from multiple legacy systems into a unified global LIMS environment.</li><li>Builds inventory from each type of controlled chamber (e.g., refrigerator, freezer, LN2, Ambient, etc.) into an inventory management system.</li></ul>Testing & Compliance<ul><li>Contribute to test planning and execution to ensure the LIMS/ELN solution meets specifications, supports bioanalytical workflows, and complies with company standards and regulatory requirements (including GxP and FDA 21 CFR Part 11).</li></ul>Documentation<ul><li>Create and maintain clear, comprehensive documentation covering requirements, processes, data flows, configurations, and user guides.</li></ul>Training & User Support<ul><li>Assist in developing and delivering training to end users adopting the new LIMS/ELN system.</li></ul>Collaboration & Communication<ul><li>Serve as a liaison between PKDM-BA labs (ATO and ASF), research teams, technology teams, and software vendors.</li><li>Foster strong collaboration across diverse groups including bench scientists, data scientists, software engineers, and data engineers.</li></ul> Qualifications & Skills:<ul><li>Bachelors in life sciences, computer sciences, or a related field</li><li>Minimum 2 years of direct experience working with laboratory software and electronic data processes in the pharma/biotech industry.</li></ul>Regulatory & Quality Knowledge<ul><li>Experience with Laboratory Information Management Systems and Electronica Laboratory Notebooks (e.g., Watson LIMS, StarLIMS, IDBS ELN, Others) would be helpful.</li><li>Experience in GxP environments and understanding of computerized system validation and regulatory frameworks (e.g., FDA 21 CFR Part 58 and 11) is desired.</li></ul>Soft Skills & Ways of Working:<ul><li>Self-driven and consistent demonstration of initiative</li><li>Ability to multi-task activities while maintaining attention to details</li><li>Excellent communication skills</li><li>Strong analytical, organizational, and problem solving abilities.</li><li>Demonstrated success collaborating with cross functional scientific and technical teams.</li><li>Adaptability, energy, and willingness to work across time zones.</li><li>Innovative mindset with a track record of driving ideas to implementation.</li><li>Ability to work effectively in a cross-functional, team matrix environment</li><li>Comfortable interacting with a diverse team with wide-ranging skillsets.</li><li>Knowledge of MS Office tools, such as Word, Excel, PowerPoint, Visio and Outlook</li><li>Knowledge of regulatory (GLP and GCP) and pharmaceutical processes is recommended</li></ul>

Associate Scientist

Antibodies

Assays

Biotech and Pharmaceutical

Business Processes

Computer Science

Customer Acquisition

Data Management

Data Science

Drug Metabolism

Ecosystems

FDA (Food and Drug Administration)

GCP (Good Clinical Practices)

GLP (Good Laboratory Practices)

Informatics

Inventory Management

Laboratory Information Management System (LIMS)

Laboratory Notebook

Laboratory Systems

Liquid Chromatography-Mass Spectrometry (LC-MS)

Metadata

Microsoft Outlook

Microsoft Visio

Pharmacokinetics

Regulations

Regulatory Requirements

Requirements Management

Small Molecules

Software Engineering

System Validation

Technical Research

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Medical Laboratory ScientistMindlance

Intern, Computer Science Emissions LabBMW Of North America LLC.

Math and Science TeacherFusion Academy

Scientist Senior AssociateThe Steely Group

Medical Laboratory ScientistIconma

Associate ScientistThe Steely Group

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