laboratory associate

Yale New Haven Health

<div>Overview: To be part of our organization, every employee should understand and share in the YNHHS Vision, support our Mission, and live our Values. These values - integrity, patient-centered, respect, accountability, and compassion - must guide what we do, as individuals and professionals, every day. 
 
At Bridgeport Hospital, we are committed to providing quality medical care and treatment that is coordinated and centered on the patient's specific needs. We strive to achieve benchmarks as a Patient Centered Medical Home and provide health care in a setting where patients are at the center of their care team. All employees of Bridgeport Hospital are part of the patients care team and contribute to the team approach of promoting access, continuous, comprehensive care and work to provide quality improvement in the care provided to their patients. 
 
Responsible for receiving and processing specimens. Accession specimens in laboratory information system. Handle incoming phone calls and assisting with general lab supply management. Work in conjunction with Medical Laboratory Scientists. 
 
EEO/AA/Disability/Veteran Responsibilities:
<ul><li><div>1. Understands and adheres to Performance Standards, Policies and Behaviors</div></li><li><div>
2. Demonstrate knowledge of department and hospital policies and procedures and their execution</div></li><li><div>
3. Handle telephone inquiries, transfer as needed</div></li><li><div>
4. Receive, accession and process specimens in order to ensure timely reporting of results. Ensures positive patient identification</div></li><li><div>
5. Perform registration in HIS as needed</div></li><li><div>
6. Process reference lab testing as needed</div></li><li><div>
7. Perform testing as needed</div></li><li><div>
8. Independently troubleshoot specimen-related problems</div></li><li><div>
9. Assist with training new employees</div></li><li><div>
10. Maintain hardware and equipment as needed</div></li><li><div>
11. Uses computer programs in laboratory and hospital-based systems to ensure accurate data entry and retrieval</div></li><li><div>
12. Perform other duties as needed</div></li><li><div>
13. Blood bank (if applicable) a.Announce MTP; assist with set up, issue, replacement of blood products. b.Select ABO Rh compatible platelets and FFP, set up on patient, print compatibility tag. c.Issue blood products after thorough review of blood product release form. d.Accept blood products back into inventory or discard returned blood products after determining suitability. e.May irradiate blood products and go to the OR to retrieve blood products</div></li><li><div>
14. Microbiology (if applicable) a.Understands sterile technique and best practices. b.Pre-analytical specimen processing includes tissue grinding, media or lysis inoculation, and manual agar streaking. c.Understands appropriate incubation environments based on specimen type and protocol. d.Operates pre-analytical instrumentation including laboratory automation systems, centrifuges, biosafety cabinets, and environmental incubation systems. e.Proficient in applicable staining techniques including Gram stain preparation.</div></li><li><div>
15. Pathology (if applicable) a.Assist with FNAs and frozen sections when applicable. Assist with office duties as needed. b.Sign off on the hazardous waste manifest when needed. c.Package and ship all AP specimens. d.Registration of all AP samples. e.Pre-analytical specimen processing includes aliquoting of specimens for additional testing f.Slide/block cover slipping, distribution, and/or filing. g.Disposal of pathology specimens h.Maintaining cytology/histology department daily and monthly maintenance charts f.Responsible for cleaning and maintenance in accordance with universal precautions g.Under direct supervision of the pathologist assistant or pathologist, preserving samples for testing h.Assist with H&amp;E slide preparation, including loading and unloading of slides into/from auto-stainer, and operating cover slipper. i.Transcribe pathology gross description and/or diagnosis.</div></li></ul>
Qualifications:

EDUCATION 
HS Diploma or equivalency exam 
EXPERIENCE 
Experience not required 
SPECIAL SKILLS 
Excellent communication skills and customer service skills. Basic computer skills Consistently interacts with coworkers and customers in a positive manner. Cooperatively and proactively assists in other areas as needed in a teamwork-oriented environment. Maintains procedure knowledge and implements all new and revised procedures in real-time. Maintains all Quality Control and Quality Assurance standards at all times. EEO/AA/Disability/Veteran.</div>

Medical Laboratory Associate I

Medical University of South Carolina

<div></div><div><div><ul><li>R-0000057931
</li> </ul></div><div></div><div><ul><li>Charleston, South Carolina
</li> </ul></div><div></div><div><ul><li>Laboratory
</li> </ul></div><div></div><div><ul><li>Clinical &amp; Research Support Services
</li> </ul></div><div></div><div><ul><li>Full Time</li></ul></div></div>
 <div>Job Description Summary
Performs moderate and high complexity testing under the general supervision of the Laboratory Manager. This position performs routine laboratory testing, quality control testing, general and instrument maintenance, calling of critical and questionable results to appropriate providers, and resulting of test using laboratory information systems. Additionally, this role performs general troubleshooting of instrumentation, communicating technical information to appropriate persons.
Entity
Medical University Hospital Authority (MUHA)
Worker Type
Employee
Worker Sub-Type
Regular
Cost Center
CC000653 CHS - Reference &amp; Specimen Referral (Main)
Pay Rate Type
Hourly
Pay Grade
Health-21
Scheduled Weekly Hours
40
Work Shift
Job Description
Performs moderate and high complexity testing under the general supervision of the Laboratory Manager. This position performs routine laboratory testing, quality control testing, general and instrument maintenance, calling of critical and questionable results to appropriate providers, and resulting of test using laboratory information systems. Additionally, this role performs general troubleshooting of instrumentation, communicating technical information to appropriate persons.
Additional Job Description
Education: Associate's or Bachelor's degree in chemical or biological sciences including 24 semester hours of science courses that include 6 semester hours of chemistry, 6 semester hours of biology, and 12 semester hours of any combination of chemical or biological sciences. Experience: None.
If you like working with energetic enthusiastic individuals, you will enjoy your career with us!
The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need.
Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees</div>

Laboratory Associate I (Reference & Specimen Referral)

Guardant Health

<div>Company Description
Guardant Health is a leading precision oncology company focused on guarding wellness and giving every person more time free from cancer. Founded in 2012, Guardant&reg; is transforming patient care and accelerating new cancer therapies by providing critical insights into what drives disease through its advanced blood and tissue tests, real-world data and AI analytics. Guardant tests help improve outcomes across all stages of care, including screening to find cancer early, monitoring for recurrence in early-stage cancer, and treatment selection for patients with advanced cancer. For more information, visit guardanthealth.com and follow the company on LinkedIn , X (Twitter) and Facebook .
Position Summary:
The Clinical Laboratory Associate (CLA) II is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions.
The nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment.
Essential Duties and Responsibilities:
In accordance with California Business and Professions Code BPC &sect; 1269, the following activities may be performed under the supervision of the laboratory director or appropriately licensed personnel:
<ul><li>Sample collection or receipt, sample preparation, labeling, handling, preservation or fixation, assay processing or preparation, and/or transportation and storage of specimens;
</li></ul><ul><li>Assist the CLSs in a licensed clinical laboratory in performing sample processing;
</li></ul><ul><li>Assist the CLSs during automated methods of patient testing;
</li></ul><ul><li>Perform routine equipment maintenance according to the laboratory&rsquo;s standard operating
</li></ul>procedures;
<ul><li>Create sample batches, print labels and label tubes and plates;
</li></ul><ul><li>Assist licensed testing personnel in troubleshooting activities;
</li></ul><ul><li>Prepare and store reagents for sample processing and sample archiving;
</li></ul><ul><li>Order and stock laboratory supplies;
</li></ul><ul><li>Print and file of laboratory records;
</li></ul><ul><li>In the case of qualitative and semi-quantitative tests, the unlicensed personnel may add the test reagent to the specimen or vice versa, but the results must be read by the laboratory director or appropriately licensed personnel.
</li></ul><ul><li>Check, monitor and resolve routine cold storage temperature and laboratory temperature and initiate a service request as necessary;
</li></ul><ul><li>Perform general laboratory tasks include cleaning of racks, laboratory equipment and benches;
</li></ul><ul><li>Document all corrective actions taken when test systems deviate from the laboratory&rsquo;s established
</li></ul>performance specifications;
<ul><li>Assist with internal audits and inspection preparation,
</li></ul><ul><li>Organize the maintain schedule of the laboratory and equipment;
</li></ul><ul><li>Ensure calibration of laboratory equipment is scheduled and performed on time;
</li></ul><ul><li>Ensure laboratory equipment is properly labeled;
</li></ul><ul><li>Write and revise standard operating procedures under supervisor instruction, as needed;
</li></ul><ul><li>Identify process improvement opportunities and report to laboratory management;
</li></ul><ul><li>Perform other duties as assigned; and
</li></ul><ul><li>Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer.
</li></ul>Qualifications:
<ul><li>Minimum of Associate degree or equivalent required;
</li></ul><ul><li>Bachelor&rsquo;s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field
</li></ul>preferred;
<ul><li>At least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred;
</li></ul><ul><li>Strong computing skills;
</li></ul><ul><li>Proficiently executed Good documentation practices;
</li></ul><ul><li>Advanced knowledge of reagent stability and storage, quality control policies, and factors that influence test results;
</li></ul><ul><li>Demonstrates strong practical reasoning and sound judgment;
</li></ul><ul><li>Skilled in making informed and effective decisions;
</li></ul><ul><li>Exhibits exceptional attention to detail and a strong commitment to precision in all tasks;
</li></ul><ul><li>Strong communicator with ability to maintain open communication with internal employees, managers;
</li></ul><ul><li>Proficient in giving and receiving constructive feedback, fostering open communication and continuous improvement;
</li></ul><ul><li>Capable of independently executing tasks with minimal direction, while maintaining a collaborative approach that avoids complete isolation;
</li></ul><ul><li>Ability to divide workload evenly among CLAs in accordance with operational needs;
</li></ul><ul><li>Ability to prioritize tasks with a high emphasis on quality and time;
</li></ul><ul><li>Proactively initiate and drive projects, consistently contributing innovative solutions and seizing opportunities for process improvement; and
</li></ul><ul><li>Ability to participate in projects, update others on progress and complete assignments as expected.
</li></ul>Work Environment:
<ul><li>Hours and days may vary depending on operational needs;
</li></ul><ul><li>Standing or sitting for long periods of time may be necessary;
</li></ul><ul><li>May be exposed to hazardous materials, blood specimens and instruments with moving parts, heating or freezing elements, and high-speed centrifugation;
</li></ul><ul><li>Repetitive manual pipetting may be necessary; and
</li></ul><ul><li>Some lifting (up to 25 pounds) may be necessary. 
</li></ul> 
Hybrid Work Model: This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies. Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays, Tuesdays, and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant, our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients.
The annualized base salary ranges for the primary location and any additional locations are listed below. This range does not include benefits or, if applicable, bonus, commission, or equity. Each candidate&rsquo;s compensation offer will be based on multiple factors including, but not limited to, geography, experience, education, job-related skills, job duties, and business need. Primary Location: Redwood City, CA Primary Location Base Pay Range: $40 - $55 Other US Location(s) Base Pay Range: $34 - $47 If the role is performed in Colorado, the pay range for this job is: $36 - $50 
<div> 
Employee may be required to lift routine office supplies and use office equipment. Majority of the work is performed in a desk/office environment; however, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment. Ability to sit for extended periods of time.
Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities, long-term conditions, mental health conditions, or sincerely held religious beliefs. If you need support, please reach out to Peopleteam@guardanthealth.com
A background screening including criminal history is required for this role. GH will consider qualified applicants with criminal arrest or conviction histories in a manner consistent with applicable law including but not limited to the LA County Fair Chance Policies and the Fair Chance Act (Gov. Code Section 12952).
Guardant Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
All your information will be kept confidential according to EEO guidelines.
 
 
To learn more about the information collected when you apply for a position at Guardant Health, Inc. and how it is used, please review our Privacy Notice for Job Applicants .
Please visit our career page at: http://www.guardanthealth.com/jobs/</div></div>

Clinical Laboratory Associate II - Thur-Sun 9pm-7:30am + 30% shift diff

Altasciences

<div>Your New Company!
 
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
As a Research Associate (RA) you will work independently in the day to day laboratory operation collecting and reviewing data for the Laboratory Sciences department. Responsibilities include supporting the activities of various service groups including ligand binding, flow cytometry, molecular biology and LCMS/MS, as needed. The RA participates in the creation of study worksheets, SOP&rsquo;s and other controlled documents as assigned, and provides support for general laboratory equipment and maintenance as assigned.
What You'll Do Here
<ul><li>Laboratory Maintenance (cleaning, ordering supplies, equipment PM, etc.).
</li><li>Collect and organize laboratory data according to the appropriate oversight document (ex: Protocol, Analytical Study Plan, SOPs).
</li><li>Create and/or revise SOP and SOP forms.
</li><li>Work independently in study-related tasks.
</li><li>Perform quality control review of laboratory and study records.
</li><li>Assist with method development activities.
</li></ul>What You'll Need to Succeed
<ul><li>BS (preferred) or AS degree in scientific discipline or equivalent education and laboratory experience
</li><li>1-3 years of relevant LC-MS laboratory experience
</li><li>Basic to Intermediate computer skills.
</li></ul>What We Offer
The pay range estimated for this position is $24.00 - $27.00 per hour. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.
Benefits
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences&rsquo; Benefits Package Includes:
<ul><li>Health/Dental/Vision Insurance Plans
</li><li>401(k)/RRSP with Employer Match
</li><li>Paid Vacation and Holidays
</li><li>Paid Sick and Bereavement Leave
</li><li>Employee Assistance &amp; Telehealth Programs
</li><li>Telework when applicable.
</li></ul>Altasciences&rsquo; Incentive Programs Include:
<ul><li>Training &amp; Development Programs
</li><li>Employee Referral Bonus Program
</li></ul>#LI-ES1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!</div>

Research Associate II, LC-MS

Robert Walters

We are seeking a Biorepository Associate to join IQVIA Laboratories at Valencia, CA.Shift Time: Monday- Friday 8am-430pmIn this role, you will assist with routine activities related to biological specimen storage, preparing and completing outbound shipments. Ensuring accuracy and compliance throughout the specimen storage and shipment workflows.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.What you&rsquo;ll be doing:<ul><li>Ensure competency within the role and full understanding of processes.</li><li>Daily use and input of specimen data into Laboratory Information System,</li><li>Complete specimen storage and shipment coordination to third party labs</li><li>Assist, as needed, with packaging of outbound shipments following the established QC process</li><li>Maintain specimen integrity, inventory and audit history within LIMS</li><li>Respond to email correspondences and support LRMS ticket requests; raise IT tickets for system issues.</li><li>Upload shipment paperwork in the LIMS and archive physical paperwork monthly</li><li>Assist with equipment maintenance, supply inventory, and workstation cleanup while following safety procedures.</li></ul>What We Are Looking For:<ul><li>High School Diploma or equivalent required.</li><li>Basic computer skills and ability to maintain effective reporting procedures.</li><li>Strong organizational and communication skills with ability to work collaboratively.</li><li>Other Equivalent combination of education, training, and experience may be accepted in lieu of degree.</li></ul>The Knowledge, Skills and Abilities needed for this role:<ul><li>Familiarity with specimen handling, QC processes, and data entry/LIMS systems.</li><li>Ability to troubleshoot IT/system issues and follow SOPs accurately.</li><li>Strong attention to detail and time management in a fast-paced environment.</li><li>Effective interpersonal skills and ability to maintain workflow under deadlines.</li></ul>What we offer you:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&rsquo; physical, mental, emotional, financial, and social well-being so they can thrive at home and at work, at any stage of their well-being journey.Pay: $19.00 - $21.00 per hourBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee discount</li><li>Flexible schedule</li><li>Health insurance</li><li>Vision insurance</li></ul>Work Location: In person

Biorepository Associate (Entry Level)

Kaiser Permanente

<div><div>Job Summary:</div>
 
Under the direct and constant supervision of a licensed person as authorized under California B&amp;PC 1269, Laboratory Assistants II performs more complex procedures defined for laboratory assistants in the RRL, such as loading samples and assisting in the operation of laboratory instruments, monitoring overdue reports and resolving problem specimens.<div> 

Essential Responsibilities:</div> 
 
<ul> 
<li>Performs all the duties and responsibilities of an RRL Lab Assistant I</li> 
<li>Prepares specimen for testing and/or send outs, including batching, creating wordlists/worksheet, pipetting, separating (serum/plasma/fluids) samples, removing fibrins/clots, centrifuging, aliquotting and preparing dilutions with the use of a calibrated pre-set pipettor</li> 
<li>Takes inventory, orders, receives, unpacks, distributes, and stocks supplies as needed</li> 
<li>Loads/unloads samples onto instruments, assists in the operation and monitoring of automated or semi-automated instruments, and notifies a CLS for any instrument alerts</li> 
<li>Assists in the performance of quality control procedures and may transcribe QC results that have been previously recorded automatically by a testing instrument</li> 
<li>Performs/assists in preventive maintenance and basic troubleshooting function, pre-analytical, analytical, and post-analytical laboratory equipment/instruments, and alerts a CLS for any suspicious outlier</li> 
<li>Reads and transcribes digital temperature, humidity, weights, etc. and alerts a CLS for any suspicious outlier</li> 
<li>Monitors overdue/pending/incomplete test reports, researches, resolves and follows through on problem specimens or patient data problems per policies and procedures</li> 
<li>Completes and maintains laboratory worksheets, preventive maintenance logs, specimen logs, labels, and other records, as required</li> 
<li>Performs specimen preservation, fixation, harvesting, plating, and staining</li> 
<li>Performs numerical matching or arrangement of pre-labeled metaphases, as applicable</li> 
Prepares cyto prep slides and/or cell blocks from specimens, as applicable 
<li>
</li> 
<li>Trains and orients new employees as necessary</li> 
<li>Performs other related duties (limited to non-licensed duties only) as necessary</li> 
<li>Detailed/specific position description of job tasks/functions may be developed by each of the laboratory departments</li> 
<li><ul>
<li>The above statements are intended to describe the general nature and the level of work being performed by the individuals assigned to this position and as such are not intended to be construed as an exhaustive list of responsibilities, duties and skills required of personnel so classified.</li></ul></li><li><div> 
Basic Qualifications:</div></li><li><div>
Experience</div></li><li><ul><li>
One year experience within the last 3 years as a Laboratory Assistant in a high volume laboratory required.</li></ul></li><li><div>
Education</div></li><li><ul><li>
High School graduate/GED required.</li></ul></li><li><div>
License, Certification, Registration</div></li><li><ul><li>
N/A</li></ul></li><li><div>
Additional Requirements:</div></li><li><ul><li>
Must be able to lift at least 20 lbs.</li></ul></li><li><div>
Notes:</div></li><li><ul><li>
This is an on call position, days and hours may vary.</li><li>
Duties includes client services tasks and may be required to work in Ancillary departments based on operational needs.</li></ul></li> 
PrimaryLocation : California,North Hollywood,Sherman Way Central Lab W 
HoursPerWeek : 1 
Shift : Variable 
Workdays : Mon, Tue, Wed, Thu, Fri, Sat, Sun 
WorkingHoursStart : 12:00 AM 
WorkingHoursEnd : 11:59 PM 
Job Schedule : Call-in/On-Call 
Job Type : Standard 
Employee Status : Regular 
Employee Group/Union Affiliation : B01|SEIU|Local 399 
Job Level : Entry Level 
Job Category : Laboratory 
Department : Sherman Way Central Lab-Bldg A - Pathology-General - 0806 
Travel : No 
Kaiser Permanente is an equal opportunity employer committed to fair, respectful, and inclusive workplaces. Applicants will be considered for employment without regard to race, religion, sex, age, national origin, disability, veteran status, or any other protected characteristic or status. 
 
For jobs where work will be performed in unincorporated LA County, the employer provides the following statement in accordance with the Los Angeles County Fair Chance Ordinance. Criminal history may have a direct, adverse, and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: 
 
<li>Consistently supports compliance and the Principles of Responsibility (Kaiser Permanente's Code of Conduct) by maintaining the privacy and confidentiality of information, protecting the assets of the organization, acting with ethics and integrity, reporting non-compliance, and adhering to applicable federal, state, and local laws and regulations, accreditation, and licensure requirements (where applicable), and Kaiser Permanente's policies and procedures.</li> 
<li>Models and reinforces ethical behavior in self and others in accordance with the Principles of Responsibility, adheres to organizational policies and guidelines; supports compliance initiatives; maintains confidences; admits mistakes; conducts business with honesty, shows consistency in words and actions; follows through on commitments.</li> 
<li>Job duties with at least occasional or possible access to: (1) patients, the general public, or other employees; (2) confidential protected health information and other confidential KP information (including employee, proprietary, financial or trade secret information); (3) KP property and assets, for example, electronic assets, medical instruments, or devices; (4) controlled substances regulated by federal law or potentially subject to diversion.</li></ul></div>

Regional Reference Laboratories Laboratory Assistant II, North Hollywood (On-call, Variable shift)

ClinLab Solutions Group

<div>
 
 Job Title: Research Associate
 
 
 
 Work Location:
 
 San Francisco County, California
 
 
 3-6 Month contract
 
 
 Summary:
 
 
 Seeking a contract Research Associate to support laboratory operations and research activities in a cell biology or molecular biology setting. The ideal candidate will have foundational laboratory skills and a strong commitment to maintaining high-quality standards in a BSL-2 environment.
 
 
 Responsibilities:
 
 <ul>
 <li>
 Perform routine mammalian cell culture tasks, including thawing, passaging, and maintenance of cell lines.
 </li>
 <li>
 Conduct basic cell line quality control procedures to ensure integrity and reliability of experimental materials.
 </li>
 <li>
 Follow established standard operating procedures (SOPs) and maintain aseptic technique at all times.
 </li>
 <li>
 Document experimental procedures and results accurately in laboratory records and databases.
 </li>
 <li>
 Assist with the preparation and organization of laboratory reagents and supplies.
 </li>
 <li>
 Collaborate with team members to support ongoing research projects and meet project timelines.
 </li>
 <li>
 Maintain a clean and safe laboratory environment in compliance with BSL-2 safety protocols.
 </li>
 <li>
 Participate in troubleshooting and optimization of laboratory protocols as needed.
 </li>
 </ul>
 
 Qualifications:
 
 <ul>
 <li>
 BS or MS in Cell Biology, Molecular Biology, or a related field.
 </li>
 <li>
 0&ndash;2 years of hands-on laboratory experience (industry experience preferred but not required).
 </li>
 <li>
 Demonstrated experience with mammalian cell culture, including routine maintenance and quality control.
 </li>
 <li>
 Ability to follow SOPs and maintain aseptic technique in a BSL-2 laboratory environment.
 </li>
 <li>
 Strong organizational and documentation skills.
 </li>
 <li>
 Excellent communication and teamwork abilities.
 </li>
 <li>
 Detail-oriented with a commitment to laboratory safety and quality standards.
 </li>
 </ul>
 
 
</div>

Research Assistant

Search 9352+ Laboratory associate jobs near you this April. New roles added regularly across leading industries. Apply today.