field_job_employment_type

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job_organization_name

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<h3>Job Description</h3>
Job DescriptionResearch Associate I – Trait Discovery Location: San Diego, CA | Full-time | Onsite Summary A biotechnology startup focused on sustainable aviation fuels is seeking a Research Associate I to support trait discovery and strain assessment efforts. This is an entry-level, hands-on laboratory role ideal for candidates with experience in cell biology, microbiology, or molecular biology who are excited to work in a fast-paced startup environment. Responsibilities
<ul>
<li>Perform aseptic, laboratory-scale cultivation of algae</li>
<li>Prepare cultivation media and vessels, including autoclaving</li>
<li>Collect routine culture measurements using spectroscopy, microscopy, and flow cytometry</li>
<li>Prepare samples and support algae strain performance and physiological assessments</li>
<li>Calibrate laboratory instruments and cultivation systems</li>
<li>Document experimental procedures, analyze data, and summarize results</li>
<li>Perform basic molecular biology techniques including PCR and gel electrophoresis</li>
<li>Work fully onsite in laboratory and greenhouse environments</li>
</ul>
 Qualifications
<ul>
<li>Bachelor’s degree in cell biology, molecular biology, biochemistry, microbiology, or related field</li>
<li>1–2 years of academic or industry laboratory experience</li>
<li>Strong aseptic technique and familiarity with biosafety cabinets</li>
<li>Ability to follow written and verbal protocols</li>
<li>Strong communication skills for reporting results and progress</li>
<li>Proficiency with Microsoft Office</li>
<li>Ability to lift up to 25 pounds</li>
</ul>
 Why Join
<ul>
<li>Opportunity to join an early-stage biotech startup</li>
<li>Hands-on experience in trait discovery and strain development</li>
<li>Collaborative lab and greenhouse environment</li>
<li>Mission-driven work supporting sustainability</li>
</ul>

Research Associate I Trait Discovery

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The&nbsp;Associate Director, Statistics - Oncology&nbsp;provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients.
This role will work a hybrid schedule in one of the AbbVie locations:
<ul>
<li>Lake County, IL</li>
<li>South San Francisco, CA</li>
</ul>
Responsibilities
<ul>
<li>Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission.</li>
<li>Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans.</li>
<li>Represent function/department on project team(s) to provide statistical input to compound/drug development and drive alignment with functional management. Partner with other functions (Clinical, Regulatory, Patient Safety, and GMA, etc.) to create development strategies for assigned projects.</li>
<li>Demonstrate extensive understanding of statistical concepts and methodology. Propose novel statistical methodological approaches to design of scientific studies. Provide sufficient detail to allow programming implementation. Ensure that all statistical analyses specified in scientific protocols and analysis plans are conducted appropriately.</li>
<li>Train and mentor staff on statistical methodology and operations. May supervise contract statisticians or junior statisticians. Gain expertise in innovative statistical methods. Assist functional leaders in recruiting qualified personnel and arranging training opportunities for professional development of staff.</li>
<li>Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.</li>
<li>Act as the liaison for statistical issues on AbbVie collaborative studies with CROs, academic institutions, government agencies, steering and/or data monitoring committees, joint ventures or licensing collaborators. Build external scientific connections which foster professional development and promote the reputation of the Statistics Department.</li>
<li>Ensure that all applicable regulatory requirements for work processes are met. Critically review regulatory submission documents. Participate in discussions with regulatory agencies as needed. Validate external statistical software to ensure compliance with SOPs and regulatory requirements</li>
<li>Significant Work Activities:&nbsp;Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</li>
</ul>
Qualifications 
<ul>
<li>MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics, Biostatistics, or a highly related field.</li>
<li>High degree of technical competence and excellent communication skills, both oral and written</li>
<li>Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others</li>
<li>Able to manage project timeline and quality of deliverables</li>
<li>Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo</li>
<li>Have strong leadership skills and experience in working/managing cross-cultural or oversea teams</li>
<li>Pharmaceutical or related industry knowledge required, including experience and understanding of drug development and life-cycle management in the regulated environment.</li>
<li>(SSG) Experience leading safety-related projects (eg, ISS, benefit-risk assessment, signal detection)</li>
<li>(GMA Stat) Competence in experimental and RWE study design, descriptive statistics, inferential statistics, statistical modeling, and statistical programming. Knowledge of methodologies for confounding control and bias minimization in observational studies preferred.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Director, Statistics

<h3>Job Description</h3>
Job Description
Join PDS Tech Commercial as a Load Research Technician in Tempe, AZ!
Summary:
Are you detail-oriented and tech-savvy? PDS Tech Commercial is seeking a Load Research Technician to support a leading organization.&nbsp;In this role, you’ll play a critical part in ensuring accurate and efficient data processing that impacts customer service, load research, and billing operations.
Key Responsibilities:
<ul>
<li>Interrogate interval data meters and process data using validation, editing, and estimation (VEE) techniques.</li>
<li>Store processed data in databases for use in customer data requests, load research studies, and special contract billing.</li>
<li>Produce data in tabular and graphical formats for publication.</li>
<li>Map new residential, commercial, and industrial loads for new customer data.</li>
<li>Develop monthly performance indicators, including variance calculations for sales and revenue quantities.</li>
<li>Complete special projects as assigned by supervisors or planning analysts.</li>
</ul>
Required Qualifications:
<ul>
<li>High school diploma required; some college coursework preferred (Associate’s degree or less).</li>
<li>Strong attention to detail and accuracy.</li>
<li>Ability to learn new software quickly.</li>
<li>Proficiency with Microsoft Office Suite.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Prior experience in data entry or technical data processing.</li>
<li>Familiarity with interval data or utility industry processes.</li>
</ul>
Why Join Us?
At PDS Tech Commercial, we believe in empowering our team members with opportunities to grow and succeed. You’ll work in a collaborative environment with a company that values innovation, precision, and professional development. We offer:
<ul>
<li>Competitive pay 27.00 /hr&nbsp;and benefits.</li>
<li>Opportunities for skill development and career advancement.</li>
<li>A supportive team culture focused on excellence and integrity.</li>
</ul>
Ready to Make an Impact?
Apply today and take the next step in your career with PDS Tech Commercial!
 Pay Details: 27.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.pdstech.com/candidate-privacy" target="_blank">https://www.pdstech.com/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Load Research Technician

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Discovery Chemistry Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to projects focused on identifying and optimizing novel peptide ligands for siRNA delivery to various tissues. This internship offers hands-on experience across the full discovery workflow, including synthesis, screening, analysis, and optimization of peptide candidates. The intern will work closely with experienced scientists and gain exposure to high-throughput screening strategies and medicinal chemistry principles within a collaborative research environment.
This is an 11-week Summer Internship Program paying $26.00 per hour for students pursuing a Masters and $27.00 per hour for students pursuing a PhD. This role requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Synthesize linear and cyclic peptides using solid-phase peptide synthesis (SPPS), both manually and on automated synthesizers.</li>
<li>Support high-throughput screening (HTS) efforts, including synthesis of combinatorial peptide libraries and screening for activity.</li>
<li>Purify and analyze peptides using chromatography (HPLC) and mass spectrometry (LC-MS).</li>
<li>Apply medicinal chemistry principles to support lead optimization, including improving peptide stability and affinity.</li>
<li>Maintain accurate experimental records using an electronic laboratory notebook (ELN).</li>
<li>Follow all EHS and laboratory safety protocols, proactively identifying chemical and physical hazards.</li>
<li>Participate in team meetings, sharing results and contributing to scientific discussions.</li>
<li>Collaborate with team members across the discovery organization.</li>
</ul>
Requirements
<ul>
<li>Currently enrolled student in a Master's or Doctorate degree program in Chemistry or Biochemistry or a related field.</li>
<li>Familiarity with analytical chemistry techniques, including HPLC and LC-MS.</li>
<li>Strong problem-solving skills and ability to quickly learn new procedures and techniques.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
<li>Willingness and ability to spend 75% of the workday in a laboratory environment and 25% at a desk.</li>
</ul>
Preferred
<ul>
<li>Experience with peptide design, synthesis, or screening.</li>
<li>Interest in drug discovery, delivery technologies, or medicinal chemistry.</li>
<li>Strong curiosity, creativity, and enthusiasm for experimental science.</li>
<li>Prior experience working in a collaborative research environment.</li>
</ul>
California pay range $10,560—$11,440 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Discovery Chemistry (Peptides)

<h3>Job Description</h3>
Job Description
Actively Screening for Chemist to join global animal health company in Lithia Springs, GA! 
Position Overview: 
The candidate will be responsible for supporting analytical research and transfer activities for drug substances and drug products with a focus on small molecule substrates. The candidate will be responsible for supporting multiple projects and will work in close collaboration with partner groups across the organization. 
Job Responsibilities:
<ul>
<li>Conduct laboratory experiments supporting analytical method transfer.</li>
<li>Perform processes and operate equipment required for large-scale monoclonal antibody (mAb) production.</li>
<li>Utilize various modern analytical tools and technologies (e.g., U/HPLC, GC, MS, Karl Fischer, dissolution, particle size, etc.).</li>
<li>Maintain equipment and problem solve as needed.</li>
<li>Understand, follow, and accurately complete process documentation to maintain a high level of product quality.</li>
<li>Understand and follow safety policies.</li>
<li>Work collaboratively with members of other departments.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS in Biological sciences or a related field</li>
<li>Previous experience in large-scale production or laboratory scale</li>
<li>3-5+ years of relevant experience</li>
<li>In depth understanding and knowledge of applications of various modern analytical tools and technologies, including modern techniques for separation science (e.g., HPLC, NMR, GC, LC/MS, Dissolution etc.)</li>
<li>Experience with automation and ELISA. </li>
<li>Good understanding of quality requirements in analytical support for clinical supplies and manufacturing transfer work.</li>
<li>Good understanding of chemistry and formulation processes</li>
<li>Excellent documentation skills for recording research work and ability to summarize results and data.</li>
<li>Practical analytical experience working with active pharmaceutical ingredients and related dosage forms.</li>
<li>A track record of analytical problem solving and method development is desired.</li>
<li>Basic understanding of the pharmaceutical development process.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Lithia Springs, GA.
Pay and Benefits
The pay range for this position is $33.00 - $55.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Lithia Springs,GA.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Chemist

<h3>Job Description</h3>
Job Description
Job Summary: We are seeking a detail-oriented and safety-conscious Chemical Plant Operator to join our team. The ideal candidate will be responsible for operating and maintaining the equipment used in our chemical production processes. This role is crucial to ensuring the safe, efficient, and high-quality production of chemical products that meet our company's standards and customer requirements.
Key Responsibilities:
<ul>
<li>Operate and Monitor Equipment: Manage and monitor chemical processing equipment to ensure optimal performance and product quality.</li>
<li>Control Chemical Processes: Adjust machine settings, valves, and controls to regulate pressure, temperature, flow rates, and chemical reactions as per established procedures.</li>
<li>Mix and Process Chemicals: Measure, mix, and process chemicals following detailed formulas and protocols to produce desired products.</li>
<li>Perform Routine Inspections: Conduct regular inspections of equipment and systems to detect and troubleshoot operational issues, ensuring that machinery operates safely and efficiently.</li>
<li>Maintain Production Logs: Accurately record production data, including quantities produced, machine performance, and any anomalies encountered during the process.</li>
<li>Adhere to Safety Protocols: Follow all safety guidelines and procedures to maintain a safe working environment, including the proper handling and storage of hazardous materials.</li>
<li>Collaborate with Maintenance Teams: Work closely with maintenance personnel to perform preventive maintenance and address any mechanical issues that may arise.</li>
<li>Ensure Compliance: Ensure that all processes comply with environmental regulations and company policies regarding chemical manufacturing.</li>
<li>Quality Control: Perform quality checks to ensure that products meet specifications and identify areas for process improvement.</li>
</ul>
Qualifications:
<ul>
<li>High school diploma or equivalent; a degree or certification in chemical engineering, process technology, or a related field is a plus.</li>
<li>Proven experience as a Chemical Plant Operator or in a similar role in a chemical manufacturing environment.</li>
<li>Strong understanding of chemical processes and equipment operation.</li>
<li>Knowledge of safety procedures and regulations related to chemical manufacturing.</li>
<li>Ability to work in a fast-paced environment and make quick, effective decisions.</li>
<li>Excellent attention to detail and strong problem-solving skills.</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to stand, walk, and move around the plant for extended periods.</li>
<li>Capable of lifting and moving heavy materials and equipment as necessary.</li>
<li>Comfortable working in environments with exposure to chemicals, heat, and noise.</li>
</ul>
Want to be considered for this opening immediately? Call our office at 713-680-9898! Candidates already registered with us, please send an updated resume to <a href="mailto:interviews@lpcpersonnel.com" target="_blank">interviews@lpcpersonnel.com</a> and reference the job title. If you are not already registered, please apply by clicking the "Apply Now" button.

Chemical Operator

<h3>Job Description</h3>
Job Description
Greetings from IT Engagements
&nbsp;
&nbsp; IT Engagements&nbsp;is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.
&nbsp;
Role: Scientist II – Cell and Molecular Biology (Contract W2 Role)
Location: Pleasanton, CA
&nbsp;
Position Overview:
<ul>
<li>Client is seeking a qualified and highly motivated individual for the role of Scientist II in BioSpecimen Acquisition and Management to support Culture Collection and Panel Production activities.</li>
<li>The BioSpecimen Acquisition and Management function at Client Diagnostic Solutions is a centralized service organization that supports the acquisition, characterization, and management of biological materials, as well as the development of select panels for clinical research and the cultivation and characterization of various microorganisms and mammalian cell lines.</li>
<li>The Scientist II position facilitates daily operations associated with fulfilling service requests for Culture Collection and panel activities, while providing best-in-class, practical biological solutions to internal customers to drive innovation at Client Diagnostic Solutions. &nbsp;</li>
</ul>
Specific Responsibilities
<ul>
<li>Under minimal supervision, execute assigned project activities using established procedures and applying scientific knowledge and accumulated experience to complete projects involving manipulation of human cell lines, microorganisms, and/or other biological materials.</li>
<li>Perform standard recombinant DNA techniques, including cloning, restriction digestion, ligation, and bacterial transformation.</li>
<li>&nbsp;Perform routine and specialized cell culture procedures using adherent and suspension immortalized cell lines.</li>
<li>Analyze plasmid DNA and RNA transcripts for purity, concentration, and quality.</li>
<li>Make recommendations to resolve problems encountered during experimental procedures.</li>
<li>Receive general direction; plan and execute own work. May act as a project lead.</li>
<li>Maintain an effective scientific knowledge base and apply broad scientific concepts to resolve problems of moderate scope and complexity.</li>
<li>Analyze alternative approaches to solve problems or develop new perspectives on existing solutions.</li>
<li>Ensure accuracy, quality, and timeliness of all assigned projects, tasks, and related activities.</li>
<li>Summarize experimental results and review conclusions with supervisor or project lead. Communicate results through written reports and presentations as needed.</li>
<li>Maintain accurate electronic records using validated systems, ensuring data is recorded in a timely, accurate, and consistent manner.</li>
<li>Perform work in accordance with established internal safety guidelines and procedures, and as specified by applicable external regulatory agencies (e.g., OSHA).</li>
<li>Participate in routine laboratory maintenance, laboratory safety activities, ISO, and QSR implementation. &nbsp;</li>
</ul>
Position Requirements &amp; Experience
<ul>
<li>Bachelor’s degree in Molecular Biology, Cellular Biology, Microbiology, or a related field with 5+ years of relevant experience, or Master’s degree in Molecular Biology, Cellular Biology, Microbiology, or a related field with 5+ years of relevant experience.</li>
<li>Experience with aseptic techniques and bacterial and/or mammalian cell culture.</li>
<li>Ability to manually manipulate samples (including plating, pipetting, labeling, and vialing) on a routine basis, with or without reasonable accommodation.</li>
<li>Experience with cloning techniques, including plasmid design and preparation, restriction enzyme digestion, ligation, bacterial transformation, and downstream processing.</li>
<li>Experience performing nucleic acid extractions (DNA/RNA), quantification, amplification, and characterization using tools such as Qubit, Nanodrop, gel electrophoresis, and PCR instruments.</li>
<li>Ability to work in a laboratory environment on a daily basis under BSL-2 laboratory conditions, with or without reasonable accommodation, including work with infectious or engineered biological materials and a variety of sample types (e.g., blood, serum, urine, stool).</li>
<li>Ability to work effectively in a dynamic, collaborative team environment with multiple stakeholders across the organization.</li>
<li>Understanding of good laboratory practices, data integrity, and documentation standards.</li>
<li>Ability to plan work independently and determine next steps within the context of an overall project.</li>
<li>Proficiency with Microsoft Office and Google applications.</li>
<li>Experience with LIMS software, electronic lab notebooks (eLN), and JMP is preferred.</li>
<li>Client-facing experience is a plus. &nbsp;</li>
</ul>
Personal Characteristics &amp; Cultural Fit
<ul>
<li>Highly organized and detail oriented.</li>
<li>Flexible and adaptable to shifting priorities, unique biological material handling requirements, and evolving organizational needs.</li>
<li>Strong written and verbal communication skills; ability to follow written and verbal instructions.</li>
<li>Passionate about biorepository management and working within a global, matrixed organization.</li>
<li>Demonstrated aptitude for cross-functional collaboration.</li>
<li>Results- and goals-oriented mindset. &nbsp;</li>
</ul>
Interview process: 1. phone (30mins) 2. In-person (1. 45 min with RRRP 2. 45 with RRP) Onsite position
&nbsp;
Thank You
<a href="mailto:vinaya@itengagements.com" target="_blank">vinaya@itengagements.com</a>

Bio Scientist II - Cell and Molecular Biology (Contract W2 Role)

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Associate Manufacturing Scientist I (third shift) will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations.
3rd shift work hours are 10 pm – 8:30 am and includes a 15% shift differential.
Responsibilities
<ul>
<li>Follow batch records, SOPs, and work instructions to detail</li>
<li>Document all operations in batch records and notebooks</li>
<li>Comply with GMP protocols</li>
<li>Assist other chemists within the CMC group during synthesis and chromatography of oligonucleotides including:
<ul>
<li>Reagent solution preparation</li>
<li>Column Packing</li>
<li>Mobile phase preparation</li>
<li>Fraction collection</li>
</ul>
</li>
<li>Operate TFF to desalt purified RNA solutions</li>
<li>Operate a lyophilizer and package solid drug substance</li>
<li>Execute processes as part of a team to ensure production timelines are kept and quality product is produced</li>
<li>Maintain a clean work space</li>
<li>Maintain safety by wearing required personal protective equipment</li>
</ul>
Requirements
<ul>
<li>BS or MS in chemistry, biochemistry, engineering, or related scientific field</li>
<li>Entry level to 3 years experience in a similar position</li>
<li>Good verbal and written communication skills</li>
<li>Ability to work in a team environment</li>
<li>Ability to pay attention to detail</li>
</ul>
Preferred
<ul>
<li>Experience working in a GMP setting with controlled documentation</li>
</ul>
Wisconsin pay range $70,000—$83,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Associate Manufacturing Scientist II (3rd Shift)

<h3>Job Description</h3>
Job Description
The European Institute of Policy Research and Human Rights is a prestigious institution that offers cutting-edge online programs designed to educate future leaders in policy research, human rights, and related disciplines. Our mission is to deliver world-class skill enhancing programs to candidates globally, equipping them with the knowledge and skills to influence policy and drive positive change in their communities.
Applications are invited for Senior Research Fellowship (for candidates enrolled / passed Masters / Doctoral in any discipline).
Program Overview
<ul>
<li>Learn and follow our methodology to draft research paper in one of the researchable areas. (No prior experience in research paper writing is required, Candidates will receive comprehensive mentorship and guidance throughout the process / tenure.) Program Certification fee of Eur498 is applicable. As a Certified Senior Research Fellow is a significant achievement a valuable addition to your CV that can impress future employers, universities, or scholarship committees. It helps set you apart with a unique edge.</li>
</ul>
What You'll Do:
<ul>
<li>Learn and Lead Groundbreaking Research: Know how to Tackle important policy issues and devise groundbreaking solutions.</li>
<li>Collaborate with Experts</li>
<li>Strategic Analysis: Utilize data to create influential policy recommendations.</li>
<li>Publish &amp; Impact: Contribute your findings to esteemed academic and policy publications.</li>
</ul>
Candidate will be choosing one of the researchable research areas for their research.
Research papers produced by candidates will be published with a Digital Object Identifier (DOI), ensuring the work is uniquely identifiable and accessible through our open-source publication portal.
Eligibility Criteria / Who Can Apply:
<ul>
<li>Open to candidates who are currently enrolled in or have completed a Masters or Doctoral program. Candidates enrolled or passed Bachelor degree but not enrolled in Masters are not eligible to apply.</li>
<li>Applicants from all academic disciplines are welcome, including but not limited to Law, Human Rights, International Relations, Management, Political Science, Social Sciences, Engineering, Medicine, Business, and related fields.</li>
<li>Working / non working professionals in any sector are encouraged to apply. This includes lecturers, professors, advocates, medical professionals, journalists, engineers, historians, managers, environmental scientists, government officials, social activists, and those involved in politics or any relevant field.</li>
<li>Candidates must demonstrate the ability to work independently in a virtual environment and effectively meet deadlines.</li>
</ul>
How to Apply
Interested candidates should submit their updated CV.
Shortlisted candidates will be contacted with complete details.
Note: Applicants are advised to submit only one application. Multiple applications for different positions or locations may result in the cancellation of all submitted applications.

(SRFP)Sr. Fellow- Research (Code:EU7250)

<h3>Job Description</h3>
Job Description
About the Role:
The Clinical Lab Supervisor plays a critical role in ensuring the accuracy and efficiency of laboratory operations for andrology and endocrinology testing in the CCRM Fertility lab. This position is responsible for overseeing laboratory staff, managing workflow, and ensuring compliance with regulatory standards. The supervisor will also be instrumental in implementing quality control measures and optimizing laboratory processes to enhance service delivery. By fostering a collaborative environment, the supervisor will support the professional development of team members while maintaining high standards of patient care. Ultimately, this role contributes to the overall mission of providing reliable and timely laboratory results that inform insurance decisions and improve client outcomes.
Minimum Qualifications:
<ul>
<li>Bachelor's degree in Clinical Laboratory Science, Chemistry, Biology or a related field (qualified for high complexity testing)</li>
<li>A minimum of 3 years of experience in a clinical laboratory setting, with at least 1 year in a supervisory role</li>
<li>Familiarity with andrology (semen analysis, IUI prep) and endocrinology (hormone testing)</li>
</ul>
Preferred Qualifications:
<ul>
<li>MLS or MLT</li>
<li>TS licensure</li>
</ul>
Responsibilities:
<ul>
<li>Oversee daily operations of the clinical laboratory, ensuring compliance with all regulatory and safety standards.</li>
<li>Hands on lab work as required
<ul>
<li>manual semen analysis (count, motility, morphology</li>
<li>IUI preparation</li>
<li>sperm cryo</li>
<li>hormone testing (Cobas analyzer)</li>
</ul>
</li>
<li>Manage and mentor laboratory staff, providing training and support to enhance their skills and performance.</li>
<li>Implement and monitor quality control procedures to ensure the accuracy and reliability of laboratory results.</li>
<li>Coordinate with other departments to streamline processes and improve overall laboratory efficiency.</li>
<li>Prepare and maintain documentation related to laboratory operations, including reports and compliance records.</li>
<li>weekend rotation</li>
</ul>
Skills:
The required skills for this position include strong leadership abilities, which are essential for managing a diverse team and fostering a positive work environment. Attention to detail is crucial in ensuring compliance with regulatory standards and maintaining the accuracy of laboratory results. Effective communication skills are necessary for collaborating with other departments and conveying important information to staff and stakeholders. Problem-solving skills will be utilized daily to address operational challenges and implement improvements in laboratory processes. Additionally, proficiency in laboratory information systems will aid in managing data and enhancing workflow efficiency.

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