field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
 Company: Central Admixture Pharmacy Job Posting Location: Irvine, California, United States Functional Area: Quality Working Model: Onsite Days of Work: Wednesday, Tuesday, Thursday, Friday, Monday Shift: 5X8 Relocation Available: No Requisition ID: 4067 
B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®.
Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit <a href="http://www.bbraunusa.com" target="_blank">www.bbraunusa.com</a>
 
Position Summary:
Performs routine functions/analysis as required by the laboratory in compliance with CAPS, and cGMP specifications. The analyst prepares test samples and performs tests according to the standard operating procedures.
Responsibilities: Essential Duties
<ul>
<li>Perform routine analysis of finished product, raw material or environmental samples according to established specifications and procedures using various laboratory apparatus under minimal supervision of senior staff.</li>
<li>Interprets and applies specifications and operating procedures when carrying out both monitoring and testing responsibilities.</li>
<li>Records data in controlled notebooks, controlled data sheets, validated spreadsheets and/or LIMS including all computational tasks and completes analysis report forms. Maintains neat and legible records and promptly and accurately inputs data into LIMS.</li>
<li>May perform routine laboratory maintenance and instrument upkeep as required. Prepares standards or test reagents according to established procedures and specifications.</li>
<li>Follows cGMPs, GLPs, SOPs, USP and FDA guidelines in all appropriate functions and notifies supervisor and/or lead of any observed discrepancies.</li>
<li>Prepare media, reagents, test samples and equipment as required. </li>
<li>Responsible for the general cleanliness and appearance of the lab by keeping laboratory equipment, supplies and environment in good operational condition.</li>
<li>Proficient or become proficient in Environmental Monitoring techniques.</li>
<li>Proficient or become proficient in Sterility Test, Bioburden, and Growth Promotion.</li>
<li>Proficient or become proficient in Bacterial Endotoxins testing using Kinetic-Turbidimetric assay.</li>
<li>Keep inventory of laboratory supplies for routine testing and special projects. </li>
</ul>
Expertise: Knowledge &amp; Skills
<ul>
<li>Understand aseptic technique.</li>
<li>Knowledge of basic chemistry principles in the quality field.</li>
<li>Must have a good understanding of documentation procedures and GMPs for the health care industry.</li>
<li>Good communication and interpersonal skills.</li>
<li>Ability to work independently or in a team. Good technical and troubleshooting skills.</li>
<li>Must be able to use computers, calculators, diagnostic test equipment and precision measuring equipment.</li>
<li>Must have organizational planning skills.</li>
<li>Excellent communication skills.</li>
<li>Must be able to get along with the other people and work as a team member.</li>
<li>Must be able to follow instructions and follow tasks through to completion.</li>
<li>Must be flexible/adaptable</li>
<li>Must be able to schedule tasks and meet deadlines.</li>
<li>Must be able to manage one's time and have a sense of urgency.</li>
</ul>
Required:
<ul>
<li>Bachelors degree and 2-3 years related experience</li>
<li>Basic understanding of Chemistry; basic knowledge in technical area as required by the specific QC lab.</li>
<li>Basic knowledge of good analytical and laboratory techniques, basic knowledge of cGMPS’s, GLP’s, SOP’s, USP, and FDA requirements.</li>
<li>Frequent travel required.</li>
<li>Apply specific skills as required by the technical specialty(s) within the department.</li>
</ul>
Desired:
<ul>
<li>Science degree and direct experience in specific laboratory work.</li>
</ul>
Schedule is (8am-5pm) Monday-Friday. Weekends, holidays, and overtime as needed
Salary range is $21.18-$25.42
While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 20 pounds.
 
The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.
B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at <a href="http://www.bbraunusa.com" target="_blank">www.bbraunusa.com</a>.
Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.
We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here.
 All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. 
Compensation details: 21.18-25.42 Hourly Wage
 
PI71ed32ad7a75-25405-38107869

QC Chemistry Associate II CAPS

<h3>Job Description</h3>
Job DescriptionJob Title: Clinical Lab Analyst Job Description
We are seeking a dedicated Clinical Lab Analyst to join our team responsible for newborn screening testing on blood spot specimens. This role involves using various methods such as immunoassay, enzyme assay, electrophoresis, HPLC, tandem mass spectrometry, and molecular methods to identify infants at risk for inherited conditions.
Responsibilities
<ul>
<li>Perform daily operations and routine maintenance, calibration, and assist in troubleshooting laboratory instruments and equipment.</li>
<li>Document and review newborn screening test data, procedures, and results.</li>
<li>Release data and reports for use by physicians and healthcare professionals.</li>
<li>Maintain standard operating procedures and prepare documentation for test verification or validation studies.</li>
<li>Perform quality control and quality assurance procedures as per established standards.</li>
<li>Recognize and troubleshoot basic laboratory method and performance issues.</li>
<li>Assemble quality control data, recognize problems, document issues, perform root cause analysis, and initiate corrective actions.</li>
</ul>
Essential Skills
<ul>
<li>Strong foundation in Chemistry, Biology, Genetics, HPLC, and mass spectrometry.</li>
<li>Bachelor’s degree in Chemistry, Biochemistry, Biology, Genetics, or a related field, or an equivalent combination of education and experience.</li>
<li>Meet Clinical Laboratory Improvement Amendments (CLIA) qualifications for high complexity testing.</li>
<li>Minimum of 3 months hands-on laboratory experience.</li>
<li>Ability to conduct high complexity testing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Certified Medical Lab Technologist or MLT is a plus.</li>
<li>Six months to one year of newborn screening (NBS) laboratory experience is desirable.</li>
<li>Basic experience with immunoassay, mass spectrometry, and molecular biology techniques.</li>
<li>Completion of college coursework in human genetics.</li>
<li>Experience in Quality Assurance and Quality Control (QA/QC).</li>
</ul>
Work Environment
The lab operates 24/7 to ensure timely testing of newborn blood specimens for potential inherited disorders. The position requires overnight shifts with a schedule of 5 days on, 4 days off, rotating through weekends and holidays. Flexibility is offered for specific weekend off requests. The typical hours are from 9:30 PM to 7:30 AM, with initial training during the day from 8:00 AM to 4:30 PM. The team consists of about 7 members, working in three separate testing areas, rotating nightly. Dress code includes long pants and closed-toed shoes.
Job Type &amp; Location
This is a Contract to Hire position based out of Ankeny, IA.
Pay and Benefits
The pay range for this position is $20.00 - $20.00/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 Ankeny,IA.
Application Deadline
This position is anticipated to close on Dec 15, 2025.
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.

Clinical Lab Analyst

<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 Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.
Responsibilities:
<ul>
<li>Leads the statistical programming activities for projects with lower complexity.</li>
<li>Leads the statistical programming activities for studies.</li>
<li>Develop SAS programs for the creation of ADaM data sets following CDISC standards.</li>
<li>Develop SAS programs for the creation of Tables, Listings and Figures.</li>
<li>Validation of ADaM data sets, Tables, Listings and Figures.</li>
<li>Create specifications for the structure of ADaM data sets for individual studies and integrated data.</li>
<li>Create documentation for regulatory filings including reviewers guides and data definition documents</li>
<li>Leads the development of standard SAS Macros and participates in the development of standard operating procedures.</li>
<li>Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.</li>
</ul>
**This is a US based remote position
Qualifications 
<ul>
<li>MS in Statistics, Computer Science or a related field with 6+ years of relevant experience OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience.</li>
<li>In-depth understanding of SAS programming concepts and techniques related to drug development.</li>
<li>Fundamental understanding of CDISC Standards.</li>
<li>Fundamental understanding of the drug development process, including experience with regulatory filings.</li>
<li>Ability to communicate clearly both oral and written.</li>
<li>Ability to accurately estimate effort required for study related programming activities.</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>
</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>

Senior Statistical Analyst (Remote)

<h3>Job Description</h3>
Job Description
Job Title: Chemical Operator
Job Description
Join our team to support the silicones manufacturing division, bringing your expertise in specialty chemicals to a dynamic and innovative environment.
Responsibilities
<ul>
<li>Support the silicones manufacturing division.</li>
<li>Handle chemicals safely and efficiently.</li>
<li>Conduct troubleshooting and resolve issues within the manufacturing process.</li>
<li>Work in laboratory settings and assist in production tasks.</li>
<li>Ensure compliance with Good Manufacturing Practices (GMP).</li>
</ul>
Essential Skills
<ul>
<li>Experience in chemical handling and manufacturing processes.</li>
<li>Technical experience or skillset.</li>
<li>Familiarity with silicones.</li>
<li>Strong troubleshooting abilities.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Associate's degree in chemistry is a plus but not required.</li>
</ul>
Work Environment
Work in a clean environment that has recently expanded with the acquisition of a new business line. Join a small, cohesive team of 30 individuals. The position offers an opportunity to transition to a permanent role. The current schedule is Monday through Friday, 5:30 am to 2:00 pm, with a shift to 7:00 am to 3:30 pm expected in January.
Job Type &amp; Location
This is a Contract to Hire position based out of Allentown, PA.
Pay and Benefits
The pay range for this position is $20.00 - $24.00/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 Allentown,PA.
Application Deadline
This position is anticipated to close on Dec 11, 2025.
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.

Chemical Operator

<h3>Job Description</h3>
Job Description
Entry Level Undergraduate Chemist needed in Mansfield, TX!
Description:
<ul>
<li>Perform Analytical Testing on R&amp;D Products</li>
<li>Keep Laboratory clean</li>
<li>Follow all regulatory guidelines</li>
</ul>
Pay:&nbsp;18.00-21.00 hourly depending on experience
Instrumentation/Testing:
<ul>
<li>Titrations</li>
<li>Ph</li>
<li>Viscosity testing</li>
<li>GC</li>
</ul>
Schedule:&nbsp;up to 20 hours a week, schedule is flexible
Contract:&nbsp;12-18 months
Education/Experience:
<ul>
<li>College Students looking to get R&amp;D experience working towards Chemistry degrees welcome</li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Mansfield, TX.
Pay and Benefits
The pay range for this position is $18.00 - $24.00/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 Mansfield,TX.
Application Deadline
This position is anticipated to close on Dec 18, 2025.
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.

Undergraduate Chemist

<h3>Job Description</h3>
Job DescriptionDescription:
&nbsp;Description
Bauer Foundation Corp. (BFC) is a Florida corporation and the U.S. subsidiary of the world-wide operating Bauer Group based in Schrobenhausen, Germany. The Bauer Group is a world- renowned foundation contractor, designer, and builder of the world’s finest foundation equipment.
BFC, as part of the Bauer construction division, is a leader in the execution of complex excavation pits, ground improvement, deep foundations, and vertical seals, utilizing the most up to date equipment and installation techniques. Bauer Foundation Corp. provides all types of foundation solutions and services for industrial, commercial, residential, and governmental construction projects. Bauer Foundation Corp. promotes Bauer services and technology throughout the entire United States.
 
BFC is looking for dynamic individuals with experience as a Project Manager - Major Projects: Geotechnical Foundation, in the special foundation industry. If you have a passion for progress, we want to hear from you!
 
Reports to: Operations Manager
Position: Full time
Schedule: up to 6 days per week, 12 hours per day
Requirements:
Job Summary:
The Project Manager - Major Projects: Geotechnical Foundation will organize, manage, and plan complex civil engineering projects. The primary role of the Project Manager is to lead the project delivery team in achieving project goals and objectives through managing resources, identify and mitigating risk, and facilitating project solutions including the project scope, schedule, and budget from pre-construction through construction and project close-out.
 
Supervisory Responsibilities:
· Oversees a team of Engineers, Superintendents, and field personnel to ensure projects are completed on time and to specifications.
· Delegates work and assignments to team members based on expertise, work experience, and time constraints.
 
Duties/Responsibilities:
· Develops project scope, goals, and deliverables to ensure project completion.
· Leads an interdepartmental team to complete an assigned project on time, to specifications, and with accuracy and efficiency.
· Outlines the tasks involved in the project and delegates accordingly.
· Conducts cost analysis, estimating expected costs for the project.
· Prepares and implements a budget based on estimates.
· Conducts risk assessments; reports identified risks to management; provides recommendations for mitigation of risk (including termination of the project if appropriate).
· Addresses questions, concerns, and/or complaints throughout the project.
· Acts as a liaison between company, clients, contractors, and vendors.
· Manages and supervises consultants, contractors, and other subject matter experts in the preparation of planning and construction documents, and in the implementation of the project.
· Communicates effectively with senior management, elected officials and their staff, stakeholders, and other public agencies.
· Ensures compliance with federal, state, local, industry, contractual, and company regulations, standards, specifications, and best practices.
· Performs other related duties as assigned.
 
Requirements:
Required Skills/Abilities:
· Willingness to travel
· Excellent verbal and written communication skills.
· Excellent interpersonal and customer service skills.
· Excellent organizational skills and attention to detail.
· Excellent time management skills with a proven ability to meet deadlines.
· Strong analytical and problem-solving skills.
· Strong supervisory and leadership skills.
· Ability to prioritize tasks and to delegate them when appropriate.
· Thorough understanding of or the ability to quickly learn about the project being developed.
· Must have a thorough understanding of project accounting and demonstrated ability to manage the schedule and budget for multiple projects at the same time.
· Proficient with Microsoft Office Suite or related software.
· Must possess a valid driver’s license and be able to operate a motor vehicle.
 
Education and Experience:
· Bachelor’s degree in Civil Engineering or Construction Management or related field.
· Minimum 8 years’ experience in special foundations/geotechnical foundations
· Experience at least 1 major project over $20M
· PMP, PgMP, CAPM, and/or comparable project management certifications highly desirable.
 
Physical Requirements:
· Prolonged periods sitting at a desk and working on a computer.
· Must be able to lift up to 15 pounds at times.
 
Compensation and benefits:
Competitive salary; commensurate with experience.
 
Benefit packages available – health insurance, life insurance, short-term disability, 401(k) plan with employer match, paid holidays and vacation, paid parental leave, and tuition assistance
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor an employment Visa at this time.
 
BAUER Foundation Corp. is an equal opportunity employer and welcomes applications from all qualified individuals. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
 
 
#LI-DNI &nbsp;&nbsp;
 
PIf5ab8e56a493-25405-37502643

Project Manager - Major Projects: Geotechnical Foundations

<h3>Job Description</h3>
Job Description
Salary, Benefits and Hiring level: $95,488 – $128,689 starting, DOE; (promotion potential to GS-13 step 10, equivalent to $147,615 in 2025) . In addition, the Pacific Council offers generously competitive insurance and retirement benefits.
Organizational Culture
At the Pacific Council, we value respect, integrity, curiosity, and collaboration. Our team is mission-driven and supportive, combining analytical rigor with a genuine commitment to sustainable fisheries and fishing communities. We work together in a transparent, collegial environment that celebrates teamwork, innovation, and diverse perspectives. 
Summary
The Pacific Fishery Management Council (Pacific Council) is one of eight regional councils established under the Magnuson–Stevens Fishery Conservation and Management Act. The Council manages fisheries in federal waters off Washington, Oregon, and California through transparent, science-based decision-making that sustains fish populations and the communities that depend on them. 
Our work covers groundfish, salmon, highly migratory species, and coastal pelagic species, and increasingly addresses issues such as climate change, offshore wind energy, and aquaculture. Council staff support this mission by conducting analyses, coordinating advisory bodies, and ensuring open, inclusive public processes in collaboration with stakeholders as well as state, tribal, and federal partners. 
Position Overview 
The Pacific Council is seeking a Fisheries Scientist (Staff Officer) with a Ph.D. or equivalent experience in fisheries science, marine biology, oceanography, ecology, or a related discipline. 
This position plays a central role in the development of scientific processes, the review of scientific analyses, and providing recommendations and insights for informing Council decisions. The successful candidate will apply strong analytical and problem-solving skills to complex fishery management issues, work collaboratively with diverse experts and stakeholders, and communicate scientific information clearly to policymakers and the public. 
Key Responsibilities 
<ul>
<li>Lead or contribute to scientific analyses, reports, and discussion papers supporting Fishery Management Plans, plan amendments, and regulatory actions.</li>
<li>Conduct or review biological, oceanographic, and ecological analyses relevant to fisheries management decisions.</li>
<li>Integrate information from stock assessments, ecosystem models, and monitoring programs into management advice.</li>
<li>Foster evidence-based decision making via the development and application of peer review processes.</li>
<li>Coordinate with state, tribal, and federal scientists to ensure analytical rigor and consistency across disciplines.</li>
<li>Facilitate and coordinate the meetings and agendas of Council advisory bodies and scientific review panels.</li>
<li>Present complex scientific information clearly and objectively to decision-makers, advisory bodies, and the public.</li>
<li>Maintain neutrality and professionalism in a dynamic, sometimes contentious policy environment.</li>
</ul>
Qualifications 
 Desired Minimums 
<ul>
<li>Ph.D. (or equivalent experience) in fisheries science, marine biology, oceanography, ecology, or a closely related field.</li>
<li>Demonstrated ability to design, conduct, or synthesize scientific analyses related to living marine resources.</li>
<li>Excellent writing and verbal communication skills, including the ability to convey complex concepts to non-technical audiences.</li>
<li>Strong organizational, analytical, and problem-solving skills.</li>
<li>Ability to work collaboratively with individuals from diverse scientific and technical backgrounds.</li>
<li>High professional and ethical standards, with a commitment to objectivity and public service.</li>
</ul>
 Additional Preferred 
<ul>
<li>Familiarity with West Coast fisheries and the Council’s management process.</li>
<li>Experience contributing to peer review, stock assessments, or ecosystem-based management.</li>
<li>Experience leading or supporting multidisciplinary or interagency projects.</li>
<li>Knowledge of federal fisheries policy frameworks and the Magnuson–Stevens Act.</li>
</ul>
Physical Demands
Staff Officers operate at the intersection of science, policy, and public engagement. The position requires occasional travel throughout the West Coast (typically 4–8 days per trip) and occasional international travel. A primarily remote work arrangement is not available. 
Work Environment
The work is primarily in an office environment. Frequent use of a keyboard and other computer hardware is required, often for lengthy periods of time. Use of other typical office equipment may also be required. Extended periods of continuous work beyond eight hours per day is often required. Lifting of light to moderately heavy boxes and equipment and unloading and loading boxes and equipment into and from vehicles, may be required. 
Hiring Requirements
Employment will be contingent upon successful completion of a background check.
 
Applications will be accepted until position is filled.

Fisheries Scientist (Staff Officer)

<h3>Job Description</h3>
Job Description
Geologist 1 or 2
 
Location:
Stillwater Mine - Nye, MT
Schedule:
Rotating Shifts: 5x4x4x5
 
Job Responsibilities and Duties:
<ul>
<li>Assist mining operations by mapping, sampling and guiding underground production headings.</li>
<li>Log and sample drill core.</li>
<li>Collect detailed geotechnical information, both in the core lab and underground mapping.</li>
<li>Utilize computer software, interpret geology and produce representative geologic maps.</li>
<li>Provide technical information on matters of ore width and grade.</li>
<li>Work cooperatively with other technical services personnel.</li>
<li>Will be required to work rotating shifts.</li>
</ul>
Qualifications and Skills:
Required: 
<ul>
<li>Leadership qualities including character, teamwork, communication, business sense and vision</li>
<li>Work performed is both underground and in an office environment. Must be able to perform all physical requirements of the underground work, which includes but is not limited to Ladder climbing and walking on uneven broken rock piles. Lifting and carrying is required (core boxes, sample bags, iron gates, etc.)</li>
<li>Operate surface and underground equipment (trucks, tractors, forklift).</li>
</ul>
Preferred:
<ul>
<li>Previous underground experience</li>
<li>Demonstrate and perform basic geological functions.</li>
<li>Organized and systematic with attention to detail and quality.</li>
<li>Observational skills for mineralogy and structural features.</li>
<li>Understand and interpret plan maps and cross-sections.</li>
</ul>
Education &amp; Experience
<ul>
<li>BS, BA or higher Geoscience degree </li>
<li>OR one to three (1-3) years of relevant experience</li>
</ul>
 
Sibanye-Stillwater is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions at Sibanye-Stillwater are based on business needs, job requirements and individual qualifications, without regard to race, color, creed, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation or preference, marital or family status, disability, genetic information, age, parental status, military service, or other non-merit factor.
 Job Posted by ApplicantPro

Geologist 1 or 2

<h3>Job Description</h3>
Job Description
We are looking for a Senior Chemical Engineer to join a state-of-the-art EV/Hybrid battery recycler. This position will be responsible for the development and implementation of new processes and products as multiple lithium-ion battery recycling facilities are established across the US, as well as the oversight of existing projects. The ideal candidate will have experience with process design, chemical synthesis, and process control. This role will be responsible for developing and implementing a wide range of projects that are critical to the company’s growth.
Primary Responsibilities:
<ul>
<li>Lead the design, installation, and commissioning of chemical processes and equipment.</li>
<li>Provide ongoing process support for plant operation and maintenance.</li>
<li>Support materials and analytical lab development and operation</li>
<li>Own process deliverables for Front End Engineering Design through EPC project phase such as flowsheets, P&amp;IDs, process modeling, control narratives, HAZOPs, etc.</li>
<li>Evaluate and recommend new process technologies to improve recycling and refining, including both technical and economics/financial considerations.</li>
<li>Work with internal and external resources to scale processes from lab to commercial</li>
<li>Support the development of new technology, processes and equipment.</li>
</ul>
Desired Qualifications:
<ul>
<li>5+ years’ experience working in an industrial chemical processing environment</li>
<li>Bachelor’s Degree in Chemical Engineering or related technical discipline</li>
<li>Experience with capital projects</li>
<li>Experience working with EPC’s to execute projects</li>
<li>Experience scaling processes from R&amp;D to Pilot to Commercial scale</li>
<li>Ability to work with and manage external resources to facilitate projects</li>
<li>Experience in hydrometallurgy, mineral extraction and separation</li>
<li>Experience in waste water treatment and pollution control systems a plus</li>
<li>Background in mining &amp; minerals and/or battery recycling processes a plus</li>
<li>Ability to travel domestically and internationally as required</li>
</ul>
Work Environment/Conditions:
Office Location: Work from Home (WFH)
Travel: 20% - 50% to plant site
Plant: Necessary to follow safety protocols and procedures in our and our customer plants. Important to interact with all levels of specialists, team leaders and department managers.

Senior Chemical Process Engineer (FILLED)

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiologist Location: Raritan, NJ Duration: 12 Months+ (Possibilities of Extension) Pay Rate: $30.50/hr. on W2 Job Description: Responsibilities:
<ul>
<li>Perform testing on intermediates, final product and water.</li>
<li> Support all non-routine testing such as validations and any other required studies.</li>
<li> Document results clearly and accurately. Interpret results by comparing against appropriate specifications and/or requirements.</li>
<li>Perform environmental monitoring (viable and non-viable).</li>
<li>Perform bioburden, endotoxin and growth promotion tests</li>
<li>Knowledge on microbiological testing, principles, theories, practices and methodology to align with current procedures and Pharmacopoeias.</li>
<li>Calibrate and maintain laboratory equipment and maintain supplies inventory levels.</li>
<li>Maintains current knowledge of quality guidelines and regulations (GxP).</li>
<li>Participate in laboratory investigations, technology transfer, validations and R&amp;D projects.</li>
</ul>
 Qualifications:
<ul>
<li>B.S. / B.A. degree or equivalent in Biology, Microbiology, Life Science or related field is required.</li>
<li>Minimum 0-2 years of laboratory experience in a regulated environment is required.</li>
<li>Experience with microbiological testing.</li>
<li>Knowledge of quality guidelines, standards and regulations (GxP).</li>
<li>Good verbal and written communication skills required</li>
<li>Experience working in a regulated environment preferred.</li>
</ul>
 #sczr2

13,571 Science Jobs