location_0_addressRegionName

location_0_addressCountryName

ONSITE

UNKNOWN

jobPosting hiringOrganization as json hashed.

ADAPTED_NOW

Scientist

Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated scientist for our formulation development laboratory. Experience in process development and technology transfer into cGMP manufacturing, familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred.

KBSkills

ACTIVE

Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated scientist for our formulation development laboratory. The focus of this position is solid oral dosage forms but other dosage form experience, especially parenteral, will be considered as this is an area of growth for the company. Must be capable of working independently from concept and product prototype through transfer to cGMP Manufacturing.  The ideal candidate will possess strong problem solving abilities, excellent customer service mindset, and a positive can do attitude. A college degree is required with at least 3 years’ experience in formulation development. Experience in process development and technology transfer into cGMP manufacturing, familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred. QCL offers competitive salaries commensurate with experience and an excellent benefits package as well as great potential for career advancement and leadership in a rapidly growing company. recblid 83xnztog6fovpz11tludbptyfhhmqb <img src="https://b.recruitology.com/beacon/view/83xnztog6fovpz11tludbptyfhhmqb/"/>

Quality Chemical Laboratories

Formulations Scientist

Analysis Skills

Current Good Manufacturing Practice (cGMP)

Customer Support/Service

Dosage Forms

Drug Manufacturing

Laboratory

Manufacturing

Problem Solving Skills

Process Development

Prototyping

Regulatory Requirements

Testing

monster

OFFSITE

Physician

As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. M3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs).

M3 Wake Research Seeks Clinical Research Physician/Principal Investigator--Part-Time HoursCompany DescriptionM3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.Due to our continued growth, we are hiring a Clinical Research Physician/ Principal Investigator at Wake Research, an M3 company. This position is 100% on-site and is located in Dallas, TX. It is a contract position, part-time hours. Typical working hours will be 8 hours per week. Preferred specialty: Gastroenterology/ Hepatology . Job DescriptionAs a Clinical Research Physician, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients, health authorities, colleagues, and biopharmaceutical companies. Your role will be focused clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborate with the team with all aspects of clinical and scientific input and safety evaluation.Essential Duties and Responsibilities:<ul><li>Provide clinical expertise into the conduct of clinical trials</li><li>Build positive relationships and networks with internal and external medical professional and local opinion leaders</li><li>Work closely with colleagues in other functions including, Regulatory Affairs, Clinical Operations and Patient Engagement</li><li>Lead and provide an oversight to a team of researchers and clinical staff involved in conduct of clinical trials</li><li>Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines</li><li>Evaluate study volunteer’s eligibility for clinical trials</li><li>Perform physical exams and assessments as required per research protocols</li><li>Complete all industry-required training</li><li>Assess study patient health through interviews and physical examinations</li><li>Communicate information to patients regarding diagnosis and treatment goals</li><li>Review all diagnostic reports and provide clinical direction to the study team</li></ul>QualificationsRequirements:<ul><li>10 years' post training experience as a physician in gastroenterology</li><li>Currently licensed to practice medicine in the state of hire with no history of license suspension or debarment</li><li>Advanced knowledge of treatment and drug interactions</li><li>Ability to build rapport with patients and biopharmaceutical sponsors</li><li>Strong attention to detail</li><li>Strong leadership qualities</li><li>Provide clinical oversite to study team</li><li>Clinical research experience</li></ul>Additional InformationAbout M3USAM3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems. Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements. Embrace the chance to drive change with M3 USA.

CS Wake Research

M3 Wake Research Seeks Clinical Research Physician/Principal Investigator--Part-Time Hours

Practice Match

Investigator

There are 26 research sites throughout the USA, offering a dedicated and wholly-owned site network with a centralized, single point of contact for site identification, study implementation and trial management, recruitment and retention, advertising, contracting, and quality control. M3 Wake Research has a 39 year history of building meaningful relationships with sponsors and CROs, and most importantly, providing excellent care for its patients.

Are you a BC Family Medicine/Internal Medicine or Emergency Medicine Physician with experience as a Principle Investigator looking to work part-time as a Sub-Investigator? M3 Wake Research has an opportunity for you in Fayetteville, North Carolina. Investigator role overview:<ul><li>Part Time (roughly 10 hours per week)</li><li>On site presence required weekly</li><li>Must be board certified </li><li>Must have experience with Sponsor Initiated Trials for Pharmaceutical studies</li></ul>M3 Wake Research has a 39 year history of building meaningful relationships with sponsors and CROs, and most importantly, providing excellent care for its patients. There are 26 research sites throughout the USA, offering a dedicated and wholly-owned site network with a centralized, single point of contact for site identification, study implementation and trial management, recruitment and retention, advertising, contracting, and quality control.

Family Medicine Sub-Investigator Fayetteville, NC at M3 Wake Research

Physician - Family Practice

Your role will be focused clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborate with the team with all aspects of clinical and scientific input and safety evaluation. Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research.

As a Clinical Research Physician, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients, health authorities, colleagues, and biopharmaceutical companies. Your role will be focused clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborate with the team with all aspects of clinical and scientific input and safety evaluation.Essential Duties and Responsibilities:<ul><li>Provide clinical expertise into the conduct of clinical trials</li><li>Build positive relationships and networks with internal and external medical professional and local opinion leaders</li><li>Work closely with colleagues in other functions including, Regulatory Affairs, Clinical Operations and Patient Engagement</li><li>Lead and provide an oversight to a team of researchers and clinical staff involved in conduct of clinical trials</li><li>Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines</li><li>Evaluate study volunteers eligibility for clinical trials</li><li>Perform physical exams and assessments as required per research protocols</li><li>Complete all industry-required training</li><li>Assess study patient health through interviews and physical examinations</li><li>Communicate information to patients regarding diagnosis and treatment goals</li><li>Review all diagnostic reports and provide clinical direction to the study team</li></ul>QualificationsRequirements:<ul><li>10 years' post training experience as a physician in family or emergency medicine (other specialties considered if seeing pediatric patients)</li><li>Currently licensed to practice medicine in the state of hire with no history of license suspension or debarment</li><li>Current board certification in specialty area</li><li>Advanced knowledge of treatment and drug interactions</li><li>Ability to build rapport with patients and biopharmaceutical sponsors</li><li>Strong attention to detail</li><li>Strong leadership qualities</li><li>Provide clinical oversight to study team</li><li>Clinical research experience</li></ul>About M3USAM3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, weve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.*M3 reserves the right to change this job description to meet the business needs of the organization

Part-Time Principal Investigator in Durham, NC for Board Certified Practicing Family Medicine Physician

INTEGRATED

PERMANENT

FULL_TIME

Flavor Technologist

Privately owned Company is seeking an experienced Food Scientist to join their team! Title: Senior Formulations Scientist -Meat/Poultry/Protein Seasoning.

Title: Senior Formulations Scientist -Meat/Poultry/Protein Seasoning Location: Fort Mill, SC Type: Full Time, Salaried with benefits Schedule: Monday-Friday Day Hours    Overview:  Privately owned Company is seeking an experienced Food Scientist to join their team! In this role, you will be provide scientific and technical knowledge Responsibilities:<ul><li>Lead projects from ideation to commercialization</li><li>Formulate, modify, and cost-reduce food products</li><li>Solve technical challenges in flavor development and applications</li><li>Replicate existing products and flavors</li><li>Conduct basic product analyses (salt, moisture, pH, granulations)</li><li>Maintain accurate records and data</li><li>Perform sensory evaluations</li><li>Participate in R&D and cross-functional meetings</li><li>Apply customer product/process knowledge to projects</li><li>Write and interpret reports, research records, and manuals</li><li>Present findings to stakeholders</li><li>Provide technical expertise to internal and external customers</li><li>Develop intellectual property ideas</li><li>Evaluate ingredient sourcing, costing, and qualifications</li><li>Guide Jr. Scientists, technologists, and technicians</li><li>Stay updated on food trends and technology</li><li>Support the Director of Culinary as needed</li></ul> Requirements: <ul><li>B.S. in Food Science, Food Engineering, or related field</li><li>5+ years in seasoning, sauce, batter/breader, or meat system formulation</li><li>1+ years in meat science and plant commercialization</li><li>Proactive with strong organization skills</li><li>Excellent communication and presentation abilities</li><li>Experience writing/reviewing technical procedures & regulations</li><li>Strong sensory evaluation skills (taste & smell)</li><li>Ability to manage multiple projects in a fast-paced setting</li></ul> Benefits:  Our client offers a comprehensive benefits package including Medical, Dental, Vision, 401k plan, yearly bonus, PTO & Holidays, company gatherings and more! #M3   Ref: #558-Scientific

<h1 style="text-align: center; color: rgba(34, 34, 34, 1); font-size: 4rem">Our Story</h1>
<h4 style="color: rgba(34, 34, 34, 1); font-size: 2.4rem">Impacting lives. It's in our DNA.</h4>
At Joulé, we believe our world is filled with possibilities – where character, integrity and commitment drive our purpose. For over 30 years, Joulé has been a trusted partner to industry leading clinical, scientific, and healthcare organizations by providing innovative workforce solutions and delivering top talent. Operating at the forefront of the life sciences arena, Joulé’s relentless approach enables our clients to rapidly and effectively execute critical initiatives and major projects. Joulé is a System One division.
Joulé consists of multiple business lines working together for client success: <a style="color: rgba(0, 0, 0, 0)" href="https://www.jouleinc.com/specialties/scientific/">scientific</a>, <a style="color: rgba(0, 0, 0, 0)" href="https://www.jouleinc.com/specialties/clinical/">clinical</a>, and <a style="color: rgba(0, 0, 0, 0)" href="https://www.jouleinc.com/specialties/healthcare/">healthcare</a> recruiting plus <a style="color: rgba(0, 0, 0, 0)" href="https://www.jouleinc.com/specialties/equipment-services/">equipment services</a>.
Since our existence, we’ve excelled in these specialized markets, and in recent years we have further narrowed the Joulé brand to exclusively represent these arenas. Joulé's services are backed by the considerable reach and resources of our parent company, System One.
<h4 style="color: rgba(34, 34, 34, 1); font-size: 2.4rem">The Business of Science</h4>
Way back before STEM was a trend, Joulé established its roots in scientific and technical disciplines. We began life as an engineering services firm, but our business has evolved considerably to where it stands today:
<ul style="color: rgba(136, 136, 136, 1); font-size: 15px">
<li>A leader in specialized workforce solutions and integrated services</li>
<li>One of the top ten largest clinical and scientific staffing firms in the U.S.</li>
<li>An ISO-certified provider of laboratory and facility support</li>
<li>An advocate for scientific, clinical, and healthcare clients and candidates alike</li>
</ul>
<h4 style="color: rgba(34, 34, 34, 1); font-size: 2.4rem">National Reach with Local Expertise</h4>
Working at the intersection of business and science, we make it easier to recruit and deploy talent for ongoing work and on-demand projects in a host of disciplines. We’re still writing our story, but our future is built on a foundation of quality delivery and personalized service.

Joulé

Senior Formulation Scientist- Seasoning Meat/poultry

Botany

Communication Skills

Cost Control

Cross-Functional

Data Quality

Food Science

Intellectual Property Development

Multitasking

Organizational Skills

Presentation/Verbal Skills

Project/Program Management

Record Keeping

Regulations

Reporting Skills

Research & Development (R&D)

Technical Writing

Toxicologist

If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.

Job Family:Scientist (Digital) Travel Required:None Clearance Required:Ability to Obtain Public Trust What You Will Do: We are currently searching for a Toxicologist. This position is to provide toxicological support for literature-based cancer hazard evaluations for possible listing in the Report on Carcinogens. The incumbent should have experience/expertise in toxicology, cancer biology and mechanisms, environmental health science, and systematic review. This is a full time (30 hours per week), on-site opportunity in Durham, NC. <ul><li>Work with staff to confirm assay results and evaluate new techniques and instruments; search literature; propose, design and test alternative assays for difficult screening targets; confirm assay results; develop secondary assays. </li><li>Submit and gain approval of laboratory animal study protocols. </li><li>Provide advice and assistance to users in designing experiments, using instrumentation, data acquisition and analysis, and preparing figures for publication. </li><li>Work with staff on the interpretation of experiments performed by research scientists. </li><li>Serves as co-lead of literature cancer evaluation teams for at least one project. </li><li>Advance the science through proposing and investigating new target projects for initiation based on novelty and relevance to human health. </li><li>Write technical reports and prepare manuscripts. </li><li>Oversee project data quality; analyze and interpret project data. </li><li>Conduct systematic review of cancer animal and mechanistic studies, including evaluating study quality and evidence integration. </li><li>Presents research at national scientific meetings and symposia. </li><li>Prepare oral presentations and posters for internal and external groups/conferences. </li><li>Co-author manuscripts on research projects; publish in peer-reviewed journals. </li><li>Review, edit, and, as needed, write first drafts of papers, posters and manuscripts. </li><li>Present results of clinical and experimental research at recognized scientific meetings by lectures and exhibits (poster sessions). </li><li>Search existing literature for new and/or relevant techniques. </li><li>Produce research reports and regularly communicate results to staff and collaborators. </li><li>Prepare information for and attend advisory, review committee and panel meetings; respond to issues and concerns </li><li>about specific applications/proposal pertaining to assigned program area. </li><li>Provide scientific and technical expertise to all visiting fellows, post-docs, and technicians. </li><li/></ul>#SOAR What You Will Need:<ul><li>At least five (5) years of experience </li><li>DABT Certification (Diplomate of the American Board of Toxicology credential) </li><li>Master’s Degree </li></ul> What Would Be Nice To Have:<ul><li>Systematic review </li><li>Knowledge of computational biology is preferred. </li><li>Toxicology </li><li>Cancer biology/carcinogenesis </li><li>Computational biology/read across </li><li>Animal cancer studies </li><li>Manuscript writing </li><li>Data Presentation </li><li>PowerPoint </li><li>Outlook </li><li>Excel </li><li>Word </li></ul> What We Offer:Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace. Benefits include: <ul><li>Medical, Rx, Dental & Vision Insurance </li><li>Personal and Family Sick Time & Company Paid Holidays </li><li>Parental Leave </li><li>401(k) Retirement Plan </li><li>Group Term Life and Travel Assistance </li><li>Voluntary Life and AD&D Insurance </li><li>Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts </li><li>Transit and Parking Commuter Benefits </li><li>Short-Term & Long-Term Disability </li><li>Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities </li><li>Employee Referral Program </li><li>Corporate Sponsored Events & Community Outreach </li><li>Care.com annual membership </li><li>Employee Assistance Program </li><li>Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.) </li><li>Position may be eligible for a discretionary variable incentive bonus </li></ul>About Guidehouse Guidehouse is an Equal Employment Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, citizenship status, military status, protected veteran status, religion, creed, physical or mental disability, medical condition, marital status, sex, sexual orientation, gender, gender identity or expression, age, genetic information, or any other basis protected by law, ordinance, or regulation. Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco. If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation. Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee.

Guidehouse

Accidental Death and Dismemberment (AD&D)

Assay Development

Assays

Biology

Cancer

Conferences

Corporate Funding

Data Analysis

Dental Insurance

Employee Assistance Plan

Environmental Health

Environmental Sciences

Experiment Design

Health Science

Human Health

Instrumentation

Insurance

Legal

Prescription Drugs

Project Evaluation

Project Tracking

Publications

Quality Management

Scientific Research

Test Design

Toxicology

Tuition Reimbursement

User Interface/Experience (UI/UX)

Vision Plan

Willing to Travel

Writing Skills

Capital Markets Placement_feed

Medical Laboratory Technician

LICENSURE/CERTIFICATION/REGISTRY/LISTING:Required: Must have Medical Technologist (MT) or Medical Laboratory Scientist (MLS) pr Specialist in Blood Bank (SBB) or Technologist in Blood Banking (BB) or Technologist in Chemistry (C) or Technologist in Hematology (H) or Technologist in Microbiology (M) or Specialist in Microbiology (SM) by ASCP Overview: The Medical Laboratory Scientist Lead analyzes human samples, such as blood, tissue, and body fluids, to determine chemical content, cell count, drug levels, blood type, and the presence of microorganisms.

Overview: <table><tbody><tr><td colspan="1"></td></tr><tr><td>The Medical Laboratory Scientist Lead analyzes human samples, such as blood, tissue, and body fluids, to determine chemical content, cell count, drug levels, blood type, and the presence of microorganisms. This role is responsible for utilizing automated equipment and specialized instrumentation to prepare samples and perform multiple complex tests that provide valuable information on diseases. This role also guides less experienced team members through training, onboarding and answering questions.</td></tr></tbody></table> Responsibilities: <table><tbody><tr><td colspan="1"></td></tr><tr><td>Ensures accurate and timely analysis of specimens using various laboratory techniques to ensure positive specimen identification while maintaining proper documentations. Performs testing of laboratory specimens (pre-analytical, analytical and post analytical) according to established laboratory policies and procedures. Collaborates with laboratory management to develop and update standard operating procedures to ensure adherence to best practices and continuous improvement in specimen processing. Monitors and troubleshoots equipment and testing processes, promptly addressing technical issues to minimize downtime and maintain reliable laboratory operations. Supports the training and onboarding of new technologists to facilitate their integration into the team and ensuring consistent competency evaluations to uphold high standards of performance. Performs other duties as assigned.</td></tr></tbody></table> Qualifications: <table><tbody><tr><td colspan="1">EDUCATION:</td></tr><tr><td>Required: Bachelor's Degree in medical technology, clinical laboratory science, or chemical, physical, or biological science.</td></tr></tbody></table> <table><tbody><tr><td colspan="1">EXPERIENCE:</td></tr><tr><td>Required: Four years of laboratory experience in a high complexity laboratory in designated specialty or subspecialty.</td></tr></tbody></table> <table><tbody><tr><td colspan="1">LICENSURE/CERTIFICATION/REGISTRY/LISTING:</td></tr><tr><td>Required: Must have Medical Technologist (MT) or Medical Laboratory Scientist (MLS) pr Specialist in Blood Bank (SBB) or Technologist in Blood Banking (BB) or Technologist in Chemistry (C) or Technologist in Hematology (H) or Technologist in Microbiology (M) or Specialist in Microbiology (SM) by ASCP</td></tr></tbody></table>

Cone Health

Medical Laboratory Scientist Lead - Core Lab

Best Practices

Blood Bank

Chemistry

Clinical Laboratory

Content Management

Continuous Improvement

Disease

Hematology

Laboratory Analysis

Laboratory Management

Laboratory Operations

Laboratory Techniques

Microbiology

Microorganism

Onboarding

Physical Chemistry

Procedure Implementation

Quality Assurance Methodology

Sample/Specimen Processing

Specimen Analysis

Specimens/Samples

Standard Operating Procedures (SOP)

Standards Development

Test Lab

Time Management

Appcast PX 2

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