analytical research chemist

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
First Shift (Days)<p></p><p><b>
Environmental Conditions</b></p>
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials<p></p><p><b>
Job Description</b></p><p></p><p>
As part of the Thermo Fisher Scientific team, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world&rsquo;s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.</p><p><br>
We are seeking an Analytical Scientist II with exceptional problem-solving skills to join our Research and Development team in High Point, NC, United States. As an Analytical Scientist III, you will have a crucial role in advancing our research initiatives and contributing to the development of innovative scientific solutions.</p><p>
Responsibilities:</p><p>
Conduct cleaning method development and validation for our wide range of products</p><ul><li>Perform routine and investigational testing in accordance with approved methods and specifications, including chemical, physical, and microbiological analyses. Evaluate results, identify trends, and support investigations related to out-of-specification or atypical findings.</li><li>Conduct additional testing as required to support quality investigations, regulatory inquiries, supplier qualification, method validation or verification, stability studies, and risk assessments, including but not limited to impurity, residual solvent, volatile, and trace-level analyses.</li><li>Ensure all testing activities comply with applicable GMP, GLP, and regulatory requirements. Accurately document results, prepare technical summaries, and communicate findings to cross-functional stakeholders. Support continuous improvement initiatives by recommending or implementing enhanced analytical approaches when necessary.</li><li>Collaborate with cross-functional teams to determine project requirements and objectives</li><li>Design and conduct experiments to assess and enhance cleaning procedures</li><li>Analyze samples and interpret data using statistical tools and software</li><li>Prepare and present technical reports and presentations to individuals and groups within and outside the organization</li><li>Ensure compliance with regulatory standards and guidelines</li><li>Contribute to the continuous improvement of analytical methodologies and processes</li><li>Stay updated with industry trends and advancements in analytical techniques</li></ul><p>
Requirements</p><p>
To be successful in this role, you should have:</p><ul><li>A BS degree with 2+ years of relative experience or MS Degree with 1 year experience, a Ph.D. in Analytical Chemistry or a related field</li></ul><p>
&middot;&middot; Proven experience in cleaning method development and validation</p><ul><li>Proficiency in using analytical instruments and software, including but not limited to LC/MS, FTIR and HPLC.</li><li>Strong knowledge of statistical analysis tools and techniques</li><li>Excellent communication and interpersonal skills</li><li>The ability to work independently and as part of a collaborative team</li></ul><p>
What Makes This Opportunity Unique?</p><ul><li>Join a world-class organization at the forefront of scientific innovation</li><li>Work in a pharmaceutical research facility with advanced technology</li><li>Collaborate with a diverse team of experts to solve complex scientific challenges</li><li>Contribute to the development of products that have a meaningful impact on global health and well-being</li><li>Benefit from a competitive compensation package and opportunities for professional growth</li></ul><p>
Equal Opportunity Employer: Thermo Fisher Scientific Inc. is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.</p><p>
Reasonable Accommodation: Thermo Fisher Scientific Inc. is committed to accommodating individuals with disabilities. If you require accommodation due to a disability, please contact us to discuss your needs.</p></div><p></p>

Analytical Scientist II, Cleaning Method Development

New York University

<div>Position Summary:
<div>
Arts &amp; Science is seeking a dedicated Financial Analyst to join the Department of Chemistry. This individual will facilitate financial transactions for departments and programs and provide internal control review of fiscal activity on operating, restricted fund, endowment, plant fund, and sponsored research accounts; implement and assist with developing internal control procedures; provide analyses for preparation of annual school budget.</div>
Qualifications:
<div><b>
Required Education:</b><br>
Bachelor's degree<br>
<br>
<b>Required Experience:</b><br>
3 years relevant experience or equivalent combination. Must include experience with forecasting, financial analysis, and budget management.<br>
<br>
<b>Preferred Experience:</b><br>
Experience in an academic/higher education setting.<br>
<br>
<b>Required Skills, Knowledge and Abilities:</b><br>
Excellent interpersonal, organizational, analytical, and problem-solving skills. Familiarity with Windows-based software applications, including proficiency with database and spreadsheet software.</div>
Additional Information:
<div>
In compliance with NYC's Pay Transparency Act, the annual base salary range for this position is USD $78,107.73 to USD $85,000.00. New York University considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/training, key skills, internal peer equity, as well as, market and organizational considerations when extending an offer. This pay range represents base pay only and excludes any additional items such as incentives, bonuses, clinical compensation, or other items.
<br>
<br>
NYU aims to be among the greenest urban campuses in the country and carbon neutral by 2040. Learn more at nyu.edu/nyugreen.<br>
<br>
NYU is an Equal Opportunity Employer and is committed to a policy of equal treatment and opportunity in every aspect of its recruitment and hiring process without regard to age, alienage, caregiver status, childbirth, citizenship status, color, creed, disability, domestic violence victim status, ethnicity, familial status, gender and/or gender identity or expression, marital status, military status, national origin, parental status, partnership status, predisposing genetic characteristics, pregnancy, race, religion, reproductive health decision making, sex, sexual orientation, unemployment status, veteran status, or any other legally protected basis. All interested persons are encouraged to apply at all levels.</div></div>

Financial Analyst - Chemistry

United Therapeutics

<div><div>California, US residents <div></div>.</div><div></div><div>
The job details are as follows:</div><div></div><div>
Who We Are</div><div></div><div>
We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.</div><div><br>
United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter&rsquo;s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).</div><div><br>
The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.<br>
<br>
Who You Are</div><div>
As an Associate/Research Scientist, Analytical Chemistry, you&rsquo;ll be a critical scientific partner at the intersection of discovery, development, and scale‑up&mdash;helping transform complex chemistry into therapies that can change lives. In this role, you&rsquo;ll work side‑by‑side with synthetic chemists to develop and execute advanced analytical methods, generate high‑quality data, and solve real‑world challenges tied to route selection, impurity control, and process understanding. You&rsquo;ll bring clarity to complexity by interpreting chromatographic data, supporting tech transfer and GMP readiness, and ensuring analytical rigor from early research through manufacturing. If you enjoy being hands‑on in the lab, thinking deeply about data, and collaborating across teams to move innovative science forward, you&rsquo;ll find both purpose and momentum here</div><div></div><div>
The Associate/Research Scientist, Analytical Chemistry supports a team of synthetic chemists by developing and executing various analytical (LC, GC, SFC, KF etc.) methods to solve complex research problems such as route scouting, process understanding, scale-up and impurity isolation/purification. This role also partners with QC, and external vendors to develop robust analytical methods, generate high-quality data, to ensure analytical readiness for scale-up, tech transfer and GMP manufacturing.</div><ul><li>
Collaborate with synthetic chemists to support isolation and characterization of API, impurities, intermediates, and markers using preparative techniques such as prep‑HPLC and SFC while meeting assigned project timelines</li><li>
Execute established analytical methods for chromatographic techniques including LC, GC, and SFC using appropriate detection such as UV, ELSD, CAD, MS, and FID</li><li>
Trend and interpret chromatography data to provide actionable insights including reaction completion, chiral selectivity, impurity profiles, and purge trends, and communicate results clearly to synthetic chemists</li><li>
Analyze samples or materials from vendors according to established or transferred analytical procedures</li><li>
Operate, calibrate, and maintain laboratory instruments and associated computer systems by coordinating with groups such as IT and OT for basic troubleshooting</li><li>
Coordinate vendor service activities including preventive maintenance, repairs, and column selection, and assist with obtaining quotes or making purchases for columns, consumables, and chemicals</li><li>
Author and review technical documentation such as analytical reports, method SOPs, method development summaries, investigations, and data packages for method transfer</li><li>
Contribute to technical documentation such as development summaries, experiment records, method notes, and invention disclosures as needed</li><li>
Ensure data quality and adherence to internal policies and scientific standards</li><li>
Review data packages such as method development reports and protocols from other departments and vendors</li><li>
Utilize scientific literature to support execution of research assignment objectives</li><li>
Drive improvements in analytical throughput and lab efficiency</li><li>
Support safety practices, chemical hygiene, and waste management while applying principles of sustainability</li></ul><div></div><div>
Minimum Requirements</div><div>
Associate Research Scientist, Analytical Chemistry R&amp;D</div><ul><li>
5+ years of relevant chemistry experience in pharmaceutical industry with a Bachelor's degree or 3+ years of relevant chemistry experience in pharmaceutical industry with a Master's degree or 0+ years of relevant chemistry experience in pharmaceutical industry with a PhD</li><li>
Foundational understanding of chromatographic techniques (LC, GC, SFC) and associated detection technologies (UV, ELSD, CAD, MS, FID), sufficient to execute established analytical methods independently</li><li>
Ability to trend and interpret chromatography data to provide actionable insights (reaction completion, chiral selectivity, impurity profiles, purge trends) and communicate results clearly to synthetic chemists</li><li>
Ability to operate, calibrate and maintain various laboratory instruments and related computers by interacting with other departments IT/OT for basic troubleshooting</li><li>
Ability to coordinate vendor service activities (PM visits, repairs, column selection) and assist with obtaining quotes/purchase for columns, consumables, and chemicals</li><li>
Ability to contribute to technical documentation such as development summaries, experiment records, and method notes; contribute to invention disclosures as needed</li><li>
Ability to utilize scientific literature for accomplishing research assignment objectives</li></ul><div></div><div>
Preferred Qualifications</div><ul><li>
Ability to analyze materials from external vendors/CDMOs using transferred procedures; confirm compliance with method requirements and report deviations</li><li>
Ability to ensure data quality and adherence to internal policies and scientific standards</li><li>
Proficient with MS Office, ChemDraw, and SciFinder</li></ul><div></div><div>
Minimum Requirements</div><div>
Research Scientist, Analytical Chemistry R&amp;D</div><ul><li>
8+ years of relevant chemistry experience in pharmaceutical industry with a Bachelor's degree or 6+ years of relevant chemistry experience in pharmaceutical industry with a Master's degree or 2+ years of relevant chemistry experience in pharmaceutical industry with a PhD</li><li>
Experience in independently leading analytical investigations, hands-on experience with HPLC/UPLC/GC method development, troubleshooting and common sample prep techniques</li><li>
Working knowledge of LC&ndash;MS (TOF) for mass-based compound characterization</li><li>
Ability to interpret analytical data in the context of chemical process development</li><li>
Sound knowledge of chromatography software: Waters Empower, Agilent MassHunter, Thermo Scientific Chromeleon and Waters ChromScope</li><li>
Clear technical writing and data storytelling (chromatogram stacking, overlays, etc.)</li><li>
Comfortable in fast-paced R&amp;D environments with shifting priorities</li><li>
Experience with chiral analysis/method development (chiral HPLC and/or SFC) is highly preferred</li></ul><div></div><div>
Preferred Qualifications</div><ul><li>
Doctor of Philosophy (PhD) in chemistry or related discipline</li><li>
Sound knowledge of MS Office, ChemDraw, and SciFinder</li><li>
Experience supporting API process development (route scouting and kilo lab)</li><li>
Experience with CAD detectors and SFC</li><li>
Experience working with external CDMOs and reviewing vendor analytical packages</li><li>
Familiarity with KF, NMR, FTIR</li><li>
Familiarity with regulatory expectations for early to late-stage development (ICH concepts, specs setting and CMC support)</li></ul><div></div><div>
Job Location</div><div>
United Therapeutics requires this candidate to be 100% on-site at our Silver Spring, Maryland location.</div><div></div><div>
The salary range for the Associate Research Scientist position is $96,500 - $130,000 per year and the salary range for the Research Scientist is $111,000 - $150,000 per year. These ranges reflect our good-faith estimate of the compensation for this role at the time of posting. An employee&rsquo;s position within the salary range will be based on factors such as education, qualifications, experience, skills, geographic location, and business needs, as well as other factors permitted by law at the time of posting. This range may be modified in the future based on company and market factors.</div><div></div><div>
At United Therapeutics, our mission and vision are one. We use our enthusiasm, creativity, and persistence to innovate for the unmet medical needs of our patients and to benefit our other stakeholders. We are bold and unconventional. We have fun, we do good.</div><div></div><div>
Eligible employees may participate in the Company&rsquo;s comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off &amp; paid parental leave benefits, disability benefits, and more. For additional information on Company benefits, please visit <div>https://www.unither.com/careers/benefits-and-amenities</div></div><div></div><div>
United Therapeutics Corporation is an Equal Opportunity Employer, including veterans and individuals with disabilities.</div></div><div></div>

Associate Research Scientist/Research Scientist, Analytical Chemistry R&D

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Office<p></p><p><b>
Job Description</b></p><p></p><p>
This is a fully remote role supporting one of our key customers. We welcome applicants from all locations within the US.</p><p>
Must be legally authorized to work in the United States without sponsorship.</p><p>
Must be able to pass a comprehensive background check, which includes a drug screening.</p><p></p><p>
Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission &ndash; to enable our customers to make the world healthier, safer, and cleaner.</p><p>
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.</p><p></p><p>
The Research Scientist acts as the sponsor representative/study monitor for one or more studies and supports the bioanalytical study phases of clinical trials.</p><p></p><p><b>
Key responsibilities:</b></p><ul><li>
Reviews trial related documentation with a link to the GxP vendor (i.e., CTP, SAP, TLF&rsquo;s, CSR, Lab manual)</li><li>
Ensures the bioanalytical vendor receives copies of trial related documentation and relevant amendments (e.g., clinical trial protocol)</li><li>
Reviews and approves study plans of bioanalytical phases of clinical trials</li><li>
Reviews and approves (if applicable) bioanalytical reports</li><li>
Oversees planned and unplanned changes to study plan and vendor procedures are documented according to vendor procedures (e.g., in amendments and deviations) and are shared with the sponsor as stipulated in the quality agreement or communication plan</li><li>
Ensures that the Clinical Trial Team is adequately informed of the project status and that relevant information (e.g., end-of-study timelines and data delivery requirements) from the Clinical Trial Team is conveyed to the project manager and bioanalytical vendor</li><li>
Escalates issues related to timelines, budget or communication to the appropriate stakeholders</li><li>
Manages oversight documentation in eTMF</li><li>
Contributes to interactions with regulatory agencies (if applicable)</li></ul><p></p><p><b>
Education and Experience:</b></p><ul><li><ul><li>PhD in Immunology or Molecular Biology and previous experience in the field of life sciences that provides the knowledge, skills, and abilities to perform the job comparable to 4+ years</li></ul></li><li>
OR</li><li>
Master&rsquo;s Degree and previous experience in the field of life sciences that provides the knowledge, skills, and abilities to perform the job comparable to 6+ years</li><li>
OR</li><li>
Bachelor's Degree and previous experience in the field of life sciences that provides the knowledge, skills, and abilities to perform the job comparable to 8+ years</li></ul><p></p><p>
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</p><p></p><p><b>
Knowledge, Skills and Abilities:</b></p><ul><li>
Experience in managing outsourced activities at external vendors required</li><li>
Strong knowledge of bioanalytical techniques specifically in biologics and antibodies assays required &middot; Experience performing PK and ADA assays required</li><li>
Experience in analyzing human samples in support of clinical trials required</li><li>
Strong understanding of GCP/GCLP guidelines and other current global regulations required</li><li>
Experience with submission documentation and regulatory interactions</li><li>
Experience with clinical immunogenicity data interpretation, writing and reviewing the Integrated Summary of Immunogenicity (ISI) and clinical study report</li><li>
Experience drafting and reviewing bioanalytical modules (2.7.1, 2.7.2) and immunogenicity sections in regulatory documents either independently or collaboration with a medical writer</li></ul><p></p><p>
Working Environment:</p><p>
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:</p><ul><li>
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>
Able to work upright and stationary for typical working hours.</li><li>
Ability to use and learn standard office equipment and technology with proficiency.</li><li>
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul></div><p></p>

Research Scientist PI - Bioanalytical

Nawah Scientific

<div>
 <strong>
  Job Brief
  <br/>
  <br/>
 </strong>
 We're seeking for
 <strong>
  Analytical Chemistry Research Assistant
 </strong>
 who will be responsible for sample testing, data recording and performing routine checks to ensure the quality and integrity of data.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  Laboratory Performance
  <br/>
  <br/>
 </strong>
 Participate in all lab performance activities and, whenever applicable, compliance of lab activities with ISO/IEC 17025/GLP requirements.
 <br/>
 <br/>
 Implementing laboratory procedures effectively to control lab activities.
 <br/>
 <br/>
 Execute the approved internal quality control program to ensure proper control of technical processes.
 <br/>
 <br/>
 Execute equipment operation protocols, intermediate check procedures, and maintenance plan.
 <br/>
 <br/>
 Record results daily and report immediately any malfunction or abnormal results.
 <br/>
 <br/>
 <strong>
  Improvement
  <br/>
  <br/>
 </strong>
 Provide suggestions for laboratory operation improvement.
 <br/>
 <br/>
 Stay up to date with Scientific updates/ regulatory requirements.
 <br/>
 <br/>
 <strong>
  Job Requirements
  <br/>
  <br/>
 </strong>
 <strong>
  Must-have
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in any of the following: Biotechnology, Science, Pharmacy or relevant field.
  </li>
  <li>
   3 Months:3 years of experience in relevant position.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Nice to have
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Training, workshop attendance, graduation projects, conference attendance/presentation, publications.
  </li>
  <li>
   Familiarity with data collection methods, statistical analysis software (e.g., SPSS, GraphpadPrism, etc).
  </li>
  <li>
   Familiarity with laboratory safety protocols and adherence to good laboratory practices (GLP).
  </li>
  <li>
   Experience with MS Office
  </li>
  <li>
   Familiarity with presentation software e.g. MS PowerPoint and Empower software for water hplc.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Offer
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Work with a supportive and energetic team in a dynamic research environment that fosters collaboration and innovation.
  </li>
  <li>
   Enjoy annual salary increases and additional benefits based on your performance and contribution.
  </li>
  <li>
   Receive an annual family bonus as a token of appreciation for your loyalty and commitment to the company.
  </li>
  <li>
   Earn a great quarterly incentive for achieving your goals and exceeding expectations.
  </li>
  <li>
   Benefit from comprehensive social and medical insurance coverage for you.
  </li>
  <li>
   Participate in an annual cycle meeting to review your progress and plan your future development.
  </li>
 </ul>
</div>


Research Assistant - Analytical Chemistry Lab

Bristol Myers Squibb

<div><b>Working with Us</b><br>
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.<br>
<br>
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .<br>
<br>
Our Chemical Process Development group is a team of organic chemists, analytical chemists, and chemical engineers working together to design novel syntheses from raw materials to supply new medicines to patients. Our scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates. The work is driven by innovative science, data-driven decision-making, and collaborative teamwork. The scientific knowledge package from the manufacturing process, design parameters, and control strategies enables regulatory filings to bring these novel medicines to patients worldwide.<br>
<br>
<b>Position Summary:
</b><br>
<br>
This Analytical Development role will be responsible for developing effective collaborations within Chemical Process Development (CPD) project teams consisting of organic chemists, chemical engineers, and analytical scientists to support an increasingly complex portfolio of small molecules and milla-molecular (ADCs, peptides, oligonucleotides) drug candidates.<ul><li>
Accountable for providing fit-for-purpose analytical methods and analyses which provide key insights and process knowledge for scale-up and process optimization studies for projects within the portfolio.</li><li>
Accountable for collaborating within project teams to provide innovative analytical approaches to help solve challenging problems encountered to support route selection and process optimization studies conducted by chemists and chemical engineers.
</li><li>Accountable for developing and transferring methods to other analytical release functions to support the timely release of clinical API batches.</li><li>
Partners with other Analytical Functions within CPD, and across Product Development to evolve, integrate and optimize analytical support to create a world-class analytical function.
</li><li>Successful candidates expected to grow and advance to become either analytical leaders or technical leads for projects within the CPD portfolio.</li></ul><b>
Key Responsibilities:</b><ul><li>
Responsible for willingly and enthusiastically working at the bench to solve analytical challenges encountered within pharmaceutical development. Can be relied upon to work independently to develop and validate methods, as well as investigate and apply innovative separation techniques such as 2DLC or CE. Seeks opportunities to publish/present work externally.</li><li>
Accountable for identifying opportunities and/or implementing solutions to improve monitoring of continuous manufacturing processes, and increasingly applying automation to improve efficiency, productivity, quality or reduce costs.
</li><li>Responsible for actively collaborating with other Key Scientists within the team. Expected to consistently display a can-do attitude and demonstrate the willingness and capability to adapt and grow within a complex and changing environment.
</li><li>Responsible for working with leadership to develop self, share best practices, work effectively to solve pharmaceutical development problems, and continuously learn and improve. Expected to demonstrate capability to advance upon the technical ladder or become an effective analytical lead within project teams.
</li></ul><b>Experience &amp; Qualifications:
</b><ul><li>Ph.D. in analytical or organic chemistry with 0-2 years of experience or M.S. in analytical or organic chemistry with 2-4 years of experience, or B.S. in analytical or organic chemistry 5-7 years of experience; Practical experience directly relevant to the role is critical to success and minimum degree requirements change relative to experience.</li><li>
Experience with chromatographic and/or spectroscopic techniques preferred.</li><li>
Experience with data science, analytical chemistry relevant modeling, AI/ML, &amp;/or programming preferred.
</li><li>Experience in working across matrixed teams highly desirable.</li><li>
Demonstrated commitment to safety.</li><li>
Excellent interpersonal, collaborative, team building, and communication skills to ensure effective collaborations within matrix teams. Demonstrated performance against cooperation principles and enterprise mindset.
</li></ul>If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
<br>
<br>
<b>Compensation Overview:</b><br>
<br>
New Brunswick - NJ - US: $99,330 - $120,366<br>
<br>
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
<br>
<br>
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
<br>
<br>
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</li><li>
<b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul><b>Work-life benefits include:
</b><br>
<br>
Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
<br>
<br>
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.<br>
<br>
<ul><li><b>Eligibility Disclosure: </b>T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul><br>
<b>Uniquely Interesting Work, Life-changing Careers</b><br>
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.<br>
<br>
<b>On-site Protocol</b><br>
<br>
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
<br>
<br>
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<b>Supporting People with Disabilities</b><br>
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BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
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<b>Candidate Rights</b><br>
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BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
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<b>Data Protection</b><br>
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We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .<br>
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R1600311 : Scientist, Analytical Development</div>

Scientist, Analytical Development

McKinsey & Company

<div>
 <strong>
  Who You'll Work With
  <br/>
  <br/>
 </strong>
 Driving lasting impact and building long-term capabilities with our clients is not easy work. You are the kind of person who thrives in a high performance/high reward culture - doing hard things, picking yourself up when you stumble, and having the resilience to try another way forward.
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 In return for your drive, determination, and curiosity, we'll provide the resources, mentorship, and opportunities you need to become a stronger leader faster than you ever thought possible. Your colleagues&mdash;at all levels&mdash;will invest deeply in your development, just as much as they invest in delivering exceptional results for clients. Every day, you'll receive apprenticeship, coaching, and exposure that will accelerate your growth in ways you won&rsquo;t find anywhere else.
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 When you join us, you will have:
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 <ul>
  <li>
   Continuous learning: Our learning and apprenticeship culture, backed by structured programs, is all about helping you grow while creating an environment where feedback is clear, actionable, and focused on your development. The real magic happens when you take the input from others to heart and embrace the fast-paced learning experience, owning your journey.
  </li>
  <li>
   A voice that matters: From day one, we value your ideas and contributions. You&rsquo;ll make a tangible impact by offering innovative ideas and practical solutions, all while upholding our unwavering commitment to ethics and integrity. We not only encourage diverse perspectives, but they are critical in driving us toward the best possible outcomes.
  </li>
  <li>
   Global community: With colleagues across 65+ countries and over 100 different nationalities, our firm&rsquo;s diversity fuels creativity and helps us come up with the best solutions for our clients. Plus, you&rsquo;ll have the opportunity to learn from exceptional colleagues with diverse backgrounds and experiences.
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  <li>
   World-class benefits: On top of a competitive salary (based on your location, experience, and skills), we provide a comprehensive benefits package to enable holistic well-being for you and your family.
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  </li>
 </ul>
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  Your Impact
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 You will deliver content expertise across topics such as maintenance, reliability and operations functions for our chemical&rsquo;s clients.
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 In this role, you will help clients build capabilities in delivery and execution, both during an active project and continuing after we&rsquo;ve shared our recommendations. You will work in teams to build the capabilities, systems and processes needed to deliver results and then ensure those results are sustained. To do this, you will bring and maintain or develop genuine expertise in the Chemicals sector across the multiple clients you will serve.
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 You will have responsibilities across all phases of our client development work, from initial business development and delivery to maintaining great relationships with clients during projects and beyond. You will collaborate closely with clients and drive analyses to provide unique insights. You will also support the development and maintenance of proprietary knowledge capabilities in conjunction with other experts in local and global practices.
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 You will be based in our Riyadh office as part of our Saudi Client Capabilities Hub.
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 You will work closely with our Global Energy and Materials practice who advises top management in the Chemicals sector locally and globally. As part of our hub, you will serve our clients across the EEMA region.
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 Our hub is part of our global Client Capabilities Networkwhich is comprised of 8000+ client serving professionals with deep specialization across industries and functions. Colleagues in our global Client Capabilities Network deliver distinctive client impact through assets and expertise and are driven by a culture of innovation.
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  Your Qualifications and Skills
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   Bachelor&rsquo;s degree in chemical, mechanical, electrical, or petroleum engineering
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   3+ years of professional experience in the petrochemical sector with comprehensive understanding of the petrochemical industry market, including downstream chemicals
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   Experience in chemical process engineering, operational improvement, project management or strategic decision-making in the petrochemical industry is a plus
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   Experience working with numbers/quantitative models
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   Strong problem-solving skills and conceptual abilities with an analytical mindset
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   Excellent business acumen and understanding of the main business, economic and financial concepts and terminology
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   Strong multitasking abilities; service-oriented personality
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   Ability to work collaboratively in a team environment; ability to work effectively with people at all levels in an organization
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  <li>
   Skills to communicate complex ideas effectively
  </li>
  <li>
   Fluency in English required, fluency in Arabic preferred
  </li>
 </ul>
</div>


Knowledge Analyst - Chemicals

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