49 Analytical Chemistry jobs in the United States

Manager, Analytical Chemistry in Albuquerque, NM
Build your future at Curia, where our work has the power to save lives.
The Manager of Analytical Chemistry is responsible for overseeing all operations within the Analytical Chemistry Laboratory. This role encompasses a wide range of duties, including personnel management (hiring, conducting performance reviews, managing performance, scheduling, etc.), budget preparation and management, and ensuring the lab is audit-ready for both regulatory bodies and customers. The Manager will also be responsible for developing and maintaining departmental metrics, representing the department in various internal and external meetings, and collaborating with both internal stakeholders and external customers to deliver exceptional service. Additionally, this position involves fostering a culture of continuous improvement, ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), and leading initiatives to enhance laboratory efficiency and effectiveness.
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.
We proudly offer
+ Generous benefit options (eligible first day of employment)
+ Paid training, vacation and holidays (vacation accrual begins on first day of employment)
+ Career advancement opportunities
+ Education reimbursement
+ 401K program with matching contributions
+ Learning platform
+ And more!
Responsibilities
+ Oversee analysts responsible for analytical testing on projects, documentation review, and investigations.
+ Support the transfer of robust analytical methods for analytical testing and maintains lab in a GMP readiness state.
+ Assign, supervise and establish daily work assignments in the group, including developing timelines, work plans, and milestones for the direct reports.
+ Identify and lead key projects for continual improvement of compliance and processes in laboratories as appropriate.
+ Supervise the analysts to maintain the inventory of reagents, reference standards, equipment, and other laboratory supplies.
+ Ensures team operates in compliance with all Quality, EH&S, and regulatory (i.e., FDA, OSHA, DEA, EPA, etc.) requirements and initiatives.
+ Manage equipment/instrument calibrations, performance verification, IQ, OQ, PQ
+ Attend safety and quality assurance meetings as required.
+ Supervise and administer OOS investigations as needed in conjunction with clients and the QA group. Provide technical incite for corrective actions as necessary.
+ Administer laboratory training sessions with technical staff as necessary.
+ Initiate Change controls and performs the necessary action items to close change control.
+ Ensure SOPs, LDS are accurate and revises as needed.
+ Lead audits inspections, client and general tours.
+ Manage analytical staff's activities in a GMP laboratory testing environment, schedule, and assign/prioritize laboratory activities aligned with organizational goals.
+ Support laboratory staffing; provide input on hiring decisions, access to training, and manage staff performance and development.
+ Represent QC cross-functionally, provide technical subject matter expertise and apply sound scientific judgment based on laboratory operations experience and knowledge.
+ Participate in internal and external audits.
+ Promote a customer service-centric environment, including pro-active communication to clients and timely follow-up with potential clients.
+ Oversee proper handling of controlled substances.
+ Keep a working knowledge of commonly prescribed methods, troubleshooting strategies, regulatory and technical industry trends.
Qualifications
+ Bachelor's degree in in Science, Chemistry, Biology or related field of study
+ Minimum of five (5) years in Analytical Chemistry, Quality Assurance or Regulatory Compliance Management
+ Minimum of two (2) years in a leadership role
+ Minimum of five (5) years in an aseptic/sterile product facility, preferred
Supervisory Responsibilities:
This role is responsible for leading and supporting a team, overseeing day-to-day operations, managing departmental goals, and ensuring adherence to organizational policies and procedures. This role also involves fostering a positive work environment, providing guidance and support to your team members, and evaluating performance to drive continuous improvement and achieve both departmental and organizational objectives.
Other Qualifications:
+ Must pass background check
+ Must pass drug screen
+ May be required to pass Occupational Health Screening
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-MM2

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials
**Job Description**
**Job Description**
Do you have a passion for innovative ideas and groundbreaking discoveries? With over $1 billion invested annually in R&D, at Thermo Fisher Scientific you'll help solve some of the world's toughest challenges, from giving cancer patients hope, ensuring safe drinking water and helping law enforcement tackle cases through forensics. We empower our teams to put science into meaningful action and give our R&D colleagues the autonomy, resources, and tools they need to take science a step beyond.
**How will you make an impact?**
The R&D Scientist II will be supporting a cross-functional team working toward the design and commercialization of new cell culture media and media supplement products. They will apply analytical chemistry skills to conduct established assays and play a role in developing novel analytical methods.
Location: Hunt Valley, MD onsite
**A Day in the Life:**
+ Operate autonomously or with limited guidance from supervisors or senior researchers.
+ Develop and support analysis of small and large molecule liquid chromatography (LC-MS) and ultra-high-performance liquid chromatography (UHPLC) assays.
+ Assist in troubleshooting existing products and work with internal and external customers to implement solutions.
+ Write protocols and reports, present data, and work across multiple groups.
**Keys to Success:**
**Education**
+ Degree in Chemistry, Chemical Engineering, Biology, Biochemistry, or other related field (Master's - or bachelor's)
**Experience**
+ 3+ years of previous experience with analytical techniques such as HPLC/UHPLC and LC-MS technology is required.
+ Method development and optimization for small and large molecule assays using LC-MS is desired.
+ Experience with GC-MS and Thermo Scientific LC-MS instruments is a plus.
+ Good understanding and working knowledge of chemistry principles, such as acid/base chemistry, sample solubility, and precipitation, as it relates to sample preparation.
**Knowledge, Skills, Abilities**
+ Ability to work both independently and in a team setting.
+ Excellent communication (verbal and written) and presentation skills.
+ Able to perform reliably under pressure while prioritizing and handling multiple projects or activities.
_We offer competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement, and a range of other employee benefits!_
_At Thermo Fisher Scientific, each one of our 100,000+ extraordinary minds have a unique story to tell. Join us and achieve our mission-enabling our customers to make the world healthier, cleaner, and safer. You'll be joining a hard-working, dedicated, and motivated team that shares your passion for exploration and discovery. With revenues of $2 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant impact to the world._
**Compensation and Benefits**
The salary range estimated for this position based in Maryland is 72,600.00- 96,800.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Our client, a leading organization in the pharmaceutical and biotechnology industry, is seeking a RResearch Associate Scientific - R&D to join their team. As a Research Associate, Analytical Chemist - R&D, you will be part of the Research & Development department supporting innovative product development initiatives. The ideal candidate will have strong analytical skills, attention to detail, and a collaborative mindset, which will align successfully in the organization.
**Job Title:** Research Associate Scientific - R&D
**Location:** Round Lake, Illinois
**Pay Range:** $25.00 to 27.00 on hourly.
Openings : 4 positions
**What's the Job?**
+ Conduct critical chemical and physical analyses on finished product R&D stability samples.
+ Support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives.
+ Perform chemical assays requiring precise analytical skills and understanding of chemistry principles.
+ Complete all testing, including special project/protocol testing, in a timely manner to meet project schedules.
+ Maintain data integrity and ensure compliance with company SOPs, FDA, cGxP, and QSR regulations.
**What's Needed?**
+ Bachelor's degree in chemistry, pharmaceutical sciences, biology, or a related scientific discipline with 6 months or more of experience.
+ Experience with analytical chemistry instrumentation such as pH, UV, titrations, Particle, TOC is preferred but not required.
+ Experience in a regulated environment with strong technical problem-solving skills.
+ Good oral and written communication skills, with a keen eye for detail.
+ Familiarity with laboratory safety, equipment maintenance, and troubleshooting instrumentation.
**What's in it for me?**
+ Opportunity to contribute to impactful projects that improve patient outcomes worldwide.
+ Work in a collaborative and innovative environment supporting professional growth.
+ On-site position with a duration of 12 months, with potential for extension or conversion.
+ Engage with sophisticated laboratory instrumentation and cutting-edge research tools.
+ Be part of a company committed to safety, quality, and continuous improvement.
**Upon completion of waiting period, consultants are eligible for:**
+ Medical and Prescription Drug Plans
+ Dental Plan
+ Vision Plan
+ Health Savings Account
+ Health Flexible Spending Account
+ Dependent Care Flexible Spending Account
+ Supplemental Life Insurance
+ Short Term and Long Term Disability Insurance
+ Business Travel Insurance
+ 401(k), Plus Match
+ Weekly Pay
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
**About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells.**
_ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

Company 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 Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
Purpose:
Technical expert that will independently investigate, identify, develop and optimize new methods/ techniques to address critical project needs. Continuously seek to improve existing laboratory methods and processes. Read and adapt literature to accomplish assignments. Demonstrate mastery of broad range of experimental techniques and methods of data analysis.
Responsibilities:
- Independently design, execute and interpret critical experiments to answer scientific questions. Understand the broad objectives of the project as well as their role in achieving those objectives, and modify experimental plan when required, to respond.
- Learn, understand and master new experimental techniques, and act as a resource or mentor for others.
- Innovate and implement new experimental protocols.
- Demonstrate a high level of proficiency in his/her field.
- Set and meet experimental timelines.
- Effectively organize and present scientific plans and data.
- Contribute to writing and conceptual framework of publications, presentations, and patents.
- Routinely read and apply relevant scientific literature. Impact projects mostly through lab and/or pilot plant based activities where applicable.
Preferred Qualifications:
- Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.
- Demonstrated ability to learn, understand and master new experimental techniques.
- Ability to multitask and work within timelines.
- Demonstrated scientific writing skills and strong verbal communication skills.
Qualifications
-BS or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience.
-Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.
-Demonstrated ability to learn, understand and master new experimental techniques.
-Ability to multitask and work within timelines.
-Demonstrated scientific writing skills and strong verbal communication skills.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
+ This job is eligible to participate in our long-term incentive programs
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
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.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$78,500 - $141,000

Our client is recruiting a Senior Scientist specializing in Analytical Chemistry for their state-of-the-art research and development facility located in Richmond, Virginia, US . This senior-level position requires a highly motivated individual to lead and execute complex analytical projects. You will be responsible for developing, validating, and implementing advanced analytical methods for the characterization of diverse chemical compounds and formulations. Expertise in a range of analytical techniques, including chromatography (HPLC, GC), mass spectrometry (LC-MS, GC-MS), spectroscopy (NMR, IR, UV-Vis), and elemental analysis, is essential.

Key responsibilities include designing experiments, interpreting data, and troubleshooting analytical challenges. You will collaborate closely with cross-functional R&D teams to support new product development, process improvements, and quality control initiatives. The ideal candidate will have a strong understanding of scientific principles, meticulous attention to detail, and the ability to manage multiple projects simultaneously. Experience with method transfer and regulatory compliance (e.g., FDA, EPA) is highly desirable.

This role demands excellent scientific judgment, strong problem-solving abilities, and effective communication skills, both written and verbal, for reporting findings to scientific and management audiences. You will also mentor junior scientists and contribute to the continuous improvement of analytical capabilities within the department. A Ph.D. in Chemistry or a closely related field with a specialization in Analytical Chemistry is required, along with a minimum of 7 years of relevant industrial or academic research experience. Experience in a regulated industry (e.g., pharmaceutical, biotechnology) is a significant advantage. This is an exciting opportunity to contribute to cutting-edge scientific discovery and innovation.

Our client is seeking a highly experienced and innovative Principal Scientist specializing in Analytical Chemistry to join their cutting-edge research and development facility in Phoenix, Arizona, US . This senior role will be instrumental in leading complex analytical projects, developing novel methodologies, and contributing to the strategic direction of the company's scientific endeavors. The ideal candidate will possess deep expertise in a wide range of analytical techniques, including chromatography (HPLC, GC), mass spectrometry (LC-MS, GC-MS), spectroscopy (NMR, IR, UV-Vis), and wet chemistry. You will be responsible for designing and executing experiments, interpreting complex data, and troubleshooting analytical challenges. Key responsibilities include mentoring junior scientists, collaborating with cross-functional research teams, authoring technical reports and publications, and presenting findings to internal and external stakeholders. This position demands a Ph.D. in Analytical Chemistry, Physical Chemistry, or a closely related field, with a minimum of 10 years of post-doctoral research experience in an industrial or academic setting. A proven track record of innovation, independent research, and successful project leadership is essential. Experience with method development, validation, and regulatory compliance (e.g., GMP, GLP) is highly desirable. You will be expected to stay abreast of the latest advancements in analytical science and to foster a culture of scientific excellence within the team. The ability to work collaboratively in a laboratory environment and to contribute to a positive team dynamic is crucial. This is a challenging and rewarding opportunity for a motivated scientist looking to make a significant impact in a leading R&D organization. The work will be conducted on-site at our state-of-the-art facilities in Phoenix, Arizona, US .

Our client is looking for a distinguished Principal Scientist in Analytical Chemistry to join their cutting-edge Scientific Research & Development division in Tampa, Florida, US . This senior role is critical in driving scientific innovation, developing new analytical methodologies, and leading complex research projects. You will be responsible for designing and executing experiments, interpreting sophisticated data, and authoring high-impact scientific publications and patents. The ideal candidate will possess a Ph.D. in Chemistry or a related field, with extensive post-doctoral or industry experience focused on advanced analytical techniques such as chromatography (HPLC, GC), mass spectrometry (LC-MS, GC-MS), spectroscopy (NMR, IR, UV-Vis), and elemental analysis. Your expertise should extend to method validation, troubleshooting complex analytical challenges, and ensuring compliance with regulatory standards (e.g., GMP, GLP). You will mentor junior scientists, manage project timelines and budgets, and collaborate with cross-functional teams including biologists, material scientists, and formulation chemists. This position requires exceptional critical thinking skills, a strong publication record, and the ability to communicate complex scientific concepts clearly to both technical and non-technical audiences. The opportunity to work with state-of-the-art instrumentation and contribute to groundbreaking discoveries makes this a highly rewarding role within a collaborative and stimulating research environment. The hybrid work model offers a balance between focused independent research and essential team interaction at our advanced facilities.

**Working with Us**
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.
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 .
RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.
RayzeBio, a Bristol Myers Squibb company, is looking for an ICP-MS Chemist at their Indianapolis manufacturing site. The person will be responsible for method development and implementation, method validation, verifications, or transfer, as well as stability testing activities to support product development at the RayzeBio manufacturing site in Indianapolis. This role will report directly to the Manager of Analytical Development at the Indianapolis site.
**Job Responsibilities:**
Essential duties and responsibilities include the following. Other duties may be assigned.
+ Develop and validate analytical methods on an Inductively Coupled Plasma Mass Spectrometry instrument (ICP-MS) for testing Elemental Impurities present in parenteral radiopharmaceutical drugs and raw materials.
+ Collaborate on the development and validation of other methods utilizing alpha spectrometers, gamma spectrometers, mass spectrometers, and ultra-high-performance chromatography.
+ Prepare analytical test methods and method validation, verification, and transfer protocols and reports in accordance with applicable guidelines and industry standards (e.g. USP, EP, and ICH).
+ Develop and maintain appropriate documentation, including notebooks, protocols, reports, standard operating procedures and associated forms, and data analysis.
+ Participate in troubleshooting and investigations of analytical issues, identify root causes, and implement corrective actions.
+ Participate in instrument qualification, calibration, and maintenance activities.
+ Work closely with other teams to ensure timely delivery of analytical results and support product development and commercialization.
+ Participate in method transfer activities from CDMO or internal research facility to QC team, ensuring accuracy and reliability of data.
+ Provide technical support to other teams or business units as required.
+ Ensure compliance with GMP regulations, safety guidelines, and quality standards.
+ Work with RSO to ensure laboratory compliance with the radiation safety programs.
+ Source and on-board analytical technologies as required.
+ Perform other duties as required by management.
+ The position is salaried. Work will be predominantly first shift, M-F, but extended hours or weekend work based on radiopharmaceutical manufacturing schedule may be required.
+ This position will require the applicant to work with and around ionizing radiation and hazardous chemicals.
**Education and Experience:**
+ B.Sc. or M.Sc. in Analytical Chemistry, Pharmaceutical Sciences, or relevant scientific field
+ Minimum 5 years of experience in analytical method development, validation, verification, and transfer in the pharmaceutical or radiopharmaceutical industry.
+ Prior extensive experience with ICP-MS, including verifying USP/ or ICHQ3D(R2) Elemental Impurities and developing and validating custom ICP-MS methods for dozens of elemental impurities that may be present in raw materials.
+ Prior experience composing or collaborating on Elemental Impurities risk assessments.
+ Prior experience in a GMP pharmaceutical testing laboratory with knowledge of GMP regulations, quality systems, and safety guidelines.
**Preferred Experience:**
+ Experience with parenteral drugs and/or radiopharmaceutical preferred but not required.
+ Experience working with the Thermo iCAP TQe ICP-MS.
+ Experience working with the Thermo Qtegra software, including building reports.
**Skills:**
+ Proficient in the use of laboratory instrumentation and Microsoft Office Suite
+ Highly motivated and organized professional with the ability to work independently or in a team environment
+ Strong analytical and problem-solving skills
+ Ability to multi-task and prioritize work based on multiple workflows
+ Ability to communicate effectively with multiple stakeholders
+ Strong written and oral communication skills
+ Excellent professional ethics, integrity, and ability to maintain confidential information.
**Physical Demands:**
While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 40 pounds. Specific vision abilities required by this job include close vision and distance vision.
This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials .
**Work** **Environment:**
The noise level in the work environment is usually moderate.
The starting compensation for this job is a range from $96,148 - $16,500 , plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit .
Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
#RayzeBio, GPS_2025, #LI-Onsite
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.
**Compensation Overview:**
Indianapolis - RayzeBio - IN: 96,148 - 116,508
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.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , 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.
**On-site Protocol**
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:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
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 . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
**Company:** Bristol-Myers Squibb
**Req Number:** R
**Updated:** :49:27.260 UTC
**Location:** Indianapolis-IN
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

Description
This role provides the QC analysis of raw materials, in-process, drug substance and drug product samples in support of our GMP manufacturing operations at the Seattle and Redmond, WA GMP facilities. These efforts support GMP manufacturing activities for biotherapeutic products.
Responsibilities:
+ Perform routine/non-routine QC testing using chromatographic and physiochemical methods.
+ Ensure timely and accurate completion of GMP documentation.
+ Collaborate with Analytical Development to generate and approve protocols, reports, and other technical documents required for the qualification and transfer of analytical methods.
+ Conduct laboratory investigations, deviations, OOS, change controls and CAPAs.
+ Support equipment qualification (IQ, OQ, PQ).
+ Create, maintain, and revise SOPs, methods and associated documents.
+ Support all operations of the QC labs including the ordering supplies and maintaining laboratory equipment and lab spaces.
+ Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on analytical related matters.
+ Participate in daily and weekly operation meetings.
Additional Skills & Qualifications
+ BS in Chemistry, Biochemistry, or related field and with 3-5 years of Quality Control experience in GMP biopharmaceutical or biotechnology industry.
+ Laboratory Experience with HPLC / UPLC chromatography systems and capillary electrophoresis (CE) techniques.
+ Familiarity with capillary electrophoresis or chromatography data systems.
+ Knowledge of GMP regulations and experience with regulatory compliance inspections.
+ Ability to adapt, work in a fast-paced environment, manage multiple projects and priorities at the same time.
+ Excellent oral/written and interpersonal communication skills; and a knowledge of Microsoft Office Suite (Excel, Word, PowerPoint).
Pay and Benefits
The pay range for this position is $42.00 - $52.00/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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Redmond,WA.
Application Deadline
This position is anticipated to close on Oct 31, 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 (% ) for other accommodation options.