339 Associate Scientist jobs in the United States

**Join Amgen's Mission of Serving Patients**
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**Associate Scientist**
**What you will do**
The Hybrid Modality Group at Amgen is seeking a highly motivated scientist in the field of Antibody Drug Conjugates (ADC) to join us in the state-of-the-art research facility at the Amgen headquarters campus located in Thousand Oaks, CA.
Let's do this. Let's change the world. In this vital role you will work at the interface of synthetic chemistry, biochemistry, and chemical biology, and apply your chemical synthesis skills in developing new antibody drug conjugates to support the advancement of drug discovery programs
+ Perform bioconjugation of antibodies, peptides, and small molecule payloads and characterize conjugates using analytical techniques, such as HPLC, LC-MS, and SEC.
+ Synthesis, purification and characterization of small molecule payloads and linkers
+ Operate and maintain standard lab equipment.
+ Document experimental plans and procedures with attention to detail in a timely manner.
+ Review, analyze, and interpret scientific data and results; and provide regular updates, documentation, and/or communication on project results
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The dedicated individual we seek is a scientist with these qualifications.
**Basic Qualifications:**
+ Master's Degree and 1+ years of relevant experience
**Or**
+ Bachelor's Degree and 3+ years of relevant experience
**Preferred Qualifications:**
+ Master's degree in Organic Chemistry, Biochemistry, or a related field
+ Demonstrated proficiency in organic synthesis including designing, executing, and optimizing chemical reactions
+ Experienced in various purification and analytical techniques including chromatography methods (e.g. HPLC, RP HPLC chromatography) and structural determination methods (e.g. NMR, MS)
+ Demonstration of good lab practices, with particular attention to safety
+ Strong written and verbal communication skills
+ Ability to work comfortably within a dynamic team of scientists and engineers with diverse technical and cultural backgrounds
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
+ A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
+ A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
+ Stock-based long-term incentives
+ Award-winning time-off plans
+ Flexible work models, including remote and hybrid work arrangements, where possible
**Apply now and make a lasting impact with the Amgen team.**
**careers.amgen.com**
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
**Application deadline**
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Actalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
+ Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.
+ Evaluate test results and decide on the acceptability of samples.
+ Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.
+ Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.
+ Ensure notebooks are reviewed promptly according to SOPs.
+ Analyze and interpret results in written and oral formats.
+ Assist in the training of new analysts.
+ Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.
+ Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.
Essential Skills
+ Proficiency in HPLC, UPLC, and UV-Vis.
+ Strong background in chemistry and analytical techniques.
+ Experience with SOPs and GMP compliance.
+ Ability to analyze and interpret data accurately.
Additional Skills & Qualifications
+ Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.
+ Ability to manage problems involving several concrete variables in standardized situations.
+ Competence in performing necessary computations and interpreting graphs.
+ Working knowledge of instrumentation software used in laboratories.
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $35.00/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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Sep 5, 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.

**Associate Scientist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. Catalent's Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology. The Associate Scientist is responsible for performing analytical research and development work in the Analytical R&D Department. The Associate Scientist work/assist on method development, method transfer, method verification and method validation under appropriate guidance along with routine release and stability testing in support of clinical development and registration activities required for the regulatory submissions. Shift: Monday-Friday 8 AM-5 PM. This position is 100% on-site in Winchester, Kentucky. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. **The Role** + Perform technical review of client's documents as required including but not limited to specification/validation reports/test methods/compliance reports etc. to perform gap analysis with respect to methods/instruments/procedures etc. for completing methods transfers from client's/or their third-party labs with guidance from supervisors/senior team members. + Analysis of finished products, in-process materials, raw materials, according to the assigned specifications, methods, and protocols according to cGLP and cGMP. Document, process, report the data as applicable to support the team in timely fashion. + Perform analysis as required to support assigned testing using KF titrations/Dissolutions/IR/UV spectrophotometers, LC to perform dissolutions/assays/BU/CU, impurities and data processing using Empower and document per applicable test methods/specification/protocols etc. with guidance from senior team members. + Use Empower software- creating instrument/processing/report methods and performing online empower calculations for assay/dissolutions/impurities etc. Knowledge of Trackwise for managing deviations and investigations and ability to manage /handle with guidance from supervisors/senior team members. + Troubleshoot and propose any method improvement requirements during the method feasibility work of client supplied methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with guidance from supervisors/senior team members. Methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with guidance from supervisors/senior team members. + Perform/assist team members in method transfers, Compendial verifications or full method validations (forced degradation and calculating mass balance/peak purity to prove stability indicating nature of the method) per applicable guidances (USP <1224>, <1225>, <1226> ICH Q2 etc.)/SOPs with guidance from the supervisors/senior team members. + Perform stability testing on developmental/clinical/registration batches as per approved test methods/stability protocols and report/document per applicable specification/stability protocols. Escalate any OOS/OOT/atypical/trending results with supervisors or concerned team members. + Other duties as assigned. **The Candidate** + Bachelor's Degree in Chemistry, Pharmaceutical Sciences or Life Sciences Required (Preferred in Analytical Chemistry). + Must have at least one year of experience in pharmaceutical industry and 1+ years of experience in analytical testing/research experience using HPLC/GC/UV, etc. + Understand analytical chemistry calculations such as concentrations (Area%, %w/w, ppm, µg/mL, etc.), molarity, Beer's Law, reference standard purity on as is, anhydrous, or dry basis etc. + Basic understanding and knowledge of analytical chemistry and chromatographic techniques (e.g., LC/GC/dissolutions) and spectroscopic (e.g., UV) analysis. + Demonstrate Knowledge and ability to understand and follow ICH guidelines (ICH Q1, Q2, Q3 etc.) including other regulatory guidelines. + Adhere and perform all lab job duties/responsibilities according to applicable SOP's related to DEA scheduled drugs, safety, waste management and housekeeping and work with the team in improvement of the processes and procedures. + Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs. Maintaining clean environment for laboratory operations. Use of and safe handling of glass canisters, chemicals, and other required equipment. **Why You Should Join Catalent** + Several Employee Resource Groups focusing on D&I + Tuition Reimbursement - Let us help you finish your degree or earn a new one! + Generous 401K match + 152 hours accrued PTO + 8 paid holidays **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers ( to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE ( .

Associate ScientistJob Description
The Associate Scientist will work within a Quality Control (QC) environment, performing product testing in a fast-paced laboratory setting. This role requires proficiency in HPLC, GC, and FTIR techniques to ensure the highest quality standards are met.
Responsibilities
+ Conduct bench-top chemistry tests, including viscosity and pH testing, to generate accurate data.
+ Test various formulations such as creams, gels, solutions, topicals, foams, and ointments.
+ Review, interpret, and execute analytical methods to ensure compliance with quality standards.
+ Collaborate with lab counterparts across multiple shifts to verify analyses and maintain consistency.
+ Escalate discrepancies to QC management if results do not align with expected outcomes.
+ Manage a fast-paced and high-pressure workload, typically running two tests per day.
Qualifications:
+ Bachelor's degree in a science field, preferably chemistry, organic chemistry, or biochemistry.
+ 6 months to 1 year of undergraduate research/lab or post-academic experience in a chemistry
+ Proficiency in HPLC and GC techniques.
Work Environment
The position operates on a 1st shift schedule, Monday through Friday, from 8am to 5pm. The work environment includes a well-equipped laboratory setting and requires adherence to a professional dress code.
Pay and Benefits
The pay range for this position is $22.00 - $22.00/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 San Antonio,TX.
Application Deadline
This position is anticipated to close on Aug 29, 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.

Kelly Science is seeking an Associate Scientist for a cell and gene therapy focused client located in the Boston, MA area.
Salary: $70,000-90,000/year
Job Duties Include:
+ Execute key Molecular Biology tasks which include nucleic acid isolation, qPCR, ddPCR, customized library preparation for DNA/RNA sequencing and library sequencing, preclinical and clinical samples for research grade and GLP/GCP compliant projects.
+ Participate in the establishment, transfer, standardization, and optimization of assays, as well as in the execution of method qualifications/validations.
+ Participate in the QA investigations of unexpected assay occurrences, deviations, and out-of-specification results in compliance with existing regulations.
+ Document experiments, results and findings in laboratory notebook and LIMS system.
+ Assist in authoring and updating of laboratory SOPs.
+ Collaborate in the setup, preventive maintenance and verification of lab equipment, and the preparation of device-related documentation (IQ/OQ, PQ and CSV documentation).
+ Contribute to laboratory maintenance tasks, including ordering and maintaining stock and resources.
Qualifications:
+ Bachelors degree in a scientific related field
+ 2-4 years of experience with molecular biology tasks such as nucleic acid isolation, qPCR, ddPCR and preparing for DNA/RNA sequencing.
+ Experience with analytical method qualification, transfer, validation and general understanding of regulatory requirements for biotherapeutics development is a plus.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:
**JOB LOCATION:** Lexington, MA
**POSITION** : Associate Scientist
**POSITION DESCRIPTION** : Takeda Development Center Americas, Inc. is seeking a Associate Scientist with the following duties: Provide hands on laboratory experience to the design and development of research assignments for a specific project or projects within the functional area; utilize a wide variety of analytical techniques to analyze samples and present the data in a timely manner either as a scientific presentation or report; understand project timelines and plan and coordinate project work with departmental, functional and external stakeholders; contribute independently to project work which may include multiple projects within functional area; generate, analyze, and interpret/communicate data; plan and implement resolutions to technical issues and instrument troubleshooting when needed; serve as a technical resource for junior staff and leverage expertise in laboratory technology as a functional resource/trainer; independently design and execute experiments, and report results; build and maintain relationships with vendors and assist with technical aspects of vendor negotiations; up to 5% domestic and international travel required.
**REQUIREMENTS:** Master's degree in Chemistry, Biology, Pharmacy, Pharmaceutical Sciences, Engineering, or a related pharmaceutical science field plus 3 years of related experience OR Bachelor's degree in Chemistry, Biology, Pharmacy, Pharmaceutical Sciences, Engineering, or a related Pharmaceutical Science field plus 5 years of related experience. Prior experience must include: Conduct molecular cloning, expression, and purification of recombinant proteins and antibodies for drug discovery, and develop protocols for the production, purification, and characterization of catalytic antibodies. Generate, analyze, and interpret data, and planned and implement solutions to technical issues, including troubleshooting laboratory instruments when needed; Analyze data from preclinical studies to evaluate the efficacy and safety of therapeutic antibodies and utilized protein engineering techniques to enhance their binding affinity and specificity. Serve as a technical resource for junior staff, leveraging expertise in laboratory technology and providing training; Provide hands-on laboratory support for the design and development of research assignments for specific projects, applying a wide range of analytical techniques to analyze samples and presenting data as scientific presentations or reports. Develop and validate in-process analytical methods (e.g., HPLC, CE, SDS-PAGE) to monitor critical quality attributes of biologics during manufacturing, ensuring regulatory compliance and consistency; Independently design and execute experiments, reporting results in a timely manner. Build and maintain relationships with vendors and assist with technical aspects of vendor negotiations.
Full time. $127,500.00 - $195,600.00 per year. Competitive compensation and benefits.
Qualified applicants can apply at . Please reference job #R0152031. EOE
Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
**Locations**
Lexington, MA
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time

Associate Scientist
Date: Aug 6, 2025
Location:
West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 61694
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**How you'll spend your day**
Teva Branded Pharmaceuticals Products R&D LLC seeks an Associate Scientist in our West Chester, PA office to:
· Troubleshoot or investigate study results, as applicable and independently author technical reports and prepare data presentations for cross-functional teams with minimal supervision.
· Support drafting regulatory filling document (IND, BLA etc).
· Perform routine cell culture experiments including seed culture expansion, bioreactor operation and clarification activities to support early and late -stage process development. This includes, but is not limited to experiments in shaker flasks, Ambr15, Ambr 250, 10L, 50L, 100L and 200L bioreactors, disc-stack centrifuge, and filtration.
· Perform equipment set-up, sterilization, daily operation, sampling and in-process tests (Ex: cell count, viability, gases, metabolites, titer).
· Record experiment results in batch records and electronic lab notebooks in compliance to Good Documentation Practices.
· Perform data analysis as needed.
· Design and conduct experiments to support upstream process development and process characterization activities under managerial supervision.
· Develop experimental plan and execute cell culture and/or harvest studies in laboratory either individually or as a part of working team.
· Maintain and troubleshoot laboratory equipment, coordinate calibration, and manage raw material stocks and supplies in collaboration with relevant internal groups.
· Lead USP projects for timeline driven deliverables in a multi-disciplinary matrix organization.
Approximately 10% domestic travel and 10% international travel required for business purposes including attending conferences and trainings.
**Your experience and qualifications**
**REQUIREMENTS:** Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology or a related field and 2 years of mammalian cell culture and bioreactor operation experience in a biopharmaceutical company.
Must have experience with:
· Chemical engineering principles;
· Process-scale up and scale-down model qualification activities;
· Early and late-stage cell culture development activities;
· Process characterization activities;
· Design of experiments (DOE) and statistical modeling; and,
· Statistical software for data analysis and statistical modeling including JMP and SIMCA.
· Approximately 10% domestic travel and 10% international travel required for business purposes including attending conferences and trainings.
Please apply at using REQ ID 61694.
**Enjoy a more rewarding choice**
We offer a competitive benefits package, including:
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
Life and Disability Protection: Company paid Life and Disability insurance.
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. 
The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.  
**Already Working @TEVA?**
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site ( internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
**Important notice to Employment Agencies - Please Read Carefully **  
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities.  All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.  
EOE including disability/veteran