quality assurance scientist

Amway

<div>
 
 Job Description
 
 
 
 Apply now
 
 
 Job Title: Formulation/Quality Scientist
 
 
 Posting Start Date: 10/23/25
 
 
 Posting Location: Ada (Grand Rapids), MI
 
 
 Requisition ID: 42130
 
 
 
 Job title: Formulation/Quality Scientist
 
 
 
 
 Department / Division: Nutrition Quality Assurance/Research &amp; Development
 
 
 
 
 Salary Grade: EXC 15
 
 
 
 
 Salary Range: $97,620 - $116,389
 
 
 
 
 Location: Ada, MI
 
 
 
 
 What Do We Need
 
 
 
 Are you passionate about working with innovative and high-quality supplement products that improve the health and wellbeing of consumers around the world? We are seeking a nutrition formulation talent, who will collaborate with a highly cross functional team to deliver formulation support for our existing nutrition portfolio. This individual will support all internally produced products offering technical support from our raw materials, through a lifecycle of finished goods production. A primary area of focus in this role involves supply continuity, offering analysis and solutions for issues that risk interrupting our product supply. This includes quality issues, regulatory changes that require reformulation, or manufacturing issues that involve troubleshooting support to maintain supply continuity.
 
 
 
 What&rsquo;s Special About This Team
 
 
 
 The Nutrition Quality Engineering group is a dynamic team of over 20 engineers across two Amway sites (Ada, Michigan and Buena Park, California). The team works in a fast-paced environment supporting internal and external manufacturing sites to ensure quality product is produced and supplied to our customers. Our team works heavily with cross functional partners such as engineering, product development, planning, suppliers, and manufacturing to prevent and address product quality issues. Our team also works with our global QA counterparts in over 10 markets across many countries. This is a talented team with deep expertise that one can learn from and build skills and competencies that promote personal and professional growth.
 
 
 
 Required Qualifications
 
 
 
 <ul>
 <li>
 BS degree (MS desired) in chemical engineering, food or pharma science or closely related discipline
 </li>
 <li>
 Minimum 1 - 3 years&rsquo; experience in nutrition, food, or pharma industry working with product formulation
 
 
 </li>
 </ul>
 
 Skills To Be Successful In The Role
 
 
 
 <ul>
 <li>
 Ability to develop solutions for technical formulation challenges
 </li>
 <li>
 Exposures in product formats such as tablets, capsules, soft gels, etc.
 </li>
 <li>
 Talent to collaborate with internal partners and external vendors to effectively and efficiently resolve issues
 </li>
 <li>
 Experience with data analysis, statistical techniques, and problem solving
 </li>
 <li>
 Comfort with lab equipment, knowledge of manufacturing equipment, and formulation talent
 
 
 </li>
 </ul>
 Amway does not provide immigration-related sponsorship for this role. Do not apply for this role if you will need Amway immigration sponsorship (e.g., H-1B, STEM OPT, TN, etc.) now or in the future.
 
 
 Apply now
</div>

Formulation/Quality Scientist

Department of General Services

<div><div><div><div><div><div><div>Are you a Scientist with interest in quality assurance, biochemistry, chemistry, and molecular biology testing?

Come join DGS as a Senior Scientist in our Newborn Screening Group!

Title: Senior Scientist (Newborn Screening) &ndash; CL538

State Role Title: Scientist II

Hiring Range: $69,000 - $83,000

Pay Band: 5

Agency: Department of General Services

Location: Richmond, VA

Agency Website: www.dgs.virginia.gov

Recruitment Type: General Public &ndash; G

DGS is seeking a Senior Scientist for our Newborn Screening Laboratory at the Division of Consolidated Laboratory Services (DCLS). This position serves as a Senior Scientist. This position oversees quality assurance (QA) efforts for the NBS Group and the performance of filter paper blood spot analysis for a variety of genetic disorders as required by the Code of Virginia.

Virginia&rsquo;s Newborn Screening Program is a partnership between DCLS and the Virginia Department of Health to screen each baby born in Virginia for certain rare yet serious metabolic and genetic disorders. Babies with these disorders may look healthy at birth but can suffer devastating consequences, even death, if the disorder goes untreated. The Newborn Screening Group works with various platforms including mass spectrometry, electrophoresis, microfluidics, automated immunoassays, and molecular techniques including polymerase chain reaction (PCR) and sequencing.

As a member of the Newborn Screening laboratory team, this Senior Scientist will support customer service efforts, oversee quality assurance efforts, review analytical results, write, review and update SOPs, train staff, act as a technical specialist and prioritize, schedule and coordinate testing performed by other staff members, as needed. This position will also participate in product evaluations, method analysis, and maintain competency according to the agency accreditation requirements. These duties are performed independently with minimal supervision from the Group Manager.

Job duties include, but are not limited to:
<ul>
<li>Independently performs moderate and highly complex testing accurately.</li>
<li>Support the DCLS Quality Management System to ensure the accuracy and integrity of DCLS laboratory test results.</li>
<li>Maintains, troubleshoots, monitors repair services for and documents instrument, equipment, method problems, and service requests.</li>
<li>Monitors and maintains a current inventory of testing supplies and materials.</li>
</ul><ul><li>In addition, some weekend and holiday work as well as on-call coverage is required.</li>
</ul>
We&rsquo;ve got great benefits!

DGS offers excellent health benefits at affordable pricing, pre-tax spending accounts, paid life insurance, paid Short- and Long-Term Disability benefits, paid holidays, vacation, and other leave benefits, wellness programs, and a state retirement plan with options for tax-deferred retirement savings including employer matching. Additionally, supplemental bus passes, ride share, or parking are available and DGS is a qualifying employer for the Public Service Loan Forgiveness Program.

Minimum Requirements
<ul>
<li>Candidate must meet the requirements for technical supervisor in a high complexity testing laboratory as defined by 42 CFR 493.1449.
</li><li>Candidate must demonstrate significant knowledge and experience in clinical laboratory testing.</li>
<li>Experience training staff.</li>
<li>Ability to communicate effectively and work in a team environment.</li>
<li>Experience operating and troubleshooting laboratory instrumentation.</li>
<li>Demonstrated ability to apply safe laboratory practices.</li>
<li>Experience with QA and QC procedures and ability to document and interpret QC data.</li>
<li>Ability to work a set schedule for Monday through Friday, with some weekend and holiday work as well as on-call coverage.</li>
</ul>
Sponsorship will not be provided for this position now or in the future. Confirmation of eligibility to work will be required at time of hire.

The selected candidate must also pass a fingerprint-based criminal background check.

Additional Considerations
<ul>
<li>Knowledge and experience with high complexity, high volume clinical laboratory testing using automated laboratory equipment.</li>
<li>Experience with Laboratory Information Management Systems (LIMS).</li>
<li>Work-related experience serving as a team leader with the ability to prioritize, schedule and coordinate laboratory testing of others.</li>
<li>Work-related experience with mass spectrometry, including LC-MS/MS.</li>
<li>Work-related experience with immunoassays, molecular biology assays, enzyme activity assays, and/or HPLC.</li>
<li>Experience leading quality assurance and quality improvement initiatives.</li>
<li>Experience preparing for CLIA audits.</li>
</ul>
Special Instructions

The online state application must contain all required information and fully respond to questions to be considered for this job opportunity. Please be sure that all of your relevant qualifications and considerations are specifically addressed in your submitted application.

Online applications should be submitted via jobs.virginia.gov.

Fax, e-mail, or mail applications will not be accepted. For assistance or computer access, please visit your local Virginia Employment Office or contact our office jobs@dgs.virginia.gov or 804-786-3910.

You will be provided with confirmation of receipt when your application has been successfully submitted. Applications will continue to be accepted until a suitable pool of candidates is received, but this position may be closed at any time after NOVEMBER 18, 2025. Please refer to the &ldquo;Your Application&rdquo; page in your account to check the status of your application for this position. Applicants in need of accommodation during the application and/or interview process may contact DGS at 804-786-3910 for assistance.

Sponsorship will not be provided for this position now or in the future. Confirmation of eligibility to work will be required at time of hire. DGS will record information from each new employee&rsquo;s Form I-9 (Employment Eligibility Verification) into the Federal E-Verify system to confirm identity and work authorization.

The selected candidate must pass a fingerprint-based criminal background check.

Blood-borne pathogen training will be provided by the employer. In order to comply with OSHA blood-borne pathogen requirements, DCLS offers the Hepatitis B vaccine.

DCLS employees are designated as essential personnel. This designation requires DCLS employees to report to the workplace or at an assigned remote location during state authorized closings or delays (i.e., weather-related closures/delays, holidays, etc.), unless otherwise instructed by management.

Due to the critical nature of the work performed by the Division of Consolidated Laboratory Services (DCLS) and the requirements and responsibilities placed upon DCLS by the Drug Free Workplace Act, Federal Select Agent Program, and DHRM Policy 1.05 Alcohol and other Drugs, it is the policy of DCLS to maintain a workplace that is free from the harmful effects of alcohol or other drugs. The unlawful or unauthorized use of drugs by DCLS employees while at work adversely impacts DCLS&rsquo;s ability to perform high quality analytical testing services and support for local, state and federal agencies that serve to protect the health, safety and security of the public. As such, DCLS strictly prohibits the manufacture, distribution, dispensation, possession or use of alcohol, marijuana, or other drugs, prohibits employees from possessing or using alcohol, marijuana or any controlled substances (including, but not limited to prescription drugs) while in state owned vehicles, in the workplace or on DCLS premises, or when performing official work duties.

Applicants that indicate they have preferential hiring rights in the form of a yellow form or blue card must submit these to our office prior to the closing of the posting, in accordance with DHRM policy 1.30. Please note that only current and former employees of the Commonwealth of Virginia that will be or have been laid off are eligible for preferential hiring rights.

The Virginia Department of General Services is an equal opportunity employer and a proud Virginia Values Veterans (V3) Certified employer. Individuals from minoritized groups, individuals with disabilities, veterans, and individuals with AmeriCorps, Peace Corps, and other national service experience are encouraged to apply.

In support of the Commonwealth&rsquo;s commitment to inclusion, we are encouraging individuals with disabilities to apply through the Commonwealth Alternative Hiring Process. To be considered for this opportunity, applicants will need to provide their AHP Letter (formerly COD) provided by the Department for Aging &amp; Rehabilitative Services (DARS), or the Department for the Blind &amp; Vision Impaired (DBVI). Service-Connected Veterans are encouraged to answer Veteran status questions and submit their disability documentation, if applicable, to DARS/DBVI to get their AHP Letter. Requesting an AHP Letter can be found at AHP Letter or by calling DARS at 800-552-5019.

Note: Applicants who received a Certificate of Disability from DARS or DBVI dated April 1, 2022- February 29, 2024, can still use that COD as applicable documentation for the Alternative Hiring Process.

Contact Information

Name: DGS Human Resources

Phone: 804-786-3910

Email: jobs@dgs.virginia.gov 
</div></div></div></div></div><div><div><div>Each agency within the Commonwealth of Virginia is dedicated to recruiting, supporting, and maintaining a competent and diverse work force. Equal Opportunity Employer</div></div></div></div></div><div></div>

Senior Scientist (Newborn Screening) - CL538

United Pharma Technologies Inc

<div>
 
 
 Position:
 
 QC Scientist
 
 
 
 Location:
 
 Massachusetts (MA)
 
 
 
 
 
 
 Job Description
 
 
 
 We are seeking a QC Scientist to support analytical testing for monoclonal antibody (mAb) programs. The ideal candidate will be responsible for executing standardised assays, data interpretation, and maintaining high-quality lab practices in a GMP environment.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Perform standardised assays for monoclonal antibodies.
 </li>
 <li>
 Conduct UPLC and CE analyses, glycan analysis, titer, mAb, and peptide mapping.
 </li>
 <li>
 Schedule laboratory work, process analytical data, and interpret results accurately.
 </li>
 </ul>
 
 
 
 
 
 Requirements
 
 
 <ul>
 <li>
 Motivated self-starter with relevant technical laboratory experience.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Experience with Mass Spectrometry.
 </li>
 <li>
 Waters BioAccord experience is a strong plus.
 </li>
 </ul>
 
 
</div>

Quality Control Scientist

Herbalife

<div>Overview:
<h2 class="jobSectionHeader">Position summary statement:</h2><div>
The Scientist, Document Control will have a key role in ensuring that both current and proposed raw material specifications meet Herbalife Nutrition's strict requirements and align with current regulatory demands. This role presents an outstanding opportunity to partner with various teams and efficiently implement raw material changes promptly.</div><h2 class="jobSectionHeader">
Detailed responsibilities/duties:</h2><ul><li>
Conduct a technical assessment of raw material documents to determine their suitability for Inner and/or Outer Nutrition.</li><li>
Collaborate and offer mentorship to Document Sourcing (Corporate and Regional) teams regarding inquiries concerning raw material specifications and documentation.</li><li>
Formulate, evaluate, and adjust raw material specifications in Agile, confirming adherence to existing requirements and regulations.</li><li>
Collaborate with Research and Development (Tech Ops, Formulation), Global Regulatory Affairs and Product Compliance (Corporate and Regional), Quality Control (QC), Product Science, and Transportation to guarantee suitability.</li><li>
Route raw material change requests and change orders in Agile, gathering necessary approvals from various departments promptly.</li><li>
Review raw materials used in new or revised formulas, ensuring raw materials and suppliers are approved for contract manufacturers.</li><li>
Collaborate with Global Regulatory Affairs and Product Compliance (both Corporate and Regional) to address country-specific testing needs.</li><li>
Collaborate with raw material suppliers or contract manufacturers to address concerns regarding raw material specifications.</li><li>
Support and offer mentorship to the Document Sourcing team.</li><li>
Inform contract manufacturers of any raw material specification changes.</li><li>
Keep all records pertaining to raw materials.</li><li>
Perform additional responsibilities as assigned.</li></ul><h2 class="jobSectionHeader">
Required qualifications:</h2><div>
Skills:</div><ul><li>
Fundamental understanding of raw material documentation and processes.</li><li>
Outstanding attention to detail to determine document acceptability.</li><li>
Goal-oriented with a history of fulfilling set requirements.</li><li>
Strong customer service and relationship-building skills.</li><li>
Excellent written and oral communication skills for cross-functional collaboration.</li><li>
Strong analytical skills to accomplish changes effectively.</li><li>
Remarkable planning and interpersonal skills to manage multiple tasks.</li><li>
Proficiency in Microsoft Office.</li><li>
Great teammate who is adaptable and comfortable with change.</li></ul><h2 class="jobSectionHeader">
Experience:</h2><ul><li>
4-5 years of experience in Quality Assurance or Quality Control within an FDA-regulated sector (21-CFR- Food, Dietary Supplement, or Drug).</li><li>
Previous experience conducting laboratory tests in Food, Dietary Supplement, Pharmaceutical, or Environmental industries.</li></ul><h2 class="jobSectionHeader">
Education:</h2><ul><li>
Bachelor&rsquo;s degree in a scientific field or equivalent experience.</li></ul></div>

Scientist, Document Control - India

Herbalife International India Pvt. Ltd.

<div>
 
 Overview
 
 
 
 Position summary statement:
 
 
 The Scientist, Document Control will have a key role in ensuring that both current and proposed raw material specifications meet Herbalife Nutrition's strict requirements and align with current regulatory demands. This role presents an outstanding opportunity to partner with various teams and efficiently implement raw material changes promptly.
 
 
 
 Detailed Responsibilities/duties
 
 
 
 <ul>
 <li>
 Conduct a technical assessment of raw material documents to determine their suitability for Inner and/or Outer Nutrition.
 </li>
 <li>
 Collaborate and offer mentorship to Document Sourcing (Corporate and Regional) teams regarding inquiries concerning raw material specifications and documentation.
 </li>
 <li>
 Formulate, evaluate, and adjust raw material specifications in Agile, confirming adherence to existing requirements and regulations.
 </li>
 <li>
 Collaborate with Research and Development (Tech Ops, Formulation), Global Regulatory Affairs and Product Compliance (Corporate and Regional), Quality Control (QC), Product Science, and Transportation to guarantee suitability.
 </li>
 <li>
 Route raw material change requests and change orders in Agile, gathering necessary approvals from various departments promptly.
 </li>
 <li>
 Review raw materials used in new or revised formulas, ensuring raw materials and suppliers are approved for contract manufacturers.
 </li>
 <li>
 Collaborate with Global Regulatory Affairs and Product Compliance (both Corporate and Regional) to address country-specific testing needs.
 </li>
 <li>
 Collaborate with raw material suppliers or contract manufacturers to address concerns regarding raw material specifications.
 </li>
 <li>
 Support and offer mentorship to the Document Sourcing team.
 </li>
 <li>
 Inform contract manufacturers of any raw material specification changes.
 </li>
 <li>
 Keep all records pertaining to raw materials.
 </li>
 <li>
 Perform additional responsibilities as assigned.
 
 
 </li>
 </ul>
 
 Skills
 
 
 
 Required qualifications:
 
 
 <ul>
 <li>
 Fundamental understanding of raw material documentation and processes.
 </li>
 <li>
 Outstanding attention to detail to determine document acceptability.
 </li>
 <li>
 Goal-oriented with a history of fulfilling set requirements.
 </li>
 <li>
 Strong customer service and relationship-building skills.
 </li>
 <li>
 Excellent written and oral communication skills for cross-functional collaboration.
 </li>
 <li>
 Strong analytical skills to accomplish changes effectively.
 </li>
 <li>
 Remarkable planning and interpersonal skills to manage multiple tasks.
 </li>
 <li>
 Proficiency in Microsoft Office.
 </li>
 <li>
 Great teammate who is adaptable and comfortable with change.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 4-5 years of experience in Quality Assurance or Quality Control within an FDA-regulated sector (21-CFR- Food, Dietary Supplement, or Drug).
 </li>
 <li>
 Previous experience conducting laboratory tests in Food, Dietary Supplement, Pharmaceutical, or Environmental industries.
 
 
 </li>
 </ul>
 
 Education
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in a scientific field or equivalent experience.
 
 
 </li>
 </ul>
 Terms of Use Privacy Policy Compliance Documents CSR Policy
</div>

Adecco

Quality Control Associate Scientist (Temporary - until February 2026) Basingstoke, UK Full-time, Temporary Contract Are you an experienced Quality Control professional looking to make an impact in a leading life sciences organisation? We have an exciting opportunity for a Quality Control Associate Scientist to join our team in Basingstoke on a temporary basis until February 2026. About the Role As a Quality Control Associate Scientist, you will play a key role in ensuring our products meet the highest standards of quality and compliance. You will carry out a range of QC testing activities in accordance with Oxoid test specifications and methods, supporting the timely and accurate release of products. Key Responsibilities <ul> <li> Perform Quality Control testing in line with Oxoid test specifications, including Level 1, 2, and 3 testing methods. </li><li> Prepare media and manage the use of autoclaves. </li><li> Complete Out of Specification (OOS) reports and assist with investigations. </li><li> Maintain accurate and up-to-date training records. </li><li> Plan, track, and control the progress of products under test, providing reliable availability dates to Planning and Customer Services. </li><li> Proactively alert the QC Team Leader to any potential issues or failures and support follow-up investigations. </li><li> Record all test results within the SAP Quality Management module. </li><li> Conduct equipment checks, cleaning, and audits to ensure compliance with quality standards. </li><li> Manage waste disposal and replenish consumables as required. </li></ul> About You We're looking for someone with: <ul> <li> Previous experience in a Quality Control or laboratory environment (ideally within life sciences, microbiology, or pharmaceuticals). </li><li> Strong attention to detail and a proactive approach to problem-solving. </li><li> Familiarity with SAP Quality Management or similar systems (desirable). </li><li> Excellent organisational and communication skills. </li><li> The ability to work effectively in a fast-paced, team-oriented environment. </li></ul> Contract Details <ul> <li> Location: Basingstoke </li><li> Contract type: Temporary (until February 2026) </li><li> Hours: Full-time </li></ul> Join a team dedicated to maintaining the highest standards of product quality and safety - and help us deliver excellence every day. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

QC Associate Scientist

US Pharmacopeia

<div>
 
 Description
 
 
 
 At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare.
 
 
 USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work&mdash;an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
 
 
 
 Brief Job Overview
 
 
 
 This is a hands-on, non-supervisory scientific position the Global Biologics department. The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies. The incumbent will provide quality and technical review of scientific documents for accuracy, clarity and compliance, manage and track reference standard stability program and organize efforts for continuous process improvements. The incumbent will also focus on supporting the reference standard suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports for confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in time-bound manner.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.
 
 
 
 The Sr. Scientist -I (RSS-Review) Has The Following Responsibilities
 
 
 
 Roles and Responsibilities
 
 
 <ul>
 <li>
 Performs technical and quality reviews of documents to ensure a high level of document quality and compliance before QA review
 </li>
 <li>
 Manages and tracks efforts for continuous process improvements.
 </li>
 <li>
 Develops and reviews SOP&rsquo;s, Operation Manuals, and training documents.
 </li>
 <li>
 Assists in investigations of quality related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring.
 </li>
 <li>
 Supports the day to day operation of the reference standard stability program.
 </li>
 <li>
 Works with internal stakeholders to develop new and innovative standards for analytical analysis of biological products.
 </li>
 <li>
 Communicates and maintains working relationships with cross functional USP departments regarding assigned projects
 </li>
 <li>
 Supports day to day operations of the RS Stability (CSU) program covering the USP Biologics RS catalog inventory.
 </li>
 <li>
 Reviews RS testing history and drafts test protocols for CSU studies and submits to labs based on designated testing requirements and schedules.
 </li>
 <li>
 Liaisons and Assists laboratories to ensure CSU testing is completed as per protocol and in timely manner.
 </li>
 <li>
 Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use.
 </li>
 <li>
 Compiles, assess current and historical stability testing data and prepare stability trend reports in a time-bound manner.
 </li>
 <li>
 Support the maintenance and updation of various databases documenting laboratory data and program determinations on suitability and Stability interval updates.
 </li>
 <li>
 Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Supporting Quality Assurance and Reference Standard Evaluation in the investigation of unexpected stability testing results
 </li>
 <li>
 Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps.
 </li>
 <li>
 Prepare, present and discuss regular work updates with Team Lead and other team members
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 
 
 <ul>
 <li>
 PhD. degree in Biochemistry/Biology/Pharmacy, or a related field Minimum of 7 to 10 years, or Masters degree in Biochemistry/Biology/Pharmacy or a related field with 11 to13 years of years of commensurate industrial experience.
 </li>
 <li>
 Demonstrated experience in Techical review of analytical documents in Quality Assurance.
 </li>
 <li>
 Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc.
 </li>
 <li>
 Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development.
 </li>
 <li>
 Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays.
 </li>
 <li>
 Excellent technical writing, presentation and oral communication skills are required.
 </li>
 <li>
 Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Knowledge of USP products and services is highly desirable.
 </li>
 <li>
 Operates collaboratively at all levels of the organization in a highly technical environment.
 </li>
 <li>
 Must be able to work in a fast-paced environment and respond to shifting priorities.
 </li>
 <li>
 Well-developed interpersonal, negotiation, conflict-resolution and listening skills.
 </li>
 <li>
 Must possess the ability to multi-task and to work effectively with a team.
 </li>
 <li>
 Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality.
 </li>
 <li>
 Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 No
 
 
 
 Benefits
 
 
 
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 
 
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Senior Scientist I, Documentary Standards (Reviewer)

Search 10000+ Quality assurance scientist jobs near you this November. New roles added regularly across leading industries. Apply today.

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