quality control scientist

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

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

Manaspurti Technologies Private Limited

Job Overview: We are seeking a skilled Food Scientist to contribute to the development, production, and improvement of our food products. The ideal candidate will possess a strong understanding of food chemistry, microbiology, and processing techniques.Responsibilities:<ul><li>Conduct research and development of new food products, from concept to commercialisation.</li><li>Optimise existing food formulations to improve taste, texture, and nutritional value.</li><li>Ensure product compliance with food safety regulations and quality standards.</li><li>Develop and implement quality control procedures and protocols.</li><li>Investigate food-related issues and implement corrective actions.</li><li>Conduct sensory evaluations and consumer testing.</li><li>Maintain accurate and detailed documentation of research and development activities.</li><li>Collaborate with other departments, such as production, marketing, and sales.</li><li>Stay updated on food industry trends, technologies, and regulations.</li></ul>Qualifications:<ul><li>Bachelor's or Master's degree in Food Science, Food Technology, or a related field.</li><li>Strong understanding of food chemistry, microbiology, and processing techniques.</li><li>Knowledge of food safety regulations and quality standards.</li><li>Excellent problem-solving and analytical skills.</li></ul>Job Types: Full-time, PermanentPay: From &#8377;15,000.00 per monthBenefits:<ul><li>Flexible schedule</li><li>Paid sick time</li></ul>Experience:<ul><li>total work: 1 year (Preferred)</li></ul>Work Location: In person

Food Scientist [Goa candidates only]

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

Kenvue

<div><div><div><div><div><div><div><div>Kenvue is currently recruiting for a:</div></div></div></div></div></div></div>
Scientist RMC Analytical
What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we&rsquo;re the house of iconic brands - including NEUTROGENA&reg;, AVEENO&reg;, TYLENOL&reg;, LISTERINE&reg;, JOHNSON&rsquo;S&reg; and BAND-AID&reg; that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage &ndash; and have brilliant opportunities waiting for you! Join us in shaping our future&ndash;and yours.
Role reports to:
Principal Scientist RMC Analytical
Location:
Asia Pacific, India, Maharashtra, Greater Mumbai
Work Location:
Fully Onsite
What you will do
Kenvue is currently recruiting for:
Scientist RMC Analytical - Mumbai
Who we are
At Kenvue, part of the Johnson &amp; Johnson Family of Companies, we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands&mdash;including NEUTROGENA&reg;, AVEENO&reg;, TYLENOL&reg;, LISTERINE&reg;, JOHNSON&rsquo;S&reg; and BAND-AID&reg; &mdash;are category leaders trusted by millions of consumers who use our products to improve their daily lives. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers&rsquo; hearts and homes.
What will you do
Position Summary
Scientist RMC Analytical
Support Analytical Qualifications and Specification Management for Raw Materials:
<ul><li>Support Analytical (Raw Material testing &amp; Characterization) projects globally and ensure on time support to various projects in Cosmetic and OTC products.</li><li>
Support Analytical stability testing for qualification projects globally and ensure on time support to various projects in Cosmetic and OTC products.</li><li>
Responsible for the calibration and maintenance of in-house equipment&rsquo;s.
</li><li>Collaborate with external partners for outsourcing activities and ensure the compliance to applicable Kenvue standards</li><li>
Participate in discussions regarding analyzing and interpreting data, drawing conclusions, and arriving at timely technical decisions</li><li>
Responsible for compliance of EOHS &amp; Quality standards in lab</li></ul>
Major Duties &amp; Responsibilities
Tasks/Duties/Responsibilities<ul><li>
Coordination of Raw Material Analytical qualification projects to ensure timely support to internal stakeholders</li><li>
Participate in various meetings with internal and external stakeholders to shape/streamline the processes</li><li>
Participate in raw material related investigations as appropriate to support internal &amp; external manufacturing sites and investigate the OOS results during Analytical qualifications.</li><li>
Draft &amp; review of technical documents like qualification reports, stability reports, technical justifications, analytical method transfer etc.</li><li>
Training and Performance assessment of third-party resources</li><li>
Provide timely updates to reporting manager and provide insights on creating new opportunities for process improvements</li></ul>
Required Minimum Education:
 A minimum of a Master&rsquo;s degree in Analytical/Organic Chemistry or BPharm or MPharm from reputed university
Required Years of Related Experience: 2-5 years in FMCG/Pharma sector
Required Knowledge, Skills and Abilities:
(Include any required computer skills, certifications, licenses, languages, etc.)<ul><li>
Advanced understanding and application of principles, concepts, and practices of Analytical Chemistry is required.</li><li>
Adequate knowledge of GMP, quality systems, SOPs, Global &amp; Country specific Regulatory requirements</li><li>
Technical skills related to interpretation of analytical data and accurate documentation of laboratory investigations and non-conformances.</li><li>
Excellent communication, organizational, and interpersonal skills</li><li>
Experience in an GxP environment is mandatory.</li><li>
Ability to collaborate with internal and external resources to meet project objectives.</li><li>
Proven record of delivering project results</li><li>
Strong analytical and problem-solving skills</li><li>
Proficiency in Microsoft office tools</li></ul>
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.</div>

Scientist RMC Analytical

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>

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

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Formulation/Quality Scientist