product development scientist

SUPRANATURALS, LLC

<div>POSITION PURPOSE AND SCOPE: 
This scientist will be responsible for developing formulas (liquid, powder, capsule), flavor work, and validating methods to support manufacturing and new products; instrumentation or equipment set up, troubleshooting, maintenance, and blend validation, and training other formulators in the lab.
 
 
ESSENTIAL RESPONSIBILITES:<ul><li>
Create new formulas for customers and formulate great tasting products</li><li>
Performs technical support for new product, to ensure product is ready for production run</li><li>
Creates the Batch Records for production runs.</li><li>
Troubleshoots any issues related to the materials of the product run</li><li>
Finds solutions to help machines run better for the product run</li><li>
Approves all changes to Batch Records</li><li>
Gather and compile supplier documentation.</li></ul> 

Note: This description is not intended to be all inclusive. Employee may be requested to perform other duties as requested.
 
 
EDUCATION AND EXPERIENCE:<ul><li>
Undergraduate degree in Food Science with 3-5 years experience in related field.</li><li>
Related manufacturing experience (5 years) primarily in formulation and flavor work.
<ul><li>We work with many pre-workout/energy brands, so experience working with caffeine is a plus.</li></ul></li></ul>
SKILLS AND ABILITIES:<ul><li>
Highly motivated, creative and independent performer with the ability to operate in a fast-paced, high pressure environment.
</li><li>Ability to interpret a variety of instructions furnished in written, oral, or schedule form.</li><li>
High ethical standards with the ability to maintain confidentiality of information.</li><li>
Excellent written and verbal communication skills.</li><li>
Strong analytical, critical thinking and communications skills.
</li><li>Ability to work both independently and in a team environment</li><li>
Must be able to follow all safety guidelines.</li></ul>
PHYSICAL DEMANDS: 
The employee may be required to lift and/or move up to 30 lbs. 
 
WORK ENVIRONMENT:<ul><li>
Laboratory environment which may include long hours standing, sitting, bending, twisting, walking, climbing stairs, strong and/or unusual odors.</li></ul> 

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Product Development Scientist

Rich Products

<div>Rich&rsquo;s, also known as Rich Products Corporation, is a family-owned food company dedicated to inspiring possibilities. From cakes and icings to pizza, appetizers and specialty toppings, our products are used in homes, restaurants and bakeries around the world. Beyond great food, our customers also gain insights to help them stay competitive, no matter their size. Our portfolio includes creative solutions geared at helping food industry professionals compete in foodservice, retail, in-store bakery, deli, and prepared foods, among others. Working in 100 locations globally, with annual sales exceeding $4 billion, Rich&rsquo;s is a global leader with a focus on everything that family makes possible. Rich&rsquo;s&reg;&mdash;Infinite Possibilities. One Family.<div><div><div><h2 class="jobSectionHeader"> 
Purpose Statement</h2></div><div>
Rich Products, a $5.5Billion food manufacturing company, is looking for a Product Development Scientist II to join our growing R&amp;D Team. In this role, you will be responsible for new product development, product maintenance and product improvement for our desserts category. 
In this role, you will collaborate with cross functional teams to ensure successful development and commercialization of new products, product improvement or cost reductions. You will conduct routine, non-routine and complex research and development activities concerned with the chemical, biological and/or physical complexity of product formulations in order to develop new products and evaluate and improve the quality of existing products and related processes. 
You will successfully partner with others cross-functionally. 
This role is based in Missouri City, TX, with expected travel of 10%.</div></div><div><div><h2 class="jobSectionHeader">
Key Accountabilities and Outcomes</h2></div><div><div>
New Product Development/Product Improvements/Cost reductions 
<ul><li>Prepares prototype and line extension products using research lab, pilot lab, manufacturing facilities and equipment, as required. Typical project assignments involve small product line extensions and iterative new products (e.g. modifying a customized product formula to create a new product).</li><li>Plans, organizes and completes projects of modest scope or are a segment of a larger project. Selects and/or develops appropriate methods for conducting projects and assists in designing experiments.</li><li>Interfaces frequently with various internal departments (i.e. Marketing, Purchasing, Engineering) and customers in accomplishing project milestones.</li><li>Selects and evaluates raw materials for experiments.</li><li>Sets-up, operates and maintains research lab equipment.</li><li>Works with outside labs, universities, ingredient suppliers and lab equipment vendors as needed by project activity.</li><li>Designs and conducts complex shelf life and storage studies, including product and package performance under various conditions and makes recommendations for appropriate adjustments in product and/or package as required.</li><li>Designs and conducts storage studies, including product and package performance under various conditions.</li><li>Performs complex measurements and statistical analysis.</li></ul></div><div>
Technical Support 
<ul><li>Presents results of complex experiments and recommendations to various groups, both internally and externally.</li><li>Orders materials for producing and evaluating complex prototypes.</li><li>Develops solutions to a variety of technical problems of moderate scope and complexity by applying extensive technical knowledge and experience.</li></ul></div><div>
Record-keeping 
<ul><li>Maintains accurate, up to date records, laboratory notebooks and computer database.</li><li>Prepare and document all plant validation trials according to department protocol.</li><li>Ensures the work environment is sanitary, safe, and orderly.</li><li>Maintains a sanitary, safe and orderly work environment.</li></ul></div></div></div><div><div><h2 class="jobSectionHeader"> 
Knowledge, Skills, and Experience</h2></div><div><ul><li>Bachelor&rsquo;s Degree in Food Science, Food Engineering or related field with 3+ years product development related experience in food preparation/food industry; OR M.S.in Food Science, Food Engineering, or related field with 2+ years product development related experience in food preparation/food industry.</li><li>Demonstrated experience developing products such as cakes, cookies, muffins, brownies, icings/glazes.</li><li>Experience in applying advanced mathematics (i.e. statistics) and their practical application required.</li><li>Broad understanding of food science (e.g. biochemistry, microbiology, nutrition, etc.) acquired through both lecture and laboratory work.</li><li>Demonstrated ability to apply technical standards, principles, theories, concepts and techniques.</li><li>Solid verbal and written communication skills and presentation skills; with all levels within an organization.</li><li>Demonstrated ability to work in a fast paced environment.</li><li>Solid PC proficiency in Microsoft Office 365 including Word and PowerPoint; intermediate to advanced proficiency level in Excel and database, statistical software (spreadsheets, computer analysis; report writing). Proficient with relevant software tools (e.g. PLM, etc.) a plus.</li><li>Ability to use presentation and project management software beneficial.</li></ul> 
Physical requirements:<ul><li>Lift up to 50 lbs.</li><li>Stand for 6 or more hours during the work day.</li><li>Ability to compare and distinguish differences in ingredients, materials, etc. through taste, smell, touch and visual inspection.</li><li>Manual dexterity required to operate various equipment such as scales, balances, etc.</li></ul>
 #LI-NT1<h1 class="jobSectionHeader">
#CORP123</h1></div></div></div> 
COMPENSATION
In accordance with state law, the rate or range provided is Rich Products Corporation, its subsidiaries and affiliates (&quot;Rich's&quot;), reasonable estimate of the base compensation for this role. The actual amount may be higher or lower, based on non-discriminatory factors such as experience, knowledge, skills, abilities, shift differential, and location. 
Annual Range/Hourly Rate
$75,510.48 - $102,161.24 
Rich Products Corporation, its subsidiaries and affiliates (&ldquo;Rich&rsquo;s&rdquo;), are committed to a policy of Equal Employment Opportunity, standing up for fairness and maintaining a culture of belonging, to provide an exceptional experience for all. We will not discriminate against an applicant or employee on the basis of race, color, religion, sex, national origin, disability, military or veteran status, or any other Federal or State legally protected classes. The information collected by this application is solely to determine suitability for employment, verify identity, and maintain employment statistics on applicants. 
Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is a change in the way things are normally done which will ensure an equal employment opportunity without imposing undue hardship on Rich&rsquo;s. Please contact Rich&rsquo;s Associate Experience Network at hrhelp@rich.com if you need assistance completing this application or to otherwise participate in the application process.</div>

Product Development Scientist II

CPS, Inc.

<div>
 The Formulation Scientist will join the R&amp;D Group in Utah, reporting to the Director of R&amp;D. The role focuses on application development of Nutraceutical oral dosage forms including hands on experience in product development, physical properties, analytical testing, technical support, and primarily for the pharmaceutical and nutraceutical markets.
 
 
 The Formulation Scientist applies formulation science knowledge to oral solid dosage forms, collaborating with marketing, sales, manufacturing, supply chain, quality, analytical labs, and other R&amp;D groups. Responsibilities include generating scientific data across lab, pilot plant, and commercial scales, becoming an in-house expert on customer usage of company products. The role involves project management, report writing, and data presentation, balancing customer-facing and laboratory-focused tasks. Travel to customer locations for visits and scale-up trials is required. The working environment spans office, laboratory, pilot production, and manufacturing setting, with occasional domestic and international travel.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Execute application development projects for customers in the nutraceutical market.
 </li>
 <li>
 Identify gaps in the company product line and generate new product ideas.
 </li>
 <li>
 Collaborate with R&amp;D team members on new product development.
 </li>
 <li>
 Validate company products through qualitative and analytical evaluations.
 </li>
 <li>
 Contribute to customer formula development programs, showcasing company ingredients in various product categories.
 </li>
 <li>
 Assess competitive product lines.
 </li>
 <li>
 Stay current with new technologies and developments.
 </li>
 <li>
 Perform tests on new samples produced in the pilot plant, comparing actual results to predictions.
 </li>
 <li>
 Source equipment and ingredients for laboratory projects.
 </li>
 <li>
 Maintain accurate R&amp;D files, project files, and lab notebooks.
 </li>
 <li>
 Perform other duties as assigned.
 </li>
 <li>
 If you&rsquo;d like to hear more about this opportunity and others we are currently working on, please contact Sam Kovacevic at skova@cps4jobs.com.
 
 
 </li>
 </ul>
 JO: 135.25KK
 
 
 Salary
 
 
 $110,000
 
 
 Benefits Available
 
 
</div>

Formulation Scientist (Nutraceuticals)

Merck

<div>Job Description
Are you enthusiastic and driven to create and lead execution of design verification testing strategies for innovative combination products?
Join our company&rsquo;s Device Product &amp; Process Development (DPPD) Team, which focuses on the design, development, and commercialization of novel biologic/drug/vaccine-device combination products for safe and effective delivery to their intended sites of action. The DPPD Team oversees the development of the device constituent within our pipeline of combination products, spanning various therapeutic areas and routes of administration, including inhalation, implantation, and injection.
The Associate Principal Scientist will lead the definition and execution of design verification strategies, and design transfers for testing readiness, which includes incoming and release tests for components and combination products. This position also supports other critical activities such as drug product and combination product final assembly processes validations. All activities will require collaboration with cross-functional teams both within and outside of Device Development &amp; Technology. The incumbent must be able to work well with employees at all levels to effectively engage and coordinate the implementation/ readiness and execution of design verification tests and methodologies in support of key development activities. Additionally, this position will require applying knowledge in drug and device product development, such as manufacturing process development and validation, design control, risk management, material and molding, design validation to create and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.
Principal Responsibilities<ul><li>
Lead, set direction, align with key stakeholders, and successfully execute, design verification strategies for assigned drug-device combination product program(s) for successful clinical introduction(s) and commercial market(s) approval(s).<ul><li>
Define design input(s)/ output(s) and lead associated combination product design verification plan, protocol(s), and report(s) that demonstrate design output(s) meet design input(s).</li><li>
Lead establishment of test methodologies, including method development and validation, internally or externally, per design verification strategy.</li><li>
Lead strategy and execution of accelerated and real time aging studies including bridging studies at the device component/ subassembly/ in-process material and combination product level.</li><li>
Lead stablishing test methodologies/ testing readiness and execution in support of critical activities such as stability studies, drug product filling process validation, combination product final assembly process validation, shipping studies, etc.</li><li>
Support establishment of incoming and release tests at the component and combination product level with key functional areas.</li><li>
Oversee design verification activities performed by external partners.</li></ul></li><li>
Proactively anticipate and resolve project obstacles and effectively communicate complex product technical challenges, design verification strategy, timelines, milestones, and risks within our Company and with external partners.</li><li>
Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs under your leadership.</li><li>
Lead/ Support clinical supplies production with respect to device component and combination product testing.</li><li>
Maintain a high level of engagement with cross-functional team members to effectively implement and successfully execute against design verification strategies.</li><li>
Stay current with new device technologies, relevant worldwide regulations, standards, and effectively share this knowledge with others.</li><li>
Enhance our Company&rsquo;s professional image and competitive advantage through publications, presentations, patents, and professional activities.</li></ul>
Qualifications
Requirements:<ul><li>
B.S. in Mechanical Engineering (or an equivalent field) + 8 years of combination product development experience; M.S. in Mechanical Engineering (or an equivalent field) + 5 years of combination product development experience; or a Ph.D. in Mechanical Engineering (or an equivalent field) + 3 years of combination product development experience.</li><li>
Leadership experience of combination product design verification programs and leading activities (e.g., strategy/ plan, protocol(s), report(s), test method development/validation, etc.) requiring cross-disciplinary project teams.</li><li>
Leadership experience with comprehensive knowledge of various aspects of device development and their interdependencies with design verification, including but not limited to, design controls, risk management, materials &amp; molding, process development and validation, secondary packaging development &amp; qualification, and design validation.</li><li>
Comprehensive understanding of drug product development in addition to device development expertise.</li><li>
Strong familiarity with regulatory landscape associated with drug delivery combination product and design verification requirements.</li><li>
Strong working knowledge of standards relevant to device components and combination products, including ISO 11608, ISO 11040, ISO 80369, as well as performance tests related to container closure integrity and dose accuracy, among others.</li><li>
Proven track record of applying analytical skills in product test method design, development, and validation.</li><li>
Working knowledge of analytical test method technology transfer process.</li><li>
Skilled in laboratory good documentation practices and electronic documentation systems.</li><li>
Self-motivated with ability to work independently.</li><li>
Proven ability to lead teams of diverse skill sets and backgrounds.</li><li>
Strong interpersonal skills and a strategic thinker; able to influence without formal authority; ability to influence and present ideas to senior leadership.</li><li>
Excellent communication, prioritization, presentation, negotiation, project management, and organizational skills.</li><li>
Willing to travel</li></ul>
Preferred experiences include:<ul><li>
Combination product drug delivery device components &ndash; plastic, metal, glass, elastomeric materials, etc. &ndash; fracture, stress-strain response, friction, hardness, surface roughness, surface energy quantification.</li><li>
Combination product sub-assemblies (including electro-mechanical) &ndash; system tear down analysis, gear ratio optimization, weakest link component identification and optimization, etc.</li><li>
Material characterization and failure mode analysis and integration with combination product risk management.</li><li>
Stress-strain testing of different materials under different environmental conditions, i.e., temperature, humidity.</li><li>
Eagerness to identify lab capability gaps, drive procurement of new equipment, and quickly upskill (also train others) on operation.</li><li>
Experience with analytical or numerical simulation.</li><li>
Excellent collaboration and ideation skills, including facilitating brainstorming sessions, developing proof of concepts, and generating feasibility data.</li></ul><ul><li>
Strong familiarity with compression/tensile testing (Instron, Zwick, Texture Analyzer), rheology (TA Instrument), metrology/non-destructive inspection (XRCT [Zeiss], Optical microscopy [Keyence], high speed imaging)</li><li>
Experience in 3D CAD (Solidworks) and rapid manufacturing techniques (machining, 3D printing) for fixture development and device redesign efforts.</li></ul>
Fluency with industry-related guidance &amp; standards:<ul><li>
21 CFR Part 4</li><li>
21 CFR 820</li><li>
21 CFR 210/ 211</li><li>
EU Medical Device Regulation</li><li>
USP &lt;1&gt;</li><li>
USP &lt;697&gt;</li><li>
FDA Guidance for Industry, Container Closure Systems for Packaging Human Drugs and Biologics</li><li>
ISO 13485</li><li>
ISO 14971</li><li>
ISO 11608</li><li>
ISO 11040</li><li>
ISO 10993</li><li>
ISO 23908</li><li>
ISO 80369</li><li>
ISTA 3A/B</li><li>
ASTM F1886</li><li>
ASTM D4169</li><li>
ASTM F1980</li></ul>
Required Skills:
Combination Products, Combination Products, Cross-Team Collaboration, Cultural Diversity, Customer Experience Design, Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Diversity Awareness, Drug Development, Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Microscopies, Negotiation, Optical Microscopy, Product Commercialization, Production Process Development, Project Management, Prototyping, Quality Management Systems (QMS), Self Motivation {+ 3 more}
Preferred Skills: 
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another&rsquo;s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.
The salary range for this role is
$139,600.00 - $219,700.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee&rsquo;s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully 
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms 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.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
11/28/2025<ul><li>A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
</li></ul> 
Requisition ID:R366313</div>

Associate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent)

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]

Harmonious Hiring

A leading company in the cosmetics and chemical industry is seeking an experienced R&amp;D Research Scientist to join its team. This role involves product formulation, ingredient research, and regulatory compliance to support the development and enhancement of cosmetic and chemical products. If you have a strong background in product development and formulation, this is a great opportunity to advance your career.Key Responsibilities:<ul><li>Develop and improve formulations for cosmetics and chemical-based products.</li><li>Conduct research on raw materials, active ingredients, and product stability.</li><li>Ensure compliance with cosmetic regulations and safety assessments.</li><li>Collaborate with internal teams to enhance product performance and innovation.</li><li>Optimize product textures, stability, and functionality through ingredient research and testing.</li></ul>Qualifications:<ul><li>Degree in Chemistry, Chemical Engineering, or a related field.</li><li>Experience in cosmetics or chemical product development.</li><li>Strong understanding of formulation design and ingredient interactions.</li><li>Knowledge of cosmetic industry regulations and safety assessments.</li><li>Ability to conduct raw material analysis and apply innovative research to product development.</li></ul>Benefits:<ul><li>Comprehensive Health Insurance</li><li>Paid Time Off (PTO)</li><li>401(k) Retirement Plan</li><li>Performance-Based Employee Awards</li><li>Reimbursement for Business-Related Expenses</li><li>Complimentary Breakfast &amp; Lunch Provided</li></ul>If you are passionate about cosmetic and chemical innovation and eager to contribute to a cutting-edge R&amp;D team, apply today.Job Type: Full-timePay: $65,000.00 - $100,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Health insurance</li><li>Paid time off</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>cosmetic and chemical product development: 2 years (Required)</li></ul>Language:<ul><li>Korean (Required)</li></ul>Work Location: In person

Korean Bilingual R&D Chemist – Cosmetics Products

Validation & Engineering Group

<div>Validation &amp; Engineering Group, Inc. (V&amp;EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
<ul><li>Process Development Sr Associate Scientist</li>
</ul>
Qualifications:
Doctorate OR, Master+ 2 years of Scientific experience OR, Bachelors + 4 years of Scientific experience
Personnel with experience in the inspection (manual/automatic), packaging area, incoming (primary containers), forensic or QC (defects).
<ul><li>Willing to work in a Process Development laboratory environment</li>
<li>Monitors field of expertise, including literature and technology development, and communicates relevant observations.</li>
<li>Understands and interprets primary components specifications and methods.</li>
<li>Demonstrates knowledge regarding metal, glass and polymer formation process and primary container components defects and classifications.</li>
<li>Performs Primary Packaging Evaluations and Glass/Polymers Forensic Analysis.</li>
<li>Introduces advanced scientific methods.</li>
<li>Develops and implements new and novel protocols to address specific issues.</li>
<li>Represent the department on project teams under supervision.</li>
<li>Initiates productive collaborations within and outside of the Process Development Department.</li>
<li>Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies.</li>
<li>Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents.</li>
<li>Participates with the external scientific community.</li>
<li>Assumes lead role in department-wide support efforts such as safety, OE and other committees. Develops and follows timelines for completing project teamwork.</li></ul></div>

ZL01-051525 Process Development Sr Associate Scientist

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