development scientist

Croda

<div>
 
 Croda is a FTSE100 organisation focused on our purpose of Smart Science to Improve Lives&trade;. With a market capitalisation of ~&pound;6 billion and nearly 6,000 employees globally, we are innovating novel and sustainable ingredients for the Textiles and Surface coatings industry through our commitment to sustainability and customer centricity.
 
 
 
 As our Industrial Specialties business looks to deliver its ambitious strategy of growth, we are looking for a Process Development Scientist to join our organisation to support the team for process development activities, technology transfer and scale-up of new products at site.
 
 
 Reporting into the Process Development Manager, you will be responsible for process development and scaling up chemistries from the Lab and from other sites of Croda.
 
 
 
 Who We&rsquo;re Looking For
 
 
 
 At Croda, we believe our people are the heart of our success. We are committed to fostering an environment where you can grow, make a meaningful impact, and thrive.
 
 
 Degree qualified in Organic Chemistry
 
 
 Strong understanding of formulations and synthesis processes.
 
 
 Proficient in process modeling, data analysis, and statistical tools.
 
 
 Hands-on experience with lab equipment, pilot plant operations, and safety systems.
 
 
 Experience with scale-up, process intensification, and/or continuous manufacturing is a plus
 
 .
 
 
 
 What You&rsquo;ll Be Doing
 
 
 
 Be part of a team that values diversity, sustainability, and continuous innovation, where your ideas and contributions matter.
 
 
 
 Design and develop robust and scalable chemical processes for new or existing products.
 
 
 Conduct laboratory experiments, interpret data, and translate results into actionable process improvements.
 
 
 Participate in the technology transfer and scale-up till plant level.
 
 
 Collaborate with cross-functional teams including R&amp;D, process engineering, manufacturing, and EHS to ensure successful process implementation.
 
 
 Support scale-up from lab to pilot and commercial production; provide technical input during plant trials.
 
 
 Identify and resolve technical challenges in manufacturing.
 
 
 Perform risk assessments and ensure compliance with safety and environmental standards.
 
 
 Develop and maintain process documentation including SOPs, batch records, and process flow diagrams.
 
 
 Monitor process performance and support continuous improvement initiatives.
 
 
 Stay current with technological advances and trends in process development and chemical engineering
 
 
 
 What We Offer
 
 
 
 Join a global organization with countless opportunities for growth and leadership.
 
 
 The successful candidate will receive a competitive salary and benefits package including:
 
 
 22 days paid holiday allowance
 
 
 Private medical insurance
 
 
 Best in class medical benefits
 
 
 Access to share plans
 
 
 Generous parental leave
 
 
 Free car parking on Croda sites
 
 
 
 Additional Information
 
 
 This is a hybrid position based at our Thane site.
 
 
 If you require any reasonable adjustments during the hiring process or experience any issues with our online application process, please email jobs@croda.com.
 
 
 
 Croda recognises employees as our strength and the diversity they bring to our workforce are directly linked to our ongoing success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including age, race, colour, religion, national origin, gender, sexual orientation, gender identity, gender expression, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs.
 
 
 
 Why Croda?
 
 
 
 At Croda, we believe our people are our difference. We are people-led, driven by the desire to do good and deliver value, a unifying principle shaped by all the great people that have travelled through Croda since our beginning in 1925. We pride ourselves on bringing together diverse teams and talents from across the globe and, guided by our values of Responsible, Innovative, and Together, we are passionate about building an inclusive, collaborative, and diverse organisation with innovation and customer focus underpinning all that we do.
</div>

Process Development Scientist

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 Scientist</li>
</ul>
Requirements:
<ul><li>Doctorate degree or Master degree and 5 years of Scientific experience OR
</li><li>Bachelor degree and 6 years of Scientific experience
</li><li>Life Sciences and/or Engineering (statistics, mathematics, systems engineering, industrial engineering)
</li></ul>Attributes:
<ul><li>Relevant work experience in data analysis or related field (eg as a statistician, data scientist, computational biologist)
</li><li>Work with large, complex data sets. Solve difficult, non-routine analysis problems, applying advanced analytical methods as needed.
</li><li>Conduct end-to-end analysis that includes data gathering and requirements specifications, processing, analysis, ongoing deliverables, and presentations
</li><li>Experience with statistical software (e.g. R, MATLAB, SAS, Jump, Minitab) and database languages (e.g. SQL)
</li><li>Experience with statistical data analysis such as linear models, multivariate analysis, and stochastic models
</li><li>Experience articulating business questions and using mathematical techniques to arrive at an answer using available data
</li><li>Demonstrated skills in selecting the right statistical tools given a data analysis problem
</li><li>Data system knowledge &ndash; OSIsoft PI / Spotfire/ OVDAS /PLM
</li></ul>Skills:
<ul><li>To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor.</li></ul>
<ul><li>Conceives and designs, executes or evaluates, and interprets experimental strategies.</li></ul>
<ul><li>Provides input to new processes to generate robust and reliable data.</li></ul>
<ul><li>Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.</li></ul>
<ul><li>Designs, monitors or conducts experimental strategies with general guidance from supervisor.</li></ul>
<ul><li>Provides data analysis and interpretation, and assesses impact of the data on the project.</li></ul>
<ul><li>Keeps current in field of scientific expertise and areas relevant to their function.</li></ul>
<ul><li>Monitors field of expertise, including literature and technology development, and communicates relevant observations.</li></ul>
<ul><li>May introduce advanced scientific methods.</li></ul>
<ul><li>Develops and implements new and novel protocols to address specific issues.</li></ul>
<ul><li>May represent the department on project teams under supervision of a senior scientific staff member.
</li></ul><ul><li>Fully bilingual (English/Spanish).</li></ul>
<ul><li>Available to work extended hours, possibility of weekends and holidays.</li></ul></div>

ZL02-100424 Process Development Scientist

Azurity Pharmaceuticals

<div>
 Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company&rsquo;s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
 
 
 Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
 
 
 
 Job Responsibilities
 
 
 
 <ul>
 <li>
 Design, conduct and or supervise formulation development, process development, process optimization, scale up and manufacturing of product.
 </li>
 <li>
 Prepare and review documents such as batch records, Batch Packaging Records, Product Development reports, SOPs, Stability protocols, Raw material specifications, Packaging material specifications and In-process/ Finished product specifications, labelling and stability loading.
 </li>
 <li>
 Review of test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals.
 </li>
 <li>
 Schedule experiments and prioritize assignments to meet project objectives and deadline.
 </li>
 <li>
 Maintain laboratory equipment and follow company safety standards.
 </li>
 <li>
 Conduct laboratory experiments and prepare reports with conclusions and recommendations.
 </li>
 <li>
 Follow current laboratory procedure and develop new laboratory procedures or improvise existing procedures to meet project objectives.
 </li>
 <li>
 Identify and manage the potential risks within complex projects in a timely fashion.
 </li>
 <li>
 Record accurate and complete experimental methods and results in compliance with good documentation practices.
 </li>
 <li>
 Act as primary scientific contact to external collaborators.
 </li>
 <li>
 Check and manage inventories of supplies and raw materials.
 </li>
 <li>
 Ensure completion of all the training on time.
 
 
 </li>
 </ul>
 
 Qualifications And Education Requirements
 
 
 
 <ul>
 <li>
 M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 3 to 6years in pharmaceutical development and scale-up of products.
 </li>
 <li>
 Preferred area of expertise is oral dosage forms precisely in Modified Release/ extended release/ targeted release/immediate release solid/Suspensions/Solutions.
 </li>
 <li>
 Global Product Development Experience with markets like US/EU/China/ROW.
 </li>
 <li>
 Experience of developing branded and differentiated products &ndash; 505(b)(2) category would be preferred.
 </li>
 <li>
 Experience of working with CROs/CDMOs would be preferred.
 </li>
 <li>
 Should be well versed with Microsoft office applications.
 
 
 </li>
 </ul>
 By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
</div>

Formulation Development Scientist

First Quality

<div>
 
 Founded over 35 years ago, First Quality is a family-owned company that has grown from a small business in McElhattan, Pennsylvania into a group of companies, employing over 5,000 team members, while maintaining our family values and entrepreneurial spirit. With corporate offices in New York and Pennsylvania and 8 manufacturing campuses across the U.S. and Canada, the companies within the First Quality group produce high-quality personal care and household products for large retailers and healthcare organizations. Our personal care and household product portfolio includes baby diapers, wipes, feminine pads, paper towels, bath tissue, adult incontinence products, laundry detergents, fabric finishers, and dishwash solutions. In addition, we manufacture certain raw materials and components used in the manufacturing of these products, including flexible print and packaging solutions.
 
 
 
 
 
 Guided by our values of humility, unity, and integrity, we leverage advanced technology and innovation to drive growth and create new opportunities. At First Quality, you&rsquo;ll find a collaborative environment focused on continuous learning, professional development, and our mission to Make Things Better&reg;.
 
 
 
 
 
 We are seeking an
 
 Associate Product Development Scientist
 
 for our
 
 First Quality Products site
 
 located in
 
 McElhattan, PA.
 
 
 
 
 
 
 
 This position is responsible for creating, developing, and implementing new and proprietary designs of absorbent-related product systems based upon business, customer, and consumer needs as well as provide support for the needs of present product systems to assure competitive performance and value.
 
 
 
 
 
 
 
 Principal Accountabilities/ Responsibilities:
 
 
 <ul>
 <li>
 Participate as a member of the Product Development team; execute projects in timely, diligent, safe, and professional manner, and contribute to the growth of the team and department.
 </li>
 <li>
 Design new products and product improvements to meet business and consumer needs.
 </li>
 <li>
 Develop new and improved materials and technologies with suppliers, and ensure all new raw materials obtain proper safety testing and clearance.
 </li>
 <li>
 Use basic Design of Experiments (DOE) techniques to develop experimental plans.
 </li>
 <li>
 Support the existing business product cost improvements through product redesigns.
 </li>
 <li>
 Provide technical support to reduce consumer complaints.
 </li>
 <li>
 Support corporate proprietary technology by documenting and patenting novel ideas.
 </li>
 <li>
 Develop new test methods to better predict and understand product performance in use.
 </li>
 <li>
 Work with more senior scientist or manager to help set project objectives.
 </li>
 <li>
 Coach and develop indirect reports to enhance team performance towards department objectives.
 </li>
 </ul>
 
 
 
 
 
 Education and experience requirements:
 
 
 <ul>
 <li>
 Four-year technical degree (e.g. Chemistry, Chemical Engineering, Mechanical Engineering, Material Science Engineering) or equivalent; additional business studies preferred.
 </li>
 <li>
 3+ years in R&amp;D inventing, developing, and implementing new products.
 </li>
 <li>
 Knowledge of and experience with developing product systems for the retail market, preferably hygiene products.
 </li>
 <li>
 Knowledge of materials used in retail absorbent products (e.g. pulp, super absorbent polymers, nonwovens).
 </li>
 <li>
 Working knowledge of consumer product converting technologies for pulp, paper, and nonwoven materials.
 </li>
 <li>
 Experience with the process of searching, evaluating, and filing patents.
 </li>
 <li>
 Experience providing direction for the physical testing of hypotheses, resulting in specific conclusions and recommendations.
 </li>
 <li>
 Able to speak, read and write the English language and have strong oral and written communication skills.
 </li>
 <li>
 Good analytical skills, with working knowledge of basic statistics.
 </li>
 <li>
 Good computer skills in Microsoft Office program.
 </li>
 <li>
 
 Able to travel ~20-30% to US and International for product and process trials.
 
 </li>
 </ul>
 
 
 
 
 
 What We Offer You
 
 
 
 We believe that by continuously improving the quality of our benefits, we can help to raise the quality of life for our team members and their families. At First Quality you will receive:
 
 <ul>
 <li>
 Competitive base salary and bonus opportunities
 </li>
 <li>
 Paid time off (three-week minimum)
 </li>
 <li>
 Medical, dental and vision starting day one
 </li>
 <li>
 401(k) with employer match
 </li>
 <li>
 Paid parental leave
 </li>
 <li>
 Child and family care assistance (dependent care FSA with employer match up to $2500)
 </li>
 <li>
 Bundle of joy benefit (year's worth of free diapers to all team members with a new baby)
 </li>
 <li>
 Tuition assistance
 </li>
 <li>
 Wellness program with savings of up to $4,000 per year on insurance premiums
 </li>
 <li>
 ...and more!
 </li>
 </ul>
 
 
 
 
 First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data.
 
 
 
 
 
 First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.
 
 
 
 
 
 For immediate consideration, please go to the Careers section at www.firstquality.com to complete our online application.
 
</div>

Associate Product Development Scientist

Syngene International Limited

<div>
 Date: 14 Oct 2025
 
 
 Location:
 
 
 IN
 
 
 Division: Discovery Services
 
 
 
 Job Title: Junior Analytical Development Scientist - OSD
 
 
 
 
 Job Location: Bengaluru
 
 
 
 
 Department: DPA &ndash; FD
 
 
 
 
 About Syngene :
 
 Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
 
 
 At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit
 
 
 
 Mandatory expectation for all roles as per Syngene safety guidelines
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
 </li>
 <li>
 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 </li>
 <li>
 Hold self and their teams accountable for the achievement of safety goals
 </li>
 <li>
 Govern and Review safety metrics from time to time
 
 
 </li>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 <ul>
 <li>
 Analytical development supporting Formulation development
 </li>
 <li>
 Routine analysis of samples
 </li>
 <li>
 Method development
 </li>
 <li>
 Instrument calibrations
 </li>
 <li>
 Documentation
 </li>
 <li>
 Report preparation
 </li>
 <li>
 Miscellaneous lab responsibilities
 
 
 </li>
 </ul>
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Candidate should have very good educational and theoretical background.
 </li>
 <li>
 Candidate should have knowledge of calibration, method development and troubleshooting using various instruments like KF auto titrator, dissolution (I, II &amp; IV), spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC
 </li>
 <li>
 Knowledge of various regulatory guidelines w.r.t. method development, product development and documentation
 </li>
 <li>
 Knowledge of method development for oral dosage forms w.r.t. tests like assay, degradation products, dissolutions, blend uniformity, content uniformity, cleaning method, etc.
 </li>
 <li>
 Knowledge of specification setting for oral dosage forms, in-process specifications as well as product specifications
 </li>
 <li>
 Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage
 </li>
 <li>
 Good understanding of Documentation as per GxP requirements
 </li>
 <li>
 Online Lab notebook writing
 </li>
 <li>
 Method development report preparation &ndash; Assay, Degradation products, Dissolution, cleaning method, etc.
 </li>
 <li>
 Method of Analysis, Test report, SOP preparation
 </li>
 <li>
 Calibration documentation
 </li>
 <li>
 Review of documents generated by peers or juniors
 </li>
 <li>
 Should be able to search scientific literature on-line
 </li>
 <li>
 Should be a team player and able to coach juniors technically
 
 
 </li>
 </ul>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 Excellence
 
 
 Integrity
 
 
 Professionalism
 
 
 
 Experience:
 
 More than 5 years up to 8 years
 
 
 
 Skills And Capabilities
 
 
 
 Candidate should have good proficiency for MS-office tools
 
 
 Should be able to search scientific literature on-line
 
 
 
 Behavioral Skills
 
 
 
 Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team.
 
 
 Good speaking-listening-writing skills, attention to details, proactive self-starter.
 
 
 Ability to work successfully in a dynamic, ambiguous environment.
 
 
 Ability to meet tight deadlines and prioritize workloads.
 
 
 Ability to develop new ideas and creative solutions.
 
 
 Should be able to work in team and flexible for working in shifts.
 
 
 Should be a focused employee.
 
 
 
 Education:
 
 M.Pharm / M.Sc
 
 
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>

Junior Analytical Development Scientist - OSD

Confidential Company

<div>
 
 
 Position Summary:
 
 
 
 We are seeking a highly skilled and motivated PhD-level R&amp;D Scientist with 3&ndash;4 years of experience in drilling fluid systems and simulation modeling. The ideal candidate will lead and contribute to the development and optimization of advanced drilling fluid technologies and digital simulation tools to enhance wellbore stability, efficiency, and sustainability in drilling operations.
 
 
 This is a strategic role for someone who combines deep technical knowledge with hands-on experience in lab research, fluid rheology, and numerical modeling.
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Lead and conduct R&amp;D projects focused on designing, testing, and improving drilling fluid systems (water-based, oil-based, synthetic-based, or polymer-based).
 </li>
 <li>
 Develop and implement simulation models (e.g., hydraulics, thermal modeling, cuttings transport, fluid loss) to predict drilling fluid performance in various well conditions.
 </li>
 <li>
 Utilize numerical tools (e.g., ANSYS, COMSOL, CFD, or custom simulators) to optimize formulations and drilling parameters.
 </li>
 <li>
 Conduct laboratory experiments to assess rheology, stability, filtration, and other key drilling fluid properties under HPHT conditions.
 </li>
 <li>
 Analyze experimental and field data to correlate simulation models with real-world performance.
 </li>
 <li>
 Collaborate with field engineers, product development teams, and clients to troubleshoot field challenges and deliver customized fluid solutions.
 </li>
 <li>
 Write technical reports, research papers, and contribute to patent filings and conference presentations.
 </li>
 <li>
 Stay updated on emerging technologies, materials, and digital innovations in drilling and well construction.
 </li>
 </ul>
 
 
 Required Qualifications:
 
 
 <ul>
 <li>
 PhD in Chemistry , Petroleum Engineering, Chemical Engineering, or a related field with a specialization in drilling fluids ..
 </li>
 <li>
 3&ndash;4 years of industry or academic R&amp;D experience focused on drilling fluid systems and simulation.
 </li>
 <li>
 Strong knowledge of fluid rheology, wellbore hydraulics, HPHT testing, and formation interactions.
 </li>
 <li>
 Strong problem-solving abilities and capability to design and conduct structured research programs.
 </li>
 <li>
 Excellent written and verbal communication skills, including the ability to present technical findings to both technical and non-technical audiences
 </li>
 </ul>
 
 
</div>

Research And Development Scientist

Grifols

<div><div><div><div><div>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. 
</div></div> 
 
</div></div>The incumbent will provide technical or scientific expertise to the development, scale-up, transfer, and/or support of production processes for plasma derived or recombinant proteins. Activities are centered on unit operations such as filtration methods, chromatography, precipitation, and process trouble shooting.

The candidate must have the ability to set and meet deadlines, multitask, and prioritize personal tasks based on project needs.

The candidate will also have a large role in maintaining the laboratory facilities in accordance with procedure. 

Primary responsibilities for role:
<ul><li>With supervision, develops actions plans in support of departmental goals.
</li></ul><ul><li>Identifies and collects data on critical process attributes.</li></ul>
<ul><li>Executes action plans independently or as part of a team.</li></ul>
<ul><li>Assists in the design of scientifically rigorous experiments. Executes and interprets results independently.</li></ul>
<ul><li>May conduct laboratory or clinical production work, as required, using standard processing and analytical equipment.
</li></ul><ul><li>Independently prepares procedures or technical reports, including data interpretation.</li></ul>
<ul><li>With supervision, prepares and effectively communicates technical results in cross-functional settings.</li></ul>
<ul><li>Develops solutions to complex technical problems within area of expertise.</li></ul> 

Knowledge, Skills, and Abilities
<ul><li>Ability to set and meet deadlines, multitask, and prioritize tasks based on project needs.</li></ul>
<ul><li>Experience performing and analyzing results from protein assays relevant to process or formulation development: SDS-PAGE, HPLC, ELISA and UV/Vis spectroscopy.</li></ul>
<ul><li>Applies scientific or engineering principles in problem solving.</li></ul>
<ul><li>Has ability to apply scientific or engineering principles and company&rsquo;s policies and procedures in completion of job tasks.
</li></ul><ul><li>Takes initiative in keeping current in area of specialization (e.g., protein purification, chromatography, filtration) and expanding knowledge base in professional area.</li></ul>
<ul><li>Experience with laboratory notebooks</li></ul>
<ul><li>Must have excellent written communication and strong oral communication skills.</li></ul>
<ul><li>Must be proficient in use MS Office Suite.</li></ul> 


Education Biochemistry, Chemistry, or relevant life science field. 

Experience 6+ years of relevant experience 

Occupational demands:

Work is performed in a clinical and/or a laboratory environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to chemicals. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits and bends neck for 4-6 hours per day. May stand and twist neck for 2-4 hours per day. Occasionally walks, bends and twists waist and squats. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Moderate lifting of 15-30lbs. with a maximum lift of 35 lbs. May reach above and below shoulder height. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Frequently works with diverse groups to obtain consensus on complex issues. Ability to apply abstract principles to solve complex conceptual issues. Performs a wide range of complex tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. 
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. 

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants in a manner consistent with the requirements of applicable state and local laws. 
Location: NORTH AMERICA : USA : NC-RTP:[[cust_building]] 

Learn more about Grifols</div>

Senior Associate Process Development Scientist II

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