<h3>Job Description</h3>
Salary: 
Join our Team!  Molded Dimensions Group is a supplier of rubber, urethane and plastic components headquartered in Port Washington, WI. With our diverse customer base, we operate in a wide variety of end markets including marine, medical, automotive, trucking and mining. What we provide is more than just a product. We pride ourselves on being the best at what we do and look for individuals that share the same passion.

We are looking for an experienced Chemist to be the company’s key knowledge resource for rubber and urethane materials for our Port Washington, WI location. Reporting to the Director of Engineering, you will work closely with customers, suppliers, Sales, Engineering, Purchasing, Manufacturing and Quality Assurance to develop and optimize rubber and urethane formulas and process parameters for performance in application, ease of processing, availability of supply, and overall cost.

Principal Duties

1.  Develops and recommends compounds/formulas/ingredients for new and existing items:

<ul>
<li> Obtains pricing, properties data, color matches, etc. from material suppliers.</li>
<li> Compounds materials, molds test pieces, performs material testing, and evaluates results to validate conformance to specification.</li>
<li> Recommends and evaluates replacements and substitutions. </li>
<li> Maintains an accurate and thorough database of all formulas, with ASTM D2000 performance specifications and typical results, specific gravities, etc.</li>
<li> Prepare technical data sheets for customers.</li>
</ul>
2.  Oversees material-related measuring, testing and processing parameters used in manufacturing:

<ul>
<li> Develops/reviews milling and mixing procedures.</li>
<li> Develops rheometer curve limit specifications.</li>
<li> Trouble-shoots material processing problems</li>
<li> Shelf-Life Inventory: Dispositions non-conforming and aged lots of material</li>
<li> Assures that Foreign Distribution product conforms to its ASTM D2000 specification.</li>
<li> Recommends metal prep methods and adhesive systems.</li>
<li> Recommends cryogenic deflashing temperatures and durations.</li>
<li> Participates in Mill Rescue Team</li>
</ul>
3.  Educates internal and external customers about materials by:

<ul>
<li> Maintaining active formula quoting guides for quoting and material selection, with overviews of properties, processability, availability and cost</li>
<li> Acting as a consultant to others on new product development, trouble-shooting existing items, investigating field failures, and purchasing processing equipment</li>
<li> Assisting in sales presentations and internal material training</li>
</ul>
4.  Oversees the materials lab:

<ul>
<li> Purchases and maintains all lab equipment and software.</li>
<li> Develops internal test methods in accordance with industry practices.</li>
<li> Maintains procedures and records.</li>
</ul>
5.  Reviews our material portfolio against market needs and industry developments, recommending new:

<ul>
<li> compounds and ingredients</li>
<li> suppliers</li>
<li> testing and production methods</li>
<li> technologies and equipment</li>
</ul>
6.  Performs other duties assigned, to include:
<ul>
<li>
<ul>
<li> Manage safety data sheets – production and lab</li>
<li> Control incoming experimental materials.</li>
<li> Environmental compliance – reach, ROHS, conflict minerals, PROP 65</li>
<li> Manage IMDS system/submissions.</li>
<li> Maintain rubber and urethane quoting guides.</li>
<li> Consult with subsidiary company on material related issues.</li>
<li> Cost reduction projects with sourcing</li>
</ul>
</li>
</ul>

Qualifications

<ul>
<li>Bachelor of Science degree in Chemistry, Chemical Engineering, or Materials Science and Engineering.</li>
<li>3-5 years industrial experience with rubber and/or urethane materials, including a thorough understanding of ASTM D2000 standards, testing procedures and equipment. Rubber formulation experience desired. </li>
<li>Strong verbal communication skills, ability to create detailed technical documentation, effective prioritization of multiple projects from multiple requestors, focus on serving internal customers, willingness to share knowledge, ability to make sound and confident decisions, analytical problem-solving skills.</li>
<li>Ability to run, or learn to run, Lab Mill.</li>
</ul>

Why MDG?  By joining the Molded Dimensions Group, you will have the opportunity to work alongside our talented and driven professionals, that embrace change and celebrate success. We work hard but know how to have fun!
keywords: compounders, rubber technology, process chemistry/chemist

Chemist

<h3>Job Description</h3>
Job Title – Chemist I
Department – Tracer Diagnostics
Reports to – Laboratory Director 

Job Summary

The Chemist is primarily responsible to perform advanced technical and analytical work involving the investigation of the chemical nature of substances and provides assistance in the implementation and maintenance of company processes. Requires use of independent judgement; performed under general directions and reviewed through observation, conferences and results achieved.
Key Areas of Responsibility
<ul>
<li>Analyzes chemical nature and make-up of various samples from different sources to provide information on compounds or quantities of compounds present using analytical techniques and instrumentation</li>
<li>Processes and records data from analytical instruments</li>
<li>Performs laboratory analyses in order to produce reliable and precise reports to support scientific investigations within the oil and gas industry</li>
<li>Assist with maintenance of analytical instruments according to specifications</li>
<li>Constructs, maintain, &amp; operate lab equipment (e.g., centrifuges, pipetting machine, pH meters)</li>
<li>Prepares chemical reagents for analyses</li>
<li>Uses multiple software programs to assist in performing analyses and preparing scientific reports</li>
<li>Assists in the development and performance of experiments to test hypotheses and improve tracer technology</li>
<li>Supervise laboratory technicians as required to maintain data analysis and reporting</li>
<li>Support and uphold HS&amp;E policies and procedures of NCS and the customer</li>
<li>Align individual goals with NCS’s corporate goals, while adhering to the NCS Promise</li>
<li>Participate in Personal Development for Success (PDS)</li>
<li>Other duties, relevant to the position, shall be assigned as required</li>
</ul>
Knowledge, Skills &amp; Abilities
<ul>
<li>Bachelor’s Degree in physical science (Chemistry Degree Preferred)</li>
<li>1-3 years of Analytical Laboratory working experience; preferred</li>
<li>Knowledge of HPLC, GC, MS and other modern analytical technologies</li>
<li>Proficient in Microsoft Office Suites</li>
<li>Ability to work in a dynamic and fast paced environment, willing to think on their own, with excellent attention to detail and ability to handle multiple tasks</li>
<li>Ability to work in the presence of odors typical of petroleum, petrochemicals and laboratory chemicals without allergic reaction or nausea</li>
<li>Ability to stand, bend and sit for extended time periods</li>
<li>Ability to work in climate and non-climate-controlled area (95% climate, 5% non-climate)</li>
<li>Ability to move or lift 50lbs</li>
</ul>
Additional Information
<ul>
<li>Status: Exempt</li>
<li>Employment Classification: Full-time, Regular</li>
<li>Work Schedule: Monday to Friday 8:00am – 5:00pm, overtime required as needed to maintain production schedule</li>
<li>Special Equipment: Laptop</li>
<li>Bonus: Eligible</li>
<li>Travel: 5% domestic travel and international travel may be required</li>
<li>Criminal background check required for all positions</li>
<li>Safety sensitive positions will require additional pre-employment testing</li>
</ul>
Core Competencies
<ul>
<li>Teamwork/Collaboration – Able to work cooperatively with other individuals</li>
<li>Service Focus – Builds &amp; maintains customer satisfaction and provides excellent service to internal &amp; external customers</li>
<li>Decision Making – Able to make decisions and solve problems of varied levels of complexity using logical, systematic, and sequential approach</li>
<li>Ethics &amp; Integrity – Trustworthiness and ethical behavior with consideration for impact &amp; consequence when making decisions/taking action</li>
<li>Problem Solving – Ability to approach a problem by using a logical, systematic, sequential approach</li>
<li>Continuous Improvement – Ongoing improvement of products, services, or processes through incremental &amp; breakthrough improvements</li>
<li>Accountability – Obligation or willingness to be answerable for an outcome</li>
</ul>

Chemist I

<h3>Job Description</h3>
JRAD is seeking candidates for an immediate fill. This position is located in Indian Head, MD.

Job Duties:
<ul>
<li>Analyzes environmental and/or air samples for Chemical contamination </li>
<li>Operates and maintains laboratory equipment (e.g., Gas and Liquid Chromatography, Mass Spectrometers, and performs basic maintenance and checks on common laboratory systems </li>
<li>Uses Laboratory Information Management System (LIMS) software for managing analytical data</li>
<li>Participates in laboratory proficiency testing activities and maintains QA/QC records to include performance charts, control limits, and detection and reporting limits for analytical methods governing use of laboratory instrumentation </li>
<li>Maintains operator manuals and procedures</li>
<li>Meticulously adheres to laboratory procedures, data management practices and safety protocols in accordance with Laboratory Quality Assurance Plans and safety policies/regulations</li>
<li> Maintains inventory of lab supplies </li>
</ul>

Travel Requirements: Ability to travel 15% of the time is required.

Required Skills and Education:
<ul>
<li>Bachelor’s Degree in Chemistry, Biochemistry, or similar, from an accredited college or university </li>
<li>At least 10 years of experience with quantitative analysis of chemical compounds</li>
<li>Must have experience with quality management standards (e.g., ISO 17025 or similar), sample preparation methods, techniques, regulations, protocols, safety measures, and the operation and maintenance of chemical laboratory instrumentation </li>
<li>Working knowledge of Microsoft Office products including Excel, Project, Word, Access, and Power Point </li>
<li>Excellent written and oral communication skills</li>
</ul>

Security Clearance:
Active Secret is required

When you work for JRAD you will never be just a number. We put people before profits! 

JRAD is committed to the health and well-being of its employees. We offer more paid time off than the average company upon hire and the following benefits are available to all full-time employees: 
<ul>
<li>Health Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Life &amp; Accidental Death and Dismemberment Insurance </li>
<li>Section 125 Flexible Spending Accounts for unreimbursed medical &amp; dependent day care </li>
<li>Disability Insurance </li>
<li>401K Plan </li>
<li>Tuition Reimbursement </li>
</ul>

JRAD is an Equal Opportunity Employer/Veterans/Disabled. 

PLEASE NOTE: Once you apply, to ensure you continue to receive important updates on your application and status, please add JRAD to your approved email list and/or check your spam and junk mail often for updates

<h3>Job Description</h3>
About the Role
We seek a highly motivated and experienced Chemist to join our ARD and Quality team. The ideal candidate will have a master’s degree in chemistry/ pharmaceutical sciences and 3-5 years of experience in a GMP environment. Expertise in HPLC with Empower, dissolution, and other analytical techniques is required.
Position Responsibilities:
<ul>
<li>Develop, validate, and implement analytical methods for the quality control of pharmaceutical products.</li>
<li>Perform routine testing of pharmaceutical products using a variety of analytical techniques, including HPLC, dissolution, and all other analytical techniques relevant to pharmaceutical product testing. </li>
<li>Troubleshoot and resolve analytical problems.</li>
<li>Generate and review analytical reports.</li>
<li>Work with other members of the team and cross-functional teams to ensure the quality and safety of pharmaceutical products.</li>
</ul>
Skills:
<ul>
<li>Strong analytical and problem-solving skills.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to work independently and as part of a team.</li>
</ul>
Education / Experience:
<ul>
<li>Master’s degree in chemistry or pharmaceutical sciences.</li>
<li>3-5 years of experience in a GMP environment.</li>
<li>Expertise in HPLC with Empower, dissolution, and other analytical techniques.</li>
</ul>
Company Overview
ANI Pharmaceuticals, Inc. is a diversified bio-pharmaceutical company serving patients in need by developing, manufacturing, and marketing high quality branded and generic prescription pharmaceutical products. Our team is focused on delivering sustainable growth by building a successful Purified Cortrophin Gel franchise, strengthening our generics business with enhanced development capability, innovation in established brands and leveraging our North American manufacturing capabilities.
At ANI Pharmaceuticals, there are opportunities to contribute to our purpose every day. We value authenticity, knowledge, and hard work, we strive to celebrate our employees in a positive environment. Our culture empowers everyone to be successful and apply our full potential.
Please note that ANI does not accept search agency or third-party emails, calls, or solicitations.  
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&lt;br&gt;&lt;b&gt;Company Description&lt;/b&gt;&lt;br&gt;&lt;br&gt;&lt;strong&gt;Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.&lt;/strong&gt;&lt;br&gt;&lt;br&gt;&lt;strong&gt;Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.&lt;/strong&gt;&lt;br&gt;&lt;br&gt;&lt;strong&gt;In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.&lt;/strong&gt;&lt;br&gt;&lt;br&gt;&lt;b&gt;Job Description&lt;/b&gt;&lt;br&gt;&lt;br&gt;The Chemist I performs testing activities as directed by Department Supervisor in accordance with all applicable company and regulatory guidelines to ensure that quoted turnaround times are met in support of monograph testing, unknown/failure analysis and other areas.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Essential Duties and Responsibilities:&lt;/strong&gt;&lt;br&gt;&lt;li&gt;Perform testing activities as directed by Department Supervisor in accordance with all applicable company and regulatory guidelines.&lt;/li&gt;&lt;li&gt;Monitor backlog and plan testing schedule to ensure quoted turnaround times are met.&lt;/li&gt;&lt;li&gt;Wet chemistry techniques utilized will include gravimetry, titrimetry, colorimetry and others as needed.&lt;/li&gt;&lt;li&gt;Instrumentation utilized may include HPLC, GC, ICP, ICP-MS, IC, and others as needed.&lt;/li&gt;&lt;li&gt;Maintain neat and accurate records.&lt;/li&gt;&lt;li&gt;Enter testing data into LIMS and monitor for QC failures.&lt;/li&gt;&lt;li&gt;Review and approve laboratory analytical data.&lt;/li&gt;&lt;li&gt;Monitor and record environmental conditions in laboratory. Alert management of any out of tolerance findings.&lt;/li&gt;&lt;li&gt;Perform calibrations/checks of laboratory equipment.&lt;/li&gt;&lt;li&gt;Maintain glassware inventory for laboratory use.&lt;/li&gt;&lt;li&gt;Maintain chemical/reagent traceability.&lt;/li&gt;&lt;li&gt;Assist with maintenance of chemical/supply inventory.&lt;/li&gt;&lt;li&gt;Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions.&lt;/li&gt;&lt;li&gt;Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and assisting with internal audit findings as assigned by Environmental Lab Supervisor or Monograph Supervisor.&lt;/li&gt;&lt;li&gt;Maintain regular attendance and punctuality.&lt;/li&gt;&lt;li&gt;Conducts all activities in a safe and efficient manner.&lt;/li&gt;&lt;li&gt;Perform other duties as assigned.&lt;/li&gt;&lt;br&gt;&lt;b&gt;Qualifications&lt;/b&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;B.S. in Chemistry or related field&lt;/li&gt;&lt;li&gt;Knowledge of WiDNR, ISO 17025 and related standards&lt;/li&gt;&lt;/ul&gt;&lt;br&gt;&lt;b&gt;Additional Information&lt;/b&gt;&lt;br&gt;&lt;br&gt;&lt;strong&gt;What we offer:&lt;/strong&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Excellent full time benefits including comprehensive medical coverage, dental, and vision options&lt;/li&gt;&lt;li&gt;Life and disability insurance&lt;/li&gt;&lt;li&gt;401(k) with company match&lt;/li&gt;&lt;li&gt;Paid vacation and holidays&lt;/li&gt;&lt;/ul&gt;&lt;br&gt;&lt;strong&gt;Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.&lt;/strong&gt;&lt;br&gt;

St. Francis Hospital Memphis 
 Saint Francis Hospital Memphis is a 510-bed acute care hospital dedicated to providing high quality, compassionate care to the Mid-South community. As a comprehensive medical center, Saint Francis Hospital Memphis features a broad spectrum of tertiary and acute care, outpatient services and specialty areas including Women’s Services, Surgical Services, Bariatric Center of Excellence and Behavioral Health. Other acute care areas include Emergency Room, Critical Care, Med/ Surge and Telemetry. 
 Student Extern PRN Nights Position Summary
 Qualified candidates are required to have successfully completed a clinical rotation in either Microbiology, Chemistry, Hematology, or Urinalysis.
 Under direct supervision of a Medical Laboratory Scientist II or a Lead, performs laboratory tests as assigned.
 Responsibilities
 Under direct supervision of a Medical Laboratory Scientist II or a Lead, processes and performs laboratory testing in sections where successful completion of clinical rotation has occurred; reviews and reports lab results, and performs operation and maintenance of laboratory instrumentation and equipment.
 Education
 Required: Currently enrolled in a NCCLS-accredited Medical Technology or Medical Laboratory Technician program and have completed all pre-clinical, core medical laboratory sciences.
2305027398 
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
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Processes and tests all types of laboratory specimens; reviews and reports lab results; performs operation, maintenance and advanced troubleshooting of laboratory instrumentation and equipment; acts as resource to other laboratory personnel.
 Essential Job Duties Ability to function in all areas of the clinical laboratory: blood bank, chemistry, hematology, microbiology, serology/immunology and urinalysis.
 Responsible for performing moderate and high-complexity testing.
 Alters or adjusts methods and procedures for the neonate, pediatric, adolescent, adult and geriatric patient.
 Performs quality control procedures and instrument checks.
 Demonstrates knowledge of expected lab values for the neonate, pediatric, adolescent, adult and geriatric patient.
 Notifies nursing unit and/or physician of critical lab values.
 Maintains accurate laboratory records on procedures performed for statistics and billing.
 Meets current documentation standards and policies.
 Interacts professionally with the Director of Clinical Laboratory, Pathologist and clinical laboratory personnel.
 Consults with other departments, as appropriate, to collaborate in patient care and performance improvement activities.
 Performs all aspects of patient care in an environment that optimizes patient safety and reduces the likelihood of medical/health care errors.
 Follows standard precautions at all times.
 Manages and operates laboratory equipment safely and correctly.
 Demonstrates knowledge of new testing methods, products, instrumentation; remains informed on all current technologies.
 Maintains current knowledge of hospital policy, CAP, JCAHO, state and other regulatory requirements.
 Demonstrates the ability to be flexible, organized and function under stressful situations.
 Demonstrates the value of team concept on a consistent basis.
 Professional Requirements: 
 Reports to work on time and as scheduled, completes work within designated time. 
 Adheres to scheduling requests of the department (Works weekends, no “special days off”, no exceptions).
 Adheres to the Customer Service Standards of Sunnyvale while representing the organization in a positive and professional manner.
 Communicates the mission, ethics and goals of the facility, as well as the focus statement of the department and complies with all organizational policies regarding ethical business practices.
 Utilizes computerized punch time system correctly.
 Completes annual education requirements and maintains regulatory requirements.
 Adheres to dress code, appearance is neat and clean and wears identification while on duty. 
 Completes in-services and returns in a timely fashion and has not missed any mandatory in-services.
 Attends at least 8 staff meetings annually, is responsible for information presented at monthly staff meetings that he/she is unable to attend.
 Actively participates in performance improvement and continuous quality improvement (CQI) activities.
Regulatory Requirements:
 Required: Bachelor’s Degree from an approved college or university and/or graduate of an accredited school of medical technology, or equivalent such as military training as defined by 42 CFR 493.1489, or have qualified at the Medical Technologist level by achieving a satisfactory grade on a HHS examination prior to 2/28/92 42 CFR 493.1491. The above meets required criteria as defined by CLIA regulations for High Complexity testing (42 CFR 493.1489 and 42 CFR 493.1491). 
 Prefer 6 months to 1 year medical laboratory technologist, clinical laboratory scientist experience in acute care facility. 
 Required: Registered in accordance with an approved certifying agency (ASCP, NCA, AMT or CSMLS). Equivalency evaluation by NACES or AICE for non-US trained personnel must be completed within 30 days of hire. Licensure, as required by State.
Language Skills:
 Ability to effectively communicate in English, both verbally and in writing. 
 Additional languages preferred.
Skills:
 Basic computer knowledge. 
 Operates the following equipment correctly and safely: microscopes, centrifuges, hematology, chemistry, and other instrumentation.
2403011434 
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
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See SonicJobs Terms &amp; Conditions at <a href="https://www.sonicjobs.com/us/terms-conditions" target="_blank">https://www.sonicjobs.com/us/terms-conditions</a> and Privacy Policy at <a href="https://www.sonicjobs.com/us/privacy-policy" target="_blank">https://www.sonicjobs.com/us/privacy-policy</a> and SonicJobs Privacy Policy at <a href="https://www.sonicjobs.com/us/privacy-policy" target="_blank">https://www.sonicjobs.com/us/privacy-policy</a> and Terms of Use at <a href="https://www.sonicjobs.com/us/terms-conditions" target="_blank">https://www.sonicjobs.com/us/terms-conditions</a>

<h3>Job Description</h3>
Who we are &amp; what we do:
At ARMOR-IIMAK, we innovate and manufacture Thermal Transfer Ribbons, Direct Thermal Films &amp; Industrial &amp; Digital Inkjet Inks for products used every day. Whether it is a large sign, advertisement displaying your company or clothing designed for a friend, team, or organization, our ink technology makes visions, a reality. As a dynamic organization with a global presence, our passion &amp; determination to design, manufacture, and sell the highest quality products across a diverse set of industries is what we do.
What you’ll do:
<ul>
<li>Support product development programs</li>
<li>Formulate inks for ink jet, thermal transfer products and other applications</li>
<li>Identify materials for innovative applications</li>
<li>Design, conduct and analyze experiments for formulation and process development and improvement</li>
<li>Make recommendations for laboratory, pilot scale and production implementations, including test plans, instrumentation, and equipment</li>
<li>Prepare documentation for manufacturing engineering and production</li>
</ul>
Who you are:
<ul>
<li>You are technically savvy, analytical, detail oriented, curious, and experimental </li>
<li>You enjoy a collaborative work environment, where you’ll interact with a wide variety of departments, but also like a balance of autonomous work as well</li>
<li>Research comes naturally to you, as you thrive when problem solving and are determined to find solutions</li>
<li>You are communicative </li>
</ul>
What you have: 
<ul>
<li>BS in Chemistry or Material Science required</li>
<li>1-3 years of experience in ink and coating formulation inkjet experience is preferred</li>
<li>Knowledge of statistics and design experiments</li>
<li>Knowledge of polymer science, printing and coating technology, digital Imaging, digital Inks or equivalent disciplines</li>
<li>Familiar with stage gate project management process</li>
<li>Excellent problem-solving and analytical skills</li>
<li>Excellent verbal, written and interpersonal communication skills</li>
<li>Strong MS Office skills</li>
<li>Fast learner, flexible, with the ability to multi-task and work within a group setting</li>
</ul>
What we offer:
<ul>
<li>Health, Vision, Dental Insurance </li>
<li>Immediate 401(k) Match</li>
<li>Wellness Program/Incentives</li>
<li>Paid Lunch Breaks</li>
<li>Paid Time Off</li>
<li>Shift Premiums</li>
<li>On-Site Fitness Facility</li>
<li>Continued Learning Opportunities </li>
<li>Tuition Assistance Program</li>
<li>Employee Appreciation Programs</li>
<li>ARMOR-IIMAK Safety Program</li>
<li>Employee Assistance Program</li>
</ul>
Pay Transparency: Additional factors such candidates work experience, education/training, job-related skills, as well as market and business considerations may influence compensation offered. 
ARMOR-IIMAK is an equal opportunity organization. We recruit, employ, train, compensate, and promote without regard to race, religion, color, national origin, age, gender, sexual orientation, gender identity, marital status, disability, protected veteran status, or any other basis protected by applicable federal, state or local law.

<h3>Job Description</h3>
Salary: DOE
Recipharm is a leading CDMO (Contract Development and Manufacturing Organization) in the pharmaceutical industry employing 9,000 employees with headquarters in Sweden. One of Recipharm’s nine research and development facilities is in Research Triangle Park, North Carolina, USA. Recipharm aspires to be the first-choice strategic partner for inhaled drug development companies worldwide.
We are seeking Chemists for our Product Development Team here at Recipharm in RTP. Our scientists and chemists work on a number of different projects for our clients. Many of our clients are small to mid-size pharma companies that focus on rare diseases to give patients with unmet medical needs better treatment options. This keeps us motivated and gives us the opportunity to make a difference and work on many different exciting, inhaled drug projects.
The level of the position will be based on qualifications and experience.

Key responsibilities will be:
<ul>
<li>Performing analytical testing associated with aerosol characterization with various inhalation devices, such as metered dose inhalers, dry powder inhalers, solutions and suspensions for nebulization, and nasal products by means of HPLC and other analytical techniques.</li>
<li>Performing product performance and physical chemical characterization testing by means of NGI collections, spray characterization, and other technologies.</li>
<li>Documenting laboratory work carefully per SOPs and cGMPs.</li>
<li>Assisting in the development and qualification of chromatography and inhalation test methods.</li>
<li>Analyzing data and writing reports, protocols, test methods, SOPs, and other documents.</li>
<li>Identifying and solving problems, recommend changes in the area of expertise.</li>
<li>Maintaining a safe work environment.</li>
</ul>
Required Qualifications:
<ul>
<li>B.S. degree in chemistry, biological sciences, pharmaceutical sciences, or related fields</li>
<li>4 to 5 years of relevant industry experience in either chromatographic analysis (HPLC) in a GMP environment or pharmaceutical or food product development.</li>
<li>A thorough understanding of general laboratory procedures to reliably conduct analyses and operate lab instrumentation.</li>
<li>Strong oral and written communication skills for reporting experimental results.</li>
<li>Proficient in Microsoft Excel and Word</li>
<li>Self-motivated, and well organized with excellent time management abilities and problem-solving skills.</li>
<li>Experience in working both independently and in a team-oriented, collaborative environment.</li>
</ul>

Preferred Qualifications:
<ul>
<li>Inhaled product testing (e.g. cascade impaction, delivered dose, spray characterization)</li>
<li>Experience with equipment such as coulometric Karl Fischer, FT-IR, osmometer, Gas Chromatograph</li>
<li>Experience with formulation &amp; process development studies utilizing small scale equipment</li>
<li>Experience from a contract lab organization</li>
</ul>
We offer a competitive compensation and benefits package including: Full Benefits (Medical, Dental, Vision, Life, Disability) 401(K) with Company Match Paid Vacation, Sick Time &amp; Parental Leave
Dependent Care FSA
Educational reimbursement program

Physical Requirements:
All Chemist positions must possess the ability to stand and/or walk for up to 8 hours a day and carry up to 25 pounds. This position involves repetitive motion of the arm, wrist, hand and fingers with the ability to feel and handle work materials for up to 8 hours per day. The position also requires the ability to carry out tasks involving extensive reaching, crouching, and bending. Day to day tasks may involve handling of and the ability to identify hazardous chemicals and materials.

**Relocation assistance is not provided for this position. Candidate must be able to commute daily to the job site**

COVID-19 considerations: Vaccinations strongly recommended for all adults.

<h3>Job Description</h3>
Benefits:
<ul>
<li>401(k)</li>
<li>Competitive salary</li>
<li>Dental insurance</li>
<li>Health insurance</li>
</ul>
 Seeking qualified Chemist w/Masters or foreign equiv degree in Pharmacy or Science or Chemistry &amp; 6 months of work experience to Perform routine manufacturing batch production record review in support of product batch release in accordance with specifications and SOPs. Review documentation associated with production operations. Ensures adequate levels of documentation are acceptable and compliant to existing procedures and audits production batch records to ensure adherence to policies, SOPs, and cGMP requirements. Qualification/Validation of manufacturing equipment to ensure the equipment meet the user requirements and Support QA Management with department strategy development, objectives and goal setting, project prioritization activities. Establish process and procedures to ensure compliance and improvement to the Quality Management System (QMS).

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