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<p><strong>Midwest candidates only!</strong></p>
<p><strong>Key Responsibilities:</strong></p>
<ul>
<li>Record and maintain analysis/records accurately.</li>
<li>Perform instrument maintenance, calibrations, quality control checks, solution preparations and solution standardizations.</li>
<li>Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues.</li>
<li>Initiate corrective actions on identified non-capable procedures or practices.</li>
<li>Communicate to supervisor concerns about standard laboratory procedures, operational problems and quality trends.</li>
<li>Promote complete customer satisfaction through quality and service to both internal and external customers.</li>
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<p><strong>Job Qualifications:</strong></p>
<ul>
<li>Bachelor’s Degree in Chemistry or Technical Science degree required.</li>
<li><strong>1-2 years of relevant experience outside of college</strong></li>
<li>Self-motivated and able to work independently as well as in a group setting.</li>
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Midwest candidates only!
Key Responsibilities:
Record and maintain analysis/records accurately.
Perform instrument maintenance, calibrations, quality control checks, solution preparations and solution standardizations.
Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues.
Initiate corrective actions on identified non-capable procedures or practices.
Communicate to supervisor concerns about standard laboratory procedures, operational problems and quality trends.
Promote complete customer satisfaction through quality and service to both internal and external customers.
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Bachelor’s Degree in Chemistry or Technical Science degree required.
1-2 years of relevant experience outside of college
Self-motivated and able to work independently as well as in a group setting.
Proficiency in computer skills and good working knowledge with all MS Office Applications.
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<p><strong>Midwest candidates only!</strong></p>
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<li>Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues.</li>
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<li>Communicate to supervisor concerns about standard laboratory procedures, operational problems and quality trends.</li>
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jimibl </p>
<div class="date-location">Aug 03, 2019 - Waterloo / Cedar Falls</div>
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<div class="job-post-details">
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<p>Our manufacturing company is looking to add a <strong>QC Chemist</strong> to their weekend night shift in the <strong>Waterloo, IA</strong> area. This <u>Chemist</u> will perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustments and/or rejection decisions.</p>
<p><strong>Midwest candidates only!</strong></p>
<p><strong>Key Responsibilities:</strong></p>
<ul>
<li>Record and maintain analysis/records accurately.</li>
<li>Perform instrument maintenance, calibrations, quality control checks, solution preparations and solution standardizations.</li>
<li>Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues.</li>
<li>Initiate corrective actions on identified non-capable procedures or practices.</li>
<li>Communicate to supervisor concerns about standard laboratory procedures, operational problems and quality trends.</li>
<li>Promote complete customer satisfaction through quality and service to both internal and external customers.</li>
</ul>
<p><strong>Job Qualifications:</strong></p>
<ul>
<li>Bachelor’s Degree in Chemistry or Technical Science degree required.</li>
<li><strong>1-2 years of relevant experience outside of college</strong></li>
<li>Self-motivated and able to work independently as well as in a group setting.</li>
<li>Proficiency in computer skills and good working knowledge with all MS Office Applications.</li>
<li>Must be willing to work the Night Weekend shift which consists of Friday/Saturday/Sunday 6pm-6am.</li>
</ul> </div>
</div>
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<p class="similar-job-title"><a href="https://www.jobs2careers.com/click.php?jid=67f8c3adc09c73eca6f808c51&ri=99455d0475194acf98d9b2ede32f00fe&job_loc=Cedar+Rapids%2CIA&q=Qc+Chemist&spl=v1%253AHhFFl2GR%252FAllAlX7%253AJLDMKF0Osi%252BwPlE7Wl9TnQ%253D%253D%253AABgHURZhOhY2lJYC08YXQD5jd04eJ8MiZ%252FpTKCL9TATUcKFexwOB5coZAtvgmJe1DuWluzlGlBSNtxpLXY%252BGARXfV5M3tyd7yKOAGWWvbfiZa6tIivm%252FSnxaFiJlXu8RIM9w2Dg%253D&encrypt=0&l=Waterloo%2C+IA&query_category_id=560000&t=simplyhired.com&jobkey-27694090763/" class="blue-link" target="_blank">The Perry Group, Lt - Design/Build PM (chemical/process engineering)</a></p>
<p class="similar-job-company">CDM Smith - <span class="text-muted">Cedar Rapids, IA</span></p>
<p class="text-muted similar-job-date">
4 days ago </p>
<p class="similar-job-title"><a href="https://www.jobs2careers.com/click.php?jid=6632b6c538cc73ecba5f5e4a1&ri=99455d0475194acf98d9b2ede32f00fe&job_loc=Hampton%2CIA&q=Qc+Chemist&spl=v1%253ACPoys9DlTf6zEI0S%253ANlJev55HfZg4Ejgl5ulOyg%253D%253D%253A09wISq7M8REfpFakoRfIcvLT0O%252Fj%252BRebFgG6sxPxWzuDWAoyhGJyjOGOcNPOfuqvdwZnc969dzlcoGNqI6HqI1bxctn5W6Q%252B%252F1WjzWRp7tqj8t1G5TpObtTBJKDLk9p1OSc%253D&encrypt=0&l=Waterloo%2C+IA&query_category_id=560000&t=simplyhired.com&jobkey-27621038214/" class="blue-link" target="_blank">Clinic Lab Assistant - New Hampton Clinic - Part Time</a></p>
<p class="similar-job-company">Trinity Health - <span class="text-muted">Hampton, IA</span></p>
<p class="text-muted similar-job-date">
4 days ago </p>
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'title' => 'Analytical Development Group Leader',
'description' => 'Company Information<br /><br /><p>You Matter to Cambrex. </p><p>Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. </p><p>Your Work Matters.</p><p>At Cambrex, we strive to build a culture where all colleagues have the opportunity to:</p><ul><li>engage in work that matters to our customers and the patients they serve </li><li>learn new skills and enjoy new experiences in an engaging and safe environment</li><li>strengthen connections with coworkers and the community</li></ul><p>We re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes medical, dental, vision, Life, LTD, retirement savings and more! Can we make this broader language, so it fits in all markets, e.g., that includes healthcare, life insurance, planning for retirement, and more! </p><p>Your Future Matters.</p><p>Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!</p><br />Job Overview<br /><br /><p>Reporting to the Director, Research and Analytical Development, the Group Leader, Analytical Development will provide management oversight and leadership to a group of approximately 5 to 8 direct reports with varying levels of degrees and experience at an industry leader.</p><br />Responsibilities<br /><br /><ul><li>Safely and efficiently manage a group of 5-8 direct reports with varying levels of experience and degrees, in order to develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products</li><li>Effectively and professionally communicate project status to internal and external clients during weekly teleconferences and email correspondence</li><li>Investigate and solve analytical technical issues</li><li>Assist with or lead efforts to transfer documented analytical methods to QC and PSG departments</li><li>Provide guidance and/or project leadership for cross-functional project teams</li><li>Provide guidance to lab personnel on safe lab practices</li><li>Perform analytical chemistry assays based on new and existing methodologies and qualify reference materials</li><li>Training staff on analytical techniques and instrumentation</li><li>Participate in the evaluation of new business opportunities</li><li>Maintain lab notebooks documenting work and writing technical reports to document analytical methods</li><li>Maintain compliance with cGMP SOPs and DEA regulations</li><li>Coordinate off-site testing as necessary</li></ul><br />Education, Experience & Licensing Requirements<br /><br /><ul><li>BS Degree in Chemistry, with analytical emphasis. Advanced degree preferred.</li><li>At least 5 years of industrial experience in a method development role and validation role with a focus on small scale pharmaceutical method validation</li><li>Demonstrated success in validating analytical methods to support production in a safe, efficient and economically viable manner</li><li>Mastery of compliance requirements within cGMP, safety, and regulatory environments required</li><li>Strong operational knowledge of analytical instrumentation including HPLC, GC, GPC, LC/MS, FTIR, UV-VIS, NMR, and data stations required</li><li>Experience in pharmaceutical laboratory experience required</li><li>Familiarity with cGMP regulations required</li><li>Working knowledge of Empower 2 beneficial</li><li>Project management experience strongly preferred</li><li>Windows based computer knowledge</li></ul><p></p><p><em>Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.</em></p><p>#CB</p><p>#LI-RD1</p>',
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'title' => 'Laboratory Scientist Non Certified',
'description' => 'Overview:<br/><p style="margin: 0px;"><strong><span style="font-size: 12pt;">UnityPoint Health - Allen Hospital </span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 12pt;">Full-Time Benefit: Night Shift. 5 on 5 off, 2 on 2 off. 1930-0700; weekend/holiday rotation</span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt;">The Laboratory Scientist, Non-Certified position is responsible for performing waived and moderate complexity laboratory tests and analyses in the hematology, special chemistry, chemistry and microbiology departments in the laboratory. The Laboratory Scientist, Non-Certified collects and processes patient specimens within the laboratory and is responsible for quality control and maintenance of laboratory equipment.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Why UnityPoint Health?</span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">? </span></p><ul><li style="margin-left: 1.25in;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Commitment </span></strong><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">to our Team </span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Weve been named a <span style="color: blue;">Top 150 Place to Work in Healthcare 2022</span> by Beckers Healthcare for our commitment to our team members.? </span></li><li style="margin-left: 1.25in;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Culture </span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">At UnityPoint Health, </span><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">you</span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;"> Come for a fulfilling career and experience </span><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;"><span style="color: blue;">a culture</span> guided by uncompromising values and unwavering belief in doing what's right for the people we serve.? </span></li><li style="margin-left: 1.25in;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Benefits </span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;"> Our competitive <span style="color: blue;">Total Rewards</span> program offers benefits options that align with your needs and priorities, no matter what life stage youre in.? </span></li><li style="margin-left: 1.25in;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Diversity, </span></strong><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Equity and Inclusion Commitment</span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;"> Were committed to ensuring you have a voice that is heard regardless of role, race, gender, religion, or sexual orientation.</span><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">?</span></li><li style="margin-left: 1.25in;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Development</span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;"> We believe equipping you with support and <span style="color: blue;">development opportunities</span> is an essential part of delivering a remarkable employment experience.? </span></li><li style="margin-left: 1.25in;"><strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Community Involvement </span></strong><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;"> Be an essential part of our core purposeto improve the health of the people and communities we serve.</span><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">?</span></li></ul><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">? </span></p><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Visit us at UnityPoint.org/careers to hear more from our team members about why UnityPoint Health is a great place to work. <span style="color: blue;"></span></span><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">? </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><br/><br/>Responsibilities:<br/><table border="1" cellspacing="0" cellpadding="0"><tbody><tr><td valign="top" width="623"><p style="margin: 0px;"><span style="font-size: 12pt;"><strong>Clinical Excellence</strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Performs waived and moderate complexity lab testing following proper laboratory procedure and follow up of critical lab values</span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Works to support testing in the department areas of chemistry, hematology, specimen collection and processing and other department areas as defined by complexity of testing.</span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Works closely with Certified Laboratory techs (MLS/MLT/MT) with lab procedures, tests and training</span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Assists with training of new staff into proper laboratory procedures and processes</span></p><p style="margin: 0px;"> </p></td></tr><tr><td valign="top" width="623"><p style="margin: 0px;"><span style="font-size: 12pt;"><strong>Quality of Care</strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Performs and verifies quality control and instrument maintenance and troubleshooting</span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Understands quality in laboratory testing</span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Follows lab regulatory requirements for CLIA, CAP and Joint Commission</span></p></td></tr><tr><td valign="top" width="623"><p style="margin: 0px;"><span style="font-size: 12pt;"><strong>Care Coordination</strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Collect, receive and process laboratory samples and sendouts following proper laboratory procedures. Includes training in phlebotomy (blood draws).</span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Registers, orders and documents patient lab orders in the LIS and HIS computer systems</span></p></td></tr><tr><td valign="top" width="623"><p style="margin: 0px;"><span style="font-size: 12pt;"><strong>Inventory/Supply Coordination</strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt;"> Perform inventory management and other miscellaneous tasks as needed</span></p></td></tr></tbody></table><br/><br/>Qualifications:<br/><ul><li><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Bachelors degree in chemical, physical, or biological science from an accredited institution</span></li><li><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">College or post graduate laboratory experience</span></li><li><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Valid drivers license when driving any vehicle for work-related reasons.</span></li><li><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Must be able to read, write and speak English</span></li><li><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Must possess basic computer skills and knowledge using word processing, spreadsheet, email and web browser</span></li><li><span style="font-size: 12.0pt; font-family: 'Verdana',sans-serif;">Use of usual and customary equipment used to perform essential functions of the position.</span></li></ul>',
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'title' => 'Analytical Development Group Leader',
'description' => '<p><p>Company Information</p><br><p> You Matter to Cambrex. </p><br><p> Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. </p><br><p> Your Work Matters. </p><br><p> At Cambrex, we strive to build a culture where all colleagues have the opportunity to: </p><br><p>+ engage in work that matters to our customers and the patients they serve </p><br><p>+ learn new skills and enjoy new experiences in an engaging and safe environment </p><br><p>+ strengthen connections with coworkers and the community </p><br><p> Were committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes medical, dental, vision, Life, LTD, retirement savings and more! Can we make this broader language, so it fits in all markets, e.g., that includes healthcare, life insurance, planning for retirement, and more! </p><br><p> Your Future Matters. </p><br><p> Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today! </p><br><p>Job Overview</p><br><p> Reporting to the Director, Research and Analytical Development, the Group Leader, Analytical Development will provide management oversight and leadership to a group of approximately 5 to 8 direct reports with varying levels of degrees and experience at an industry leader. </p><br><p>Responsibilities</p><br><p>+ Safely and efficiently manage a group of 5-8 direct reports with varying levels of experience and degrees, in order to develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products </p><br><p>+ Effectively and professionally communicate project status to internal and external clients during weekly teleconferences and email correspondence </p><br><p>+ Investigate and solve analytical technical issues </p><br><p>+ Assist with or lead efforts to transfer documented analytical methods to QC and PSG departments </p><br><p>+ Provide guidance and/or project leadership for cross-functional project teams </p><br><p>+ Provide guidance to lab personnel on safe lab practices </p><br><p>+ Perform analytical chemistry assays based on new and existing methodologies and qualify reference materials </p><br><p>+ Training staff on analytical techniques and instrumentation </p><br><p>+ Participate in the evaluation of new business opportunities </p><br><p>+ Maintain lab notebooks documenting work and writing technical reports to document analytical methods </p><br><p>+ Maintain compliance with cGMP SOPs and DEA regulations </p><br><p>+ Coordinate off-site testing as necessary </p><br><p>Education, Experience & Licensing Requirements</p><br><p>+ BS Degree in Chemistry, with analytical emphasis. Advanced degree preferred. </p><br><p>+ At least 5 years of industrial experience in a method development role and validation role with a focus on small scale pharmaceutical method validation </p><br><p>+ Demonstrated success in validating analytical methods to support production in a safe, efficient and economically viable manner </p><br><p>+ Mastery of compliance requirements within cGMP, safety, and regulatory environments required </p><br><p>+ Strong operational knowledge of analytical instrumentation including HPLC, GC, GPC, LC/MS, FTIR, UV-VIS, NMR, and data stations required </p><br><p>+ Experience in pharmaceutical laboratory experience required </p><br><p>+ Familiarity with cGMP regulations required </p><br><p>+ Working knowledge of Empower 2 beneficial </p><br><p>+ Project management experience strongly preferred </p><br><p>+ Windows based computer knowledge </p><br><p> Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. </p><br><p> #CB </p><br><p> #LI-RD1 </p><br></p>',
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'title' => 'The Perry Group, Lt - Design/Build PM (chemical/process engineering)',
'description' => '<p><strong>33873BR</strong></p><p><strong>Requisition ID:</strong></p><p>33873BR</p><p><strong>Business Unit:</strong></p><p>LPG</p><p><strong>Job Description:</strong></p><p>** We are open to having this opening be based at any of our CDM Smith offices located in the United States. We are also considering partial or full remote schedules for this position. **</p><p>Louis Perry Group, a CDM Smith company, is seeking an experienced Engineer/Project Manager with a chemical / process engineering background. This Project Manager will have particular responsibility to lead projects in the chemical / oil & gas market for heavy industrial clients, as well as potential other projects.</p><p>A Project Manager is an experienced Engineer who can plan, organize, and control the activities of the project as well as his/her own activities to best accomplish the successful completion (on time and within prescribed budget) of all projects assigned to him/her while operating within the guidelines established by the President. Qualities of a Project Manager would include maturity, judgement, leadership, experience, and project success.</p><p>Primary Duties and Responsibilities:</p><p> Defines the scope of individual projects. Directly responsible for the quality control and design concept of the plans and specifications following our Quality Management System (QMS).</p><p> Maintains the engineering budget, scope of work, and engineering schedule</p><p> Communicates and coordinates with all involved in the project</p><p> Develops integrated tasks to accomplish individual projects</p><p> Coordinates and monitors the technical work of each task</p><p> Coordinates the project with outside consultants</p><p> Makes recommendation of award to client</p><p> Coordinates the frequency of periodic visits by firm representative(s)</p><p> Reviews all documents prepared for each project</p><p> Monitors progress toward deliverable schedules</p><p> Works closely with personnel from Engineering departments as necessary to ensure fulfillment of contract requirements</p><p> Schedules design meetings and weekly progress meetings</p><p> Attends pre-bid meeting and tabulate bid results</p><p> Reviews and approves all Engineering (Design) Change Notices, when appropriate for the project</p><p> Reviews and approves all Contractor monthly requisitions for payment</p><p> Prepares monthly reports</p><p> Prepares project closeout meeting</p><p> Develops trust and confidence of clients</p><p> Reports to upper management any matters that jeopardize the success of the project</p><p> Seeks follow-up business for each project</p><p> Upon completion of the project, is available to the field engineers, contractors and inspectors for consultation regarding the construction phase of the project</p><p><strong>Job Title:</strong></p><p>The Perry Group, Lt - Design/Build PM (chemical/process engineering)</p><p><strong>Group:</strong></p><p>PGL</p><p><strong>Employment Type:</strong></p><p>Regular</p><p><strong>Minimum Qualifications:</strong></p><p>The Project Manager must have:</p><p> Bachelor s degree, and</p><p> Ten (10) or more years of relevant work experience, and</p><p> PMP (PMI), CCM or DBIA certification is required (within 12 months of hire or promotion onto the Approved Project Manager list)</p><p><strong>Preferred Qualifications:</strong></p><p> Bachelor's degree in chemical or mechanical engineering degree w/ process experience</p><p> experience in EPC (engineering, procurement and construction) / Design-Build firms for heavy industrial clients</p><p><strong>EEO Statement:</strong></p><p>The Perry Group, Ltd. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, pregnancy and pregnancy-related conditions, sexual orientation, gender identity, national origin, age, marital status, disability, citizenship status, genetics, protected veteran status or any other characteristics protected by applicable law.</p><p><strong>Job Site Location:</strong></p><p>United States - Nationwide</p><p><strong>Agency Disclaimer:</strong></p><p>All vendors must have a signed CDM Smith Placement Agreement from the CDM Smith Recruitment Center Manager to receive payment for your placement. Verbal or written commitments from any other member of the CDM Smith staff will not be considered binding terms. All unsolicited resumes sent to CDM Smith and any resume submitted to any employee outside of CDM Smith Recruiting Center Team (RCT) will be considered property of CDM Smith. 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In addition, CDM Smith may conduct drug testing for designated positions.</p><p>Background checks are conducted after an offer of employment has been made in the United States. The timing of when background checks will be conducted on candidates for positions outside the United States will vary based on country statutory law but in no case, will the background check precede an interview.</p><p>CDM Smith will conduct interviews of qualified individuals prior to requesting a criminal background check, and no job application submitted prior to such interview shall inquire into an applicant's criminal history. If this position is subject to a background check for any convictions related to its responsibilities and requirements, employment will be contingent upon successful completion of a background investigation including criminal history. 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Bachelor’s Degree in Chemistry or Technical Science degree required.
1-2 years of relevant experience outside of college
Self-motivated and able to work independently as well as in a group setting.
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<h1>QC Chemist</h1>
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jimibl </p>
<div class="date-location">Aug 03, 2019 - Waterloo / Cedar Falls</div>
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<p>Our manufacturing company is looking to add a <strong>QC Chemist</strong> to their weekend night shift in the <strong>Waterloo, IA</strong> area. This <u>Chemist</u> will perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustments and/or rejection decisions.</p>
<p><strong>Midwest candidates only!</strong></p>
<p><strong>Key Responsibilities:</strong></p>
<ul>
<li>Record and maintain analysis/records accurately.</li>
<li>Perform instrument maintenance, calibrations, quality control checks, solution preparations and solution standardizations.</li>
<li>Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues.</li>
<li>Initiate corrective actions on identified non-capable procedures or practices.</li>
<li>Communicate to supervisor concerns about standard laboratory procedures, operational problems and quality trends.</li>
<li>Promote complete customer satisfaction through quality and service to both internal and external customers.</li>
</ul>
<p><strong>Job Qualifications:</strong></p>
<ul>
<li>Bachelor’s Degree in Chemistry or Technical Science degree required.</li>
<li><strong>1-2 years of relevant experience outside of college</strong></li>
<li>Self-motivated and able to work independently as well as in a group setting.</li>
<li>Proficiency in computer skills and good working knowledge with all MS Office Applications.</li>
<li>Must be willing to work the Night Weekend shift which consists of Friday/Saturday/Sunday 6pm-6am.</li>
</ul> </div>
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