quality control analyst

Kernovo Pharmaceutical Industries

<p>Pharmaceutical quality control analyst</p><p>Job Type: Full-time</p><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>total work: 1 year (Preferred)</li></ul><p>Work Location: In person</p>

Quality Control Analyst

Virginia Commonwealth University

<div><div><div><h3 class="jobSectionHeader"><b>Quality Control Analyst
</b></h3><div><div><ul><li>45001279
</li></ul></div><div><ul><li>907 Floyd Avenue, MCV Main Campus, Virginia, United States, 23284
</li></ul></div><div><ul><li>Legal, Audit and Compliance
</li></ul></div><div><ul><li>Staff
</li></ul></div><div></div><div><ul><li>VP Research MBU</li></ul></div></div><div><br>
</div>
<div><p><b>Department</b> <b>Summary:</b></p>
<p>
At the VCU Office of the Vice President for Research and Innovation, our mission is to foster transformative research, discovery, and innovation at Virginia Commonwealth University through service excellence.<br>
<br>
We partner with faculty in all schools and departments as they seek funding, plan studies, establish collaborations, calculate budgets, submit grant applications, negotiate industry contracts, and secure patents and licensing agreements.<br>
<br>
Our commitment to supporting and elevating the research community at VCU has resulted in record levels of sponsored research and has placed VCU among the nation&rsquo;s premier public research universities.<br>
<br>
Through our passion for discovery and willingness to take on challenges, we continue to advance the work that matters most and position the university as a national leader in research, innovation, creativity, and scholarship.</p>
<p><b>
Duties &amp; Responsibilities:</b></p>
<p>
The Quality Control Analyst will evaluate the Human Research Protection Programs (HRPP) effectiveness and develop quality improvement activities to continuously measure, assess, and improve program compliance with federal regulations, applicable state regulations, and institutional HRPP policies and practices to protect human research participants. The position focuses primarily on review and monitoring of the activities, policies, procedures, and records for the following groups:</p>
<ul>
<li>IRB</li>
<li>HRPP education and outreach</li>
<li>HRPP staff</li>
<li>HRPP</li>
</ul>
<p><b>Typical Duties</b></p>
<ul>
<li>Provide one-on-one and group consultation</li>
<li>Communicate with the research community (IRB members, Investigators, support staff), facilitating timely information dissemination</li>
<li>Collaborate with colleagues on policies and procedures and communicate changes to the research community</li>
<li>Assist in planning, coordinating, and conducting audit, consulting, or special engagements of the HRPP under the direction of the assistant director.</li>
<li>Engagement planning responsibilities include gaining an understanding of the program or research review, evaluating risks and controls, developing objectives and engagement scope, and participating in the drafting of reports</li>
<li>Engagement coordination responsibilities include managing time and workload to meet established milestones and due dates, proofreading work for completeness and accuracy, and reporting any significant issues to the team lead that could cause completion delays</li>
<li>Support program goals to measure and improve the quality, effectiveness, and efficiency of the HRPP</li>
<li>Manage quarterly reviews to assess HRPP quality, efficiency, and effectiveness</li>
<li>Act as a backup to assist the HRPP team with the reviews of study applications and workflow</li>
<li>Establish an Education Plan, execute the plan, and track progress across both campuses with our stakeholders and research community.</li>
</ul>
<p><b>Qualifications:</b></p>
<p><b>
Only those who do not require current or future sponsorship for employment will be considered</b></p>
<p>
Minimum Qualifications</p>
<ul>
<li>Bachelor&rsquo;s degree and 1 to 3 years of relevant professional experience or equivalent combination of education, experience, and training</li>
<li>Ability to communicate clearly and effectively both verbally and in writing to all levels of management</li>
<li>Knowledge of federal, state, and university regulations</li>
<li>Effective interpersonal skills and ability to interact professionally with department and client personnel</li>
<li>Proficiency in Microsoft Office applications</li>
<li>Ability to maintain integrity, objectivity, independence, and confidentiality</li>
<li>Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU</li>
</ul>
<p>Preferred Qualifications</p>
<ul>
<li>Master's degree in a related field, Certified IRB Professional (CIP) and a Minimum of 5 years&rsquo; experience in related field.</li>
</ul>
<p><b>Salary Range: </b>65,000 - 68,000</p>
<p><b>
Benefits</b>: All full-time university staff are eligible for VCU&rsquo;s robust benefits package that includes comprehensive health benefits, paid annual and holiday leave granted up front, generous tuition benefits, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more.</p>
<p><b>
Unit:</b> VP Research MBU</p>
<p><b>
Department:</b> Human Research Protection</p>
<p><b>
FLSA Exemption Status:</b> Exempt<br>
<br>
<b>Hours per Week: </b>40</p>
<p><b>
Restricted Position: </b>No</p>
<p><b>
ORP Eligible: </b>No</p>
<p><b>
Flexible Work Arrangement: </b>Hybrid</p>
<p><b>
University Job Title: </b>25221N - Analyst LG 1</p></div></div></div></div><p></p>

Acino International AG

<p>Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and we operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard-to-reach areas of the world.</p><p>We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our Quality team in Dubai, UAE Site- Acino Pharmaceuticals FZ LLC </p><p>Quality Control Analyst will be responsible for performing analytical testing, maintaining laboratory resources, ensuring compliance with quality and safety standards, and supporting product release, method transfers, and validations. He /She will work with advanced analytical instruments, uphold data integrity principles, and ensure full compliance with GMP requirements to maintain product quality, safety, and efficacy.</p><p> Job Responsibilities </p><ul><li>Perform analysis of raw materials, packaging materials, bulk products, finished products, in-process samples, stability samples, process/cleaning validation samples, and miscellaneous samples as per approved methods and protocols.</li><li>Ensure all activities comply with GLP, GMP, and ALCOA  principles.</li><li>Operate major analytical instruments including HPLC, GC, Dissolution Apparatus, UV-Vis Spectrophotometer, and IR.</li><li>Perform daily verification, calibration, and routine maintenance of instruments as per SOPs.</li><li>Maintain an up-to-date inventory of reference standards, working standards, impurity standards, analytical columns, reagents, chemicals, and consumables.</li><li>Conduct qualification of working standards against reference or primary standards.</li><li>Prepare volumetric solutions and standardize them for routine use.</li><li>Prepare, review, and update SOPs, test methods, and specifications as needed.</li><li>Record all data accurately, clearly, and in real-time following GLP requirements.</li><li>Report and support investigations for any OOS, OOT, incidents, or non-compliance activities.</li><li>Initiate and support Change Control, CAPA, and Deviation processes as required.</li><li>Follow safety procedures and use the recommended PPE for all QC activities.</li><li>Ensure compliance with EHS policies and safe work practices in the laboratory.</li><li>Support analytical validation/verification and cleaning validation studies.</li><li>Participate in laboratory improvement initiatives.</li><li>Carry out additional tasks assigned by the QC Manager in line with department objectives.</li></ul><p> Qualifications & Skills: </p><ul><li>Bachelor's degree in chemistry, pharmaceutical sciences, or related discipline.</li><li>1-3 years of experience in a pharmaceutical QC laboratory.</li><li>Hands-on experience with HPLC, GC, Dissolution, UV, and IR instruments.</li><li>Knowledge of LIMS and SAP systems is preferred.</li><li>Good understanding of GMP, GLP, and data integrity principles (ALCOA ).</li><li>Strong attention to detail, analytical thinking, and problem-solving skills.</li><li>Effective communication and teamwork abilities.</li></ul><p>This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</p><p> Please apply via our HR system here. </p>

BOK Financial

<div><div>Req ID: 77365</div>
<div>Location: Tulsa -TUL</div>
<div>Areas of Interest: Risk Management, BSA/AML</div>
<div>Pay Transparency Salary Range: Not Available</div>
<div>Application Deadline: 01/02/2025</div>
<div>BOK Financial Corporation Group includes BOKF, NA; BOK Financial Securities, Inc. and BOK Financial Private Wealth, Inc. BOKF, NA operates TransFund and Cavanal Hill Investment Management, Inc. BOKF, NA operates banking divisions: Bank of Albuquerque; Bank of Oklahoma; Bank of Texas and BOK Financial&reg;.</div>
<div><div><div><h2 class="jobSectionHeader">
Bonus Type</h2>
</div><div><div>Discretionary</div></div></div><div><div><h2 class="jobSectionHeader">
Summary</h2>
</div><div><p>
We've built a culture at BOK Financial where amazing people (like you) can bring their best, be their best and work for the best. You've come to the right place to grow your career.</p>
</div></div><div><div><h2 class="jobSectionHeader">
Job Description</h2>
</div><div><div>
The Quality Control Analyst is primarily responsible for performing, documenting, and managing, all quality assurance processes related to the Bank Secrecy Act, Anti-Money Laundering, Office of Foreign Asset Control, and USA Patriot Act requirements.</div>
</div></div><div><div><h2 class="jobSectionHeader">
Team Culture</h2>
</div><div><p>
A career with BOK Financial will provide you opportunities and benefits that can only come from working for a trusted industry leader. Work with amazing, energetic team members and a company dedicated to your success, growth, and advancement.</p>
</div></div><div><div><h2 class="jobSectionHeader">
How You'll Spend Your Time</h2>
</div><div><ul><li>You will utilize previous audit/testing review experience to implement quality approaches, perform and document assigned audit control reviews, and conduct testing based on detailed operating procedures and processes. You will identify audit issues, exceptions, and patterns and escalate to BSA management and business line management for resolution, and formally document control/audit findings.</li>
<li>You will communicate quality control/audit test findings to the Director of BSA/AML Assessments and the BSA/AML Officer through monthly quality reports. You will participate in quality control/audit review exercises with managers and appropriate personnel to discuss audit patterns or trends, and present testing results and recommendations to resolve defects as directed.</li>
<li>You will participate in special projects, such as research, analysis of BSA testing results or issues, training, reading literature in order to become more knowledgeable about current banking, regulatory and audit issues, and performing other tasks as necessary to carry out daily responsibilities. You will maintain a high level of expertise in specific areas of testing.</li>
<li>You will review, prepare and submit Quality Control test results to the Financial Crimes Department. You will review test results on audit findings, and respond within the required Service Level timeframes and regulatory expectations to ensure that appropriate sampling and documentation are met.
</li><li>You will work with the Director of BSA/AML Assessments to identify areas of risk and make recommendations for policies and procedures on operational improvements, processes for BSA/AML compliance, quality control and any additional training essential to mitigate risk. You will seek ways to assist the Bank in strengthening controls while remaining compliant and improving efficiency.
</li></ul></div></div><div><div><h2 class="jobSectionHeader">Education &amp; Experience Requirements</h2>
</div><div><p>
This level of knowledge is normally acquired through completion of a Bachelor&rsquo;s Degree in Finance or Business Accounting, or related field of study and 2-3 years of directly related experience in audit/testing/review experience preferably serving financial institutions and/or with a bank internal audit or account department, and/or with federal regulatory agency, along with 3+ years of experience of compliance or financial crimes background or equivalent work experience of 6-8 years. A minimum of two hours of continuing education is required each month on industry-related topics or technical skills related to the role.</p><br>
<div></div>
<p>SKILLS:
</p><ul><li>Knowledge of Bank Secrecy Act and various other related anti-money laundering regulations including the Office of Foreign Asset Control and the USA Patriot Act.</li>
<li>Strong aptitude and adherence of bank policies and procedures to ensure the quality of the end state results are communicated effectively to address deficiencies to ensure all aspects of the Financial Crimes Department meet internal and external regulatory expectations.
</li><li>Strong aptitude for analyzing data to identifying patterns and trends.
</li><li>Proven ability to communicate concisely, document and articulate department and/or employee performance trends to address training program gaps, performance issues, or identify individual employee reinforcement training needs or requirements.</li>
<li>Knowledge of federally recognized examination procedures to evaluate compliance with applicable federal and state laws and regulations.
</li><li>Broad knowledge and understanding of all facets of banking.
</li><li>Strong analytical ability and organizational skills; Problem solving and root cause identification skills; Strong decision making abilities.
</li><li>Excellent leadership ability and team building skills.
</li><li>Ability to prioritize and multi-task, and demonstrated ability to meet deadlines.
</li><li>Strong PC and software skills and an aptitude for learning bank operating systems</li>
</ul>
</div></div></div><div>BOK Financial Corporation Group is a stable and financially strong organization that provides excellent training and development to support building the long term careers of employees. With passion, skill and partnership you can make an impact on the success of the bank, customers and your own career!<br>
Apply today and take the first step towards your next career opportunity!<br>
<br>
The companies in BOK Financial Corporation Group are equal opportunity employers. We are committed to providing equal employment opportunities for training, compensation, transfer, promotion and other aspects of employment for all qualified applicants and employees without regard to sex, race, color, religion, national origin, age, disability, pregnancy status, sexual orientation, genetic information or veteran status.</div>
<div>Please contact recruiting_coordinators@bokf.com with any questions.</div></div>

Teva Pharmaceuticals

<div><div><div><div><p>Apply now &raquo;</p>
</div></div><div><div><div><div><div><p>Quality Control Analyst
</p></div></div></div></div><div></div><div><div><div><div><b>Date: </b>Nov 27, 2025
</div></div></div></div><div><div><div><div><b>Location:
</b>Chennai, India, 600113
</div></div></div></div><div><div><div><div><b>Company: </b>Teva Pharmaceuticals
</div></div></div></div><div><div><div><div><b>Job Id: </b>64273
</div></div></div></div><div><div><div><div><div><div><div><div><b>Who we are</b></div>
</div><div>Together, we&rsquo;re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It&rsquo;s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world&rsquo;s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization&rsquo;s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we&rsquo;re always looking for new ways to continue making a difference, and new people to make a difference with.</div></div><div><div><div><b>
How you&rsquo;ll spend your day</b></div>
</div><div><ul><li>To perform Stability analysis.</li>
<li>Maintenance of operating instruments / equipment.</li>
<li>To maintain the assigned Laboratory workplace, instruments and equipment etc.</li>
<li>To adhere Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure.</li>
<li>Responsible for handling , operating and maintaining HPLC / UV and related instruments to ensure optimal performance.</li>
<li>Adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure.</li>
<li>Performing stability testing (Assay, RS &amp; Dissolution) of all formulations by HPLC and UV techniques.</li>
<li>Preparing samples and executing the same as per the Method of Analysis and Verification of sample set sequence in applicable software&rsquo;s.</li>
<li>Interpreting chromatographic data and ensuring proper documentation of all analytical activities in compliance with GLP / GDP requirements</li>
<li>Reporting of interpreted data in line with specification, compliance and regulatory standards and maintaining data integrity throughout the analytical lifecycle.</li>
<li>Evaluation of reported results and reporting of any abnormal results to the supervisor ontime.</li>
<li>Handling of laboratory software's.</li>
<li>Ensure to use safety apparels and PPEs while working in the laboratory.</li>
<li>Ensure timely completion of assigned training.</li>
</ul></div></div><div><div><div><b>Your experience and qualifications</b></div>
</div><div><ul><li>M.Sc., Chemistry</li>
<li>7+ years of experience</li>
</ul></div></div><div><div><div><b>Make a difference with Teva Pharmaceuticals</b></div>
</div></div><div></div><div><div><div><b>Already Working @TEVA?</b></div>
</div><div><div>
If you are a current Teva employee, please apply using the internal career site available on &quot;Employee Central&quot;. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
</div><div>The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.</div></div></div><div><div><div><b>
Teva&rsquo;s Equal Employment Opportunity Commitment</b></div>
</div><div>Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.</div></div></div>
</div></div></div></div></div><p></p><div><p>Apply now &raquo;</p></div></div></div><div></div>

<div><div><div><div><p>Apply now &raquo;</p>
</div></div><div><div><div><div><div><p>Quality Control Analyst II
</p></div></div></div></div><div></div><div><div><div><div><b>Date: </b>Nov 27, 2025
</div></div></div></div><div><div><div><div><b>Location:
</b>Chennai, India, 600113
</div></div></div></div><div><div><div><div><b>Company: </b>Teva Pharmaceuticals
</div></div></div></div><div><div><div><div><b>Job Id: </b>64340
</div></div></div></div><div><div><div><div><div><div><div><div><b>Who we are</b></div>
</div><div>Together, we&rsquo;re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It&rsquo;s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world&rsquo;s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization&rsquo;s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we&rsquo;re always looking for new ways to continue making a difference, and new people to make a difference with.</div></div><div><div><div><b>
How you&rsquo;ll spend your day</b></div>
</div><div><ul><li>Detailed description of MAIN tasks and responsibilities:</li><li>Performing Stability analysis, Method transfer, Method Validation and review of analytical documents.</li><li>Preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports and any document related to stability analysis, method transfer and method validation in compliance with current guidelines. Review and maintenance of all logbooks of the department</li><li>Preparation of departmental SOP&rsquo;s in compliance with current guidelines. Review of departmental SOP&rsquo;s, training of analysts and other technical staff and review validation of data transfer, data management using computer systems.</li><li>Preparation and review of validation protocols in compliance with current guidelines.</li><li>Calibration and validation of all instruments / equipments.</li><li>Entry of stability sample results in LIMS &amp; SAP.</li><li>Handling of LSCMS software</li><li>Initiation of Quality Forms in Track wise Harmony, documents in Glorya EDMS and CAPA in Trackwise Harmony.</li></ul></div></div><div><div><div><b>
Your experience and qualifications</b></div>
</div><div><ul><li>M. Pharmacy</li><li>10 years and 7 months of experience</li></ul></div></div><div><div><div><b>
Teva&rsquo;s Equal Employment Opportunity Commitment</b></div>
</div><div>Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.</div></div></div>
</div></div></div></div></div><p></p><div><p>Apply now &raquo;</p></div></div></div><div></div>

Quality Control Analyst II

Syndy Pharma

<p>Looking for QC cum QA who can do below responsibilities:</p><ul><li>English &amp; Telugu are mandatory</li><li>Good Knowledge in MS Office.</li><li>Raw Material Inspection</li><li>Product Testing like pH, viscosity, texture, fragrance, and color consistency etc.</li><li>Regulatory Compliance</li><li>Calibration and Maintenance of equipment&rsquo;s &amp; instruments.</li><li>Documentation</li></ul><p>Job Types: Full-time, Permanent, Fresher</p><p>Pay: &#8377;18,000.00 - &#8377;20,000.00 per month</p><p>Application Question(s):</p><ul><li>Have you done Bachelors in Pharma (B.Pharma) ?</li></ul><p>Experience:</p><ul><li>QA/QC: 1 year (Required)</li></ul><p>Language:</p><ul><li>English (Required)</li><li>Telugu (Required)</li></ul><p>Work Location: In person</p>

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