qc analyst

Globant

<div>
 At Globant, we are working to make the world a better place, one step at a time. We enhance business development and enterprise solutions to prepare them for a digital future. With a diverse and talented team present in more than 30 countries, we are strategic partners to leading global companies in their business process transformation.
 <br/>
 <br/>
 We are looking for a
 <strong>
  QA Automation Analyst
 </strong>
 who shares our passion for innovation and change. This role is critical to helping our business partners evolve and adapt to consumers' personalized expectations in this new technological era.
 <br/>
 <br/>
 <strong>
  What will help you succeed:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   At least 8 years of experience in Quality Assurance;
  </li>
  <li>
   Proficiency in bug tracking and test management tools (Jira, Xray);
  </li>
  <li>
   Strong knowledge of QA methodologies, tools, and processes.
  </li>
  <li>
   Strong Experience in following skills ;-
  </li>
  <li>
   Playwright or Cypress
  </li>
  <li>
   JavaScript / TypeScript
  </li>
  <li>
   API Automation + Web Automation
  </li>
  <li>
   Docker
  </li>
  <li>
   CI/CD integration
  </li>
  <li>
   Good to have: CMS platform experience and exposure to AI tools in testing workflows.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 This job can be filled in
 <strong>
  Egypt/Jordan
 </strong>
 .
 <br/>
 <br/>
 Create with us digital products that people love. We will bring businesses and consumers together through AI technology and creativity, driving digital transformation to impact the world positively.
 <br/>
 <br/>
 At Globant, we believe in fostering a diverse and inclusive workplace where everyone feels valued and respected. We are an Equal Opportunity Employer committed to creating a thriving and inclusive environment for all employees and candidates, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected characteristic. If you need any assistance or accommodations due to a disability, please let us know by applying through our Career Site or contacting your assigned recruiter.
 <br/>
 <br/>
 We may use AI and machine learning technologies in our recruitment process. Compensation is determined based on skills, qualifications, experience, and location. In addition to competitive salaries, we offer a comprehensive benefits package. Learn more about our commitment to diversity and inclusion and Globant&rsquo;s Benefits.
 <br/>
 <br/>
</div>


QC Analyst, Egypt - Remote - MENA

Avid Bioservices

<div><div>Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.<br>
</div><div><b>Your Role:</b>
</div><div>The <b>Analyst, Quality Control</b> will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment.</div><ul><li>
Perform and review routine assays for HPLC, ELISA/cell-based immunoassays, and/or electrophoresis (SDS-PAGE/IEF) with strict adherence to written analytical test procedures.</li><li>
Perform aseptic sampling, visual inspection, pH, conductivity, osmolality, and spectrophotometry.</li><li>
Review, revise and write test methods, standard operating procedures. In addition to performing QC testing, the Analyst may support validation projects, investigations, and method development projects.</li><li>
Other functions include but are not limited to writing study protocols and reports; training other analysts; working with other departments in developing, revising, and implementing QC procedures and policies.</li><li>
Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions.</li><li>
Participate in regulatory inspections.</li><li>
Support continuous improvement initiatives.</li><li>
Other duties as assigned.</li></ul><div><b>
Minimum Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree in biology, biochemistry, chemistry or equivalent scientific field or a minimum of 2 years of relevant, hands-on experience working in a QC or analytical lab or equivalent combination of education/experience.</li><li>
Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential.</li><li>
Must be proficient with ELISA, Analytical Biochemistry or chemistry.</li></ul><div><b>
Position Type/Expected Hours of Work:</b>
</div><div>This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00a.m. to 5:00p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary.</div><div></div><div><b>
Compensation:</b>
</div><div>We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
</div><div></div><div>The compensation range for this role is $26.73-$30.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
</div><div></div><div><b>Who you are:</b>
</div><ul><li>You have a &quot;bring it on!&quot; team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.</li></ul><ul><li>
Your written and verbal skills are out of this world, and you communicate with clarity and confidence.</li><li>
You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.</li><li>
You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.</li></ul><div><b>
Physical Demands &amp; Work Environment:</b>
</div><div>In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.</div></div>

Analyst, Quality Control (Airway)

<div><div>Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
</div><div>
</div><div><b>Your Role:</b>
</div><div>The <b>Quality Control In-Process Analyst</b> will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment for the Quality Control In-Process team.</div><ul><li>
Perform basic compendial test methods without supervision and with strict adherence to written protocols, analyze data and report results.</li><li>
Formulate buffers and reagents for the purpose of performing test methods.</li><li>
Write and revise test methods and procedures.</li><li>
Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and endotoxin by LAL.</li><li>
Perform water testing and raw material sampling and testing.</li><li>
Perform QC testing for lot release, stability, development/validation projects, and investigations.</li><li>
Other functions include writing study protocols and reports.</li><li>
Work with other departments in developing, revising and implementing QC procedures and policies.
</li><li>Should be aware of company cGMPs as well as industry regulations that apply to all job functions.
</li><li>Perform sample pick up and sample locating without supervision and with strict adherence to written protocols.</li><li>
Other duties as assigned.</li></ul><div><b>
Minimum Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree or 2-4+ years of biotech industry experience working in a QC or analytical lab.
</li><li>Must have experience with analytical testing, writing reports, GMPs, and regulatory audits.
</li><li>Experience with most, if not all the methodologies listed above.
</li><li>Experience with basic maintenance and troubleshooting of analytical instrumentation is highly desirable.</li></ul><div><b>
Position Type/Expected Hours of Work:</b></div><ul><li>
This is a full-time position operating Sunday through Wednesday or Wednesday to Saturday on a 4x10(4 days x 10 hours) schedule.
</li><li>Will have an adaptable schedule to accommodate operational and scheduling demands.</li><li>
Availability needed for overtime and weekend shifts as necessary.</li></ul><div><b>
Compensation:</b>
</div><div>We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
</div><div>
</div><div>The compensation range for this role is $26.73 to $35.63 hourly, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
</div><div>
</div><div><b>Who you are:</b>
</div><ul><li>You have a &quot;bring it on!&quot; team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.</li><li>
Your written and verbal skills are out of this world, and you communicate with clarity and confidence.</li><li>
You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.</li><li>
You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.</li></ul><div><b>
Physical Demands &amp; Work Environment:</b>
</div><div>In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.</div></div>

Analyst (In-Process), Quality Control

Takeda Pharmaceuticals

<div><p>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.</p><p></p><h2 class="jobSectionHeader"><b>
Job Description</b></h2><p></p><h1 class="jobSectionHeader"><b>
About the role:</b></h1><p>
As a Quality Control Analyst II, you will execute and review routine in-process, drug substance, and stability test methods in a timely manner. You will use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS, SoftmaxPro, Charles River Endoscan, MODA, and Empower).</p><p></p><p>
This shift will be working from Saturday to Tuesday.</p><p></p><h1 class="jobSectionHeader"><b>
How you will contribute:</b></h1><ul><li>
Maintain lab operations (including cleaning, ordering of supplies, reagent preparation, stocking, waste disposal).</li><li>
Conduct test methods including samples generated for facility monitoring (i.e., Environmental Monitoring and Critical Utilities), in-process, drug substance, and stability.</li><li>
Own and author quality system events (i.e., laboratory investigations, deviations, CAPA&rsquo;s and change controls).</li><li>
Demonstrate a functional and basic theoretical understanding of laboratory operations and Standard Operating Procedures (SOP&rsquo;s).</li><li>
Work within laboratory environment for extended periods of time, conducting facility monitoring (i.e., Environmental Monitoring and Critical Utility Monitoring) and product tests, reviewing data, maintaining laboratory materials and instruments and other laboratory functions as required.</li><li>
Complete all testing, including special project and protocol testing in a timely and appropriate manner.</li><li>
Maintain data integrity and ensure compliance with company SOP&rsquo;s, specifications, and cGMP regulations.</li><li>
Independently exercise judgment within generally defined Quality Control (QC) procedures and practices in selecting methods and techniques to troubleshoot problems and/or formulate solutions.</li><li>
Decisions have moderate impact on future QC processes and procedures that impact batch disposition.</li><li>
Initiate and own laboratory investigations, basic complexity low and medium risk deviations, CAPA&rsquo;s, and change controls of moderate scope within the electronic Quality Management System.</li><li>
Participate in cross-functional teams.</li><li>
Draft studies and investigations of moderate scope and work on problems where the situation or data requires a review of identifiable factors.
</li><li>Author new SOP&rsquo;s and initiate changes to existing procedures.</li><li>
Train new QC Analysts on routine procedures and practices.</li><li>
May be required to work overtime or be assigned to a different shift as needed.</li><li>
Perform equipment maintenance and calibrations as required.</li><li>
Complete mandatory training within required timeframe.</li><li><div>
Perform other duties as assigned.</div></li></ul><p></p><h1 class="jobSectionHeader"><b>
What you bring to Takeda:</b></h1><div><ul><li>
Bachelor&rsquo;s or master&rsquo;s degree in any Life Sciences with relevant laboratory coursework</li><li>
3-6 years of relevant experience preferred.</li><li>
Previous experience in a regulated environment preferred.</li><li>
Must understand laboratory instrumentation.</li><li>
Must be able to communicate effectively with managers and peers.</li><li>
Must be able to read, write, and converse in English.</li><li>
Must have basic computer skills. General use of word processing, spreadsheets, databases, etc. for the purposes of work execution, training, performance management, and self-service.</li><li>
Good interpersonal skills and able to work effectively and efficiently in a team environment.</li><li>
Knowledge of cGMP manufacturing</li><li>
Knowledge of chemical, biological and/or microbiological safety procedures.</li><li>
Must display eagerness to learn and continuously improve.</li></ul><p></p><h1 class="jobSectionHeader"><b>
Important Considerations:</b></h1><p>
At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:</p><ul><li>
Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.</li><li>
Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.</li><li>
Work in a cold, wet environment.</li><li>
Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.</li><li>
Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.</li><li>
Stand or sit -&gt; Must be able to remain in a stationary or standing position for extended periods of time in both office and laboratory environment.</li><li>
Carry weight, lifting - Frequently moves laboratory materials and portable instruments weighing up to 30 pounds.</li><li>
Climb - Occasionally ascends/descends step ladders to reach materials and/or stairs to collect samples.</li><li>
Dexterity/balance &ndash; required to gown for cleanroom work, balance and dexterity are required.</li><li>
May be required to participate in an on-call rotation for off-shift coverage or occasionally work off-shift hours to help support a 24-7 manufacturing department.</li><li>
Willingness to travel to various meetings or training, this could include overnight trips.</li><li><div>
Requires 0-5% travel.</div></li></ul><p></p><h1 class="jobSectionHeader"><b>
More about us:</b></h1><p>
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.</p><p></p><p>
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.</p><p></p><p>
#GMSGQ #ZR1 #LI-MA1</p></div><p></p><p><b>
Takeda Compensation and Benefits Summary</b></p><p></p><div><p>
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.</p></div><p></p><p><b>
For Location:</b></p>
Brooklyn Park, MN<p></p><p><b>
U.S. Hourly Wage Range:</b></p>
$24.76 - $38.87<p><br>
The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location.</p><p></p><p>
U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.</p><p></p><p><b>
EEO Statement</b></p><p><i>
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.</i></p><p></p><h2 class="jobSectionHeader"><b>
Locations</b></h2>
Brooklyn Park, MN<p></p><h2 class="jobSectionHeader"><b>
Worker Type</b></h2>
Employee<p></p><h2 class="jobSectionHeader"><b>
Worker Sub-Type</b></h2>
Regular<p></p><h2 class="jobSectionHeader"><b>
Time Type</b></h2>
Full time<p></p><p><b>
Job Exempt</b></p>
No</div><p></p>

Quality Control Analyst II

Smith+Nephew

<div><p><b>Life Unlimited. </b>At Smith+Nephew we design and manufacture technology that takes the limits off living.
</p><p></p><p><b>Site Quality Systems Coordinator
</b></p><p>The Site Quality Systems Coordinator is responsible for the administration, maintenance, and continuous improvement of laboratory quality systems, including the Laboratory Information Management System (LIMS) and analytical instrumentation. This role ensures data integrity, regulatory compliance, and efficient laboratory operations across both networked (software-integrated) and standalone instruments in a GMP regulated pharmaceutical environment.
</p><p></p><p>The Senior QC Analyst will collaborate closely with chemists, microbiologists, laboratory staff, and IT partners to ensure that systems and instrumentation
</p><p></p><p><b>U.S. </b><b>Sponsorship or H1B transfer is not available for this role
</b></p><p></p><p><b>What will you be doing?
</b></p><p><b>LIMS Administration &amp; Management
</b></p><ul><li>Serve as system administrator for LIMS, including user access, roles, workflows, and configuration.
</li><li>Manage sample lifecycle workflows, test specifications, and data reporting within LIMS.
</li><li>Coordinate LIMS updates, patches, and validation activities (IQ/OQ/PQ).
</li><li>Troubleshoot system issues and liaise with IT and vendors for resolution.
</li>Ensure compliance with 21 CFR Part 11, ALCOA+ data integrity principles, and internal policies.<br>
<li>
<br>
</li></ul><p><b>Instrumentation Oversight (Integrated &amp; Standalone)
</b></p><ul><li>Oversee lifecycle management of laboratory instruments (e.g., HPLC, GC, UV, balances).
</li><li>Ensure proper data capture from both:
<ul><li>Integrated systems (instrument software connected to LIMS/CDS)
</li><li>Standalone systems (manual data entry or local software)
</li></ul></li><li>Maintain instrument inventory, qualification status, and calibration schedules.
</li><li>Support instrument validation and software validation activities.
</li></ul><p></p><p><b>Data Integrity &amp; Compliance
</b></p><ul><li>Ensure secure, accurate, and attributable data handling across all systems.
</li><li>Review audit trails, electronic records, and user activity for compliance.
</li><li>Develop and enforce procedures for hybrid systems (paper + electronic records).
</li>Lead or support data integrity investigations and remediation efforts.<br>
<li>
<br>
</li></ul><p><b>Quality Systems &amp; Documentation
</b></p><ul><li>Develop, review, and maintain SOPs related to LIMS, instrumentation, and data handling.
</li><li>Support deviation investigations, CAPAs, and change control related to lab systems.
</li><li>Participate in internal and external audits (FDA, EMA, MHRA, etc.).
</li>Maintain system validation documentation and traceability matrices.<br>
<li>
<br>
</li></ul><p><b>System Integration &amp; Improvement
</b></p><ul><li>Coordinate integration between LIMS, Chromatography Data Systems (CDS), and other lab software.
</li><li>Identify opportunities for automation and process efficiency.
</li>Lead or support digital transformation initiatives within the lab.<br>
<li>
<br>
</li></ul><p><b>Training &amp; Support
</b></p><ul><li>Train laboratory personnel on LIMS, instrument software, and data integrity practices.
</li><li>Provide ongoing user support and troubleshooting.
</li><li>Develop training materials and ensure training compliance.
</li></ul><p></p><p><b>What will you need to be successful?
</b></p><p></p><p><b>Minimum Requirements
</b></p><p><b>Education
</b></p>Bachelor&rsquo;s degree in Chemistry, Biology, Pharmaceutical Sciences, or related field is required.<br>
<ul><li>
<br>
</li></ul><p><b>Experience
</b></p><ul><li>3&ndash;7+ years in a GMP pharmaceutical laboratory environment.
</li><li>Hands-on experience with LIMS (e.g., LabWare, STARLIMS, Thermo SampleManager) is required.
</li><li>Experience with analytical instrumentation and associated software (e.g., CDS systems like Empower or OpenLab) is required.
</li><li>Experience supporting regulatory inspections is preferred.
</li></ul><p></p><p><b>Knowledge:
</b></p><ul><li>Strong understanding of 21 CFR Part 11, Data Integrity (ALCOA+), CSV (Computer System Validation), Experience with system validation (IQ/OQ/PQ), knowledge of audit trails, user access controls, and electronic records
</li><li>Familiarity with both networked and standalone instrument data management.
</li>Knowledge of SQL or data querying tools is a plus.<br>
<li>
<br>
</li></ul><p><b>Competencies
</b></p><ul><li>Strong problem-solving and troubleshooting abilities
</li><li>Excellent communication and cross-functional collaborationSystem
</li>High attention to detail and organizational skills Documentation Quality<br>
<li>
</li></ul><p><br>
<b>You Unlimited.
</b></p><p>We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
</p><ul><li><b>Inclusion and Belonging - </b>Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website (https://www.smith-nephew.com/).
</li><li><b>Your Future: </b>401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement
</li><li><b>Work/Life Balance: </b>Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day
</li><li><b>Your Wellbeing: </b>Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program
</li><li><b>Flexibility: </b>Hybrid Work Model (For most professional roles)
</li><li><b>Training: </b>Hands-On, Team-Customized, Mentorship
</li><li><b>Extra Perks: </b>Discounts on fitness clubs, travel and more!
</li></ul><p></p><p>Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
</p><p></p><div><p>Stay connected by joining our Talent Community .
</p><p></p><p>We're more than just a company - we're a community! Follow us on L inkedIn to see how we support and empower our employees and patients every day.
</p></div><p></p><div><div><p>Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into <b>You </b><b>. </b><b>Unlimited </b><b>. </b>, life, culture, and benefits at S+N.
</p></div><p></p><div><p>Explore our website and learn more about our mission, our team, and the opportunities we offer.</p></div></div></div><p></p>

Site Quality Systems Coordinator (Fort Worth, TX)

Hikma Pharmaceuticals

<div>
 Job description:
 <br/>
 <br/>
 <p>
  <strong>
   Description:
  </strong>
 </p>
 <p>
  <strong>
   &nbsp;
  </strong>
  We are looking for a talented&nbsp;
  <strong>
   Quality Control Analyst
  </strong>
  &nbsp;to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritized and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.
 </p>
 <p>
  &nbsp;
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Performs wet and instrumental analysis (HPLC, UV, GC, FTIR) of raw materials, in-process and finished products.
  </li>
 </ul>
 <ul>
  <li>
   Performs physical testing and chemical analysis of Pharmaceutical Packaging Material.
  </li>
  <li>
   Troubleshoots and resolves operations issues.
  </li>
  <li>
   Prepares and standardizes volumetric solutions, reagents and indicators Internal calibration of instruments according to work instructions.
  </li>
  <li>
   Validation of the assay methods of finished products.
  </li>
  <li>
   Participates in validation of facilities and manufacturing processes
  </li>
  <li>
   <strong>
    Job Location: Badr City - Cairo
   </strong>
  </li>
  <li>
   <strong>
    Employment Type:&nbsp;Contingent worker / Temp-to-Hire
   </strong>
  </li>
 </ul>
 <p>
  &nbsp;
  <strong>
   Qualifications:
  </strong>
 </p>
 <p>
  We are looking for candidates whose experience and skills align closely with the qualifications outlined below:
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in pharmacy or science with grade Very good.
  </li>
 </ul>
 <ul>
  <li>
   Fresh Graduate
  </li>
  <li>
   Fluency in English, both written and verbal
  </li>
  <li>
   Excellent computer skills and data analysis knowledge.
  </li>
  <li>
   Good documentation practices and technical writing
  </li>
 </ul>
</div>


Quality Control Analyst (Contingent worker / Temp-to-Hire)

Hikma

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Description:</b></p>
<p><b>
 </b>We are looking for a talented <b>Quality Control Analyst</b> to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritized and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</p>
<p>
 <b>Key Responsibilities:</b></p>
<ul>
<li>Performs wet and instrumental analysis (HPLC, UV, GC, FTIR) of raw materials, in-process and finished products.</li>
</ul><ul><li>Performs physical testing and chemical analysis of Pharmaceutical Packaging Material.</li>
<li>Troubleshoots and resolves operations issues.</li>
<li>Prepares and standardizes volumetric solutions, reagents and indicators Internal calibration of instruments according to work instructions.</li>
<li>Validation of the assay methods of finished products.</li>
<li>Participates in validation of facilities and manufacturing processes</li>
<li><b>Job Location: Badr City - Cairo</b></li>
<li><b>Employment Type: Contingent worker / Temp-to-Hire</b></li>
</ul>
<p> <b>Qualifications:</b></p>
<p>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</p>
<ul>
<li>Bachelor&rsquo;s degree in pharmacy or science with grade Very good.</li>
</ul><ul><li>Fresh Graduate</li>
<li>Fluency in English, both written and verbal</li>
<li>Excellent computer skills and data analysis knowledge.</li>
<li>Good documentation practices and technical writing</li>
</ul></div></div></div></div><div><div><div><div>Location:
Giza, EG</div></div></div></div></div></div></div><p></p>

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