research laboratory specialist

Sidra

<div><p><b>JOB SUMMARY<br>
</b></p><p></p><p>The Research Specialist I &ndash; Flow Cytometry Core Lab Tech at Sidra Medicine performs all the activities required in the position, and should be eligible or/and hold QCHP license. The incumbent executes under senior supervision laboratory tests necessary for research and clinical activities in the Core. Performs routine and moderately complex scientific laboratory technical work, selecting and applying laboratory procedures and techniques to assignments with clear, specific objectives. Assignments may require investigation of a number of variables and complex features. S/he works with general supervision. The incumbent is required to exercise judgment in making technical decisions related to delegated tasks and escalating complex issues. The incumbent supports the team in Clean Room activities and in Good Manufacturing Practice operations for cell therapy and gene therapy products for clinical and research based on Good Laboratory Practice, in the development and validation of simple and moderately complex laboratory procedures for the manufacturing of cell and gene therapy products. The incumbent observes and maintains a high standard of laboratory health, safety procedures; works based to the institutional, departmental and Flow Cytometry Core&rsquo;s regulations/values/policies/procedures/instructions/protocols/designs and current professional standards and guidelines. Follows MoPH, professional, certification and accreditation bodies requirements.<br>
</p><p></p><p><b>KEY ROLE ACCOUNTABILITIES
</b></p><p><b>Clinical activities performed:
</b></p><ul><li>Peripheral blood and other tissues processing.
</li><li>Clinical assays.
</li><li>All necessary clinical grade testing for product quality control and quality control equipment used for the purpose.
</li><li><p>Clinical activity varies based on projects, the time spent in clinical related tasks is 40% or more.<br>
</p></li></ul><p></p><p><b>Research activities performed </b><i>:
</i></p><ul><li>Basic and complex research activities in addition to the above clinical activities.
</li>Other basic and complex research activities related to biomedical science.<br>
<li>
</li></ul><p></p><p><i>Note: the incumbent does not interact directly with the patient.
</i></p><p>In line with the activities briefly described above, s/he will be also accountable for the following:
</p><ul><li>Contributes to the delivery of departmental goals, through personal effort in own work area.
</li><li>Actively participates and responsibly performs the technical activities, pre-analytical, and analytical work in the labs: R&amp;D, production and testing. Under senior supervision designs, validates new methods and testing and clinical assays.
</li><li>Defines long term, medium and short term priorities and in daily work plan in accordance with the line manager reporting also outcomes, success and issues.
</li><li>Initiates, performs, reviews and troubleshoots quality control of reagents and test systems.
</li><li>Ensures and validates pre-existing assays for laboratory.
</li><li>Ensures assays comply with current regulations in Qatar or/and with international ones.
</li><li>Liaises with manager and ARC colleagues on production and outcomes, on appropriateness of tests and results.
</li><li>Maintains, monitors, records and reports tests results.
</li><li>Collaboratively maintains laboratory information system (e.g. LIMS/ELN).
</li><li>Maintains laboratory supplies inventory by checking stock to determine inventory level in assigned areas; anticipating needed supplies; and if requested placing and expediting orders for supplies; verifying receipt of supplies.
</li><li>Ensures that any difficulties or problems affecting service provision are reported promptly to colleagues, senior staff and line manager.
</li><li>Understands and adheres to process improvement principles and processes, for example, following standard work and maintaining a robust inventory concept in work area realizing that all processes are driven by the needs of the customer.
</li><li>Participates actively in Core meetings and if required in Quality Systems development/ improvement.
</li><li>Proposes changes to SOPs, relating to duties/ accountabilities, and under the instruction from the line manager drafts new versions or produces new operating procedures as addressed.
</li><li>Responsible for maintaining competencies required in Flow Cytometry Core and performs in accordance with laboratory and Sidra policy to provide accurate lab activities.
</li><li>Operates and maintains complex and basic instruments and equipment used in the laboratory, and properly sets up, calibrates, maintains, operates and shuts down such instruments (as needed);
</li><li>Maintains competence in Laboratory Information System that is crucial to the quality operations of the laboratory and patient care.
</li><li>Operates and performs daily preventive maintenance of equipment according to written procedures and documents; reports equipment malfunctions and requests service as necessary.
</li><li>Participates in research and development as directed.
</li><li>Maintains competence in Laboratory Information System and in Laboratory Management System that is crucial to the quality operations of the laboratory and patient care.
</li><li>Actively participates in Quality Improvement Programs essential to ensure that laboratory testing is accurate, timely and meets customer needs.
</li><li>Maintains policies and procedures for adherence to the current professional standards.
</li><li>Works with quality representative to develop systems to deliver quality services which satisfy Quality standards requirements.
</li><li>Accomplishes all the organizational mandatory requirements (i.e. Learning and Development requirements, use of PPE, etc.)
</li><li>Adheres to Sidra&rsquo;s standards as they appear in the Code of Conduct and Conflict of Interest policies.
</li><li>Adheres to and promotes Sidra&rsquo;s Values.
</li></ul><p><i>In view of the evolving needs and opportunities within Sidra, this position may be required to perform other duties as assigned and reporting relationships may vary.<br>
</i></p><p></p><p><b>QUALIFICATIONS, EXPERIENCE AND SKILLS &ndash; SELECTION CRITERIA<br>
</b></p><p></p><p><b>Education
</b></p><p>Bachelor&rsquo;s Degree in Biomedical Sciences/ Clinical Laboratories or other relevant program.
</p><p><b>Experience
</b></p><p>3+ years&rsquo; experience in a research laboratory environment including:
</p><ul><li>Experience in cell cultures
</li><li>Experience in flow cytometry procedures
</li><li>Experience in molecular biology procedures
</li>Experience in proteins detection.<br>
<li>
</li></ul><p></p><p><b>Certification and Licensure
</b></p><p><b>Essential
</b></p><p>Eligibility for Licensure in the State of Qatar.
</p><p><b>Preferred
</b></p><p>License recognized in Qatar, EU, US or Canada.<br>
</p><p></p><p><b>Job Specific Skills and Abilities.
</b></p><p><b>Essential
</b></p><ul><li>Cell culture of primary blood cells, as lymphocytes
</li><li>Molecular biology procedures, as nucleic acids extraction, PCR, RT-PCR
</li><li>Flow cytometry stainings and basic data analysis
</li><li>Protein detection / functional assays
</li><li>Demonstrated excellent communication and interpersonal skills.
</li><li>Openness to teach and interact with other staff members.
</li><li>Proficiency with Microsoft Office suite.
</li><li>Fluency in written and spoken English
</li></ul><p><b>Preferred
</b></p><ul><li>Experience in bacterial cloning.
</li><li>Flow cytometry acquisition of samples.</li></ul></div>
<br><div><div>About US</div>
<div><div>Sidra Medicine a healthy population is essential to a strong, prosperous society, and throughout 2020, Sidra continued to provide uninterrupted comprehensive specialist healthcare services for children and young people; and exceptional maternity, gynecology, and reproductive medical services for women, previously unavailable in Qatar and the region.&rdquo; &ndash; H.H Sheikha Moza bint Nasser, Chairperson of Qatar Foundation
</div><div>Sidra Medicine represents the vision of Her Highness Sheikha Moza bint Nasser who serves as its Chairperson. This high-tech facility is home to world-class patient care, scientific expertise, and educational resources.</div></div></div><div></div>

Research Specialist I - Research Specialist I – Flow Cytometry Core Lab Tech.

The General Hospital Corporation

<div>Site: The General Hospital Corporation<p></p><p><br>
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.</p><br>
<p></p>
The Research Specialist in the Therapeutics Program team in the Center for
<br>
Computational and Integrative Biology is a motivated and detail-oriented member who drives and conducts multiple research projects aimed at developing candidate therapeutic agents, principally small molecules with some biologics.
<br>
The projects involve characterizing and performing preclinical evaluations of small molecules, primarily aimed at understanding in vitro potency against target and off-target receptors. Work with biologics involves protein engineering, pharmacokinetics and pharmacodynamics.
<br>
<br>
The incumbent will work collaboratively and independently, reporting to the principal investigator and must work effectively within a fast-paced team environment and build and maintain positive relationships and interactions with other researchers.<p></p><p><b><br>
Job Summary</b></p>
Functioning independently and under the direction of the principal investigator, performs high-level, complex scientific research experiments. On a regular basis, contributes to scientific literature, reports, journals, and presentations, and investigates, creates, and develops new methods and technologies for research advancement.<br>
<br>
Does this position require Patient Care? No<br>
<br>
Essential Functions<br>
<ul><li>Investigates, creates, and develops new methods and technologies for research advancement.
</li></ul><br>
<ul><li>Contributes to scientific literature, reports, journals and presentations.
</li></ul><br>
<ul><li>Develops proposals and study plans, and coordinates the institutional and external reviews of these proposals.
</li></ul><br>
<ul><li>Responsible for supervising routine reports of laboratory studies, particularly as stipulated in material transfer agreements or corporate-sponsored research agreements, to be distributed to industry scientific counterparts and academic collaborators.
</li></ul><br>
<ul><li>Reports on the progress of work at weekly laboratory seminars. Semi-autonomously writes up experimental work for grant applications, book chapters, and journal publications.
</li></ul><br>
<ul><li>Responsible for preparing summaries of laboratory studies for meeting presentations and publications.
</li></ul><br>
<ul><li>Calculates, transcribes, analyzes, and prepares figures of data using advanced statistical techniques.
</li></ul><br>
<ul><li>Semi-autonomously identifies, interprets, and applies findings and methods from scientific literature relevant to projects.</li></ul><p></p><div><div><div><div><div><div><div><p><b><br>
Qualifications</b></p></div></div></div></div></div></div></div><div>
Education<br>
Master's Degree Related Field of Study required<br>
<br>
Can this role accept experience in lieu of a degree? No<br>
<br>
Licenses and Credentials<br>
<br>
Experience<br>
Experience in an academic or laboratory research setting 3-5 years required<br>
<br>
Knowledge, Skills and Abilities<br>
<ul><li>Must be a problem solver willing to take the initiative and prioritize tasks, thereby ensuring the smooth and efficient conduct of several projects simultaneously.</li><li>A high degree of computer literacy in order to use various spreadsheet, database, accounting and word processing programs to assist in administrative, grant proposal preparation, and research reporting activities.</li><li>Excellent organizational skills in order to formulate, implement, and monitor a number of interrelated tasks.</li><li>Ability to exercise discretion and good judgment in handling of sensitive and confidential information.</li><li>Ability to work under deadline pressure and prioritize work from several sources.</li><li>Excellent interpersonal skills for internal and external communications.</li></ul></div><p></p><div><div><div><div><div><div><div><p><b><br>
Additional Job Details (if applicable)</b></p></div></div></div></div></div></div></div><p></p><div><div><div><div><div><div><div><p><b><br>
Remote Type</b></p></div></div></div></div></div></div></div>
Onsite<p></p><div><div><div><div><div><div><div><p><b><br>
Work Location</b></p></div></div></div></div></div></div></div>
185 Cambridge Street<p></p><div><div><div><div><div><div><div><p><b><br>
Scheduled Weekly Hours</b></p></div></div></div></div></div></div></div>
40<p></p><div><div><div><div><div><div><div><p><b><br>
Employee Type</b></p></div></div></div></div></div></div></div>
Regular<p></p><div><div><div><div><div><div><div><p><b><br>
Work Shift</b></p></div></div></div></div></div></div></div>
Day (United States of America)<p></p><p><b><br>
Pay Range</b></p>
$63,252.80 - $102,596.00/Annual<p></p><p><b><br>
Grade</b></p>
7<br>
<p></p>
At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.<p></p><div><div><div><div><div><div><div><p><b><br>
EEO Statement:</b></p></div></div></div></div></div></div></div>
1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran&rsquo;s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.<p></p><h2 class="jobSectionHeader"><b><br>
Mass General Brigham Competency Framework</b></h2><div><div><p>
At Mass General Brigham, our competency framework defines what effective leadership &ldquo;looks like&rdquo; by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.</p></div></div></div>

Research Specialist

Nawah Scientific

<div>
 <strong>
  Job Brief
  <br/>
  <br/>
 </strong>
 We're seeking for
 <strong>
  R&amp;D Methodology Specialist
 </strong>
 who will be responsible for sample testing, data recording and performing routine checks to ensure the quality and integrity of data.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  Laboratory Performance
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Participate in all lab performance activities and, whenever applicable, compliance of lab activities with ISO/IEC 17025/GLP requirements.
  </li>
  <li>
   Implementing laboratory procedures effectively to control lab activities.
  </li>
  <li>
   Execute the approved internal quality control program to ensure proper control of technical processes.
  </li>
  <li>
   Execute equipment operation protocols, intermediate check procedures, and maintenance plan.Record results daily and report immediately any malfunction or abnormal results.
  </li>
  <li>
   Implement environmental monitoring program to affirm compliance with laboratory safety protocols and international regulations and maintain clean laboratory conditions.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  External Customers
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provides, when required, clarifications and answers to customer inquiries to attain customer satisfaction.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  External Suppliers and Services
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Report on the unavailability of any lab supplies and write purchasing requests for missed products including supplies specifications.
  </li>
  <li>
   Analyze Proficiency Test (PT) samples according to provider instructions and document sample results.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Improvement
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provide suggestions for laboratory operation improvement.
  </li>
  <li>
   Stay up to date with Scientific updates/ regulatory requirements.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Sample Testing Activities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Analyze laboratory samples according to laboratory procedures, customer test request, and Lab head instructions to produce reliable results.
  </li>
  <li>
   Read and record samples results in appropriate technical forms.
  </li>
  <li>
   Execute method verification/validation protocols.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Must-have
  <br/>
  <br/>
 </strong>
 <strong>
  Job requirements:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in any of the following: Biotechnology, Science, Pharmacy or relevant scientific speciality.
  </li>
  <li>
   At least 4 years of Methodology experience in Pharmaceutical company or QC laboratories.
  </li>
  <li>
   Good command of both written and spoken in English.
  </li>
  <li>
   Strong attention to detail and accuracy in analytical work.
  </li>
  <li>
   Adhere to ICH, WHO, USP, and cGMP requirements in daily work.
  </li>
  <li>
   Effective communication and teamwork skills.
  </li>
  <li>
   Good problem-solving and troubleshooting skills.
  </li>
  <li>
   Ability to handle multiple projects and meet deadlines.
  </li>
  <li>
   Detail-oriented with strong documentation practices.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Nice To Have
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience in HPLC/GC operations.
  </li>
  <li>
   Familiarity with chromatographic and spectroscopic techniques.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Offer
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Work with a supportive and energetic team in a dynamic research environment that fosters collaboration and innovation.
  </li>
  <li>
   Enjoy annual salary increases and additional benefits based on your performance and contribution.
  </li>
  <li>
   Receive an annual family bonus as a token of appreciation for your loyalty and commitment to the company.
  </li>
  <li>
   Earn a great quarterly incentive for achieving your goals and exceeding expectations.
  </li>
  <li>
   Benefit from comprehensive social and medical insurance coverage for you.
  </li>
  <li>
   Participate in an annual cycle meeting to review your progress and plan your future development.
  </li>
 </ul>
</div>


Research Specialist - R&D Methodology Lab

Anotech

<div>
 <p>
  <strong>
   Job Purpose:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Responsible for overseeing and managing all aspects of preparing all necessary laboratory equipment, Manuals and Operating Procedures, and ensuring the laboratory is available and fully operational for plant Start-up: personnel, equipment and adequate supply of chemicals and consumables. Reports directly to the Commissioning &amp; Start-up Methods Lead. The Laboratory Specialist shall develop and implement the permanent Laboratory Information Management System. They shall also ensure mentorship and training of the routine operation laboratory personne
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   l
  </strong>
 </p>
 <p>
  <strong>
   Job Responsibilitie
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  s:
 </p>
 <p>
  Commissioning and Start-up preparat
 </p>
 <ul>
  <li>
   ionEnsure design meets all the operational and HSE requireme
  </li>
  <li>
   ntsOrganize laboratory equipment reception and equipment storage. Follow-up on missing and downgraded equipment with Contractor and / or Vendor commissioning procedures, test plans, and system handover documentat
  </li>
  <li>
   ionActively participate in the laboratory pre-commissioning and commissioning. Record punch items and follow-up on punch list clearance with the objective of ensuring the laboratory is available to support plant start
  </li>
  <li>
   -upIdentify potentially required specific analyses which will not be possible on site, and elaborate means and procedures to perform those analyses (sub-contracting to third party laborator
  </li>
  <li>
   iesReview and adjust (with equipment Vendor), calibration of all the laboratory equipm
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  ent
 </p>
 <p>
  Commissioning and Start-up execu
 </p>
 <ul>
  <li>
   tionSupervise Commissioning of all the laboratory equip
  </li>
  <li>
   mentEnsures Laboratory is available and fully operational for plant start-up: personnel, equipment and adequate supplies of chemicals and consuma
  </li>
  <li>
   blesImplement laboratory waste handling in line with site waste management philosophy validated by the HSE depart
  </li>
  <li>
   mentDuring early operation, supervising all laboratory work methods, test analyses, data interpretation, analysis of products quality, refrigerant and effluent w
  </li>
  <li>
   asteDuring early operation, direct and co-ordinate all sampling and testing activities of laboratory, including determining methods of analysis, problem solving and troubleshooting upcoming is
  </li>
  <li>
   suesHandover an established and fully operational laboratory facility to the routing laboratory opera
  </li>
  <li>
   tionAssistance for closed loop start-up and monitoring of the fluid quality in
  </li>
  <li>
   sideParticipate to commissioning activities: Network cleanliness monitoring during flushing operation (closed loops, chemical injection lines); lubricant or hydraulic fluids cleanliness anal
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   ysis
  </strong>
 </p>
 <p>
  <strong>
   Qualifications And Experi
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   ence:
  </li>
  <li>
   Master&rsquo;s Degree in Chemical or Petroleum Engin
  </li>
  <li>
   eering15+ years&rsquo; experience in the Oil &amp; Gas industry with a full understanding of laboratory activities and procedures, expertise in laboratory discipline. Experience in projects with large onshore plants and LNG plants is
  </li>
  <li>
   a plus5+ years in an LNG plant laboratory in a supervisory role in a multi-cultural envir
  </li>
  <li>
   onmentTechnical Competencies: Production operations, Laboratory activities, Process operations, Regulations, Certifications, Commissioning and start-up of O&amp;G facilities, Safety of personnel and installations, Maintenance / Inspection, SIMOPS, Operational contract management, Construction, instal
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  lation
 </p>
</div>


CSU - Laboratory Specialist

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>Laboratory Validation Specialist
</b></p><p>The Laboratory Validation Specialist is responsible for validations supporting the Quality Control laboratories. Primarily the role is responsible for the validation, verification, and/or qualification of test methods used in the laboratories, analytical instruments, and computerized systems used in a GMP-regulated pharmaceutical environment. This role ensures that test methods, equipment, and processes are compliant with regulatory requirements, including method validation standards, data integrity standards and computer system validation (CSV), while supporting reliable and accurate laboratory operations. This role also serves as a Quality Control representative for other site validations that requiring Quality Control support.
</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>Validation
</b></p><ul><li>Lead and execute qualification activities for laboratory instruments (e.g., dissolution, spectroscopy systems).
</li><li>Develop and execute validation protocols for methods.
</li><li>Manage execution of IQ/OQ/PQ protocols for new and existing equipment.
</li>Represent QC in the development, review, and execution of validation supporting other site projects and processes.<br>
<li>
<br>
</li></ul><p><b>Data Integrity &amp; Compliance
</b></p><ul><li>Ensure compliance with ALCOA+ data integrity principles.
</li><li>Review audit trails, electronic records, and system access controls.
</li><li>Support and lead data integrity assessments and gap remediation plans.
</li>Participate in regulatory inspections and audits.<br>
<li>
<br>
</li></ul><p><b>Documentation &amp; Quality Systems
</b></p><ul><li>Author, review, and approve validation protocols, reports, SOPs, and work instructions.
</li><li>Support deviations, investigations, CAPAs, and change control related to validation activities.
</li>Maintain validation lifecycle documentation in accordance with GMP requirements.<br>
<li>
<br>
</li></ul><p><b>Risk Management &amp; Lifecycle Approach
</b></p><ul><li>Apply risk-based validation approaches per GAMP 5 guidelines.
</li><li>Perform impact and risk assessments for changes to validated systems.
</li>Ensure continued process verification and system performance monitoring.<br>
<li>
<br>
</li></ul><p><b>Cross-Functional Collaboration
</b></p><ul><li>Work closely with R&amp;D, QA, QC, Manufacturing, IT, Metrology, and Engineering teams.
</li><li>Interface with vendors for system implementation, validation support, and troubleshooting.
</li>Provide technical guidance on validation requirements and best practices.<br>
<li>
<br>
</li></ul><p><b>Training &amp; Continuous Improvement
</b></p><ul><li>Train laboratory personnel on validated systems and compliance expectations.
</li><li>Identify opportunities for process improvements and efficiency in validation practices.
</li><li>Support digitalization and automation initiatives in the lab.
</li></ul><p></p><p><b>What will you need to be successful?
</b></p><p><b>Education:
</b></p>Bachelor&rsquo;s degree in Chemistry, Biology, Engineering, Computer Science, or related scientific field.<br>
<ul><li>
<br>
</li></ul><p><b>Experience:
</b></p><ul><li>2&ndash;6+ years in pharmaceutical, biotech, or regulated laboratory environments.
</li><li>Experience with laboratory test method validation, equipment qualification and/or CSV.
</li><li>Familiarity with LIMS, CDS (e.g., Empower, OpenLab), or other lab systems.
</li><li>Experience supporting regulatory inspections is preferred.
</li>Experience with automation or system integration (LIMS/ERP) is a plus.<br>
<li>
<br>
</li></ul><p><b>Knowledge:
</b></p><ul><li>GMP (Good Manufacturing Practices)
</li><li>Test Method Validation
</li><li>Computer System Validation (CSV)
</li><li>21 CFR Part 11 / EU Annex 11
</li><li>GAMP 5 guidelines
</li><li>Data Integrity (ALCOA+)
</li><li>Experience with validation lifecycle documentation (URS, IQ/OQ/PQ)
</li><li>Understanding of audit trails, electronic signatures, and system security
</li><li>Knowledge of risk management tools (e.g., FMEA) is a plus.
</li></ul><p></p><p><b>Competences:
</b></p><ul><li>Strong analytical and problem-solving skills
</li><li>Attention to detail and documentation accuracy
</li>Effective communication and teamwork across departments<br>
<li>
<br>
</li></ul><p><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>

Laboratory Validation Specialist (Fort Worth, TX)

Diageo

<div><p><b>Job Description :</b></p><div><div><div><p><b>
About us</b></p><p></p><p>
With over 200 brands sold in nearly 180 countries, we&rsquo;re the world&rsquo;s leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you&rsquo;ll test new ideas, learn and grow, and unlock a brighter, more exciting future.</p><p></p><p>
Join us to create a career worth celebrating.</p><p></p><p><b>
About the Function</b></p><p>
Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo&rsquo;s 30,000+ people work in Supply Chain and Manufacturing. It&rsquo;s an intricate and sophisticated operation that&rsquo;s the product of logistical, manufacturing, and technical collaborations.
</p><p></p><p>Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We&rsquo;re committed to realising our &lsquo;Society 2030: Spirit of Progress&rsquo; goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we&rsquo;ll help you to thrive in our inclusive culture.</p><p></p><p><b>
About the role</b></p><p>
We are looking for <b>Laboratory Specialist </b>to join our team at our <b>Nevsehir Factory</b>. The ideal candidate will ensure the creation of warehouses for quality control, reporting, and records of raw materials, packaging materials, auxiliary features, semi-finished products, and finished products in accordance with company rules, legal requirements, local and global standards and quality plans. Maintaining the control and continuity of the Quality Food Safety management system in the factory where the company works.</p><p></p><p><b>
Role Responsibilities</b></p><ul><li><p>
Perform analyses of all types of materials and substances, such as raw materials, semi-finished products, finished products, etc., according to experimental instructions and technical specifications.</p></li><li><p>
Inform the supervisor and initiate corrective actions when nonconformities are detected in the analysis results of samples analyzed in the laboratory, and follow up on the process.</p></li><li><p>
Check the compliance of all parameters affecting product quality.</p></li><li><p>
Handle customer complaints, analyze and control non-compliant products, participate in root cause analysis studies, and conduct product, defect, and statistical studies.</p></li><li><p>
Perform statistical analysis and error analysis related to the analyses and controls conducted.</p></li><li><p>
Participate in necessary activities for establishing the HACCP Food Safety System in the factory and perform required checks to ensure the continuity of the system.</p></li><li><p>
Conduct periodic GMP field inspections (e.g., GMP audits, FSSC 22000 field audits), initiate corrective actions for identified nonconformities, and follow up on the process.</p></li><li><p>
Participate in projects related to quality, food safety, and other topics.</p></li></ul><p></p><p><b>
Experience / skills required</b></p><ul><li><p>
Associate degree (2-year) in Chemistry, Food Technology, Laboratory, or a related field</p></li><li><p>
Preferably 0&ndash;3 years of experience in laboratory analysis or quality control</p></li><li><p>
Basic knowledge of laboratory equipment and analytical methods</p></li><li><p>
Familiarity with quality and food safety systems such as HACCP and GMP is an asset</p></li><li><p>
Experience in handling non-conforming products and supporting corrective actions is a plus</p></li><li><p>
Basic understanding of data recording, reporting, and simple statistical analysis</p></li><li><p>
Attention to detail and strong sense of responsibility in following procedures and instructions</p></li><li><p>
Ability to work in a structured environment in compliance with technical specifications</p></li><li><p>
Good communication skills and ability to work collaboratively with cross-functional teams</p></li><li><p>
Open to learning, proactive, and disciplined working approach</p></li><li><p>
Basic level of English is preferred</p></li></ul><p><b><br>
Diversity statement</b></p><p></p><p>
Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.</p><p></p><p>
We embrace diversity in the broadest possible sense. This means that you&rsquo;ll be welcomed and celebrated for who you are just by being you. You&rsquo;ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.</p><p></p><p>
Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.</p><p></p><p>
Feel inspired? Then this may be the opportunity for you.</p></div></div></div><p></p><p><b>
Worker Type :</b></p>
Regular<p></p><p><b>
Primary Location:</b></p>
Nevsehir Plant<p></p><p><b>
Additional Locations :</b></p><p></p><p><b>
Job Posting Start Date :
</b></p>2026-03-26</div>

Laboratory Specialist

<div><p><b>Job Description :</b></p><p><b>
Job Description :</b></p><div><div><div><p><b>
About us</b></p><p></p><p>
With over 200 brands sold in nearly 180 countries, we&rsquo;re the world&rsquo;s leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you&rsquo;ll test new ideas, learn and grow, and unlock a brighter, more exciting future.</p><p></p><p>
Join us to create a career worth celebrating.</p><p></p><p><b>
About the Function</b></p><p>
Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo&rsquo;s 30,000+ people work in Supply Chain and Manufacturing. It&rsquo;s an intricate and sophisticated operation that&rsquo;s the product of logistical, manufacturing, and technical collaborations.
</p><p></p><p>Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We&rsquo;re committed to realising our &lsquo;Society 2030: Spirit of Progress&rsquo; goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we&rsquo;ll help you to thrive in our inclusive culture.</p><p></p><p><b>
About the role</b></p><p>
We are looking for <b>Laboratory Specialist </b>to join our team at our <b>Alasehir Factory</b>. The ideal candidate will ensure the creation of warehouses for quality control, reporting, and records of raw materials, packaging materials, auxiliary features, semi-finished products, and finished products in accordance with company rules, legal requirements, local and global standards and quality plans. Maintaining the control and continuity of the Quality Food Safety management system in the factory where the company works.</p><p></p><p><b>
Role Responsibilities</b></p><ul><li><p>
Perform analyses of all types of materials and substances, such as raw materials, semi-finished products, finished products, etc., according to experimental instructions and technical specifications.</p></li><li><p>
Inform the supervisor and initiate corrective actions when nonconformities are detected in the analysis results of samples analyzed in the laboratory, and follow up on the process.</p></li><li><p>
Check the compliance of all parameters affecting product quality.</p></li><li><p>
Handle customer complaints, analyze and control non-compliant products, participate in root cause analysis studies, and conduct product, defect, and statistical studies.</p></li><li><p>
Perform statistical analysis and error analysis related to the analyses and controls conducted.</p></li><li><p>
Participate in necessary activities for establishing the HACCP Food Safety System in the factory and perform required checks to ensure the continuity of the system.</p></li><li><p>
Conduct periodic GMP field inspections (e.g., GMP audits, FSSC 22000 field audits), initiate corrective actions for identified nonconformities, and follow up on the process.</p></li><li><p>
Participate in projects related to quality, food safety, and other topics.</p></li></ul><p></p><p><b>
Experience / skills required</b></p><ul><li><p>
Associate degree (2-year) in Chemistry, Food Technology, Laboratory, or a related field</p></li><li><p>
Preferably 0&ndash;3 years of experience in laboratory analysis or quality control</p></li><li><p>
Basic knowledge of laboratory equipment and analytical methods</p></li><li><p>
Familiarity with quality and food safety systems such as HACCP and GMP is an asset</p></li><li><p>
Experience in handling non-conforming products and supporting corrective actions is a plus</p></li><li><p>
Basic understanding of data recording, reporting, and simple statistical analysis</p></li><li><p>
Attention to detail and strong sense of responsibility in following procedures and instructions</p></li><li><p>
Ability to work in a structured environment in compliance with technical specifications</p></li><li><p>
Good communication skills and ability to work collaboratively with cross-functional teams</p></li><li><p>
Open to learning, proactive, and disciplined working approach</p></li><li><p>
Basic level of English is preferred</p></li></ul><p><b><br>
Diversity statement</b></p><p></p><p>
Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.</p><p></p><p>
We embrace diversity in the broadest possible sense. This means that you&rsquo;ll be welcomed and celebrated for who you are just by being you. You&rsquo;ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.</p><p></p><p>
Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.</p><p></p><p>
Feel inspired? Then this may be the opportunity for you.</p></div></div></div><p></p><p><b>
Worker Type :</b></p>
Regular<p></p><p><b>
Primary Location:</b></p>
Alasehir Plant<p></p><p><b>
Additional Locations :</b></p><p></p><p><b>
Job Posting Start Date :
</b></p>2026-04-10</div>

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