academic writer & scientific quality assurance specialist Jobs in Istanbul

academic writer & scientific quality assurance specialist

administrative affairs specialist Jobs in Istanbul

administrative affairs specialist

content specialist

customer services and quality assurance lead Jobs in Istanbul

customer services and quality assurance lead

kalite ve veri analitiği yönetici yardımcısı / yetkilisi Jobs in Istanbul

kalite ve veri analitiği yönetici yardımcısı / yetkilisi

academic writer scientific quality assurance specialist

Blueclip

<div>
 <p>
  As Blueclip, we started our journey to bring the most creative minds and the know-how together to deliver great works.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About Our Search
  </strong>
 </p>
 <p>
  We are currently looking for an
  <strong>
   Academic Writer &amp; Scientific Quality Assurance Specialist
  </strong>
  to join our client who is a biotech company specializing in bioinformatics solutions for rare diseases and cancer, leveraging Next Generation Sequencing (NGS) data.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Their cloud-based software, SEQ Platform, is currently used in more than 25 countries and has been adopted by over 450 hospitals and laboratories. To date, it has played a critical role in diagnosing rare diseases for over 300,000 patients and is a leading biotechnology company with a vision of developing products to provide personalized treatment recommendations for cancer patients, helping them live longer and healthier lives. diseases and the development of personalized treatment strategies for cancer.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Role Overview
  </strong>
 </p>
 <p>
  As an
  <strong>
   Academic Writer &amp; Scientific Quality Assurance Specialist
  </strong>
  , you will be responsible for developing their scientific communications and ensuring scientific accuracy across publications, conference materials, and product documentation.
 </p>
 <p>
  <br/>
 </p>
 <p>
  This role is ideal for a
  <strong>
   PhD graduate or post-doctoral researcher
  </strong>
  looking to transition from academia to a dynamic biotech environment. You will work closely with internal teams, collaborators, and global scientific partners to uphold the company&rsquo;s academic excellence.
 </p>
 <p>
  <br/>
 </p>
 <p>
  The position requires a strong scientific foundation, excellent writing skills, and the ability to communicate complex ideas clearly and effectively. Occasional international travel for conferences and collaboration meetings will be expected.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  ● Develop and publish high-quality scientific materials, including journal articles, posters, white papers, and conference submissions
 </p>
 <p>
  ● Draft and edit grant proposals and collaboration project documents
 </p>
 <p>
  ● Act as the scientific voice in academic and research environments
 </p>
 <p>
  ● Communicate with journal editors, conference organizers, and collaborators
 </p>
 <p>
  ● Review and validate the scientific accuracy of product-related materials
 </p>
 <p>
  ● Ensure consistency with current literature and methodological rigor in all outputs
 </p>
 <p>
  ● Support benchmarking studies and scientific audits to maintain quality standards
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  ● PhD in
  <strong>
   Genetics, Molecular Biology, Genomic Medicine, Bioinformatics
  </strong>
  , or a related field
 </p>
 <p>
  ● Strong publication record and experience in scientific writing and presentations
 </p>
 <p>
  ● Excellent command of
  <strong>
   academic English
  </strong>
  (written and spoken)
 </p>
 <p>
  ● Highly organized, detail-oriented, and proactive in leading scientific projects
 </p>
 <p>
  ● Ability to collaborate effectively with both
  <strong>
   technical and clinical teams
  </strong>
 </p>
 <p>
  ● Willingness to travel domestically and internationally for conferences and workshops
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What&rsquo;s in It for You?
  </strong>
 </p>
 <p>
  ● Opportunities for
  <strong>
   international exposure
  </strong>
  and collaboration
 </p>
 <p>
  ● Clear growth path toward
  <strong>
   scientific leadership
  </strong>
 </p>
 <p>
  ● Competitive
  <strong>
   salary
  </strong>
  and
  <strong>
   performance-based bonus
  </strong>
  structure
 </p>
 <p>
  ● A mission-driven environment contributing to
  <strong>
   real clinical impact
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Ready to leave a mark? Apply now! 🚀
 </p>
</div>


Academic Writer & Scientific Quality Assurance Specialist

MANN+HUMMEL

<div>
 <strong>
  Role Summary
  <br/>
  <br/>
 </strong>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 The job incumbent is responsible for all product and pricing management activities and supports the growth of the Automotive Aftermarket BU.
 <br/>
 <br/>
 The role will be to be accountable for all the processes within the product and pricing management functions.
 <br/>
 <br/>
 <strong>
  Main Tasks
  <br/>
  <br/>
 </strong>
 <strong>
  Product Management
  <br/>
  <br/>
 </strong>
 Range Management
 <br/>
 <br/>
 <ul>
  <li>
   Responsible for continuously expanding our multibrand product portfolio for all segments (passenger cars, commercial vehicles, off-highway applications) to achieve a defined market and competitive market coverage.
  </li>
  <li>
   Increase range to achieve targeted market coverage, via expansion of globally available range to local range, as well as new part developments
  </li>
  <li>
   Prioritization and assessment of found gaps in the product range according to relevance for the respective vehicle and sales potential
  </li>
  <li>
   Responsible for Life Cycle Management in CDB.
   <br/>
   <br/>
  </li>
 </ul>
 Research
 <br/>
 <br/>
 <ul>
  <li>
   Maintenance of vehicle information, such as equipment information and OE references, and their technical evaluation at component level, including 1st step checking for identical product solutions available within portfolio or defining range gaps.
  </li>
  <li>
   Additionally, define the technical requirements as basis for the product development, considering OE and vehicle information.
  </li>
  <li>
   Creation of market requirements in internal catalogue system and specify the local requirement in terms of demand, cost and specification.
  </li>
  <li>
   Gathering of market, competitor and VIO information via market research
   <br/>
   <br/>
  </li>
 </ul>
 New Product Introduction (NPI)
 <br/>
 <br/>
 <ul>
  <li>
   Initiation of internal process for new part development (workflows), define the requirements and resources to meet target SOP.
  </li>
  <li>
   Responsible for all PM related tasks within the NPI process.
  </li>
  <li>
   Lead/coordinate cross-functional product development process/teams to achieve faster Time2Market.
  </li>
  <li>
   Activate K &amp; N Type + Linkages TR on PARTS.
  </li>
  <li>
   Create bulletins for all region/country related NPI&rsquo;s and share via Salesforce Marketing Cloud.
   <br/>
   <br/>
  </li>
 </ul>
 Sales Support
 <br/>
 <br/>
 <ul>
  <li>
   Support local team (sales, pricing, marketing, CS, ..) and customers in product-related queries, new product information, and catalog data requirements.
  </li>
  <li>
   Support at fairs, exhibitions, and customer events
   <br/>
   <br/>
  </li>
 </ul>
 Quality Management
 <br/>
 <br/>
 <ul>
  <li>
   Manage quality claims via Dealer Portal.
  </li>
  <li>
   Communicate respective locations and create SAP QM tickets to follow up process.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Pricing Management
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Analyze and review current internal cost and pricing structure (intercompany price list, price waterfall, customer buying price, competitor selling price) and other marketing intelligence data to improve prices and develop a multi-branding price orientation for all responsible territories/regions.
  </li>
  <li>
   Align and implement pricing strategy in responsible markets.
  </li>
  <li>
   Checking what is relevant to our market, defining &amp; extending, pricing via monthly SOP reporting.
  </li>
  <li>
   Based on sales input and market data, construct Gross Price List for different segments, e.g., CV Specialist, OHI Specialist, Compressor Specialist, and Tender projects, and prepare customer price lists.
  </li>
  <li>
   Monitor sales and profitability, e.g., GMS, CGMS, discount impacts on sales, lost sales due to uncompetitiveness.
  </li>
  <li>
   Escalate potential cost-related requests to the Product Management Team for cost-down reviews.
  </li>
  <li>
   Consolidate, analyze, and review current triple net prices in the region for price harmonization.
  </li>
  <li>
   Upload price changes in the system &ndash; SAP price maintenance e.g., promotions, special price, tenders
  </li>
  <li>
   Review of special price requests for tender business and track win/lost sales
  </li>
  <li>
   Work with and support sales on discounts and/or net selling price for sales campaigns and promotions.
  </li>
  <li>
   Monthly maintenance of MRA Tool, SAP/PARTS CMC Tool via results of market research.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Your Profile
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Successfully completed academic degree or education with a technical or economic-scientific focus.
  </li>
  <li>
   5+ years of professional experience in product management and/or pricing management
  </li>
  <li>
   Possess detailed knowledge of Microsoft office
  </li>
  <li>
   Fluency in business English (written and spoken)
  </li>
  <li>
   Communication skills and ability to work in team
  </li>
  <li>
   Ability to work under pressure
  </li>
  <li>
   Time management, prioritization skills
  </li>
  <li>
   Co-ordination of quality topics within the group
  </li>
  <li>
   Annual budget planning for NPIs and project wise budget planning + request
  </li>
  <li>
   Experience in coordination of project management activities with Capex requirement
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills
  <br/>
  <br/>
 </strong>
 Product Design
 <br/>
 <br/>
 Market Research
 <br/>
 <br/>
 Product Development
 <br/>
 <br/>
 Product Management
 <br/>
 <br/>
 Marketing Planning
 <br/>
 <br/>
 Merchandising
 <br/>
 <br/>
 Marketing Strategies
 <br/>
 <br/>
 Brand Management
 <br/>
 <br/>
 Literacy
 <br/>
 <br/>
 External Communications
 <br/>
 <br/>
</div>


Senior Product and Pricing Specialist

Herbalife

<div>Overview:
<p><b>
Quality Assurance Specialist &ndash; EMEA</b></p><p></p><p><b><br>
Herbalife Europe Limited, Istanbul 34752, Turkey</b></p><p></p><p><b><br>
About the Team:</b></p><p>
This role sits within a small regional team based in Istanbul, where you will be the sole QA specialist for the Turkish office. At the same time, you will be part of the wider EMEA Quality Department, which operates from regional hubs in Venray, Netherlands, and Krakow, Poland.</p><p></p><p><b><br>
About the role:</b></p><p>
We are looking for a Quality Assurance Specialist with knowledge of the Turkish market. In this role, you will be responsible for ensuring that all products distributed in Turkey meet Herbalife&rsquo;s quality and compliance requirements.</p><p></p><p><b><br>
In this role you will:</b></p><ul><li>
Ensure local production meets Herbalife quality requirements, including providing support, conducting audits, and visiting pilot production sites.</li><li>
Inspect incoming products to verify compliance and develop improvement plans when deviations occur. This includes implementing and performing finished product inspections in local Turkish warehouses.</li><li>
Verify that appropriate transportation and warehouse controls are in place, with particular attention to temperature monitoring.</li><li>
Support the development and launch of new products.</li><li>
Identify, document, and resolve quality concerns and deviations.</li><li>
Conduct audits of contract manufacturers and warehouses.</li><li>
Communicate product quality issues across the organization.</li><li>
Prepare and deliver weekly and monthly quality reports to management.</li><li>
Act as a strong advocate for quality standards within the country.</li><li>
Travel to warehouses as required, with occasional visits to contract manufacturers.</li><li>
Oversee regional quality compliance at all levels, including production at contract manufacturing sites, and address any quality issues that arise.</li></ul><div></div><p><b><br>
Our requirements:</b></p><ul><li>
Minimum of 3 years&rsquo; experience in Quality Assurance</li><li>
Fluent in English both written and speaking.</li><li>
CV also needs to be in English and not Turkish for us to consider (please note all CVs in Turkish will be rejected)</li><li>
Proficient in basic Microsoft applications</li><li>
Experience with Oracle is an advantage</li><li>
Bachelor&rsquo;s degree (or higher) in a life sciences field</li></ul><p></p><p><b><br>
What we offer:</b></p><ul><li>
Hybrid working (3 days office per week) Working Hours Monday to Friday 8.30 -17.30</li><li>
International environment.</li><li>
Life Insurance employee only covered by the Company</li><li>
Private Health Insurance employee only covered by the Company</li><li>
Meal allowance</li><li>
Transportation Allowance</li><li>
Performance Bonus - based on full achievement of specified company goals and personal performance and % based on grade</li><li>
Extra hours off - wellness hours 15h per year</li><li>
Temporary remote working opportunity</li><li>
Up to 50% of discounts for Herbalife products</li><li>
Free products in the office</li></ul><p></p><p><b><br>
Who we are:</b></p><p>
Herbalife is a global nutrition company that has helped people pursue a healthy, active life since 1980. Our nutrition, weight management and personal care products are available exclusively to and through dedicated independent Members in more than 90 countries.</p><p>
Our company offers a culture focused on people, their needs, relationships and careers &ndash; helping talents grow and giving them a chance to change lives.</p><p></p><p><br>
Learn more: https://www.herbalife.com</p></div>

Quality Assurance Specialist - EMEA

Abdi Ibrahim Pharmaceuticals

<div>
 <p>
  Abdi &Idot;brahim Global Pharm, the Kazakhstan affiliate of Abdi &Idot;brahim, is seeking a highly qualified Production Manager to lead and oversee all production operations at our site in
  <strong>
   Almaty
  </strong>
  . The role will be based in Almaty and requires a strong, results-oriented leader who can drive operational excellence, ensure full compliance with GMP and regulatory standards, and promote continuous performance improvement in a dynamic manufacturing environment.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Lead and supervise all production operations to ensure timely, efficient, and high-quality output.
  </li>
  <li>
   Ensure full compliance with GMP, HSE requirements, and company SOPs across all production activities.
  </li>
  <li>
   Manage production teams across multiple shifts, maintaining workforce efficiency, discipline, and a strong safety culture.
  </li>
  <li>
   Collaborate closely with Planning, Quality Assurance, Maintenance, and Engineering teams to meet production targets and minimize downtime.
  </li>
  <li>
   Ensure optimal workload distribution across all production areas and efficient use of equipment and personnel.
  </li>
  <li>
   Track, analyze, and optimize key production KPIs such as yield, OEE, waste, and batch cycle times.
  </li>
  <li>
   Support technology transfer, scale-up, and validation activities for new products in collaboration with R&amp;D and technical teams.
  </li>
  <li>
   Complies with quality system documentation requirements, analyzes causes of nonconformities, and participates in implementing corrective and preventive actions.
  </li>
  <li>
   Drive continuous improvement initiatives using Lean and operational excellence tools.
  </li>
  <li>
   Contribute to production budgeting, capacity planning, and resource optimization.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Pharmacy, Chemical Engineering, or a related scientific/technical field.
  </li>
  <li>
   Minimum 8 years of pharmaceutical production experience
  </li>
  <li>
   Strong knowledge of GMP standards and experience in regulated pharmaceutical manufacturing environments.
  </li>
  <li>
   Strong leadership, communication, and team management skills.
  </li>
  <li>
   Strong know &ndash; how of pharmaceutical production technologies (granulation, compression, coating, mixing, filling, packaging, etc.).
  </li>
  <li>
   Ability to manage multi-shift operations and drive team performance.
  </li>
  <li>
   Fluency in English both written and spoken; knowledge of Russian is an asset.
  </li>
 </ul>
 <p>
 </p>
</div>


Production Manager - Kazakhstan

<div>
 <p>
  Abdi &Idot;brahim, founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry, with 5,500 employees. Since 2002, Abdi &Idot;brahim has led Turkey&rsquo;s pharmaceutical industry with a strong vision and today exports to over 70 countries. Committed to being a responsible corporate citizen, the company prioritizes sustainability across all business processes, aligning its mission with societal needs. Its 2025 vision is to remain a wholly local company while becoming one of the top 100 pharmaceutical companies globally.
 </p>
 <p>
  We are seeking a motivated
  <strong>
   MSAT
  </strong>
  <strong>
   Specialist
  </strong>
  to join our monoclonal antibody production team. In this role, you will be a part of the downstream processing operations, ensuring the highest standards of quality, efficiency, and innovation in the purification of monoclonal antibodies. You will work in a talented team, collaborate cross-functionally, and contribute to the success of our bioprocessing pipeline.
 </p>
 <p>
  We are looking for an
  <strong>
   MSAT
  </strong>
  <strong>
   Specialist
  </strong>
  to join our Drug Substance Production team at the Biotechnological Production Facility (AbdiBio) on the Esenyurt campus.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   The requirements for the successful candidate are:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s / master's degree in biological science discipline.
  </li>
  <li>
   Excellent command of English.
  </li>
  <li>
   6&ndash;8 years of core work experience in biosimilar manufacturing or the biotech industry.
  </li>
  <li>
   Provide technical support for USP/DSP operations, such as fermentation, cell culture, purification, and Chromatography.
  </li>
  <li>
   Provide technical support for cell culture (USP) and protein purification (DSP) operations in a GMP setting.
  </li>
  <li>
   Support process monitoring, data trending, and deviation investigations during routine manufacturing.
  </li>
  <li>
   Participate in tech transfer, scale-up, and process optimization activities.
  </li>
  <li>
   Familiarity with &Auml;KTA chromatography systems and Unicorn software.
  </li>
  <li>
   Understanding of protein purification principles, resin packing/unpacking, and column integrity checks.
  </li>
  <li>
   Knowledge of Quality Management Systems such as Change Control, Deviation, Risk assessment, ICH guidelines and CAPA.
  </li>
  <li>
   Strong communication and interpersonal skills.
  </li>
  <li>
   Knowledge of cGMP.
  </li>
  <li>
   Adherence to cGMP compliance in all operations.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   The key duties of the successful candidate are:
  </strong>
 </p>
 <ul>
  <li>
   Understanding and execution of well-defined procedures within a GMP manufacturing facility.
  </li>
  <li>
   Strong understanding of biologics processes (USP/DSP), GMP, and regulatory guidelines Operation and troubleshooting of equipment such as chromatography skids, TFF systems, peristaltic pumps, and pressure vessels.
  </li>
  <li>
   Preparation and handling of process solutions under aseptic and cleanroom conditions.
  </li>
  <li>
   Adherence to Standard Operating Procedures, logbooks, and Batch Manufacturing Records (BMR).
  </li>
  <li>
   Review the CMC document sections.
  </li>
  <li>
   Preparation of validation protocols, buffer, Media and product hold protocols.
  </li>
  <li>
   Proficient in data analytics, statistical tools (e.g., Minitab), and scientific writing.
  </li>
  <li>
   Work closely with cross-functional teams including Production, QA, QC, and Engineering.
  </li>
 </ul>
 <p>
 </p>
</div>


AbdiBio Manufacturing Science and Technology Specialist

Ferring Pharmaceuticals, Inc.

<div><div>Job Description:</div><div>
Regulatory Affairs Associate</div><div></div><div>
At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women&rsquo;s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.</div><div>
Joining our Regulatory team, you will be part of an empowering and collaborative culture where your work plays a key role in ensuring patient safety, regulatory compliance and sustainable access to medicines. By working closely with cross-functional teams and external stakeholders, you will support regulatory excellence, life-cycle management and the consistent maintenance of our portfolio. Your contribution helps ensure that high-quality therapies remain available, compliant and trusted throughout their entire life cycle.</div><div></div><div>
Ferring+You</div><div></div><div>
We are looking for a Regulatory Affairs Associate to join our team and take a key role in regulatory compliance, quality assurance, document governance, and cross-functional business support in line with local regulations and global procedures, reporting directly to the Regulatory Affairs Manager.</div><div></div><div>
Your day at Ferring</div><ul><li><div>
Act as Document Accountable Person (DAP) and Document Controller (DC), ensuring document lifecycle management, consistency, and compliance</div></li><li><div>
Serve as the main local regulatory contact and manage regulatory compliance activities</div></li><li><div>
Coordinate new drug approvals, including dossier preparation, submissions, and follow-up with local Health Authorities</div></li><li><div>
Manage regulatory submissions, variations, renewals, and product lifecycle activities</div></li><li><div>
Support and coordinate regulatory inspections and maintain validity of licenses and certificates</div></li><li><div>
Monitor regulatory intelligence, assess impact, and proactively communicate regulatory changes</div></li><li><div>
Ensure timely and accurate updates in global and local regulatory systems (e-CTD, Veeva Vault, Track Wise, etc.)</div></li><li><div>
Prepare, review, and approve artworks and labeling to support submissions and product launches</div></li><li><div>
Review promotional and non-promotional materials in line with local regulations and global procedures</div></li><li><div>
Support Quality Management System (QMS) implementation and sustainability, including local market release</div></li><li><div>
Support regulatory and pricing applications, including document coordination and pricing data monitoring</div></li></ul><div></div><div>
Behind our collaboration&hellip;There&rsquo;s you</div><ul><li><div>
University degree in Pharmacy</div></li><li><div>
Min. 2-3 years of practical experience in regulatory and quality assurance</div></li><li><div>
Know-how of interactions with regulatory authorities</div></li><li><div>
Experience with e-CTD, Veeva Vault, Track Wise, and pricing is a plus</div></li><li><div>
Eager to learn personality, team player approach, attention to details</div></li><li><div>
Fluent in English language (written and verbal)</div></li></ul><div></div><div>
People come first at Ferring</div><div></div><ul><li><div>
Get inspired from our commitment to advocate for everyone&rsquo;s right to build a family, no matter who you are, where you live or who you love</div></li><li><div>
Our inclusive support package &ndash; &ldquo;Building Families at Ferring&rdquo; provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role</div></li><li><div>
Parental leave for both birthing and non-birthing parents</div></li><li><div>
Extended support on family building journey</div></li></ul><div></div><div>
Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member&rsquo;s contributions. Imagine the power of your career when it&rsquo;s Ferring + You.</div><div></div><div>
Behind our purpose&hellip; There&rsquo;s you</div><div>
If our mission and your vision are aligned, please apply.</div><div>
We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status.</div><div></div><div>
Location:</div>
Ferring Turkey</div>

Regulatory Affairs Associate

<div>
 <p>
  <strong>
   Abdi &Idot;brahim,
  </strong>
  founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi &Idot;brahim has been the leader of Turkey&rsquo;s pharmaceutical industry since 2002 with its powerful vision.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Today, Abdi &Idot;brahim operates in 17 countries outside T&uuml;rkiye, exports to more than 70 countries ranging from Canada to European Union member states, from North Africa to Asia. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi &Idot;brahim focuses on sustainability in all its business processes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are looking for an "
  <strong>
   <em>
    Analytical Development Analyst/Specialist
   </em>
  </strong>
  " to join our R&amp;D Center located in Esenyurt.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Graduated from Chemistry or Chemical Engineering departments,
  </li>
  <li>
   Preferably holding or currently pursuing a Master&rsquo;s degree in Analytical Chemistry or Pharmaceutical Chemistry,
  </li>
  <li>
   Minimum 2 years of analytical experience is required for the specialist role,
  </li>
  <li>
   Excellent command of English (both written and verbal),
  </li>
  <li>
   Strong teamwork and communication skills,
  </li>
  <li>
   Knowledge and hands-on experience in analytical method development, method validation, and stability studies,
  </li>
  <li>
   Ability to follow up-to-date scientific publications and regulatory guidelines in English,
  </li>
  <li>
   Analytical thinker with strong problem-solving orientation.
  </li>
 </ul>
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 </p>
 <p>
  <strong>
   Job Description
  </strong>
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 </p>
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  <li>
   Conduct literature research for raw materials and finished products related to newly approved product development projects,
  </li>
  <li>
   Perform analytical method development, validation, and required testing activities, and prepare corresponding reports in compliance with applicable requirements,
  </li>
  <li>
   Carry out stability analyses for new products, prepare and evaluate stability reports in line with regulations,
  </li>
  <li>
   Prepare analytical documentation sections of registration dossiers in CTD format for submission to the Ministry of Health.
  </li>
 </ul>
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R&D Analytical Development Analyst/Specialist

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