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academic writer & scientific quality assurance specialist

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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

Boston Scientific

<div><p><b>Additional Locations:</b> N/A</p><p><b>
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance</b></p><p>
At Boston Scientific, we&rsquo;ll give you the opportunity to harness all that&rsquo;s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we&rsquo;ll help you in advancing your skills and career. Here, you&rsquo;ll be supported in progressing &ndash; whatever your ambitions.</p><p></p><p><b><br>
Business Development Specialist - Endobariatrics - Turkey</b></p><p></p><p><b><br>
Purpose Statement</b></p><p><br>
Responsible for increasing the number of patients treated with, and/or the market share of, franchise products across the assigned territory. The role focuses on building and leveraging relationships with <b>Key Opinion Leaders (KOLs), hospital administration, and medical societies</b>, while developing and implementing <b>education and training programs</b> for physicians and hospital staff covering patient identification, referral, implant, and follow-up procedures. Accountable for achieving <b>sales growth</b> and supporting therapy adoption across medical sectors. May also include responsibility for the <b>Distributor market</b>.</p><p></p><p><b><br>
Key Responsibilities</b></p><p></p><ul><li><b><br>
Market &amp; Business Awareness</b></li><li><ul><li>
Maintain awareness of industry, competition, healthcare, and economic trends.</li><li>
Adjust franchise business plans to reflect market conditions.</li></ul></li></ul><p></p><ul><li><b><br>
Business Development &amp; Sales Strategy</b></li><li><ul><li>
Identify new business opportunities and accounts via relationships with KOLs and academic/research institutions.</li><li>
Develop and execute sales strategies to grow the number of patients treated and increase market share.</li><li>
Present economic benefits of growing patient numbers to hospital executives and decision-makers.</li><li>
Manage contract designs and negotiations across all products and solutions in the territory.</li></ul></li></ul><p></p><ul><li><b><br>
Education &amp; Clinical Support</b></li><li><ul><li>
Train physicians and hospital staff on patient identification, referral, implant, follow-up, and ongoing monitoring.</li><li>
Ensure increasing patient treatment and clinical success through educational initiatives.</li><li>
Attend and participate in customer, company, and industry forums or courses.</li></ul></li></ul><p></p><ul><li><b><br>
Collaboration &amp; Team Support</b></li><li><ul><li>
Work closely with sales teams to maintain relationships with economic buyers in key accounts.</li><li>
Educate local sales teams to take over projects after successful implementation.</li><li>
Collaborate with HEMA and HS&amp;P to remove barriers and implement tools (e.g., patient identification systems).</li></ul></li></ul><p></p><ul><li><b><br>
Quality &amp; Compliance</b></li><li><ul><li>
Serve as an interface between customers and the sales organization to address complaints and issues.</li><li>
Guide the local leadership team to ensure compliance with Boston Scientific Quality System and local quality requirements.</li></ul></li></ul><p></p><p><b><br>
What we can offer to you:</b></p><ul><li>
Attractive benefits package.</li><li>
Inspirational colleagues and culture.</li><li>
Fast growing and innovative environment.</li><li>
A team-oriented company culture.</li><li>
International opportunities.</li><li>
Excellent training/development programs.</li></ul><p></p><p><b><br>
Requisition ID: </b>618679</p><p></p><p><br>
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most &ndash; united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do &ndash; as a global business and as a global corporate citizen.</p><p></p><p><br>
So, choosing a career with Boston Scientific (NYSE: BSX) isn&rsquo;t just business, it&rsquo;s personal. And if you&rsquo;re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!</p></div>

Business Development Specialist, Turkey

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</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

Mann+Hummel

<div></div><div><div><div><div><p>Senior Product and Pricing Specialist</p>
<p>Istanbul, T&uuml;rkei | Marketing | Berufserfahrene | Unbefristet | December 12, 2025</p><div></div><div><div><div><div><div><br>
</div></div></div></div></div></div></div></div><div></div><div><div><div><div><div><div><div><div>As worldwide experts in filtration, MANN+HUMMEL develop solutions for vehicles, industrial applications, clean air inside vehicles and the sustainable use of water. With team spirit and an open culture of communication, we are continuously working towards achieving our vision of &lsquo;leadership in filtration&rsquo;. Become part of our team.</div>
</div></div></div></div></div></div></div><div><div><div>Job Description
</div></div><div><div><div><div><div><div>Role Summary</div></div><div><p>
The job incumbent is responsible for all product and pricing management activities and supports the growth of the Automotive Aftermarket BU.</p><p>
The role will be to be accountable for all the processes within the product and pricing management functions.</p><div>
#LI-Onsite</div></div></div><div><div><div>
Main Tasks</div></div><div><p>
Product Management</p><p>
Range Management
</p><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.</li></ul><p>
Research
</p><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</li></ul><p>
New Product Introduction (NPI)</p><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.</li></ul><p>
Sales Support</p><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</li></ul><p>
Quality Management</p><ul><li>
Manage quality claims via Dealer Portal.</li><li>
Communicate respective locations and create SAP QM tickets to follow up process.</li></ul><p>
Pricing Management</p><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.</li></ul></div></div><div><div><div>
Your Profile</div></div><div><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</li></ul></div></div><div><div><div>
Skills</div></div><div><div>
Product Design</div><div>
Market Research</div><div>
Product Development</div><div>
Product Management</div><div>
Marketing Planning</div><div>
Merchandising</div><div>
Marketing Strategies</div><div>
Brand Management</div><div>
Literacy</div><div>
External Communications</div></div></div></div>
</div></div></div><div><div><div><div><div><div><div><div>Are you full of ideas? Are you keen to take on responsibility and really achieve something? Then our doors are open to you. This company lives out its values, gives people the freedom to use their own initiative, and offers many development exciting opportunities and many exciting projects &ndash; all of which awaits you here.</div></div></div></div></div></div></div></div></div>

Senior Product and Pricing Specialist

LivaNova

<div><div>As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow&mdash;because at LivaNova, we don&rsquo;t just treat conditions &mdash; we aspire to alter the course of lives.</div><div>
POSITION SUMMARY</div><div>
The primary objective of the Field Clinical Specialist (FCS) is to provide in-house and field-based clinical and technical training/support for medical devices for the assigned country and therapeutic areas. The candidate will be responsible for training health care professionals in the use of pre and post market medical devices and associated surgical procedures; installing, upgrading, and troubleshooting the Company's products in the field; programming devices and providing technical expertise in the development of new products. The candidate will perform these duties and develop the necessary training materials in compliance the Company&rsquo;s policies.</div><div>
ESSENTIAL JOB FUNCTIONS</div><ul><li>Surgical case coverage, follow-up support and troubleshooting of the assigned LivaNova Products.</li><li>Conducting patient in-services for products.</li><li>Conducting required training for new and existing investigative centers.</li><li>Conducting training of LivaNova employees.</li><li>Develops, implements, and manages product and system training for all commercial personnel including new hire training, systems training, product launch and ancillary follow-up trainings.</li><li>Identifying, strategizing and implementing ongoing training needs.</li></ul><div>
Clinical and Technical Support</div><ul><li>Represents LivaNova for his/her respective field during surgeries, implants, device programming and etc.</li><li>Demonstrates expertise in all aspects of medical devices and troubleshooting techniques</li><li>Provides support and follow-ups in hospitals and clinics, as specified in study protocols or through commercialization efforts</li><li>Receives technical inquiries from customers, distributors and employees. Researches solutions to questions or problems.</li><li>Provides support as needed for surgeries, reprogramming, troubleshooting, follow-up, etc</li></ul><div></div><div>
Educational/Research Support</div><ul><li>Builds professional and technical knowledge by engaging with customers, attending scientific conferences, educational workshops, delivering presentations and training to field personnel and reviewing professional publications</li><li>Regularly educates and updates physicians/clinicians and clinic follow-up staff on new product releases of device systems and features, including both hardware and software modifications</li><li>Liaison between R&amp;D and physicians to coordinate beta testing&ndash; develop protocols and recruit centers</li><li>Facilitate submission of research for presentations; work with internal contacts and physicians to prepare scripts, slides, overheads, PowerPoint presentations</li><li>Aid physicians with technology &ndash; literature searches, engineering, LivaNova technology</li><li>Maintain open, effective communication with all LivaNova functions, including Regulatory Assurance, Quality Assurance, Compliance and Product Development, as well as with employees</li><li>Create and update instructions for use, physician and patient manuals, and other system documentation as required such as translations.</li><li>Generate literature/training materials &ndash; create tech memos, facilitate Sales and Marketing personnel with Marketing literature review</li><li>Assist sales to identify and target physicians</li><li>Travel may be extensive, up to 80%, including international trips</li></ul><div></div><div>
KNOWLEDGE, SKILLS &amp; ABILITIES</div><div>
Candidate must have:</div><ul><li>Ability to communicate effectively with health care professionals</li><li>Ability to instruct/coach others on use of products and clinical applications</li><li>Strong interpersonal skills and professional demeanor</li><li>Effective problem solving and trouble shooting skills</li><li>Excellent organizational skills</li><li>Ability to prioritize under pressure</li><li>Solid MS Office skills including PowerPoint</li><li>The ability to manage multiple tasks simultaneously</li><li>English level as of B2 or Upper Intermediate (including medical terminology) is considered a must</li></ul><div></div><div>
EDUCATION</div><div>
Bachelor's degree in health care related field. Advanced degree in health sciences or engineering preferred.</div><div>
EXPERIENCE</div><div>
Prefer prior experience of at least 3+ years as a field clinical role, technical representative, technology trainer or clinical trainer in medical device field. Must have surgical experience</div><div>
Welcome to impact. Welcome to innovation. Welcome to your new life.</div></div>

Field Clinical Specialist NM

Field Clinical Specialist - NM

Perrigo France

<div>
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 <br/>
 Regulatory Affairs, Associate Specialist
 <br/>
 <br/>
 Location:
 <br/>
 <br/>
 Istanbul, TR, 34732
 <br/>
 <br/>
 At Perrigo, we are driven by our mission to
 <em>
  <strong>
   Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All
  </strong>
 </em>
 . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing
 <strong>
  <em>
   The Best Self-Care for Everyone
  </em>
 </strong>
 , we are the people behind the brands you trust. We are Opill&reg;, Compeed&reg;, Solpadeine&reg;, NiQuitin&reg;, ACO&reg;, and many more.
 <strong>
  We Are Perrigo
 </strong>
 . We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
 <br/>
 <br/>
 Join us on our One Perrigo journey as we evolve to win in self-care.
 <br/>
 <br/>
 <strong>
  Description Overview
  <br/>
  <br/>
 </strong>
 In this role you will be responsible for the hands on regulatory activities required to maintain existing commercial products, and support in making correct and timely new product applications of Perrigo products on the Turkish market. You will support to ensure compliance with the existing legislation for Medicines, Medical Devices, Biocides and Cosmetics. Another key aspect of the role will be supporting in the achievement of the overall Regulatory, Quality &amp; Safety objectives and timely realization of operational activities. In this position you collaborate closely with the Corporate Regulatory and Turkish Commercial colleagues to strive to help the customer the best.
 <br/>
 <br/>
 <strong>
  Scope of the Role
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Support in the management of change by preparing applications and technical files in support of existing commercial product regulatory maintenance;
  </li>
  <li>
   Support in the regulatory activities on new product development (NPD), including artwork approvals, label claims and associated supporting documentation;
  </li>
  <li>
   Develop and approve label specifications (master text and local artwork text) in compliance with SOPs, as well as promotional materials from a regulatory perspective;
  </li>
  <li>
   Maintain regulatory files and data systems in compliance with SOPs;
  </li>
  <li>
   Represent regulatory affairs in project meetings with both Perrigo staff and external contacts;
  </li>
  <li>
   Follow up on changes in (inter)national regulations and legislations, and support in the interpretation, communication and implementation;
  </li>
  <li>
   Liaise with Corporate Regulatory, responding to regulatory queries and providing and review of registration documents as necessary for the Turkish and/or European territory;
  </li>
  <li>
   Support in the communication with local regulatory authorities regarding license applications and notice of change.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience Required
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University Degree in a Scientific Subject;
  </li>
  <li>
   Minimum of 2 years work experience within Regulatory Affairs required, within at least one of the following categories Medical Devices, Biocides, Cosmetics and Medicines;
  </li>
  <li>
   Excellent communicator in Turkish and English;
  </li>
  <li>
   Proficient computer skills esp. Microsoft (word, excel, powerpoint); experience with Veeva, TVT, Trackwise is an asset;
  </li>
  <li>
   Eye for detail, punctual, well organized;
  </li>
  <li>
   Being flexible and adaptable to change;
  </li>
  <li>
   Ability to support several concurrent projects/products simultaneously;
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
 <br/>
 <br/>
 Find out more about
 <strong>
  Total Rewards
 </strong>
 at Perrigo.
 <br/>
 <br/>
 <strong>
  Hybrid Working Approach
  <br/>
  <br/>
 </strong>
 We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
 <br/>
 <br/>
 We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more
 <strong>
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Regulatory Affairs, Associate Specialist

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