quality officer

Mahalaxmi Group

Job Description &ndash; Quality Officer (Pimpri Site)Company: Mahalaxmi Group Location: Pimpri Department: Quality AssuranceAbout UsMahalaxmi Group is a dynamic real estate organization committed to delivering high-quality housing solutions with a focus on customer satisfaction. We aim to create exceptional experiences for our clients while maintaining professionalism, transparency, and efficiency in all our processes.Position OverviewThe Quality Officer will be responsible for monitoring construction quality, ensuring adherence to approved drawings, specifications, and company standards.Key Responsibilities<ul><li>Conduct quality inspections for all ongoing construction works.</li><li>Ensure materials used meet required specifications.</li><li>Prepare quality checklists and maintain inspection records.</li><li>Identify defects, non-conformities, and implement corrective actions.</li><li>Coordinate with site engineers, contractors, and vendors for quality compliance.</li><li>Verify work completion as per drawings and standards.</li><li>Support QA documentation and audit requirements.</li></ul>Requirements<ul><li>Diploma/B.E. in Civil Engineering.</li><li>2&ndash;4 years of quality monitoring experience in construction.</li><li>Knowledge of construction materials, techniques, and QA standards.</li><li>Understanding of QMS processes.</li></ul>Skills Required<ul><li>Strong analytical and inspection skills.</li><li>Knowledge of construction quality benchmarks.</li><li>Good documentation and reporting abilities.</li><li>Problem-solving and decision-making skills.</li><li>Coordination and communication skills.</li></ul>Job Types: Full-time, PermanentPay: &#8377;30,000.00 - &#8377;40,000.00 per monthBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

Quality Officer

VARQ PACKAGES PVT LTD

VARQ Packages Pvt. Ltd. Location: Pakistan Job Type: Full TimeAbout UsVARQ Packages Pvt. Ltd. is a leading packaging and printing company committed to delivering high-quality products to our clients. We pride ourselves on maintaining rigorous quality standards and continuous improvement in all production processes. We are seeking a motivated and skilled Quality Officer to join our Quality Control and Assurance team.Position DetailsDesignation: Quality Officer Department: Quality Control and AssuranceResponsibilities:Core Quality Responsibilities<ul><li>Develop, implement, and enforce the company&rsquo;s Quality Policy.</li><li>Conduct detailed inspections of all incoming materials including paper, board, reels, master cartons, and flexo inks.</li><li>Maintain accurate records, inspection reports, and documentation for all incoming materials and production quality checks.</li><li>Take timely actions on rejected or non-conforming materials.</li><li>Perform quality inspections before, during, and after bulk production.</li><li>Carry out final inspections at output and dispatch according to AQL standards.</li><li>Inspect and monitor production processes for paper cups, glasses, bags, and napkins to ensure compliance with quality standards.</li><li>Oversee and execute all quality control and quality assurance activities including inspections, audits, and testing.</li><li>Ensure production processes are aligned with the Quality Management System (QMS).</li><li>Implement corrective and preventive actions whenever required.</li><li>Respond promptly to quality-related inquiries.</li><li>Ensure continuous improvement of production processes, systems, and quality standards.</li></ul>Coordination and Reporting<ul><li>Coordinate with Planning, Sales, and Design departments to ensure quality expectations are met.</li><li>Monitor daily production records and maintain accurate documentation.</li><li>Prepare and submit quality reports for management review.</li><li>Report all quality findings, issues, and updates directly to the CEO.</li><li>Ensure customer satisfaction by addressing and rectifying customer complaints effectively.</li></ul>Team and Leadership Responsibilities<ul><li>Supervise, train, motivate, and guide the Quality Team.</li><li>Provide leadership to ensure all QC staff understand and follow quality procedures.</li><li>Promote a culture of quality and continuous improvement across the organization.</li></ul>Requirements:Education: Graduate Experience: Minimum 3 years in Quality Control or Assurance; candidates with experience in the packaging industry will be preferred. Age Range: 25-40 yearsSkills:<ul><li>Strong knowledge and understanding of Quality Management Systems (QMS)</li><li>Good decision-making and problem-solving skills</li><li>Excellent communication and reporting abilities</li><li>Leadership skills and ability to manage a team effectively</li></ul>How to Apply:Interested candidates should apply by sending their resume to hr@varq.org with the subject line: QC OFFICERJob Type: Full-timeWork Location: In person

Normeca International

Medical Manager Normeca International AS invites &ldquo;Quality Officer&rdquo; to work in connection with the launch of our project in Pakistan &ldquo;Mobile Multi Diagnostic Clinic / Mini Hospital&rdquo; under the management of the Islamic Development Bank (ISDB) and in cooperation with the Government in Islamic Republic of Pakistan. The clinics will cover general diagnostic and minor surgical procedures, and they are all located in large mobile trailers. The clinics are fully equipped with modern medical equipment and ancillary units such as kitchen, laundry, dining room, conference rooms, etc. The Clinics are operating in KPK and Sindh Regions.Normeca International AS is seeking a meticulous and experienced Quality Officer to join our team. This role is critical in ensuring the highest standards of quality and compliance within our Mobile Medical Units (MMUs) operating in the rural areas of Pakistan. The successful candidate will be responsible for overseeing and following up on the MMUs' services and operations in the field.Key Responsibilities:<ul><li>Develop and implement quality assurance policies and procedures to ensure compliance with healthcare regulations and standards within the MMUs.</li><li>Conduct regular audits and inspections of MMU operations, patient care, and staff performance.</li><li>Monitor and analyze quality metrics to identify areas for improvement in MMU services.</li><li>Collaborate with healthcare professionals to develop and implement quality improvement initiatives for the MMUs.</li><li>Provide training and education to MMU staff on quality standards and best practices.</li><li>Investigate and resolve quality-related issues and complaints in the field.</li><li>Maintain accurate and detailed records of quality assurance activities and findings related to the MMUs.</li><li>Prepare and present quality reports to management.</li><li>Stay updated with the latest developments in healthcare quality standards and regulations.</li><li>Foster a culture of continuous improvement and patient safety within the MMUs.</li></ul>Qualifications:<ul><li>Bachelor&rsquo;s degree in healthcare administration, quality management, or a related field.</li><li>Proven experience as a Quality Officer or in a similar quality assurance role in healthcare.</li><li>Strong knowledge of healthcare regulations, quality standards, and best practices.</li><li>Excellent analytical and problem-solving skills.</li><li>Strong attention to detail and organizational skills.</li><li>Excellent communication and interpersonal skills.</li><li>Ability to work independently and as part of a team.</li><li>Proficiency in MS Office (Word, Excel, Outlook).</li><li>Proficiency in English is mandatory.</li><li>Willingness to work in non-standard conditions in rural areas and travel to various field locations.</li></ul>What We Offer:By becoming part of our team, you will join an excellent medical team and help change the world for the better for many people in Pakistan. What you will receive:<ul><li>Opportunity to develop and gain experience of international standard.</li><li>Accommodation and three meals a day while on travel.</li><li>Free medical care for you and your family in our clinic.</li><li>Competitive salary and medical insurance.</li></ul>Scope of Work: Full time Place of Work: HQ Islamabad, PakistanIf you are a dedicated and skilled Quality Officer with a passion for ensuring excellence in healthcare, we encourage you to apply. Join us in our mission to bring quality healthcare to underserved communities through our Mobile Medical Units.Job Types: Full-time, ContractWork Location: In person

Fiesta Consultants

iesta Group of Companies is hiring a Quality Officer for Graphics who will lead, train, and manage a creative team. The ideal candidate must have strong graphic design skills, the ability to build and supervise a 5&ndash;7 member team, and ensure high-quality delivery of all design tasks.This is a leadership + quality control role for someone willing to train, guide, and grow a design department.Key Responsibilities:<ul><li>Provide graphics training to team members (beginners &amp; intermediate designers).</li><li>Build and lead a team of 5&ndash;7 graphic designers.</li><li>Ensure quality control of all graphic design tasks.</li><li>Guide team on design standards, templates, formatting, and brand guidelines.</li><li>Ensure timely completion of assigned tasks.</li><li>Set creative direction and maintain consistency in all outputs.</li><li>Assist in presentation designs, documentation, and visual content creation</li></ul>Required Skills:<ul><li>Strong command over PowerPoint and Microsoft Word.</li><li>Expertise in Adobe tools, including:</li></ul>&#10004; Photoshop &#10004; Illustrator &#10004; InDesign &#10004; Premiere Pro (optional)<ul><li>Understanding of:</li></ul>&#10004; Callibry &#10004; Millium &#10004; Affinity Publisher<ul><li>Excellent quality checking skills.</li><li>Leadership &amp; training capability.</li></ul>Eligibility Criteria:<ul><li>Must be open to learning and upgrading skills.</li><li>Must have experience in graphic design and team supervision.</li><li>Strong communication and training skills.</li><li>Ability to handle pressure and meet deadlines.</li></ul>Salary &amp; Benefits:<ul><li>Fixed Salary: Rs. 25,000/month</li><li>Professional work environment</li><li>Growth and leadership opportunities</li><li>Skill enhancement &amp; training support</li></ul>Job Type: Full-timePay: From Rs25,000.00 per monthWork Location: On the road

Quality Officer Graphics

<div>We manufacture and supply reliable, high-quality medicines and vaccines to meet patients&rsquo; needs and drive our performance.Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it&rsquo;s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Operational Quality Officer 
 
You will help ensure high-quality manufacturing and compliance on the shop floor. You will work closely with production, quality and engineering colleagues. We value attention to detail, clear communication and a practical mindset. You will grow through hands-on experience, coaching others and supporting investigations. This role gives you the chance to make a real impact on patient safety while building your quality assurance career at GSK.
Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
<ul><li>Monitor production activities to confirm compliance with Good Manufacturing Practices and GSK quality standards.
</li><li>Review batch documentation for completeness, accuracy and adherence to approved procedures.
</li><li>Sample and release intermediate, bulk and finished materials following approved plans.
</li><li>Support investigations for deviations, out-of-specification results and customer complaints, including gathering facts and contributing to root cause analysis.
</li><li>Participate in internal audits and routine self-inspection activities and track corrective actions to closure.
</li><li>Coach operators and production teams to embed a quality mindset and improve operational practices.
</li></ul>Why you?
 Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
<ul><li>Bachelor&rsquo;s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or a related science degree; or equivalent professional qualification.
</li><li>Minimum 1 year of experience in a regulated manufacturing or quality environment
</li><li>Practical knowledge of current Good Manufacturing Practices (GMP).
</li><li>Strong documentation skills with attention to accuracy and completeness.
</li><li>Clear verbal and written communication skills in Arabic and a good command of English.
</li><li>Willingness to work on-site and participate in shift-based operations as required.
</li></ul>Preferred Qualifications:
If you have the following characteristics, it would be a plus:
If you have the following characteristics, it would be a plus:
<ul><li>2 or more years&rsquo; experience in operational quality, production quality or quality assurance.
</li><li>Familiarity with batch record review, sampling plans and in-process control testing.- Experience with internal audits, deviation management and CAPA systems.
</li><li>Understanding of validation concepts (IQ/OQ/PQ) and basic equipment qualification.
</li><li>Basic computer skills including MS Word and Excel and familiarity with electronic quality systems.
</li><li>Experience coaching or training production teams to improve compliance and performance.
</li></ul>Working pattern
This position is on-site at our manufacturing site. The role may require shift work and occasional weekend support to align with production schedules.
What we value
We look for people who act with integrity, take ownership and collaborate openly. You will be supported to learn and develop through hands-on coaching and formal training. We welcome candidates who value inclusion, speak up when something matters, and help create a safe and respectful workplace.
Ready to apply?
If this role matches your strengths and career goals, we would love to hear from you. Apply now to join our Operational Quality team and help us unite science, technology and talent to get ahead of disease together.
Why GSK?
 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information:
 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Operational Quality Officer

<div>
 
 Site Name:
 
 Saudi Arabia - Jeddah
 
 
 
 Posted Date:
 
 Nov 27 2025
 
 
 GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.
 
 
 We manufacture and supply reliable, high-quality medicines and vaccines to meet patients&rsquo; needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it&rsquo;s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
 
 
 
 Operational Quality Officer
 
 
 
 You will ensure operational quality and compliance on the manufacturing shop floor in Saudi Arabia. You will work closely with production, quality, laboratory and engineering teams to identify and resolve quality issues quickly. We value practical problem solvers who act with integrity, communicate clearly, and help teams improve how they work every day. This role offers strong on-the-job learning, visible impact on product quality and patient safety, and the chance to grow with GSK&rsquo;s mission of uniting science, technology and talent to get ahead of disease together.
 
 
 
 Responsibilities:
 
 
 
 This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
 
 
 
 <ul>
 <li>
 Provide day-to-day quality oversight on the shop floor during production shifts to ensure compliance with cGMP, QMS and local regulatory requirements.
 </li>
 <li>
 Review and support approval-ready batch documentation, including finished goods records and associated quality checks.
 </li>
 <li>
 Support incident and deviation investigations by collecting data, analysing root cause and tracking corrective and preventive actions.
 </li>
 <li>
 Perform focused internal audits and level 1 oversight activities to identify non-conformances and drive timely closure of actions.
 </li>
 <li>
 Conduct spot checks, environmental monitoring reviews and good documentation practice checks to maintain quality standards.
 </li>
 <li>
 Work with production, QC, and Logistics to identify risks, propose mitigations and support timely product release.
 
 
 
 </li>
 </ul>
 
 
 Why you?
 
 
 
 
 
 Basic Qualifications:
 
 
 
 
 We are looking for professionals with these required skills to achieve our goals:
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree or diploma in pharmacy, life sciences, biotechnology, chemistry, engineering or a related technical field; or equivalent practical experience.
 </li>
 <li>
 Minimum of 2 years&rsquo; experience in a pharmaceutical manufacturing environment with exposure to quality and GMP practices.
 </li>
 <li>
 Practical knowledge of Good Manufacturing Practice (GMP), Quality Management Systems (QMS) and good documentation practices.
 </li>
 <li>
 Experience supporting deviations, investigations, CAPA and batch record review.
 </li>
 <li>
 Good written and spoken English; Arabic language skills are an advantage.
 </li>
 <li>
 This role is on-site in Saudi Arabia and requires regular presence on the shop floor and shift coverage.
 </li>
 <li>
 Experience coaching or mentoring colleagues to build quality awareness.
 
 
 
 </li>
 </ul>
 
 Preferred Qualifications:
 
 
 
 
 If you have the following characteristics, it would be a plus:
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in science or pharmacy
 </li>
 <li>
 Experience with environmental monitoring, OOS/OOT investigations or assurance activities.
 </li>
 <li>
 Familiarity with electronic batch records, SAP or quality management software.
 </li>
 <li>
 Strong attention to detail and an ability to work collaboratively across teams.
 </li>
 <li>
 Experience participating in regulatory inspections or preparing inspection responses.
 
 
 
 </li>
 </ul>
 شركة جلاكسو سميث كلاين فيالمملكة العربية السعودية ملتزمة بدعم رؤية 2030 والأجندة الوطنية للمملكة العربية السعودية بما في ذلك التوطين، تماشياً مع سياسات التوظيف والتدريب وتطوير القدرات الوطنية السعودية. نقوم بتصنيع وتوريد أدوية ولقاحات موثوقة وعالية الجودة لتلبية احتياجات المرضى ودفع أدائنا. سلّمت شبكتنا المكونة من 37 موقعًا لتصنيع الأدوية واللقاحات 1.7 مليار عبوة دواء و409 مليون جرعة لقاح في عام 2024، للمساهمة في تأثير إيجابي على صحة ملايين الأشخاص .
 
 
 سلاسل التوريد لدينا ليست مجرد عنصر أساسي في عملياتنا؛ بل هي حيوية لإيصال ابتكاراتنا إلى المرضى بأسرع شكل وأكثر كفاءة وفاعلية ممكنة. تعمل التكنولوجيا على تحويل طريقة تصنيعنا للأدوية واللقاحات، مما يمكّننا من زيادة السرعة والجودة وسعة توريد المنتجات. نحن بحاجة لأفضل العقول والقدرات لمساعدتنا في رحلتنا لصنع منتجات أكثر تعقيدًا، مستفيدين من قوة تقنيات التصنيع الذكي بما في ذلك الروبوتات، الحلول الرقمية والذكاء الاصطناعي لخدمة المرضى.
 
 
 مسؤول جودة تشغيلية
 
 
 ستضمن الجودة التشغيلية والامتثال على أرضية التصنيع في المملكة العربية السعودية. ستعمل عن كثب مع فرق الإنتاج والجودة والمختبر والهندسة لتحديد مشكلات الجودة وحلها بسرعة. نقدر أصحاب الحلول العملية الذين يتصرفون بنزاهة، ويتواصلون بوضوح، ويساعدون الفرق على تحسين طريقة عملهم يوميًا. يوفر هذا الدور فرصة قوية للتعلم أثناء العمل، وتأثيرًا مرئيًا على جودة المنتج وسلامة المرضى، وفرصة للنمو مع مهمة جلاكسو سميث كلاينفي توحيد العلوم والتكنولوجيا والمواهب للتقدم معًا في مواجهة الأمراض
 
 
 المسؤوليات:
 
 
 سيمنحك هذا الدور الفرصة لقيادة أنشطة رئيسية لتطوير مسارك المهني. تشمل هذه المسؤوليات بعض ما يلي:
 
 
 
 <ul>
 <li>
 توفير إشراف جودة يومي على أرضية التصنيع خلال نوبات الإنتاج لضمان الامتثال لممارسات التصنيع الجيدة ، ونظم إدارة الجودة والمتطلبات التنظيمية المحلية
 </li>
 <li>
 مراجعة ودعم توثيق الدُفعات الجاهز للموافقة، بما في ذلك سجلات السلع النهائية وفحوصات الجودة المرتبطة بها
 </li>
 <li>
 دعم تحقيقات الحوادث والانحرافات من خلال جمع البيانات، تحليل السبب الجذري وتتبع إجراءات التصحيح والوقاية
 </li>
 <li>
 أداء تدقيقات داخلية مركزة وأنشطة إشراف من المستوى الأول لتحديد حالات عدم المطابقة ودفع إغلاق الإجراءات في الوقت المناسب.
 </li>
 <li>
 إجراء فحوصات مفاجئة، مراجعات رصد البيئة وفحوصات ممارسات التوثيق الجيدة للحفاظ على معايير الجودة
 </li>
 <li>
 العمل مع فرق الإنتاج، مراقبة الجودة وفريق الخدمات اللوجستيةلتحديد المخاطر، اقتراح التخفيفات ودعم إصدار المنتج في الوقت المناسب
 
 
 
 </li>
 </ul>
 لماذا أنت؟ المؤهلات الأساسية:
 
 
 نبحث عن محترفين يمتلكون المهارات المطلوبة التالية لتحقيق أهدافنا:
 
 
 
 <ul>
 <li>
 درجة بكالوريوس أو دبلوم في الصيدلة، أو علوم الحياة، أو التكنولوجيا الحيوية، أو الكيمياء، أو الهندسة، أو مجال تقني ذي صلة؛ أو ما يعادلها من خبرة عملية.
 </li>
 <li>
 خبرة لا تقل عن سنتين في مجال تصنيع الأدوية، مع خبرة في الجودة وممارسات التصنيع الجيد (GMP).
 </li>
 <li>
 معرفة عملية بممارسات التصنيع الجيدة (GMP)، وأنظمة إدارة الجودة (QMS)، وممارسات التوثيق الجيدة.
 </li>
 <li>
 خبرة في دعم الانحرافات، والتحقيقات، ومراجعة سجلات الدفعات، وتحليل المخاطر والتحليل المحاسبي.
 </li>
 <li>
 إجادة اللغة الإنجليزية تحدثًا وكتابةً؛ وتُعدّ إجادة اللغة العربية ميزة إضافية.
 </li>
 <li>
 يتطلب هذا المنصب حضورًا ميدانيًا في المملكة العربية السعودية، ويتطلب تواجدًا منتظمًا في المصنع وتغطية الورديات.
 </li>
 <li>
 خبرة في تدريب أو توجيه الزملاء لتعزيز الوعي بالجودة.
 
 
 
 </li>
 </ul>
 المؤهلات المفضلة:
 
 
 إذا كانت لديك الخصائص التالية فسيشكل ذلك ميزة إضافية:
 
 
 
 <ul>
 <li>
 درجة بكالوريوس في العلوم أو الصيدلة.
 </li>
 <li>
 خبرة في مجال الرصد البيئي، وتحقيقات OOS/OOT، أو أنشطة ضمان الجودة.
 </li>
 <li>
 إلمام بسجلات الدفعات الإلكترونية، ونظام SAP، أو برامج إدارة الجودة و PowerBI
 </li>
 <li>
 دقة عالية في التفاصيل، والقدرة على العمل التعاوني مع الفرق.
 </li>
 <li>
 خبرة في المشاركة في عمليات التفتيش التنظيمية أو إعداد ردود التفتيش.
 
 
 
 </li>
 </ul>
 
 Why GSK?
 
 
 Uniting science, technology and talent to get ahead of disease together.
 
 
 
 GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
 
 
 People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
 
 
 
 Contact information:
 
 
 
 You may apply for this position online by selecting the
 
 Apply now
 
 button.
 
 
 
 Important notice to Employment businesses/ Agencies
 
 
 
 GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
</div>

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