Abrar Admin

Hikma

<p></p><div><div><div><div><div><div><div>Description:
<div><b>Job</b></div>
<div><b>
Location: Cherry Hill, NJ</b></div>
<div><b>
Job Type: Full-time</b></div>
<div><b>
Req ID:</b></div><br>
<div></div>
<div>
</div><div><b>Description:</b></div>
<div>
We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Supervisor, Microbiology. In this role, you will be responsible for the supervision of microbiologists performing pharmaceutical microbiological procedures and the accuracy of test results and raw data generated. The qualified candidate must possess a strong background in sterility testing using isolator technology, sterility testing validation, Biological Indicator studies, water system sampling and testing, bioburden testing, Bacterial Endotoxin Testing (BET), bioburden and BET validation testing, microbial identifications, disinfectant studies, Antimicrobial Effectiveness Testing (AET) and AET validation, growth promotion testing of media/diluents, preparation of cryopreserved microbial cultures, and media/diluent preparation. The qualified candidate must have experience interacting with the FDA and other regulatory/audit groups. This position will be responsible for resolving technical/equipment problems, implementing corrective/preventive actions, writing/ revising standard operating procedures, forms, protocols, test methods and change controls, and providing guidance to less senior staff.</div><br>
<div></div>
<div><b>
Key Responsibilities:</b></div>
<ul>
<li>Control the workflow of the microbiology laboratory by supervising, planning, organizing, and directing the activities of the group to support production, stability program, technical services, and R&amp;D. Ensure adequate supplies and equipment are available for testing and maintain expenses at or below budget. Analyze workflow, prepare metrics, and make recommendations to improve productivity and efficiency of group and generate cost savings.</li>
<li>Enforce policies and procedures by monitoring the testing techniques and accuracy of all records and documentation that is done in the lab to ensure compliance. Ensure that team members are properly trained and proficient before allowing them to perform any tasks. Review laboratory records for accuracy, completeness, compliance, and conformance to specifications. Approve laboratory records and ensure initiation of laboratory events and investigations as required. Ensure compliance in the group and keep the department ready for both internal and external audits.</li>
<li>Oversee instrument/equipment maintenance and calibration programs. Troubleshoot and resolve instrument/equipment problems. Ensure maintenance and calibrations are done in accordance with required schedule. Develop proposals for new laboratory systems and equipment. Execute validation studies, prepare summary reports, and change controls. Stay current on laboratory instruments and methods. Ensure completion of all protocols, validations, and summary reports in a timely manner.</li>
<li>Prepare and/or revise SOPs to ensure compliance with regulations and current practices. Keep current on regulations and industry best practices pertaining to the group and update SOPs to improve compliance. Prepare and execute change controls as needed to support changes to the program.</li>
<li>Make appropriate staffing recommendations, support laboratory cross-training efforts, evaluate team member performance, perform appraisals, and ensure team members have development plans.</li>
<li>Resolve deviations. Investigate and/or work closely with investigators to determine root cause of deviations. Prepare all necessary reports in a timely manner to meet compliance requirements and business needs.</li>
<li>Interact with FDA and other regulatory/audit groups. Working knowledge of FDA regulations and application of GLPs and GMPs</li></ul><br>
<div></div>
<div><b>
Qualifications:</b></div>
<div>
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:</div>
<ul>
<li>Must have a BS and 7 years of pharmaceutical microbiology experience or a MS and 5 years of pharmaceutical microbiology experience. Must have 3-5 years of supervisory experience.</li>
<li>Excellent organizational and project management skills and ability to handle multiple projects.</li>
<li>Excellent writing and computer skills and ability to present data in a logical manner.</li>
<li>Excellent interpersonal communication, influencing, negotiation skills.</li>
<li>Understanding of scientific strategies and ability to invent new methods or new avenues of investigation.</li>
<li>Demonstrated effectiveness in task completion, decision making, and problem solving.</li>
<li>Working knowledge of FDA regulations, application of GLPs and GMPs. Experience interacting with personnel from regulatory agencies</li></ul><br>
<div></div>
<div><b>
Preferred Qualifications:</b></div>
<div>
Pharmaceutical Microbiology experience with injectable/aseptic manufacturing preferred.</div><br>
<div></div>
<div><b>
Compensation:</b></div>
<div>
Base Salary: $66,600 to $133,0750 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.</div><br>
<div></div>
<div><b>
What We Offer</b></div>
<ul>
<li> Clean climate-controlled working environment</li>
</ul><ul><li>Annual performance bonus potential</li>
<li>401k employer match up to 6% of your contributions</li>
<li>23 vacation/personal days</li>
<li>11 paid Company holidays</li>
<li>Generous healthcare benefits</li>
<li>Employee discount program</li>
<li>Wellbeing rewards programs</li>
<li>Safety and Quality is a top organizational priority</li>
<li>Career advancement/growth opportunities</li>
<li>Tuition Reimbursement</li>
<li>Maternity and Parental Leave</li></ul><br>
<div></div>
<div><b>
Equal Opportunity Employer:</b></div>
<div>
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.</div>
</div></div></div></div><div><div><div><div>Location:
Bedford, OH, US, 44146<br>
</div></div></div></div><p><br>
<b>Nearest Major Market: </b>Cleveland</p></div></div></div><p></p>

Supervisor, Quality Control Microbiology

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Location: Saudi Arabia, Riyadh</b></p>
<p><b>
Job Type: [Full-time]</b></p>
<div><b>
Hashtag: #LI-NA1</b></div><br>
<div></div>
<div><b>
About Us:</b></div>
<div>
For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</div><br>
<div></div>
<div>
As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.</div><br>
<div></div>
<div><b>
Description:</b></div><br>
<div></div>
<div>
We are looking for a talented <b>Project &amp; maintenance Engineer (Oncology plant) </b>to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</div><br>
<div></div>
<div>
If you want to be part of a team that cares about impact, this is the place for you.</div><br>
<div></div>
<div><b>
Key Responsibilities:</b></div><br>
<p></p>
<ul>
<li>Installation and qualification of production lines and utilities, and transition into managing the facility&rsquo;s maintenance and engineering operation.</li>
<li><b>Project Phase: </b>Oversee the installation of production machinery and industrial utilities (HVAC, Purified Water, CW, CA, BMS ..etc.) , as well as support design to manage and update layouts and technical drawings using <b>AutoCAD
</b></li><li><b>Qualification phase: </b>Support the execution of IQ/OQ/PQ protocols for Utilities and production lines.
</li><li><b>Operations: </b>Manage assets and maintenance scheduling using <b>SAP</b></li></ul><br>
<div></div>
<div>
 </div><div><b>2. Major Tasks &amp; Technical Project Management
</b></div><ul><li>Lead electrical scope for installation of new machines and production lines.</li>
<li>Manage revamping, upgrading, and modification of existing systems.</li>
<li>Execute major corrective actions and permanent engineering solutions.</li>
<li>Prepare technical specifications for electrical components and automation systems.</li>
<li>Review supplier offers and performs technical evaluations.</li>
<li>Coordinate installation, commissioning, FAT/SAT support, and qualification activities.</li>
<li>Ensure projects are delivered within timeline, scope, and compliance requirements.</li></ul><br>
<div></div>
<div><b>
3. Preventive &amp; Reliability Programs
</b></div><ul><li>Develop and optimize preventive maintenance strategies.</li>
<li>Implement predictive maintenance initiatives (thermal scanning, condition monitoring).</li>
<li>Monitor reliability KPIs (MTBF, MTTR, downtime trends).</li>
<li>Ensure proper documentation in CMMS.</li></ul><br>
<div></div>
<div><b>
4. GMP &amp; Compliance
</b></div><ul><li>Ensure compliance with GMP and pharmaceutical regulatory standards.</li>
<li>Support change control, deviation investigation, and CAPA implementation.</li>
<li>Maintain technical documentation and validation support records.</li></ul><br>
<div></div>
<div><b>
Core Competencies
</b></div><ul><li>Advanced troubleshooting and automation expertise.</li>
<li>Technical project coordination.</li>
<li>Reliability engineering mindset.</li>
<li>Leadership and decision-making capability.</li>
<li>Compliance and safety awareness.</li></ul><br>
<div></div>
<div><b>
Qualifications:</b></div>
<div><b>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</b></div><br>
<div></div>
<div><b>
Education: </b>Bachelor&rsquo;s degree in Mechanical <b>or </b>Electro-mechanical Engineering.</div>
<div><b>
Background: </b>Industrial background is a must, pharmaceutical is an advantage
</div><div><b>Skills: </b>High proficiency in AutoCAD and a strong grasp of industrial utilities (HVAC , Steam , CW , CA ...etc.)
</div><div><b>Systems: </b>Experience with SAP (Maintenance/Asset Management modules) is highly preferred.<b>
</b></div><div><b>Experience</b>: 3-5 years.</div><br>
<div></div>
<div><b>
Learn more about Hikma in KSA </b><b>hikma-ksa-factsheet-aug-2025-en.pdf</b></div>
</div></div></div></div><div><div><div><div>Location:
Riyadh, SA, 11564</div></div></div></div></div></div></div><p></p>

Maintenance & Project Engineer

<p></p><div><div><div><div><div><div><div>Description:
<div><b>Location: Saudi Arabia, Riyadh</b></div>
<div><b>
Job Type: [Full-time]</b></div>
<div><b>
Hashtag: #LI-NA1</b></div><br>
<div></div>
<div><b>
About Us:</b></div>
<div>
For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</div><br>
<div></div>
<div>
As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.</div><br>
<div></div>
<div><b>
Description:</b></div><br>
<div></div>
<div>
We are looking for a talented <b>Electrical Technician (Oncology plant) </b>to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</div><br>
<div></div>
<div>
If you want to be part of a team that cares about impact, this is the place for you.</div><br>
<div></div>
<div><b>
Key Responsibilities:</b></div><br>
<div></div>
<ul>
<li>Support the new plant project by performing electrical installations and wiring for production lines during the project phase, and provide ongoing electrical and automation support once the plant becomes operational.</li>
</ul><ul><li><b>Installation: </b>Execute electrical installation, panel connections, and support the commissioning of PLC-driven machinery.
</li><li><b>Maintenance: </b>Carry out routine inspections and repairs on different automation systems
</li><li><b>Data Entry: </b>Use <b>SAP </b>to log maintenance activities and manage spare parts.</li></ul><br>
<div></div>
<div>
 </div><div><b>Core Competencies
</b></div><ul><li>Troubleshooting and electrical expertise.</li>
<li>Safety awareness.</li>
<li>GMP and pharmaceutical regulatory standards.</li></ul><br>
<div></div>
<div><b>
Qualifications:</b></div><br>
<div></div>
<div><b>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</b></div><br>
<div></div>
<div><b>
Education: </b>Diploma degree in electrical or Industrial automation is preferred.
</div><div><b>Background: </b>Previous experience in industrial environment is a must, Previous experience in Pharmaceuticals is an advantage.
</div><div><b>Skills: </b>Ability to read electrical &amp; pneumatic schematics and troubleshoot industrial control systems.
</div><div><b>Systems: </b>Familiarity with SAP is preferred.
</div><div><b>Experience</b>: 3-5 years.</div><br>
<div></div>
<div><b>
Learn more about Hikma in KSA </b><b>hikma-ksa-factsheet-aug-2025-en.pdf</b></div><br>
<p></p>
</div></div></div></div><div><div><div><div>Location:
Riyadh, SA, 11564</div></div></div></div></div></div></div><p></p>

Electrical Technician

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Job Description:</b></p>
<ul>
<li>They fix application and system problems or any issues that are disrupting the application service that business users depend on.</li>
<li>Act as a first line support for the business users.</li>
<li>This role will be responsible for ensuring support levels from both management and users. You will need to track, solving and report support issues and search for solutions to these issues.</li>
<li>Fill the knowledge gaps in SAP modules as required for the current assignment.</li>
<li>In case of major knowledge deficits, raise reports to the corporate team.</li>
<li>Analysis support issues and take ownership of issue investigation and resolution</li>
<li>Involve in Support Pack testing.</li>
<li>Proposals or issues are escalated to the Application Support Team Leader.</li>
<li>Reporting recurring problems and suggesting their solution to the Application Support Team Leader.</li>
<li>Responsible for uploading all basic data at all SAP modules.</li>
</ul>
<p><b>Qualifications:</b></p>
<ul>
<li>Degree in Computer Science, Engineering or equivalent.</li>
<li>Minimum 2 to 4 years of hands-on experience at SAP application support in most of SAP modules.</li>
<li>Deep business functional capabilities and expertise.</li>
<li>Ability to write business documents and training manuals</li>
</ul></div></div></div></div><div><div><div><div>Location:
Giza, EG</div></div></div></div></div></div></div><p></p>

Senior IT Applications

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Job</b><br>
<b>Location:</b> Dubai, United Arab Emirates.<br>
<b>Department:</b> Medical Affairs - Biotechnology<br>
<b>Reports to:</b> Associate Director, Medical</p><br>
<p></p>
<p><b>
Job Purpose:</b></p>
<p>
The Sr MSL is a field-based medical expert role focused on developing and maintaining peer-to-peer relationships with key medical experts. This role will primarily support the company biotechnology franchise. The Sr MSL will collaborate with physicians and other medical experts to provide field observations to internal stakeholders and ensure that health care professionals have the most up to date information as the clinical development programs mature this role will be reporting to the MENA Medical Associate Director Biotechnology.</p>
<p>
This is a field-based job with 80% of the time allocated to the field and nearly 20% travel time.</p><br>
<p></p>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li>Develop and maintain peer-to-peer collaborations and relationships with key medical experts in the Biotechnology community.</li>
<li>Develop territory field medical plan and TLs Interaction plans based on therapeutic area objectives and TLs needs.</li>
<li>Support clinical development initiatives including site identification, trial recruitment, registry, and presentation of final approved data.</li>
<li>Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training, and speaker development.</li>
<li>Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders.</li>
<li>Support the medical community with up-to-date medical information, robust disease expertise, and product information.</li>
<li>Communicate clinical insights on new data to the company medical Affairs and to inform medical strategy for the assigned therapeutic area.</li>
<li>Train internal &amp; external stakeholders on key scientific and medical topics in relevant therapeutic area.</li>
<li>Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements.</li>
<li>Generate tactical regional plans to provide needs based, value-added support of the medical and scientific community in-line with company goals.</li>
<li>Uses systems to strategically map, identify, profile, and prioritize thought leaders in line with the medical plan and goals.</li>
<li>Maintain accurate reporting and documentation of MSL activities.</li>
<li>Provide medical and scientific information to respond to KOLs' technical questions about company`s product.</li>
<li>Lead meetings with KOLs to discuss relevant scientific literature and address their enquiries.</li>
<li>Make educational presentations to senior doctors and researchers, for example on clinical trial data.</li>
<li>Feed information back to marketing and sales colleagues to help develop marketing materials and commercial strategy.</li>
<li>Keep up to date with the latest scientific research and clinical data relevant to the company`s molecules.</li>
<li>Share safety information with the pharmacovigilance division.</li>
<li>Comply with all internal &amp; external regulations and codes that apply to medical, regulatory and compliance perspectives.</li>
<li>Support for the development of Medical Plans.</li>
<li>Support for management of clinical studies including Company Investigational Studies (CISs) &amp; Investigator Initiated Studies (IISs).</li>
<li>Supports product pre-launch, launch, and post-launch activities and communication plans within medical strategy and tactical plans.</li></ul><br>
<p></p>
<p><b>
Qualifications &amp; Experience:</b></p>
<ul>
<li>5-8 years of experience in the pharmaceutical industry.</li>
<li>A minimum of 2 years of experience in medical as MSL, Regulatory Affairs and/or Pharmacovigilance is preferred.</li>
<li>Business acumen courses/training is a plus.</li>
<li>Clinical research experience and GCP certification is a plus.</li>
<li>National experience is a Preferred.</li>
<li>Biotech experience is a plus.</li>
<li>Candidates must understand compliance considerations and demonstrate ability to work compliantly in a field-based role, within the medical organization, as well as across the commercial organization.</li>
</ul></div></div></div></div><div><div><div><div>Location:
Sharjah, AE</div></div></div></div></div></div></div><p></p>

Sr. Medical Science Liaison

<p></p><div><div><div><div><div><div><div>Description:
<div><b>Location:</b> Giza &ndash; 6th of October City</div>
<div><b>
Job Type:</b> [Full-time, Contract]</div>
<div><b>
Hashtag:</b> #LI-OB1</div><br>
<div></div>
<div><b>
About Us:</b></div>
<div>
For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</div><br>
<div>
</div><div>As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.</div><br>
<div>
</div><div><b>Description:</b></div><br>
<div></div>
<div>
This job is responsible for visiting doctors to promote particular products, disseminate product information and convey company messages to achieve monthly sales targets.</div><br>
<div></div>
<div><b>
Key Responsibilities:</b></div><br>
<div></div>
<ul><li>Follows all relevant Sales procedures so that work is carried out in a controlled and consistent manner.</li></ul>
<ul><li>Follows the day-to-day operations related to own job in the Sales function to ensure continuity of work.</li></ul>
<ul><li>Visits doctors in private clinics or hospitals on a daily basis to promote particular products, disseminate product information and convey company messages to achieve monthly sales target.</li></ul>
<ul><li>Collates accurate and prompt basic sales information and enters them on the CRM system on a daily basis to be revised by the Field Sales Supervisor.</li></ul>
<ul><li>Coordinates and communicates with sales representatives and direct manager on a daily basis to achieve sales targets.</li></ul>
<ul><li>Acquires the necessary knowledge of all of the company&rsquo;s products and/or services in order to help increase sales.</li></ul>
<ul><li>Complies with all relevant safety, quality, health and environmental procedures and code of conduct to ensure a healthy and safe work environment.</li></ul><br>
<div></div>
<div><b>
Qualifications:</b></div><br>
<div></div>
<div>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</div><br>
<div></div>
<ul><li>B.Sc. degree in Pharmacy or equivalent.</li></ul>
<ul><li>1 - 3 years of related experience</li></ul><br>
<div></div>
<div><b>
Learn more about Hikma in Egypt </b><b>hikma-egypt-factsheet_-en-sep-2025.pdf</b></div><br>
<div></div>
</div></div></div></div><div><div><div><div>Location:
EG</div></div></div></div></div></div></div><p></p>

Medical Representative - Injectables

Join Hikma and explore 6   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.