Laboratory Specialist Jobs in Algeria 2026

Up to 5 years Naukri Gulf

Microbiology Analyst

On-site - Algeria - Alger 21 August 2026

Manufacturing & Production

Perform microbiological analyses of raw materials, semi-finished products, finished products, stability products, and packaging materials. Conduct monitoring. Perform analyses of subcontracted products. Follow and update the stability study calendar. Perform validation of analytical methods. Execute validation of cleaning methods. Conduct microbiological control of the laboratory environment and production areas. Validate culture media. Conduct control of quality control and production laboratory personnel. Perform media fill tests. Draft and update quality control procedures, reports, and protocols. Ensure the proper functioning of quality control laboratory equipment. Contribute to the implementation of the quality assurance system and continuous improvement. Perform routine calibration and standardization activities. Collect samples of substances, pharmaceutical products, and pharmaceutical water if necessary.Desired Candidate ProfileMaster 2, Engineering degree, or Bachelor's degree +5 in microbiology, biotechnology, or a similar field. Knowledge of classical microbiological techniques and quality standards applicable in the pharmaceutical industry. Ability to work in a team, scientific rigor, and organizational skills. Good command of IT tools and laboratory management software. Strict adherence to laboratory procedures and safety regulations. Excellent analytical, synthesis, and written communication skills.

3 to 6 years Naukri Gulf

Quality Laboratory Technician

On-site - Algeria - Alger 19 June 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph"><ul> <li>Quality Laboratory Technician</li><li> </li><li>Perform quality controls in accordance with internal procedures.</li> <li>Perform analyses and controls of raw materials, work-in-progress products and finished products. </li> <li>Ensure the monitoring, recording and traceability of results. </li> <li>Identify and report non-conformities. </li> <li>Participate in corrective actions and continuous improvement. </li> <li>Ensure compliance with quality standards, hygiene and good practices. </li> <li>Maintain the organization and smooth operation of the laboratory.</li> </ul> <ul> <li>Training in Biology, Chemistry, Quality Control, Laboratory or similar field. </li> <li>Prior experience in the pharmaceutical industry or in a laboratory is an asset. </li> <li>Rigour, organizational skills and analytical mind. </li> <li>Ability to work in a team. </li> <li>My mastery of office software.</li> </ul> <ul> <li>A professional and evolving work environment. </li> <li>An opportunity to join a dynamic team. </li> <li>Support for integration. </li> <li>Transport assured</li> </ul>S tif Ouled Sabor</div></section>

Bayt

Technical Support Consultant

Remote - Algeria 29 July 2026

Customer Service

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Who are we? SupportYourApp is a global Intelligent Support-as-a-Service leader, partnering with tech companies and industry leaders like MasterCard, Calm and MacPaw in 30+ countries since 2010 to deliver secure customer and technical support. We operate globally, supporting clients in 60 languages across diverse industries. So what if you had a chance to be a part of the world’s leading SaaS, software, or hardware solutions? Join our community as a Technical Support Consultant today and thrive in a multicultural and multilingual environment while enjoying your home office. Unlock your potential by mastering new skills and achieving challenging goals in cooperation with our People First management approach. Excited? Let’s see what it takes. What you will do: Deliver outstanding technical support via chats and emails; Manage customer support tickets and maintain a 24-hour response SLA; Attend regular engineering planning sessions to stay informed on upcoming releases, migrations and product changes; Prepare and lead recurring support retrospectives, identifying customer trends and helping Engineering prioritize improvements; Review AI chatbot conversations and optimize Inkeep rules, workflows and responses to improve support quality; Maintain and improve customer-facing documentation and self-service resources in GitBook; Improve support systems and processes, including Zendesk workflows, automations and Linear ticket management; Keep up with evolving tools and technology; Handle sensitive customer data with care and security; Apply the latest and greatest customer happiness practices; Maintain deep understanding of client solutions and meet KPI. What you need to succeed in this role: Excellent English communication skills (at least C1 for both spoken and written); At least 1–2 years of proven experience in a Technical Support role; Experience translating technical issues for non-technical users (high EQ); Experience reproducing and troubleshooting complex technical issues using browser tools, logs, and changelogs; Solid understanding of engineering workflows, including releases, migrations, and potential user impact; Ability to clearly distinguish product bugs from user environment issues and third-party limitations; Experience escalating incidents with structured documentation (impact, timeline, reproduction steps); Experience reading logs (e. g, Jason) in tools like Grafana; Familiarity with marketplace or reselling platforms AI-first mindset, using AI tools to reduce repetitive work and improve support efficiency Hands-on experience with Zendesk and Linear (or similar ticket-tracking systems); Strong organizational skills, including tracking patterns, running retrospectives, and turning insights into actionable feedback; Personal computer (at least 8Gb of RAM) with a stable internet connection (minimum 50 Mbps–download and 40 Mbps–upload). Will be a great plus: Experience with CRM systems; Familiarity with reselling/marketplace platforms. Benefits: Fixed schedule : Monday–Tuesday, Friday from 9 AM–5 PM, and Wednesday–Thursday 12 PM–8 PM, EDT; Opportunity to cooperate fully remotely; Inclusive international environment; Compensation in USD; Rewards for referring friends; Balance between project workload and personal time, but also – internal health policy; Responsive leadership interested in your development and long-lasting cooperation; Greenhouse conditions for self-development; A culture built on trust, with no time-tracking requirements. *The items listed in this section may vary depending on the terms of your engagement. Certain benefits and conditions typically apply to employees; independent contractors may not be eligible for all of these. The specific terms, including compensation, benefits, and work conditions, will be clearly defined in your agreement if selected. You can learn more about the company and its culture by visiting our official website and social pages on Facebook, Instagram, and LinkedIn. So if you're a proactive Support Specialist who thrives on solving problems, ensuring customer satisfaction, and delivering outstanding service, don't miss this opportunity and send us your CV in English to collaborate with us! Over 1500+ specialists who already deliver exceptional customer experiences collaborating with SupportYourApp. Know someone perfect for the role? Refer them and get rewarded! We adhere to the principles of equal treatment of candidates and prohibit discrimination on any grounds protected by law. Your personal data will be processed as described in the SupportYourApp Candidate Privacy Notice . Internal job code: 3G3 </div>

1 to 5 years Naukri Gulf

Chemist Engineer

On-site - Algeria - Alger 28 July 2026

Engineering

Execute analysis and control work on precious metal samples and others, baths, treated effluents within workshops or from third-party organizations. Return products (waste or others) to the store. Control the adjustment of laboratory equipment parameters. Ensure the cleaning of laboratory equipment and utensils at the end of the shift. Report equipment and laboratory material breakdowns and/or stoppages. Respect the safety rules and instructions in force within the unit. Make proposals for the improvement of the quality of the work environment and others. Take charge of the expertise of precious metals. Execute any task entrusted by management.Desired Candidate ProfileMaster's degree (Bac +5) and experience in a similar role. If you meet these requirements, please submit your CV by clicking on the "Apply" tab.

1 to 5 years Naukri Gulf

Physico-Chemical Analyst

On-site - Algeria - Alger 20 August 2026

Engineering

Perform physicochemical analyses according to established protocols within the framework of pharmaceutical and medical production. Participate in the implementation and optimization of analytical methods in collaboration with the methods department. Ensure quality control of raw materials, in-process products, and finished products. Write accurate and detailed analysis reports, respecting standards and regulatory requirements. Contribute to the maintenance and calibration of laboratory equipment. Collaborate closely with production and research teams to guarantee product conformity. Ensure compliance with hygiene, safety, and good laboratory practices.Desired Candidate Profile<ul><li>Master's degree (Master 2), Engineering degree or equivalent (Bac +5) in Chemistry,</li><li>Knowledge of physico-chemical analysis techniques (chromatography, spectroscopy, titration, etc.).</li><li>Mastery of computer tools and laboratory management software.</li><li>Ability to work in a team, sense of organization and scientific rigor.</li><li>Good written and oral communication skills in French; knowledge of English is a plus.</li><li>Strict adherence to quality, safety and confidentiality standards.</li></ul>

1 to 5 years Naukri Gulf

Physico-Chemical Analyst

On-site - Algeria - Alger 20 August 2026

Engineering

Perform physicochemical analyses according to established protocols within the framework of pharmaceutical and medical production. Participate in the implementation and optimization of analytical methods in collaboration with the methods department. Ensure quality control of raw materials, in-process products, and finished products. Write accurate and detailed analysis reports, respecting standards and regulatory requirements. Contribute to the maintenance and calibration of laboratory equipment. Collaborate closely with production and research teams to guarantee product conformity. Ensure compliance with hygiene, safety, and good laboratory practices.Desired Candidate Profile<ul><li>Master's degree (Master 2), Engineering degree or equivalent (Bac +5) in Chemistry,</li><li>Knowledge of physico-chemical analysis techniques (chromatography, spectroscopy, titration, etc.).</li><li>Mastery of computer tools and laboratory management software.</li><li>Ability to work in a team, sense of organization and scientific rigor.</li><li>Good written and oral communication skills in French; knowledge of English is a plus.</li><li>Strict adherence to quality, safety and confidentiality standards.</li></ul>

1 to 5 years Naukri Gulf

Physico-Chemical Analyst

On-site - Algeria - Alger 20 August 2026

Engineering

Perform physicochemical analyses according to established protocols within the framework of pharmaceutical and medical production. Participate in the implementation and optimization of analytical methods in collaboration with the methods department. Ensure quality control of raw materials, in-process products, and finished products. Write accurate and detailed analysis reports, respecting standards and regulatory requirements. Contribute to the maintenance and calibration of laboratory equipment. Collaborate closely with production and research teams to guarantee product conformity. Ensure compliance with hygiene, safety, and good laboratory practices.Desired Candidate Profile<ul><li>Master's degree (Master 2), Engineering degree or equivalent (Bac +5) in Chemistry,</li><li>Knowledge of physico-chemical analysis techniques (chromatography, spectroscopy, titration, etc.).</li><li>Mastery of computer tools and laboratory management software.</li><li>Ability to work in a team, sense of organization and scientific rigor.</li><li>Good written and oral communication skills in French; knowledge of English is a plus.</li><li>Strict adherence to quality, safety and confidentiality standards.</li></ul>

2 to 4 years Naukri Gulf

Head of Quality Control Laboratory Soci t de Production Pharmaceutique

On-site - Algeria - Alger 9 June 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph"><ul> <li>Validates and approves the analysis results of raw materials upon their arrival in the store, products in progress and finished products. </li> <li>Informs his hierarchical superior in order to reject the raw material upon receipt or to stop production if the materials or products do not conform to official standards, or if there are interactions between the different components. </li> <li>Supervises the tests carried out by chemists working under his authority, who are required to verify and evaluate the quality and compliance with the relevant regulations. </li> <li>S ensures the diffusion of the active ingredient in the body and searches for possible impurities in the raw materials or degradation products by testing the product under extreme conditions. </li> <li>Verifies the reliability of raw data, analyzes trends and proposes corrective or preventive and/or improvement actions. </li> <li>Ensures strict compliance with GMP and GLP, and HSE rules within the laboratory. </li> <li>S ensures the metrological monitoring of the control equipment. </li> <li>Establishes and monitors the effective application of the directives, rules, operating methods and procedures in force for the laboratory's activities. </li> <li>Ensures proper management of stocks of reagents, culture media and laboratory consumables. </li> <li>Participates in the development of action plans, their implementation and their monitoring. </li> <li>Detects and reports all anomalies and proposes corrective and/or preventive actions. </li> <li>Develops, maintains and distributes to various users the documentation relating to the specifications. </li> <li>Directs and coordinates the various activities of the laboratory. </li> <li>D defines action programs designed to improve the laboratory's performance and implements measures to achieve greater efficiency in the activity. </li> <li>Signs the analysis reports and ensures their transmission.</li> </ul> <ul> <li> Basic training: State engineer / Master 2 in analytical and microbiological chemistry or equivalent.</li> <li> Professional training: Quality control of pharmaceutical products, MS Office, pharmaceutical analysis laboratory equipment, metrology.</li> </ul> </div></section>

1 to 3 years Naukri Gulf

Quality Control Engineer

On-site - Algeria - Alger 31 July 2026

Manufacturing & Production

Perform in-process quality controls (In Process) according to cosmetic GMP (ISO 22716). Water parameter control: Perform regular analyses (pH, hardness, conductivity, etc.) of treated water. Transmit samples to the laboratory for microbiological testing. Record test results and corrective actions. Verify the conformity of raw materials, semi-finished products, and finished products on the manufacturing and packaging lines. Perform controls: visual inspection, pH, viscosity, density, weight, PF & PSF moisture. Monitor treated water analysis and report anomalies. Collect and correctly identify samples according to the control plan. Release PSF after analysis. Prepare PSF, PF & treated water samples. Contact external laboratory for analysis needs. Monitor and control reports and sheets prepared by packaging controllers. Fill in and validate control records in real-time. Immediately report any anomaly or non-conformity and block production if necessary. Verify the batch file in terms of physico-chemical & microbiological control sheets of (PSF, PF). Classification of samples from produced batches in the sampling room.Desired Candidate ProfileResponsibilities: Guarantee the reliability and accuracy of controls performed during production. Ensure complete traceability of controls and samplings. Respect quality, safety, and hygiene procedures in the production area. Participate in investigations in case of detected non-conformity. Contribute to corrective and preventive actions (CAPA) related to In-Process control. Be versatile in the laboratory, perform multiple laboratory functions, be flexible and able to switch from one activity to another according to priorities, while respecting quality and safety standards.Authorities: Authority to stop an ongoing operation if a non-conforming product is detected. Authority to report any non-conformity or deviation to Quality and Production managers.Required Skills and Knowledge: Knowledge of Good Manufacturing Practices (ISO 22716). Mastery of physico-chemical and visual quality controls during production. Knowledge of cosmetic manufacturing and packaging processes. Notions of hygiene, health, and safety at work (HSE). Ability to detect and report deviations quickly. Analytical mind, rigor, and precision.Training & Experience: Bac +3 in Chemistry, Biology, or equivalent. Experience in quality control in cosmetic, pharmaceutical, or agri-food production desired (1-2 years). Training in cosmetic GMP and workplace safety.Necessary medical examinations: Hiring medical visit (aptitude for handling materials and products). Periodic medical visits according to regulations and job type.

Bayt

Medical Science Liaison

On-site - Algeria 27 June 2026

Sales

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.  Summary We are seeking a highly motivated and scientifically driven professional to join our team as a Medical Science Liaison / Scientific Affairs Specialist. In this role, you will act as a trusted scientific partner, providing expert medical and product knowledge to internal and external stakeholders. You will engage with healthcare professionals, key opinion leaders (KOLs), and scientific communities to exchange insights, interpret clinical data, and support evidence-based decision-making. The ideal candidate brings strong scientific acumen, excellent communication skills, and the ability to navigate complex medical environments while maintaining the highest standards of ethics and compliance. Essential Duties & Responsibilities <ul><li>Maintain a strong understanding of clinical conditions, disease states, therapies, treatment landscapes, and guidelines </li><li>Critically evaluate medical literature and clinical evidence, translating complex data into clear, balanced insights </li><li>Establish and maintain effective relationships with KOLs, healthcare professionals, scientific societies, and regulatory authorities </li><li>Act as a credible scientific resource, supporting evidence exchange both internally and externally </li><li>Gather and analyze insights on scientific, clinical, and industry trends through various engagement channels </li><li>Communicate complex scientific information in a clear, concise, and structured manner to diverse audiences </li><li>Collaborate cross-functionally across departments, regions, and stakeholders to achieve shared goals </li><li>Support internal teams with scientific and product expertise across a broad range of activities </li><li>Contribute to strategic decision-making and provide solutions to complex challenges within scope of responsibility </li><li>Ensure compliance with policies and regulations, contributing to patient safety and company integrity </li><li>Build strong, trust-based relationships with stakeholders, positioning the company as a valued partner </li><li>Demonstrate adaptability, agility, and a proactive approach to professional development </li><li>Travel extensively (up to 70%) to support field engagement and stakeholder interactions </li></ul> Qualifications & Experience <ul><li>Bachelor’s degree (or equivalent) in health, medical, or life sciences </li><li>Minimum of 3 years’ experience in a hospital setting, pharmaceutical, or medical device industry </li><li>Strong knowledge of clinical environments, disease states, and treatment practices </li><li>Proven ability to evaluate and interpret scientific and clinical data </li><li>Excellent communication and presentation skills with the ability to adapt style to different audiences </li><li>Strong collaboration and teamwork capabilities across multidisciplinary and multicultural environments </li><li>Demonstrated decision-making skills with a focus on risk mitigation and compliance </li><li>High level of integrity, ethics, and professionalism </li><li>Business acumen and strategic mindset </li><li>Self-motivated, agile, and eager to learn and grow </li></ul> Languages: <ul><li>Excellent written and verbal communication skills in French, English, and Arabic </li></ul> Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. </div>

Naukri Gulf

Chemist

On-site - Algeria - Alger 15 June 2026

Engineering

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Perform laboratory analyses. Check product conformity. Write analysis reports. Comply with safety standards.</div></section><section>Desired Candidate ProfileBachelor's degree (Bac+3) or Master's degree (Bac+5) in Chemistry. Rigor, precision and analytical skills.</section>

Naukri Gulf

Pharmacy Preparer

On-site - Algeria - Alger 22 June 2026

Logistics, Supply Chain & Procurement

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Prepare different batches of medications. Know and identify the different products of the production unit and the associated manufacturing and packaging processes. Identify the characteristics of the products to be manufactured (liquid, dry, and paste forms) and the various raw materials. Proceed with cleaning the tank and filling it with osmosis water, start the preparation with agitation, and finally take a sample for laboratory analysis. Supply with raw material and identify the conformity of a product or raw material with respect to the given specifications (laboratory analysis test). Identify the roles of the different components of the product(s) to be manufactured. Identify the steps of the entire manufacturing process. Identify the equipment and peripherals used in his activity. Report any deviation in the process and immediately inform his hierarchy. Establish the link between the characteristics of the raw materials and the observed malfunctions. Execute the tasks of his work by strictly applying the procedures, GMP and hygiene and safety rules. Diagnose, intervene and propose corrective actions adapted in case of anomaly, deviation or malfunction on the manufacturing equipment used within his scope of competence and authorization.</div></section><section>Desired Candidate ProfileLicense or Master 1 in Chemistry, Biology or Process Engineering or equivalent. Knowledge of GMP and GLP standards and notions in metrology. Professional experience desirable. Male profile.</section>

Naukri Gulf

Production Concrete Agent

On-site - Algeria - Alger 11 June 2026

Logistics, Supply Chain & Procurement

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Follow and control the daily production of concrete (batching, quantity, quality). Ensure traceability of deliveries (production orders, delivery notes). Ensure compliance with technical specifications (formulation, temperature, delivery time). Communicate with site teams to coordinate needs.</div></section><section>Desired Candidate ProfileTraining in civil engineering, laboratory, or equivalent experience in concrete production. Rigor, organizational skills, reactivity.</section>

1 to 6 years Naukri Gulf

Pharmacist Assistant

On-site - Algeria - Alger 5 August 2026

Sales

Draft pharmaceutical dossiers in collaboration with the Pharmaceutical Administration Department (DAR). Draft and prepare technical release dossiers. Ensure coordination with the National Laboratory for the Control of Pharmaceutical Products (LNCPP) for batch release. Draft and implement procedures related to your activity. Ensure compliance with Good Practices and that all company activities comply with current pharmaceutical regulations. Report on your activities to the Technical Director Pharmacist and propose improvements as needed. Participate in the implementation of the quality policy, the development and management of the quality system. Provide scientific and regulatory expertise to the relevant departments: development, quality, production, marketing, and sales. Participate in the implementation of necessary changes (change management procedure). Conduct investigations at the production and laboratory levels following reported anomalies and non-compliant results. Participate in the handling of complaints and pharmacovigilance cases. Verify and monitor batch records. Participate in regulatory and informational monitoring. Draft and update specifications (PA, PF and excipients).Desired Candidate ProfileDoctor of PharmacyExperience in a similar position

Naukri Gulf

Stock and Supply Manager

On-site - Algeria - Alger 4 June 2026

Logistics, Supply Chain & Procurement

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Ensures the design and maintenance of an input database. Coordinates annual and multi-year forecasts for all factory purchases. Ensures the purchase of raw materials, packaging items, spare parts, consumables, laboratory reagents, etc. Adjusts procurement programs within the framework of stock regulation. Ensures that all purchases comply with quality, price, and deadline requirements. Ensures the proper management of operations related to the preparation of import files (bank domiciliation, transit) when requested. Organizes the supply chain, sets up a delivery schedule, and maintains permanent contact with suppliers.</div></section><section>Desired Candidate ProfileBasic training: Bachelor's or Master's degree in management/economics or equivalent. Professional training: general management, MS Office, Sage, implemented management software.</section>

1 to 3 years Naukri Gulf

Chef de Partie

On-site - Algeria - Alger 6 August 2026

Administration

Prepare ingredients and carry out preparations according to recipes. Respect manufacturing procedures and HACCP standards. Ensure the tidiness and cleaning of the laboratory. Control the quality of raw materials and preparations. Participate in stock management.Desired Candidate Profile1 year of experience in food preparation is desired. Sense of organization and speed of execution. Respect for hygiene rules.

5 to 10 years Naukri Gulf

General Dentist

On-site - Algeria - Alger 29 July 2026

Healthcare & Medical

Perform consultations, clinical examinations, and diagnoses. Carry out current conservative and surgical dental care. Design, prepare, and place fixed prostheses (crowns, bridges, veneers, etc.). Develop treatment plans adapted to patient needs. Ensure post-treatment follow-up and oral health prevention. Collaborate with the prosthetics laboratory and other health professionals.Desired Candidate Profile<ul><li>Diploma of Doctor of Dental Medicine.</li><li>Minimum 5 years of experience in a dental practice or clinic.</li><li>Excellent mastery of fixed prosthetics.</li><li>Registration with the Order of Dental Surgeons (if applicable).</li></ul>

1 to 6 years Naukri Gulf

Laboratory and Chemical Products Engineer

On-site - Algeria - Alger Tuesday

Engineering

Participate in the control and validation of the construction plan. Participate in the formalization of all documents related to testing, commissioning & startup. Participate in monitoring the project execution schedule. Participate in the overall physical progress of project activities. Participate in controlling the application of HSE procedures on the construction site. Control the establishment of temporary infrastructures related to construction (camps & work execution means). State Engineer Laboratory & Chemical Products Corrosion Inspection. Mastery of the English language is desirable. Experience in the Oil and Gas sector.Desired Candidate Profile

1 to 5 years Naukri Gulf

Inventory and Supply Manager

On-site - Algeria - Alger 27 July 2026

Logistics, Supply Chain & Procurement

Ensures the design and maintenance of an input database. Coordinates annual and multi-year forecasts for all factory purchases. Ensures the purchase of raw materials, packaging items, spare parts, consumables, laboratory reagents, etc. Ensures the adjustment of supply programs within the framework of stock regulation. Ensures that all purchases comply with quality, price, and deadline requirements. Ensures the proper management of operations related to the preparation of import files (bank domiciliation, transit) when requested. Organizes the supply chain, sets up a delivery schedule, and maintains permanent liaison with suppliers.Desired Candidate ProfileBasic training: Bachelor's or Master's degree in management/economics or equivalent. Professional training: general management, MS Office, Sage, implemented management software.

1 to 6 years Naukri Gulf

HSE Supervisor

On-site - Algeria - Alger 10 August 2026

Research & Development

Main duties: Ensure the implementation, monitoring, and improvement of Hygiene, Safety, and Environment (HSE) systems in accordance with regulatory, normative (ISO 22716), and internal requirements, in order to guarantee the protection of personnel, products, and the environment. Responsibilities: Hygiene and GMP (ISO 22716) Supervise the application of hygiene rules in production areas. Ensure compliance of HSE practices with cosmetic GMP. Raise staff awareness of good hygiene practices and safe behaviors. Safety Identify, assess, and control occupational risks. Monitor prevention and safety plans. Check personal protective equipment (PPE). Manage emergency situations (fire, accident, evacuation). Environment: Ensure the monitoring of discharges, waste, and effluents in accordance with regulations. Implement actions to reduce environmental impacts. Contribute to the sustainable management of resources. Management and Monitoring: Organize and conduct internal HSE audits. Develop and monitor HSE performance indicators. Ensure ongoing HSE training and awareness for staff. Propose and manage corrective and preventive actions. Responsibilities related to staff health: Organize and monitor pre-employment and periodic medical examinations in collaboration with occupational health services. Monitor the application of hygiene rules and the use of personal protective equipment (PPE). Define and monitor procedures for preventing occupational risks (chemical, physical, ergonomic, biological). Supervise awareness campaigns on health, hygiene, and safety at work. Authority to order the cessation of any activity deemed dangerous to personnel or the environment. Authority to demand the immediate implementation of corrective and preventive HSE actions. Authority to conduct or supervise HSE audits and incident follow-up. Required Skills and Knowledge: Proficiency in Good Manufacturing Practices (ISO 22716) and HSE standards. Knowledge of health, safety, and environmental regulations. Risk identification, assessment, and management techniques. Knowledge of safety procedures in the laboratory, production, and logistics. Proficiency in HSE document management and audit tools. Analytical skills, rigor, and decision-making ability. Ability to train and raise awareness among staff. Training & Experience: Hygiene, Safety, Environment, Chemistry, or equivalent. HSE experience in an industrial, cosmetic, pharmaceutical, or food processing environment preferred (1 year). GMP training in cosmetics and occupational safety recommended. Medical examinations required: Pre-employment and periodic medical check-ups for all staff in conjunction with occupational health services.Monitoring of skills for high-risk positions according to regulations and the nature of the work. Documentation to be known: Normative and regulatory: ISO 22716 (Good Manufacturing Practices for Cosmetics), current regulations (safety, hygiene, and environment). Internal: Quality Manual and Company Quality Policy, internal HSE procedures (prevention, safety, waste management, PPE management), incident, accident, and risk management procedures, internal and external audit procedures, HSE records (incident reports, control sheets, indicators), performance indicators (KPIs): Accident and incident rate among staff, compliance with HSE procedures by different departments, number of HSE audits carried out and conformity of corrective actions, percentage of staff trained in HSE rules, compliance with ISO 22716 standards and current regulations. Workplace: factory located in Ouled Moussa, Boumerdes province, AlgiersDesired Candidate Profile<ul><li>Hygiene, Safety, Environment, Chemistry, or equivalent.</li><li>HSE experience in an industrial, cosmetic, pharmaceutical or agri-food environment preferred (1 year).</li><li>Training in GMP cosmetics and occupational safety recommended.</li><li>Mastery of Good Manufacturing Practices (ISO 22716) and HSE standards.</li><li>Knowledge of regulations concerning hygiene, safety and the environment.</li><li>Risk identification, assessment and management techniques.</li><li>Knowledge of safety procedures in laboratory, production and logistics.</li><li>Mastery of HSE document management and audit tools.</li><li>Analytical mind, rigor and decision-making ability.</li><li>Staff training and awareness capabilities.</li></ul>

Laboratory Specialist Jobs in Algeria

Microbiology Analyst

Quality Laboratory Technician

Technical Support Consultant

Chemist Engineer

Physico-Chemical Analyst

Physico-Chemical Analyst

Physico-Chemical Analyst

Head of Quality Control Laboratory Soci t de Production Pharmaceutique

Quality Control Engineer

Medical Science Liaison

Chemist

Pharmacy Preparer

Production Concrete Agent

Pharmacist Assistant

Stock and Supply Manager

Chef de Partie

General Dentist

Laboratory and Chemical Products Engineer

Inventory and Supply Manager

HSE Supervisor

Site Owners

Employers

Job Seekers

Laboratory Specialist Jobs in Algeria

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