1 848 Pharmaceuticals jobs in Bahrain
Regulatory Affairs Manager - Pharmaceuticals
89012 Al Seef
BHD90000 Annually
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Posted 1 day ago
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Job Description
Our client, a rapidly expanding pharmaceutical company committed to developing innovative healthcare solutions, is seeking a highly skilled and experienced Regulatory Affairs Manager to join their esteemed team in Salmabad, Northern, BH . This pivotal role requires a strategic thinker with a comprehensive understanding of global pharmaceutical regulations and a proven ability to navigate complex submission processes. You will be responsible for developing and implementing regulatory strategies, ensuring compliance with all relevant health authority requirements, and managing the submission of new drug applications and variations. Key responsibilities include preparing and reviewing regulatory documentation, liaising with regulatory agencies, providing regulatory guidance to cross-functional teams, and staying abreast of evolving regulatory landscapes. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Life Sciences, or a related field, along with at least 7 years of progressive experience in pharmaceutical regulatory affairs. Demonstrable experience with major regulatory bodies such as the FDA, EMA, and other international agencies is essential. Excellent written and verbal communication skills, strong analytical capabilities, and meticulous attention to detail are paramount. The ability to manage multiple projects simultaneously, prioritize effectively, and work collaboratively within a team environment is crucial. This role offers an exciting opportunity to contribute to the successful launch of groundbreaking pharmaceutical products and to influence regulatory policy. Our client values a proactive approach to problem-solving and a commitment to ethical practices. This hybrid role combines the benefits of in-office collaboration with the flexibility of remote work, offering a balanced work environment. We are looking for a leader who can champion regulatory excellence and drive compliance throughout the organization. If you are a dedicated professional passionate about shaping the future of medicine through strategic regulatory management, we encourage you to apply.
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0
Clinical Research Associate - Pharmaceuticals
2602 Al Malikiyah, Northern
BHD70000 Annually
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Posted 4 days ago
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Our client, a prominent pharmaceutical company, is looking for a dedicated and detail-oriented Clinical Research Associate (CRA) to contribute to groundbreaking drug development efforts. This role, based in Hidd, Muharraq, BH , will involve overseeing and managing clinical trials, ensuring adherence to protocols, regulatory guidelines, and Good Clinical Practice (GCP). The CRA will play a vital part in the entire trial lifecycle, from site selection and initiation to monitoring and close-out. Responsibilities include conducting site visits to assess patient safety, data accuracy, and regulatory compliance, developing and implementing study protocols, managing trial documentation, and collaborating with investigators, study coordinators, and other stakeholders. The successful candidate will possess excellent analytical skills, meticulous attention to detail, and strong organizational abilities. This position requires a solid understanding of clinical trial processes, pharmaceutical industry regulations, and medical terminology. The ability to travel to clinical sites is essential for this hybrid role. We are seeking professionals who are passionate about advancing medical treatments and improving patient outcomes. You will have the opportunity to work on diverse therapeutic areas and contribute to the development of life-saving medications. The ideal candidate is proactive, a problem-solver, and committed to ethical research practices. Join a forward-thinking organization that values innovation and invests in its employees' growth. This role offers a competitive salary and benefits package, along with the chance to make a significant impact in the pharmaceutical sector from our base in Hidd, Muharraq, BH .
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1
Clinical Research Scientist (Pharmaceuticals)
5432 Zallaq, Southern
BHD95000 Annually
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Posted 4 days ago
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Our client, a groundbreaking pharmaceutical company at the forefront of medical innovation, is seeking a highly specialized Clinical Research Scientist to join their fully remote research and development team. This critical role will focus on designing, implementing, and monitoring clinical trials to evaluate the safety and efficacy of novel pharmaceutical compounds. You will be responsible for a wide range of activities, including protocol development, data analysis, regulatory submissions, and scientific publications. The ideal candidate will possess a deep understanding of clinical trial methodologies, pharmaceutical development processes, and relevant regulatory guidelines.
As a Clinical Research Scientist, you will collaborate with a multidisciplinary team of clinicians, statisticians, and regulatory affairs specialists to advance drug candidates through the development pipeline. Your ability to interpret complex scientific data, contribute to study design, and ensure the ethical and scientific integrity of clinical research is paramount. This is a fully remote position that demands exceptional analytical skills, strong communication abilities, and a meticulous approach to scientific research. You will contribute to significant advancements in healthcare by bringing life-saving therapies to patients.
Key Responsibilities:
As a Clinical Research Scientist, you will collaborate with a multidisciplinary team of clinicians, statisticians, and regulatory affairs specialists to advance drug candidates through the development pipeline. Your ability to interpret complex scientific data, contribute to study design, and ensure the ethical and scientific integrity of clinical research is paramount. This is a fully remote position that demands exceptional analytical skills, strong communication abilities, and a meticulous approach to scientific research. You will contribute to significant advancements in healthcare by bringing life-saving therapies to patients.
Key Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific validity and regulatory compliance.
- Oversee the conduct of clinical trials, including site selection, monitoring, and data management.
- Analyze clinical trial data, interpret results, and prepare comprehensive reports.
- Collaborate with biostatisticians to develop statistical analysis plans.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Author scientific manuscripts for publication in peer-reviewed journals.
- Stay abreast of the latest scientific literature, clinical advancements, and regulatory updates in the pharmaceutical industry.
- Manage relationships with external investigators, key opinion leaders, and contract research organizations (CROs).
- Ensure adherence to Good Clinical Practice (GCP) guidelines and other relevant regulations.
- Provide scientific and technical expertise to cross-functional teams.
- Ph.D. or Master's degree in Pharmacology, Medicine, Biology, or a related life science field.
- Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
- Proven experience in designing and managing clinical trials (Phase I, II, or III).
- In-depth knowledge of drug development processes and regulatory affairs (e.g., FDA, EMA).
- Strong analytical and statistical interpretation skills.
- Excellent written and verbal communication skills, with a track record of scientific publications.
- Ability to work independently and effectively in a remote team environment.
- Proficiency in clinical data management systems and statistical software.
- Strong project management and organizational skills.
- Passion for scientific discovery and improving patient outcomes.
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2
Clinical Research Associate (Pharmaceuticals)
BH-609 Galali
BHD70000 Annually
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Posted 4 days ago
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Our client, a renowned pharmaceutical company dedicated to improving patient lives through innovative therapies, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in Sanad, Capital, BH . This is an essential on-site role where you will play a pivotal part in the successful execution of clinical trials, ensuring data integrity and adherence to regulatory standards.
As a CRA, you will be responsible for monitoring clinical trial sites, verifying the accuracy and completeness of data, and ensuring that trials are conducted according to protocol, Good Clinical Practice (GCP) guidelines, and other applicable regulations. Your duties will include site initiation visits, routine monitoring visits, and close-out visits. You will build strong relationships with investigators and site staff, providing them with the necessary support and guidance to ensure smooth trial operations. This role requires excellent organizational skills, attention to detail, and the ability to manage multiple tasks simultaneously. You will also be responsible for resolving data queries, ensuring timely submission of trial-related documentation, and reporting any adverse events or protocol deviations.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A minimum of 3-5 years of direct experience as a CRA in the pharmaceutical industry is required. Thorough understanding of clinical trial processes, GCP, ICH guidelines, and regulatory requirements is essential. Excellent communication, interpersonal, and problem-solving skills are necessary to effectively interact with site personnel, internal teams, and regulatory authorities. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. The ability to travel to assigned clinical sites as needed is a prerequisite for this position.
This is a fantastic opportunity to contribute to meaningful clinical research and advance your career within a leading pharmaceutical organization. Our client is committed to fostering a collaborative work environment and supporting the professional development of its employees. If you are a dedicated professional with a passion for clinical research and a commitment to upholding the highest ethical and scientific standards, we encourage you to apply for this exciting opportunity in Sanad, Capital, BH .
As a CRA, you will be responsible for monitoring clinical trial sites, verifying the accuracy and completeness of data, and ensuring that trials are conducted according to protocol, Good Clinical Practice (GCP) guidelines, and other applicable regulations. Your duties will include site initiation visits, routine monitoring visits, and close-out visits. You will build strong relationships with investigators and site staff, providing them with the necessary support and guidance to ensure smooth trial operations. This role requires excellent organizational skills, attention to detail, and the ability to manage multiple tasks simultaneously. You will also be responsible for resolving data queries, ensuring timely submission of trial-related documentation, and reporting any adverse events or protocol deviations.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A minimum of 3-5 years of direct experience as a CRA in the pharmaceutical industry is required. Thorough understanding of clinical trial processes, GCP, ICH guidelines, and regulatory requirements is essential. Excellent communication, interpersonal, and problem-solving skills are necessary to effectively interact with site personnel, internal teams, and regulatory authorities. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. The ability to travel to assigned clinical sites as needed is a prerequisite for this position.
This is a fantastic opportunity to contribute to meaningful clinical research and advance your career within a leading pharmaceutical organization. Our client is committed to fostering a collaborative work environment and supporting the professional development of its employees. If you are a dedicated professional with a passion for clinical research and a commitment to upholding the highest ethical and scientific standards, we encourage you to apply for this exciting opportunity in Sanad, Capital, BH .
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3
Clinical Research Scientist - Pharmaceuticals
604 Al Muharraq
BHD7200 Annually
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Posted 4 days ago
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Job Description
Our client, a leading biopharmaceutical company, is seeking a highly motivated Clinical Research Scientist to join their expanding research and development division. This role offers a unique opportunity to contribute to cutting-edge drug development programs. You will be responsible for the design, execution, and interpretation of clinical trials, ensuring adherence to scientific protocols and regulatory guidelines. Key duties include developing clinical study protocols, managing investigator sites, overseeing data collection and analysis, and preparing comprehensive study reports.
The successful candidate will collaborate closely with cross-functional teams, including regulatory affairs, data management, biostatistics, and medical affairs, to ensure the successful progression of clinical programs. You will also be involved in presenting research findings at scientific meetings and contributing to publications in peer-reviewed journals. A critical aspect of this role is staying abreast of the latest scientific advancements and therapeutic trends within the pharmaceutical industry.
We are looking for individuals with a Ph.D. or Master's degree in a relevant scientific discipline (e.g., pharmacology, biology, medicine) and a minimum of 5 years of experience in clinical trial management and drug development. Strong understanding of GCP (Good Clinical Practice) and relevant regulatory requirements (e.g., FDA, EMA) is essential. Excellent analytical, communication, and interpersonal skills are required to effectively interact with internal stakeholders and external investigators. This hybrid role offers a blend of office-based collaboration and remote work flexibility, located in the strategic area of Sitra, Capital, BH . Join us and be part of a team that is committed to bringing life-changing therapies to patients.
The successful candidate will collaborate closely with cross-functional teams, including regulatory affairs, data management, biostatistics, and medical affairs, to ensure the successful progression of clinical programs. You will also be involved in presenting research findings at scientific meetings and contributing to publications in peer-reviewed journals. A critical aspect of this role is staying abreast of the latest scientific advancements and therapeutic trends within the pharmaceutical industry.
We are looking for individuals with a Ph.D. or Master's degree in a relevant scientific discipline (e.g., pharmacology, biology, medicine) and a minimum of 5 years of experience in clinical trial management and drug development. Strong understanding of GCP (Good Clinical Practice) and relevant regulatory requirements (e.g., FDA, EMA) is essential. Excellent analytical, communication, and interpersonal skills are required to effectively interact with internal stakeholders and external investigators. This hybrid role offers a blend of office-based collaboration and remote work flexibility, located in the strategic area of Sitra, Capital, BH . Join us and be part of a team that is committed to bringing life-changing therapies to patients.
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4
Clinical Research Associate - Pharmaceuticals
478 Northern, Northern
BHD75000 Annually
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Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their fully remote team. This crucial role involves overseeing and managing clinical trials from initiation to completion, ensuring compliance with protocols, regulations, and ethical standards. You will be responsible for monitoring trial sites, verifying data accuracy, and ensuring patient safety throughout the research process. This position requires a deep understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements in drug development. You will act as the primary liaison between the sponsor and the investigational sites, facilitating effective communication and problem-solving. Key responsibilities include site selection, initiation, monitoring, and close-out visits, as well as ensuring timely data collection and query resolution. The ideal candidate possesses a strong background in clinical research, excellent organizational skills, and the ability to manage multiple priorities effectively in a remote environment. You must be meticulous, detail-oriented, and committed to upholding the highest standards of research integrity. Strong analytical and problem-solving skills are essential, as is the ability to build rapport and trust with site staff. This is an exceptional opportunity to contribute to life-saving medical advancements and advance your career in the pharmaceutical industry with the flexibility of a remote role. A Bachelor's degree in a life science, nursing, or a related field is required, along with significant experience as a CRA. Proficiency in clinical trial management software and electronic data capture (EDC) systems is necessary. We are looking for an independent, proactive, and adaptable professional who can thrive in a challenging yet rewarding environment.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trials.
- Ensure compliance with study protocols, SOPs, and GCP guidelines.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Monitor patient safety and report adverse events according to regulatory requirements.
- Serve as the primary point of contact between study sites and the sponsor.
- Facilitate communication and resolve issues at investigational sites.
- Train site staff on study procedures and protocols.
- Review and reconcile source documents and case report forms (CRFs).
- Ensure timely submission of study-related documentation.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA).
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
- Experience with various therapeutic areas is a plus.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Excellent monitoring, auditing, and problem-solving skills.
- Strong communication, interpersonal, and organizational abilities.
- Ability to travel as required (if applicable, though this role is remote, some site visits may occur).
- Ability to work independently and manage time effectively in a remote setting.
- Valid driver's license and clean driving record.
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5
Senior Formulation Scientist - Pharmaceuticals
1030 Bilad Al Qadeem, Capital
BHD105000 Annually
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Posted 4 days ago
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Our client is a renowned pharmaceutical company dedicated to advancing healthcare through cutting-edge research and development. We are actively searching for a highly experienced Senior Formulation Scientist to join our innovative team. This role is fully remote, allowing our experts to contribute their specialized knowledge from anywhere. As a Senior Formulation Scientist, you will be pivotal in the development of novel drug delivery systems and formulations for a diverse pipeline of pharmaceutical products. Your deep understanding of pharmaceutics, chemistry, and regulatory requirements will be essential in transforming scientific discoveries into safe and effective medicines.
Responsibilities:
Qualifications:
This pivotal role is located in the vicinity of Tubli, Capital, BH , but is a fully remote position. Join our client's dedicated team and contribute to the development of life-saving therapies.
Responsibilities:
- Design, develop, and optimize pharmaceutical formulations (e.g., oral, injectable, topical) for various therapeutic areas.
- Conduct pre-formulation studies, including characterization of active pharmaceutical ingredients (APIs) and excipients.
- Perform formulation development experiments, stability studies, and drug release testing.
- Scale up formulations from laboratory to pilot and commercial manufacturing.
- Troubleshoot formulation and process-related issues.
- Collaborate with analytical development, process development, and regulatory affairs teams.
- Prepare comprehensive documentation for regulatory submissions (e.g., IND, NDA).
- Stay abreast of the latest scientific advancements, technologies, and regulatory guidelines in pharmaceutical formulation.
- Mentor junior scientists and provide technical guidance.
- Contribute to intellectual property development and patent filings.
Qualifications:
- Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.
- Minimum of 7 years of progressive experience in pharmaceutical formulation development.
- Proven expertise in developing various dosage forms and drug delivery systems.
- Strong understanding of physical chemistry, materials science, and analytical techniques relevant to formulation.
- Experience with GMP manufacturing principles and regulatory requirements (FDA, EMA).
- Excellent problem-solving, critical thinking, and experimental design skills.
- Proficiency in relevant software and laboratory equipment.
- Strong written and verbal communication skills, including technical writing.
- Ability to work independently, manage projects, and collaborate effectively in a remote setting.
- Demonstrated leadership potential and ability to mentor junior team members.
This pivotal role is located in the vicinity of Tubli, Capital, BH , but is a fully remote position. Join our client's dedicated team and contribute to the development of life-saving therapies.
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6
Lead Research Scientist - Pharmaceuticals
111 Hamad Town, Northern
BHD120000 Annually
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Posted 4 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking an exceptional Lead Research Scientist to spearhead innovative drug discovery initiatives. Based in our state-of-the-art facility in Hamad Town, Northern, BH , this role is pivotal in advancing our pipeline of life-changing therapies. You will lead a team of dedicated researchers, guiding experimental design, data analysis, and interpretation to achieve project milestones. Responsibilities include developing novel research strategies, managing laboratory operations, and ensuring compliance with regulatory standards. The Lead Research Scientist will also be responsible for authoring scientific publications and presenting findings at international conferences. Collaboration with internal departments, such as clinical development and regulatory affairs, will be key to successful project progression. The ideal candidate possesses a Ph.D. in a relevant scientific discipline (e.g., Molecular Biology, Pharmacology, Chemistry) and a minimum of 7-10 years of progressive research experience in the pharmaceutical industry, with demonstrated leadership capabilities. A strong publication record and a deep understanding of drug discovery principles, target validation, and preclinical development are essential. This is a unique opportunity to make a significant impact on patient lives by driving scientific innovation within a leading pharmaceutical organization located in Hamad Town, Northern, BH .
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7
Quality Control Analyst - Pharmaceuticals
1011 Jbeil
BHD65000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical manufacturer, is seeking a detail-oriented and experienced Quality Control Analyst to join their esteemed team in Janabiyah, Northern, BH . This role is integral to ensuring the quality, safety, and efficacy of our pharmaceutical products. The Quality Control Analyst will perform a variety of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment and techniques. Responsibilities include method development and validation, data analysis, documentation of results, and ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements. You will collaborate closely with the R&D, production, and regulatory affairs departments to address any quality deviations and implement corrective actions. The ideal candidate will possess a strong background in analytical chemistry, a meticulous approach to work, and a thorough understanding of pharmaceutical quality control principles. This is an excellent opportunity to contribute to the production of high-quality medicines within a respected organization.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform a wide range of analytical tests on raw materials, intermediates, and finished pharmaceutical products.
- Utilize various analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and titration equipment.
- Develop, validate, and transfer analytical methods according to pharmacopeial standards and regulatory guidelines.
- Analyze test results, interpret data, and prepare accurate and comprehensive reports.
- Document all laboratory activities, results, and deviations in accordance with GMP and company SOPs.
- Ensure proper calibration, maintenance, and qualification of laboratory equipment.
- Participate in Out-of-Specification (OOS) investigations and contribute to the development of corrective and preventative actions (CAPAs).
- Collaborate with production and R&D teams to resolve quality-related issues.
- Maintain a safe working environment and adhere to all safety protocols and procedures.
- Stay updated on current Good Manufacturing Practices (cGMP) and relevant regulatory requirements.
- Assist in the preparation for internal and external audits.
- Contribute to continuous improvement initiatives within the QC laboratory.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
- Hands-on experience with analytical techniques such as HPLC, GC, FTIR, and dissolution testing.
- Strong understanding of GMP, ICH guidelines, and other relevant regulatory standards.
- Proficiency in data analysis, interpretation, and documentation.
- Excellent attention to detail and accuracy in laboratory work.
- Strong written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
- Familiarity with Bahraini pharmaceutical regulations is an advantage.
- Proficiency in MS Office Suite and laboratory information management systems (LIMS).
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8
Quality Assurance Manager - Pharmaceuticals
24007 Jbeil
BHD115000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a prominent pharmaceutical manufacturer, is seeking a highly skilled and experienced Quality Assurance Manager to ensure adherence to the highest standards of quality and regulatory compliance. This role is pivotal in maintaining the integrity and safety of pharmaceutical products throughout their lifecycle. You will be responsible for developing, implementing, and managing the company's Quality Management System (QMS), ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant international regulatory standards. The ideal candidate will have a strong background in pharmaceutical quality assurance, auditing, and regulatory affairs. You will lead a team of QA professionals, overseeing all quality-related activities, including batch record review, deviation investigations, CAPA management, change control, and internal/external audits. Key responsibilities include developing and delivering training programs on quality systems, identifying potential risks, and implementing strategies to mitigate them. Experience with validation activities (process, cleaning, analytical method) and electronic quality management systems (eQMS) is essential. You will also play a key role in preparing for and hosting regulatory inspections from agencies such as the FDA, EMA, and local health authorities. This position is based in our facility in Janabiyah, Northern, BH , and requires a hands-on approach to quality oversight. Strong leadership, excellent analytical skills, and meticulous attention to detail are crucial. You must be able to communicate effectively with all levels of the organization, as well as external regulatory bodies. A commitment to continuous improvement and fostering a robust quality culture is paramount. This is an exceptional opportunity to lead quality initiatives in a dynamic and critical industry.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure compliance with GMP, GLP, and other relevant regulatory standards.
- Oversee batch record review, deviation investigations, and CAPA management.
- Conduct and manage internal and external audits.
- Lead validation activities for processes, equipment, and analytical methods.
- Prepare the company for and host regulatory inspections.
- Develop and deliver quality training programs for employees.
- Identify and assess quality risks, implementing mitigation strategies.
- Manage the change control process to ensure product integrity.
- Foster a strong quality culture throughout the organization.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. Master's degree preferred.
- Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, GLP, and international regulatory requirements.
- Proven experience in managing QMS, audits, and regulatory inspections.
- Experience with validation protocols and eQMS software.
- Strong leadership, analytical, and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work effectively in a manufacturing plant environment.
- Attention to detail and commitment to quality excellence.
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