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regulatory co ordinator evening shift

Minerva Research Solutions

<div>Employment Type: Full-Time, On-site 
Shift: Evening 
Timings: 6 PM to 2 AM 
Candidates with relevant background will be preferred. 
 
Company Overview: 
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle. 
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Job Purpose: 
 
The Coordinator - Regulatory Affairs is responsible for working as a team member of regulatory professionals in ensuring regulatory compliance of company products and activities, including the preparation and submission of regulatory documents, the management of regulatory inspections, and the development and implementation of regulatory strategies. 
 
Key Responsibilities:<ul><li>
Working as a regulatory professional to ensure effective and efficient regulatory support for the company's products and activities.</li><li>
Develop and implement regulatory strategies that support the company's business objectives and ensure compliance with relevant regulations and guidelines.</li><li>
Manage the preparation and submission of regulatory documents, including regulatory filings, registrations, and certifications.</li><li>
Coordinate and manage regulatory inspections and audits, and ensure appropriate corrective and preventive actions are taken in response to any findings.</li><li>
Keep abreast of changes in regulatory requirements and guidelines, and communicate these changes to relevant stakeholders in a timely manner.</li><li>
Build and maintain positive relationships with regulatory authorities and other external stakeholders.</li><li>
Provide regulatory guidance and support to cross-functional teams, including product development, clinical research, manufacturing, and quality assurance.</li><li>
Collaborate with internal and external stakeholders to develop and implement regulatory policies and procedures that support the company's overall goals and objectives.</li><li>
Ensure timely and accurate reporting of regulatory activities and metrics.</li></ul>
Qualifications:<ul><li>
Bachelor's degree in a scientific discipline, preferably in life sciences, chemistry, or pharmacy.</li><li>
01 years of experience in regulatory affairs, fresh graduates will also be preferred</li><li>
In-depth knowledge of global regulatory requirements and guidelines for pharmaceuticals, medical devices, or other regulated products.</li><li>
Excellent communication, interpersonal, and problem-solving skills.</li><li>
Ability to work independently and manage multiple projects simultaneously.</li><li>
Strong attention to detail and accuracy.</li><li>
Experience working in a fast-paced, deadline-driven environment.<div>
</div></li></ul>uD7bCmnj9E</div>

Regulatory Co Ordinator(Evening Shift)

<div>Employment Type: Full-Time, On-site 
Shift: Evening 
Timings: 6 PM to 2 AM 
Candidates with relevant background will be preferred. 
 
Company Overview: 
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle. 
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Job Purpose: 
 
The Coordinator - Regulatory Affairs is responsible for working as a team member of regulatory professionals in ensuring regulatory compliance of company products and activities, including the preparation and submission of regulatory documents, the management of regulatory inspections, and the development and implementation of regulatory strategies. 
 
Key Responsibilities:<ul><li>
Working as a regulatory professional to ensure effective and efficient regulatory support for the company's products and activities.</li><li>
Develop and implement regulatory strategies that support the company's business objectives and ensure compliance with relevant regulations and guidelines.</li><li>
Manage the preparation and submission of regulatory documents, including regulatory filings, registrations, and certifications.</li><li>
Coordinate and manage regulatory inspections and audits, and ensure appropriate corrective and preventive actions are taken in response to any findings.</li><li>
Keep abreast of changes in regulatory requirements and guidelines, and communicate these changes to relevant stakeholders in a timely manner.</li><li>
Build and maintain positive relationships with regulatory authorities and other external stakeholders.</li><li>
Provide regulatory guidance and support to cross-functional teams, including product development, clinical research, manufacturing, and quality assurance.</li><li>
Collaborate with internal and external stakeholders to develop and implement regulatory policies and procedures that support the company's overall goals and objectives.</li><li>
Ensure timely and accurate reporting of regulatory activities and metrics.</li></ul>
Qualifications:<ul><li>
Bachelor's degree in a scientific discipline, preferably in life sciences, chemistry, or pharmacy.</li><li>
01 years of experience in regulatory affairs, fresh graduates will also be preferred</li><li>
In-depth knowledge of global regulatory requirements and guidelines for pharmaceuticals, medical devices, or other regulated products.</li><li>
Excellent communication, interpersonal, and problem-solving skills.</li><li>
Ability to work independently and manage multiple projects simultaneously.</li><li>
Strong attention to detail and accuracy.</li><li>
Experience working in a fast-paced, deadline-driven environment.<div>
</div></li></ul>TWsHfCzrUG</div>

NCCI

Registered Staff Nurse is required for Evening and Night shift on urgent basis.Education: BSN or General Nursing DipomaExperience: 2 to 5 years in ward, ICU and emergencyGender: Only FemaleInterested candidates may send their resumes to hr@ncci.org.pk and kindly mention their shift in subject line like Evening / Night shift.Salary: depends upon his/ her education / experience.Job Type: Full-timePay: Up to Rs40,000.00 per monthAbility to commute/relocate:<ul><li>Karachi: Reliably commute or planning to relocate before starting work (Preferred)</li></ul>Education:<ul><li>High School (Preferred)</li></ul>Work Location: In person

Staff Nurse

<div>JOB DESCRIPTION: 
 
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.<h3 class="jobSectionHeader">
Role Summary</h3>
As a QA Associate, you will play a vital role in maintaining the accuracy, compliance, and quality of clinical trial data. This includes quality control, eSource/template building, EDC data entry, and supporting the team in preparing for regulatory inspections.<h3 class="jobSectionHeader">
Key Responsibilities</h3><ul><li>
Perform ongoing quality checks to ensure data accuracy and compliance with SOPs, protocols, GCP, and regulatory requirements.</li><li>
Build eSource templates tailored to study protocols and ensure standardization.</li><li>
Enter and verify data in Electronic Data Capture (EDC) systems.</li><li>
Identify and document errors or deviations; support resolution and continuous quality improvement.</li><li>
Help generate quality reports and support risk assessments in collaboration with the clinical team.</li><li>
Contribute to CAPA development and share quality learnings across protocols/programs.</li><li>
Review key study documents for consistency and regulatory readiness.</li><li>
Assist in inspection preparation and support internal quality reviews.</li><li>
Resolve queries and prepare study-specific documentation and questionnaires.</li><li>
Participate in QA projects and support cross-functional teams as needed.</li></ul><h3 class="jobSectionHeader">
Qualifications</h3><ul><li>
Medical or clinical background (Pharm-D, MBBS, BDS strongly preferred).</li><li>
Familiarity with FDA, GCP, ICH guidelines and IRB processes.</li><li>
1+ year experience in QA/QC or clinical research preferred.</li><li>
Proficient in documentation, data systems, and basic regulatory concepts.</li><li>
Detail-oriented with strong communication and time management skills.</li><li>
Able to work effectively in a fast-paced, collaborative environment.</li><li>
Knowledge of HIPAA and data privacy in clinical settings.</li></ul>
Benefits:<ul><li>
Competitive salary and performance-based bonuses.</li><li>
Medical health insurance coverage.</li><li>
Employees Old-age benefits coverage.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional, and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul>
Openings:
04 positions 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
Evening Shift (06 PM to 02 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
nWYcKJ0v5I</div>

Clinical Trials Quality Assurance Associate (Night)

1AZ0 Marketing (Pvt) Ltd.

1AZ0 Marketing Pvt Ltd.Call Center RepresentativesOnly 10 positions / vacancies are left. Location: Gulshan e Iqbal, Karachi.Skills:Excellent communication skills in English language. Ability to work at Night Shift. Candidate should have leading capabilities. Punctual and hard worker.Pick &amp; Drop is available for femalesShift: Night/ Evening ShiftSalary: Basic: upto Rs 35,000 + Commission, Bonuses, and AllowancesJob Types: Full-time, Part-timeJob Types: Full-time, ContractPay: Rs35,000.00 - Rs40,000.00 per monthApplication Question(s):<ul><li>Do you live near Gulshan-e-Iqbal, Karachi?</li></ul>Language:<ul><li>english with fluency (Required)</li></ul>Work Location: In person

Call Center Agents/ CSR- Evening Shift (Females Only)

SKC JAPAN

Japanese Car Sales &amp; Customer Support Representative (Evening Shift)Location: Gulshan-e-Iqbal, Karachi (On-Site)Market: Japanese Car Sales &ndash; East Caribbean RegionShift: 4:00 PM to 1:00 AM (PKT)Type: Full-timeAre you an experienced sales or customer support professional looking to grow your career in an international market? SKC Japan is expanding and looking for enthusiastic, driven individuals with 3&ndash;4 years of experience in sales, customer support, or telemarketing to join our dynamic team.We specialize in exporting high-quality Japanese vehicles to the East Caribbean Islands &mdash; and we&rsquo;re looking for someone who&rsquo;s excited to make an impact in a global business.Key Responsibilities:* Convert inbound and outbound leads into successful vehicle sales* Deliver prompt and professional customer service across phone, chat, and email* Build relationships with clients and manage post-sale support* Resolve issues efficiently while maintaining customer satisfaction* Promote value-added services to increase customer conversionWorking Hours:4:00 PM &ndash; 1:00 AM (Pakistan Time)Ideal for individuals comfortable with evening shifts and international client interaction.What We Offer:Competitive base salary (open to discussion based on experience) + high commission per saleFree dinner during shiftWeekends off (Saturday &amp; Sunday)Career growth and professional development opportunitiesA supportive, collaborative work environmentApply Now!Send your resume to: hr@skcjapan.com or message us directly.Join a fast-growing international team and take your career to the next level!Job Type: Full-timePay: Rs65,000.00 - Rs100,000.00 per monthWork Location: In person

Japanese Car Sales & Customer Support Representative (Evening Shift)

Lumenco Canada

Apply only if you can work in Evening and Night ShiftJob DescriptionWe are seeking an experienced e-Commerce Data Specialist with at least 2 years of proven experience in the relevant field. The ideal candidate will have strong expertise in handling large product inventories, data categorization, and listing thousands of products across e-commerce platforms. This role requires advanced computer skills, excellent attention to detail, and the ability to work with complex software used for data uploads and website management.Experience with e-commerce platforms such as Shopify, Magento, or WooCommerce is highly preferred.Collaborate with teams to optimize listings and identify process improvements for efficient scalingKey Responsibilities&middot; Manage and update large product inventories.&middot; Categorize, format, and upload product data accurately to front-end platforms.&middot; Work with complex software tools and spreadsheets to ensure smooth data flow.&middot; Coordinate tasks efficiently and meet deadlines.Skills &amp; Requirements&middot; Minimum 2 years of experience in a relevant e-commerce data role.&middot; Proficiency in MS Excel (advanced functions, data handling, formatting).&middot; Strong English communication skills (written and verbal).&middot; Tech-savvy and able to adapt quickly to new software/tools.&middot; Excellent organizational and coordination skills.&middot; Ability to work the Evening shift (3 PM &ndash; 12 AM).&middot; Education: Bachelor&rsquo;s degree (minimum requirement).Preferred Qualifications&middot; Hands-on experience with Shopify, Magento, WooCommerce, or other major e-commerce platforms.&middot; Strong problem-solving skills and ability to work independently with minimal supervision.Job Type: Full-timePay: Rs45,000.00 - Rs50,000.00 per monthEducation:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Ecommerce Data Entry: 2 years (Required)</li></ul>Language:<ul><li>English (Required)</li></ul>Work Location: In person

e-Commerce Data Specialist

Explore 766+ Regulatory co ordinator evening shift in Karachi this September. Find roles across top companies and apply now to boost your career.

766 regulatory co ordinator evening shift jobs IN Karachi

Regulatory Co Ordinator(Evening Shift)

Regulatory Co Ordinator(Evening Shift)

Staff Nurse

Clinical Trials Quality Assurance Associate (Night)

Call Center Agents/ CSR- Evening Shift (Females Only)

Japanese Car Sales & Customer Support Representative (Evening Shift)

e-Commerce Data Specialist