content writer (night shift) Jobs in Karachi

content writer (night shift)

operations coordinator

administrative coordinator Jobs in Karachi

administrative coordinator

back office coordinator

clinical trials quality assurance associate (night) Jobs in Karachi

clinical trials quality assurance associate (night)

regulatory co ordinator evening shift

Minerva Research Solutions

<div>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.</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 (07 PM to 03 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
bK2MpLypay</div>

Regulatory Co Ordinator(Evening Shift)

<div>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.</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 (07 PM to 03 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
qnZ28Ahk2D</div>

New Era Industries SMC Pvt Ltd

Sales CoordinatorLocation: Tariq Road, KarachiCompany: New Era Industries SMC PVT LIMMITEDSalary: Rs. 50,000 &ndash; Rs. 70,000 per monthAbout UsNew Era Industries SMC PVT LIMMITED is one of the leading names in premium uPVC windows, doors, and ducting solutions. With rapid growth in the building materials sector, we are looking for a dynamic Sales Co-Ordinator to join our team and play a vital role in driving client satisfaction, supporting sales operations, and ensuring smooth project execution.Key Responsibilities<ul><li>Coordinate with the sales team for leads, quotations, and client follow-ups.</li><li>Maintain client records and update them on order status.</li><li>Liaise with production, supply chain, and accounts for timely execution.</li><li>Prepare and manage sales reports, documentation, and records.</li><li>Support sales team in achieving monthly &amp; quarterly targets.</li><li>Ensure excellent customer service and after-sales support.</li></ul>RequirementsEducation: Bachelor&rsquo;s degree minimum.Experience: 2+ years in sales coordinationAge: 25 &ndash; 35 years (Male candidates only).Skills:<ul><li>Good communication &amp; client-handling skills.</li><li>Strong computer literacy (MS Office, WhatsApp/Email).</li><li>Ability to coordinate across multiple departments &amp; meet deadlines.</li></ul>What We Offer<ul><li>Competitive Salary Package</li><li>Medical Facility for employees</li><li>Professional growth &amp; career advancement opportunities</li><li>Exposure to premium building materials &amp; uPVC industry projects</li><li>Supportive and growth-driven work culture</li></ul>Job Types: Full-time, Contract Contract length: 12 monthsPay: Rs50,000.00 - Rs70,000.00 per monthApplication Question(s):<ul><li>Current Salary</li><li>Expected Salary</li><li>Age</li></ul>Work Location: In person

sales Coordinator

WebNike

Webnike is looking for talented and experienced Academic Research Writers for a full-time position in evening shift/night shiftRequirements:<ul><li>Bachelors/Masters degree in Finance/Statistics/Economics/Business/ Medicine/Accounting/Healthcare/Law etc</li><li>At least 1-2 Years of relevant experience in research writing (Technical/Non-Technical subjects).</li><li>Must be able to deliver high-quality papers with 100% plagiarism-free content.</li><li>Proficient in using MS Word, MS Excel, and Adobe Acrobat.</li><li>General understanding of common referencing styles such as APA and MLA.</li><li>Commendable knowledge of various online search engines and libraries.</li></ul>As a employee at WebNike you will also be entitled for Provident fund, Annual leaves, performance bonus and EOBIDetails:Shift: Evening/NightJob Type: Full-timeApplication Question(s):<ul><li>This is an office based position in Karachi, no remote work will be offered. Are you interested?</li></ul>Experience:<ul><li>Research Writer: 1 year (Preferred)</li></ul>Work Location: In person

Academic Research Writer Male

Webnike is looking for talented and experienced Research writers for a full-time position in evening shift and night shift.Requirements:Bachelors/Masters degree in Finance/Statistics/Economics/Business/ Medicine/Accounting/Healthcare/Law etcAt least 1-2 Years of relevant experience in research writing (Technical/Non-Technical subjects).Must be able to deliver high-quality papers with 100% plagiarism-free content.Proficient in using MS Word, MS Excel, and Adobe Acrobat.General understanding of common referencing styles such as APA and MLA.Commendable knowledge of various online search engines and libraries.As a employee at WebNike you will also be entitled for Provident fund, Annual leaves, performance bonus and EOBIDetails:Shift: Evening/NightLocation: Gulshan-e-Iqbal, KarachiJob Type: Full-timeApplication Question(s):<ul><li>This is an office based position in Karachi, no remote job would be offered are you interested?</li></ul>Experience:<ul><li>academic writer: 1 year (Required)</li></ul>Work Location: In person

Research Writer (Office based)

Webnike is looking for talented and experienced Research Analyst for a full-time position in evening shift and night shift.Requirements:<ul><li>Bachelors/Masters degree in Finance/Statistics/Economics/Business/ Medicine/Accounting/Healthcare/Law etc</li><li>At least 1-2 Years of relevant experience in research writing (Technical/Non-Technical subjects).</li><li>Must be able to deliver high-quality papers with 100% plagiarism-free content.</li><li>Proficient in using MS Word, MS Excel, and Adobe Acrobat.</li><li>General understanding of common referencing styles such as APA and MLA.</li><li>Commendable knowledge of various online search engines and libraries.</li></ul>As a employee at WebNike you will also be entitled for Provident fund, Annual leaves, performance bonus and EOBIDetails:Shift: Evening/NightLocation: Gulshan-e-Iqbal, Karachi.Job Type: Full-timeApplication Question(s):<ul><li>Are you from Karachi?</li><li>This is an Office based job, no remote option will be given. Are you interested</li></ul>Experience:<ul><li>Research Writer: 1 year (Required)</li></ul>Work Location: In person

Research Analyst (Karachi)

E Data Solutions

We Are Hiring Fresh &amp; Energetic Youngsters For Outbound Lead Generation Projects.Start Your Career In A Reputed Call Center.Built Your Speaking, Listening &amp; Communication Skills.Fixed Salary 25000.Attendance Bonus 5000.Handsome Fixed Salary Package additional Commissions + Daily, Weekly &amp; Monthly Promotions.Candidate Must Speak &amp; Understand Basic English.Candidate Must Be Under 28 Year.Fresh &amp; Experienced both are welcome.Evening Shift Available:Evening Shift Hours: 6 PM to 12:30 AMWalk &amp; Interview Monday to Saturday 7:00 pm to 11:00 pmIF YOU WANT TO EARN &amp; LEARN IN A FRIENDLY ENVIRONMENT. . . Feel free to drop your resume.You will get a call to schedule your interview.Contact: 0315-2807729 or 0312-0012288(FOR MORE INFO CALL BETWEEN 6PM to 11PM)Job Types: Full-time, Contract, Internship, Fresher Contract length: 6 monthsPay: From Rs25,000.00 per monthWork Location: In person

Call Center Agents !!

Explore 814+ Regulatory co ordinator evening shift in Karachi this November. Find roles across top companies and apply now to boost your career.

814 regulatory co ordinator evening shift jobs IN Karachi

Regulatory Co Ordinator(Evening Shift)

Regulatory Co Ordinator(Evening Shift)

sales Coordinator

Academic Research Writer Male

Research Writer (Office based)

Research Analyst (Karachi)

Call Center Agents !!