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via SmartRecruiters Job Search
schedule_type: Full-time
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Description:
• The execution and analysis of experiments and analytical procedures.
• Displays an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures.
• Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision.
• Plans and prioritizes concurrent experimental procedures. Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results.
• May provide oral presentations on results to other department members.
• Works under active supervision.
Responsibilities:
• The conducting cell culture experiments using small scale (i.e. shake flasks, spin tubes, well plates) platforms and bench top bioreactors, running biochemical assays, and performing routine lab duties.
• The individual will also be responsible for designing experiments, monitoring cell culture parameters and documenting all studies. Experience in a basic biology lab setting, including aseptic techniques is a plus.
• Excellent oral and written communication skills are required.
• Must be able to work well independently and contribute as a member of a team.
Required Skills:
• the Commercial Cell Culture Development (CCCD) department is responsible for the development, characterization, scale-up, and transfer of cell culture processes for late stage clinical and commercial manufacturing of therapeutic proteins and antibodies.
• In addition, the department provides technical expertise and support for improving the performance of commercial manufacturing processes.
• Our department is seeking to employ a motivated individual for a 12-month temporary position.
• This individual will work with a team of scientists and engineers to develop/optimize mammalian cell culture processes.
Qualifications
B.S. degree in Biology, Bioengineering, or related field and a minimum of 1 to 3 year of molecular biology and/or mammalian cell culture laboratory experience.
Additional Information
Show more details...
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Description:
• The execution and analysis of experiments and analytical procedures.
• Displays an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures.
• Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision.
• Plans and prioritizes concurrent experimental procedures. Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results.
• May provide oral presentations on results to other department members.
• Works under active supervision.
Responsibilities:
• The conducting cell culture experiments using small scale (i.e. shake flasks, spin tubes, well plates) platforms and bench top bioreactors, running biochemical assays, and performing routine lab duties.
• The individual will also be responsible for designing experiments, monitoring cell culture parameters and documenting all studies. Experience in a basic biology lab setting, including aseptic techniques is a plus.
• Excellent oral and written communication skills are required.
• Must be able to work well independently and contribute as a member of a team.
Required Skills:
• the Commercial Cell Culture Development (CCCD) department is responsible for the development, characterization, scale-up, and transfer of cell culture processes for late stage clinical and commercial manufacturing of therapeutic proteins and antibodies.
• In addition, the department provides technical expertise and support for improving the performance of commercial manufacturing processes.
• Our department is seeking to employ a motivated individual for a 12-month temporary position.
• This individual will work with a team of scientists and engineers to develop/optimize mammalian cell culture processes.
Qualifications
B.S. degree in Biology, Bioengineering, or related field and a minimum of 1 to 3 year of molecular biology and/or mammalian cell culture laboratory experience.
Additional Information
Show more details...
via SmartRecruiters Job Search
schedule_type: Full-time
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Description:
• Responsible for the execution and analysis of experiments and analytical procedures.
• Provides assistance in the execution of experiments and analytical procedures by performing routine scientific procedures and experiments according to detailed protocols. Integrates, compiles, and tabulates data and reports results to supervisor.
• Assignments are task-oriented with detailed instructions.
• Follows standard practices to obtain data. Contributes to the completion of routine technical tasks.
• Failure to achieve results can normally be overcome without serious effect on schedules and programs.
Examples of projects are as follows:
• Validation Study to support the use of viable tubing at various lengths. The intent of this validation study would be to show that the length of tubing does not have an adverse impact on recovery rates for viable organisms.
• This task would involve assessing all site production areas to determine the length of tubing used, developing a study to validate both the shortest and longest length, documented and then driving a protocol through the review and approval cycle, conducting the study in an appropriate location on site, writing report containing the results and then driving through report review and approval cycles.
• A change control may also be needed to ensure the report is referenced in appropriate documentation.
• Implementation of an alternate EM media to replace DE Neutralizing agar.
Skills:
• Candidate should have experience in project management, technical writing skills (reports, protocols, documents), some experience in or at least an understanding of validation concepts with some experience in a pharmaceutical environment.
• should include, strong written and verbal communication skills. Systems to be use include, but are not limited to: Trackwise, e-doc (author, reviewer, approver), MASTER, Pharmnet, SAP, LIMS, ISOtrain.
Qualifications
• Candidate should possess Bachelor's degree in related field or comparable Experience 1-3 years
Additional Information
Show more details...
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Description:
• Responsible for the execution and analysis of experiments and analytical procedures.
• Provides assistance in the execution of experiments and analytical procedures by performing routine scientific procedures and experiments according to detailed protocols. Integrates, compiles, and tabulates data and reports results to supervisor.
• Assignments are task-oriented with detailed instructions.
• Follows standard practices to obtain data. Contributes to the completion of routine technical tasks.
• Failure to achieve results can normally be overcome without serious effect on schedules and programs.
Examples of projects are as follows:
• Validation Study to support the use of viable tubing at various lengths. The intent of this validation study would be to show that the length of tubing does not have an adverse impact on recovery rates for viable organisms.
• This task would involve assessing all site production areas to determine the length of tubing used, developing a study to validate both the shortest and longest length, documented and then driving a protocol through the review and approval cycle, conducting the study in an appropriate location on site, writing report containing the results and then driving through report review and approval cycles.
• A change control may also be needed to ensure the report is referenced in appropriate documentation.
• Implementation of an alternate EM media to replace DE Neutralizing agar.
Skills:
• Candidate should have experience in project management, technical writing skills (reports, protocols, documents), some experience in or at least an understanding of validation concepts with some experience in a pharmaceutical environment.
• should include, strong written and verbal communication skills. Systems to be use include, but are not limited to: Trackwise, e-doc (author, reviewer, approver), MASTER, Pharmnet, SAP, LIMS, ISOtrain.
Qualifications
• Candidate should possess Bachelor's degree in related field or comparable Experience 1-3 years
Additional Information
Show more details...
via SmartRecruiters Job Search
schedule_type: Contractor
Company Description
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations...
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables
Company Description
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations...
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Title: Quality Inspector
Duration: 6 Months
Location: Northborough, MA
Position over view:
• Monitors and/or performs inspection and control of products and materials.
• Performs product and/or component inspections in accordance with specifications and SOP.s.
• Samples, inspects, and releases components and raw materials as per SOP.s and specifications.
• Monitors various stages of processing along with the appropriate paperwork in compliance with specifications.
• Maintains raw materials, in-process and finished goods retain storage areas.
• May conduct simple testing in accordance with defined standard operating procedures.
• Contact with outside vendors as necessary.
• Filing and archiving study related documents, includes lifting of boxes (~25 - 40 lbs).
• Demonstrated ability in the application of the requisite skills to perform the required tasks of the position.
• Receives general instructions on routine assignments under general supervision.
• Receives detailed instructions on new work, which may be closely supervised and reviewed.
• The work environment characteristics described here are representative of those an employee to encounters while performing the essential functions of this job.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Job has potential for biohazard exposure.
• Experience 1-3 years.
SKILLS Over viewed:
• Multi-task oriented with the ability to change focus quickly
• cGMP experience/knowledge is preferred.
• Quality Inspection experience is preferred.
• Proficiency in Microsoft Office Suite is a must (especially Microsoft Word and Excel)
High organizational skills preferred.
Qualifications
Education over viewed:
• Associates Degree or Bachelor's Degree preferred
Additional Information
All your information will be kept confidential according to EEO guidelines Show more details...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations...
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Title: Quality Inspector
Duration: 6 Months
Location: Northborough, MA
Position over view:
• Monitors and/or performs inspection and control of products and materials.
• Performs product and/or component inspections in accordance with specifications and SOP.s.
• Samples, inspects, and releases components and raw materials as per SOP.s and specifications.
• Monitors various stages of processing along with the appropriate paperwork in compliance with specifications.
• Maintains raw materials, in-process and finished goods retain storage areas.
• May conduct simple testing in accordance with defined standard operating procedures.
• Contact with outside vendors as necessary.
• Filing and archiving study related documents, includes lifting of boxes (~25 - 40 lbs).
• Demonstrated ability in the application of the requisite skills to perform the required tasks of the position.
• Receives general instructions on routine assignments under general supervision.
• Receives detailed instructions on new work, which may be closely supervised and reviewed.
• The work environment characteristics described here are representative of those an employee to encounters while performing the essential functions of this job.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Job has potential for biohazard exposure.
• Experience 1-3 years.
SKILLS Over viewed:
• Multi-task oriented with the ability to change focus quickly
• cGMP experience/knowledge is preferred.
• Quality Inspection experience is preferred.
• Proficiency in Microsoft Office Suite is a must (especially Microsoft Word and Excel)
High organizational skills preferred.
Qualifications
Education over viewed:
• Associates Degree or Bachelor's Degree preferred
Additional Information
All your information will be kept confidential according to EEO guidelines Show more details...
via JobLeads
posted_at: 10 days agoschedule_type: Full-time
Dashboard Controller at Makro job in Meadowdale, Gauteng | CareerJunction Your privacy
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Dashboard Controller at Makro job in Meadowdale, Gauteng | CareerJunction Your privacy
This site uses cookies and similar technologies to collect and process personal data that recollects your activities and preferences. Some of the personal data, stored on your device, is processed by trusted service providers. We do this to personalise our site, services and the adverts you are shown on and... off our website. Click 'I accept' to consent to the use of these technologies or 'Settings' if you wish to manage your settings. You can always change the setting by going to the Cookie Policy page. Necessary cookies enable core functionality such as security, network management, and accessibility. You may disable these by changing your browser settings, but this may affect how the website functions.
× Location In All Categories
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Dashboard Controller at Makro
Makro
• Undisclosed
• Permanent Junior position
• Meadowdale, Gauteng
• Posted 04 May 2023 by Makro
• Expires in 33 days
• Job 2516363
Save Apply Now About the position
Summary
To accurately assign, monitor and manage customer orders right through to completion whilst meeting customer SLA.
Order Management
? 100% Execution of orders on both day and night shift
? Ensure that order fulfilment is managed daily using the appropriate Order Management Platform
? Manage Stock Handler productivity (picking and packing) right through to order completion ? Monitor hourly and daily picking & packing tasks; and address poor performance and inefficiencies within the picking & packing process
? Manage all pick & pack exceptions, and out of stock items for all Order Management Platforms
? Adhere to the returns policy for all orders types
? Adhere to the customer non collection process for all order types
? Adhere to the reverse pick process
? Ensure risk factors are minimized with the storage of partially picked and incomplete orders ? There should be no Manual Picking, Packing nor Validation
? Ensure all Departmental High Risk and all other applicable Registers are completed and reconciled daily as per the Company Processes
Fulfilment Optimization & Customer Service
? Prepare nightshift handover checklist & register and ensure the associated high-risk inventory is ready
? Ensure necessary finance approvals have been granted for all night shift orders
? Complete and communicate the demand plan for all day and night shift orders to the Delivery Coordinator
? Report back to call centre on customer complaints and ensure in store issues are resolved to minimise customer complaints.
? Adhere to the FIFO (First In First Out) per order principle
Teamwork and SelfManagement
? Follow through to ensure that Massmart personnel quality and productivity standards are consistently and accurately maintained
? Demonstrate consistent application of group and company procedures and policies
? Plan and prioritize, demonstrating abilities to manage competing demands
? Demonstrate abilities to anticipate and manage change
? Work with the broader core and site HR teams to support the overall HR strategy
? Check the Approved Work Schedule and notify Management of personnel not at work daily
Minimum Academic, Professional Qualifications & Experience required for this position
? Matric with relevant retail administration certificates
? Experience
? 1- 2 years' experience in retail administration
Desired Skills:
• order management
• Stock Control
• picking
• Customer Service
Desired Work Experience:
• 1 to 2 years
Desired Qualification Level:
• Grade 12 / Matric
Apply Now Makro
View employer profile
See all Makro jobs
EMAIL ME JOBS LIKE THIS
Share This Job
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Dashboard Controller at Makro Show more details...
This site uses cookies and similar technologies to collect and process personal data that recollects your activities and preferences. Some of the personal data, stored on your device, is processed by trusted service providers. We do this to personalise our site, services and the adverts you are shown on and... off our website. Click 'I accept' to consent to the use of these technologies or 'Settings' if you wish to manage your settings. You can always change the setting by going to the Cookie Policy page. Necessary cookies enable core functionality such as security, network management, and accessibility. You may disable these by changing your browser settings, but this may affect how the website functions.
× Location In All Categories
Share This Job
Dashboard Controller at Makro
Makro
• Undisclosed
• Permanent Junior position
• Meadowdale, Gauteng
• Posted 04 May 2023 by Makro
• Expires in 33 days
• Job 2516363
Save Apply Now About the position
Summary
To accurately assign, monitor and manage customer orders right through to completion whilst meeting customer SLA.
Order Management
? 100% Execution of orders on both day and night shift
? Ensure that order fulfilment is managed daily using the appropriate Order Management Platform
? Manage Stock Handler productivity (picking and packing) right through to order completion ? Monitor hourly and daily picking & packing tasks; and address poor performance and inefficiencies within the picking & packing process
? Manage all pick & pack exceptions, and out of stock items for all Order Management Platforms
? Adhere to the returns policy for all orders types
? Adhere to the customer non collection process for all order types
? Adhere to the reverse pick process
? Ensure risk factors are minimized with the storage of partially picked and incomplete orders ? There should be no Manual Picking, Packing nor Validation
? Ensure all Departmental High Risk and all other applicable Registers are completed and reconciled daily as per the Company Processes
Fulfilment Optimization & Customer Service
? Prepare nightshift handover checklist & register and ensure the associated high-risk inventory is ready
? Ensure necessary finance approvals have been granted for all night shift orders
? Complete and communicate the demand plan for all day and night shift orders to the Delivery Coordinator
? Report back to call centre on customer complaints and ensure in store issues are resolved to minimise customer complaints.
? Adhere to the FIFO (First In First Out) per order principle
Teamwork and SelfManagement
? Follow through to ensure that Massmart personnel quality and productivity standards are consistently and accurately maintained
? Demonstrate consistent application of group and company procedures and policies
? Plan and prioritize, demonstrating abilities to manage competing demands
? Demonstrate abilities to anticipate and manage change
? Work with the broader core and site HR teams to support the overall HR strategy
? Check the Approved Work Schedule and notify Management of personnel not at work daily
Minimum Academic, Professional Qualifications & Experience required for this position
? Matric with relevant retail administration certificates
? Experience
? 1- 2 years' experience in retail administration
Desired Skills:
• order management
• Stock Control
• picking
• Customer Service
Desired Work Experience:
• 1 to 2 years
Desired Qualification Level:
• Grade 12 / Matric
Apply Now Makro
View employer profile
See all Makro jobs
EMAIL ME JOBS LIKE THIS
Share This Job
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Dashboard Controller at Makro Show more details...
via SmartRecruiters Job Search
schedule_type: Full-time
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Order ID : 43017
Location : South San Francisco, CA
Duration : 8+ Months
Job Title : Scientist I
Job Description:
• Contribute to Pharmacovigilance and Risk Management planning for designated products by preparation of safety surveillance strategy and highlighting and tracking potential issues
• Prepare and review periodic safety reports (PBRER / PSUR, DSUR, EU renewal and other Annual Safety Reports) in accordance with regulatory requirements and standard operating procedures
• Support the preparation and maintenance of safety sections of the Company Core Data Sheet
• Conduct/support signal detection and evaluation according to SOPs and guidelines
• Provide safety content review of clinical protocols, study reports, Investigators Brochure and other related documents to ensure alignment with CDP
• Contribute to regulatory agency submissions (IND applications, NDAs, MAA’s, Variations, Renewals) by reviewing safety data and preparing relevant sections of the filing documents and submission packages
• Participate in or provide input for Drug Safety Monitoring Boards or independent monitoring committee meetings, as applicable
• The Safety Scientist should develop a clear understanding of the safety issues and a thorough knowledge of the from the drug mode of action, to enable support the SSL
• The timely medically and scientifically sound development of the clinical safety portions of a product development plan (PDP) and develop an understanding of the safety profile of the assigned product
Skills:
• Strong knowledge of international drug regulation including GCP, GVP and GMP
• Prior industry experience in drug safety, clinical development or medical affairs is desirable
• MD candidates - clinical practice experience (at least 3 years preferred, may include residency)
• Good knowledge of pharmacovigilance practices
• Good knowledge of US and EU pharmacovigilance regulatory requirements
Qualifications
Education:
• MS or MD, PhD or PharmD Preferred, or equivalent qualification Show more details...
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Job Order ID : 43017
Location : South San Francisco, CA
Duration : 8+ Months
Job Title : Scientist I
Job Description:
• Contribute to Pharmacovigilance and Risk Management planning for designated products by preparation of safety surveillance strategy and highlighting and tracking potential issues
• Prepare and review periodic safety reports (PBRER / PSUR, DSUR, EU renewal and other Annual Safety Reports) in accordance with regulatory requirements and standard operating procedures
• Support the preparation and maintenance of safety sections of the Company Core Data Sheet
• Conduct/support signal detection and evaluation according to SOPs and guidelines
• Provide safety content review of clinical protocols, study reports, Investigators Brochure and other related documents to ensure alignment with CDP
• Contribute to regulatory agency submissions (IND applications, NDAs, MAA’s, Variations, Renewals) by reviewing safety data and preparing relevant sections of the filing documents and submission packages
• Participate in or provide input for Drug Safety Monitoring Boards or independent monitoring committee meetings, as applicable
• The Safety Scientist should develop a clear understanding of the safety issues and a thorough knowledge of the from the drug mode of action, to enable support the SSL
• The timely medically and scientifically sound development of the clinical safety portions of a product development plan (PDP) and develop an understanding of the safety profile of the assigned product
Skills:
• Strong knowledge of international drug regulation including GCP, GVP and GMP
• Prior industry experience in drug safety, clinical development or medical affairs is desirable
• MD candidates - clinical practice experience (at least 3 years preferred, may include residency)
• Good knowledge of pharmacovigilance practices
• Good knowledge of US and EU pharmacovigilance regulatory requirements
Qualifications
Education:
• MS or MD, PhD or PharmD Preferred, or equivalent qualification Show more details...
via SmartRecruiters Job Search
schedule_type: Contractor
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Duration: 8 Months +
• The Research Associate/Senior Research Associate will execute ongoing process development activities for the clinical manufacturing of gene therapy products in compliance with all current regulatory and corporate quality guidelines.
• This individual collaborates with all supporting groups and departments to ensure technical and operational requirements are established and maintained in order to meet all relevant company, site and departmental development goals.
• Job Responsibilities:
• Carry out experiments supporting the generation of a purification strategy for the production of viral gene therapy vectors.
• The individual will analyze/interpret results and may recommend additional experiments that expand process knowledge and improve process performance.
• Participate in process scale-up activities, including execution of manufacturing scale runs; may act as a subject matter expert supporting the transfer of process technology to both internal and external clinical manufacturing groups.
• Author protocols, technical reports, data analysis summaries, and SOP's
• Use scientific principles and experiential knowledge to solve complex problems in creative and practical ways.
• Apply state-of-the art principles and theories in area of responsibility to develop processes and advance programs.
• Evaluate new technologies and make recommendations for their implementation in Gene Therapy process development.
• Adheres to and supports all safety programs by ensuring personnel safety training is completed and safety equipment is available.
Qualifications
Skills: Basic Qualifications:
Minimum 3 years of relevant experience in the purification of biologics.
Must have demonstrated skills and working knowledge of the unit operations associated with biologics manufacturing - column chromatography (operation of manual and automated chromatography systems), TFF, depth filtration).
Preferred Qualifications:
Ability to opreate in a dynamic, fast-paced, safety conscious, multi-product development and manufacturing environment with shifting priorities.
Strong commitment to accountability for self and departmental staff for completion of objectives in accordance with established plans.
Education:
Research Associate: Bachelor's degree and 2 or more years.
Master's and 1-2 years; Senior Research Associate: Bachelor's degree and 5 or more years.
Master's and 3 or more years
If you are interested send your updated resume along with below details.
Full Name:
Expected Pay Rate:
DOB (MM/DD):
Availability:
Visa Status:
Address:
Thanks & Regards
Khadeer Khan|Clinical & Scientific Recruitment Specialist
Phone: 973-241-1381 Ext 3079
www.linkedin.com/in/khadeermohmmed
Additional Information
All your information will be kept confidential according to EEO guidelines Show more details...
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Duration: 8 Months +
• The Research Associate/Senior Research Associate will execute ongoing process development activities for the clinical manufacturing of gene therapy products in compliance with all current regulatory and corporate quality guidelines.
• This individual collaborates with all supporting groups and departments to ensure technical and operational requirements are established and maintained in order to meet all relevant company, site and departmental development goals.
• Job Responsibilities:
• Carry out experiments supporting the generation of a purification strategy for the production of viral gene therapy vectors.
• The individual will analyze/interpret results and may recommend additional experiments that expand process knowledge and improve process performance.
• Participate in process scale-up activities, including execution of manufacturing scale runs; may act as a subject matter expert supporting the transfer of process technology to both internal and external clinical manufacturing groups.
• Author protocols, technical reports, data analysis summaries, and SOP's
• Use scientific principles and experiential knowledge to solve complex problems in creative and practical ways.
• Apply state-of-the art principles and theories in area of responsibility to develop processes and advance programs.
• Evaluate new technologies and make recommendations for their implementation in Gene Therapy process development.
• Adheres to and supports all safety programs by ensuring personnel safety training is completed and safety equipment is available.
Qualifications
Skills: Basic Qualifications:
Minimum 3 years of relevant experience in the purification of biologics.
Must have demonstrated skills and working knowledge of the unit operations associated with biologics manufacturing - column chromatography (operation of manual and automated chromatography systems), TFF, depth filtration).
Preferred Qualifications:
Ability to opreate in a dynamic, fast-paced, safety conscious, multi-product development and manufacturing environment with shifting priorities.
Strong commitment to accountability for self and departmental staff for completion of objectives in accordance with established plans.
Education:
Research Associate: Bachelor's degree and 2 or more years.
Master's and 1-2 years; Senior Research Associate: Bachelor's degree and 5 or more years.
Master's and 3 or more years
If you are interested send your updated resume along with below details.
Full Name:
Expected Pay Rate:
DOB (MM/DD):
Availability:
Visa Status:
Address:
Thanks & Regards
Khadeer Khan|Clinical & Scientific Recruitment Specialist
Phone: 973-241-1381 Ext 3079
www.linkedin.com/in/khadeermohmmed
Additional Information
All your information will be kept confidential according to EEO guidelines Show more details...
via SmartRecruiters Job Search
schedule_type: Contractor
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe
Company Description
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Duties: Clinical Laboratory Sciences Department.
• The primary responsibility in this position is routine laboratory testing and analysis of patient samples using established standard operating procedures, tabulating results, and helping with the preparation of patient data reports using a LIMS.
Skills: Qualifications:
• The ideal candidate will have a Bachelor's degree in Chemistry, Biotechnology or Medical Technology with 3+ year's direct experience using LC or MS or MS methods, software, and instruments in clinical chemistry or regulated bioanalysis applications.
Qualifications
• Bachelor's degree in Chemistry, Biotechnology or Medical Technology with 3+ year's direct experience
Additional Information Show more details...
Makro Scientific...
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
Duties: Clinical Laboratory Sciences Department.
• The primary responsibility in this position is routine laboratory testing and analysis of patient samples using established standard operating procedures, tabulating results, and helping with the preparation of patient data reports using a LIMS.
Skills: Qualifications:
• The ideal candidate will have a Bachelor's degree in Chemistry, Biotechnology or Medical Technology with 3+ year's direct experience using LC or MS or MS methods, software, and instruments in clinical chemistry or regulated bioanalysis applications.
Qualifications
• Bachelor's degree in Chemistry, Biotechnology or Medical Technology with 3+ year's direct experience
Additional Information Show more details...
via Learn4Good
posted_at: 9 days agoschedule_type: Full-time
Accounts Manager at Makro job in Meadowdale, Gauteng | Career Junction
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Accounts Manager at Makro job in Meadowdale, Gauteng | Career Junction
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Accounts Manager at Makro
Makro
• Undisclosed
• Permanent Intermediate position
• Meadowdale, Gauteng
• Posted 08 Mar 2023 by Makro
• Expires in 34 days
• Job 2507571
Save Apply Now
About the position
Department Budget Control:
? Over all responsible to the monitoring of FTE and contracts budgets in line with Company
Requirements ? Ensure that a monthly expense analyses is completed, variances noted and explanations provided
Customer Accounts Incidental:
? Ensure that incidentals are settled within 72 hours, debtors (both internal and external) queries are handled promptly.? Daily reconciliation of customer accounts? Daily clearing of incidental account is done? Ensure daily monitoring, authorizing and control of COD customer purchases and the COD processes? Ensure all COD Cards are accounted for daily and weekly
Trade Debtors:
? Ensure in-store support and payment processing on a daily basis? Ensure that no incidental trade debtor to be processed without debtor completing the COD trade agreement form.? All store related queries and issues relating to trade debtors are resolved daily/weekly/monthly? Customer limit increases to liaise with head office immediately? Liaison with Head Office in accordance to Company Standards and Audit requirements?
Daily/Weekly report on short payments send to relevant people? Trade debtors cards must be authorized with authorization letters to be traded with
Gift Vouchers Control:? Ensuring the receipting, and issuing of Gift Cards via POS system? Ensuring a zero balance in the gift card debtors suspense account? Ensuring the monthly recon is completed
Ledger Account Month End:? Ensure accurate accounting for the following accounts for month end
Ledger Account Recons:
? Accounts to be reconciled and signed off to Head Office (Finance Department) every month as per stipulated timeframe.
Unredeemed Credit Notes:? Ensure the daily posting of all adjustment journals for redeemed Inter-Branch credit notes.? Maintain clearing account 161305? Ensure all credit notes treated as cash are deleted from the back office report daily/weekly/monthly? Ensure the completion of the monthly credit note recon
Staff Purchases:? Ensure that staff purchases card is controlled and account reconciled and cleared monthly? Ensure the authorization together with a copy of the staff buying card is obtained when loading a staff purchase? Ensure staff members keep within their authorized limits? Ensure that all refunds relating to staff purchases is refunded back to the staff purchase account and no cash, gift card or credit note has been issued
Requirements
Desired
Skills:
• Attention to detail
• Financial Skills
• Managing budgets
Desired Work
Experience:
• 2 to 5 years Wholesale & Trading
• 5 to 10 years Account Management
Desired Qualification Level:
• Diploma
Employer & Job
Benefits:
• Provident Fund
• Medical Aid
Apply Now
Makro
View employer profile
See all Makro jobs
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Your privacy...
This site uses cookies and similar technologies to collect and process personal data that recollects your activities and preferences. Some of the personal data, stored on your device, is processed by trusted service providers. We do this to personalise our site, services and the adverts you are shown on and off our website. Click 'I accept' to consent to the use of these technologies or 'Settings' if you wish to manage your settings.
You can always change the setting by going to the Cookie Policy page. Necessary cookies enable core functionality such as security, network management, and accessibility. You may disable these by changing your browser settings, but this may affect how the website functions.
× Location In All Categories
Share This Job
Accounts Manager at Makro
Makro
• Undisclosed
• Permanent Intermediate position
• Meadowdale, Gauteng
• Posted 08 Mar 2023 by Makro
• Expires in 34 days
• Job 2507571
Save Apply Now
About the position
Department Budget Control:
? Over all responsible to the monitoring of FTE and contracts budgets in line with Company
Requirements ? Ensure that a monthly expense analyses is completed, variances noted and explanations provided
Customer Accounts Incidental:
? Ensure that incidentals are settled within 72 hours, debtors (both internal and external) queries are handled promptly.? Daily reconciliation of customer accounts? Daily clearing of incidental account is done? Ensure daily monitoring, authorizing and control of COD customer purchases and the COD processes? Ensure all COD Cards are accounted for daily and weekly
Trade Debtors:
? Ensure in-store support and payment processing on a daily basis? Ensure that no incidental trade debtor to be processed without debtor completing the COD trade agreement form.? All store related queries and issues relating to trade debtors are resolved daily/weekly/monthly? Customer limit increases to liaise with head office immediately? Liaison with Head Office in accordance to Company Standards and Audit requirements?
Daily/Weekly report on short payments send to relevant people? Trade debtors cards must be authorized with authorization letters to be traded with
Gift Vouchers Control:? Ensuring the receipting, and issuing of Gift Cards via POS system? Ensuring a zero balance in the gift card debtors suspense account? Ensuring the monthly recon is completed
Ledger Account Month End:? Ensure accurate accounting for the following accounts for month end
Ledger Account Recons:
? Accounts to be reconciled and signed off to Head Office (Finance Department) every month as per stipulated timeframe.
Unredeemed Credit Notes:? Ensure the daily posting of all adjustment journals for redeemed Inter-Branch credit notes.? Maintain clearing account 161305? Ensure all credit notes treated as cash are deleted from the back office report daily/weekly/monthly? Ensure the completion of the monthly credit note recon
Staff Purchases:? Ensure that staff purchases card is controlled and account reconciled and cleared monthly? Ensure the authorization together with a copy of the staff buying card is obtained when loading a staff purchase? Ensure staff members keep within their authorized limits? Ensure that all refunds relating to staff purchases is refunded back to the staff purchase account and no cash, gift card or credit note has been issued
Requirements
Desired
Skills:
• Attention to detail
• Financial Skills
• Managing budgets
Desired Work
Experience:
• 2 to 5 years Wholesale & Trading
• 5 to 10 years Account Management
Desired Qualification Level:
• Diploma
Employer & Job
Benefits:
• Provident Fund
• Medical Aid
Apply Now
Makro
View employer profile
See all Makro jobs
EMAIL ME JOBS LIKE THIS
Share This Job
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Accounts Manager at Makro Show more details...
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