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Position Description

To perform the Quality Assurance & Regulatory duties for the drug products distributed by Globyz
Pharma. Reporting to Vice President of Quality and Regulatory Affairs, you will be responsible for
performing the day to day activities for the inspection and release of drug products and Controlled drug
products, received at Globyz Pharma. You will ensure that SOP procedures are implemented and
followed at Globyz pharma for the product receipt, storage, inspection and shipping. Review the data
and ensure that product storage environments are controlled and maintained for the storage of drug
products as per manufacturer’s instructions at Globyz facility.
The focus will be to ensure that documentation for the Quality systems (Deviation, Change Controls
Customer Complaints), SOP revision and training are completed in timely fashion as per Globyz polices
and meet regulatory requirements.

Responsibilities:

• • Perform the day to day activities of quality department.
  • Perform Quality Inspection and release of received goods, (products, Packaging materials) and
    complete GMP documents on a timely fashion.
  • Perform Daily Temperature Monitoring of product storage areas at Globyz Pharma and report
    any excursions / alarms to management and initiate investigation as per Globyz’ polices.
  • Print the weekly summary of Temperature data from electronic system and review and sign and
    file accordingly.
  • Maintain the original approved SOP binder at Globyz Pharma and initiate the SOP review on or
    before its next due date as per Globyz Pharma policies.
  • Maintain the training records of entire GMP staff. When applicable initiate the training of new
    and / or revised SOP.
  • Participate in the Quality systems; deviation, change controls and customer complaints
    processes. Participate in investigation and complete reports in timely fashion.
  • Participate in self inspection program and document the observations and follow up of CAPA.
  • Perform periodic review of completed logs of PEST Control, Cleaning and Sanitation.
  • Coordinate, improve and sustain the activities in the quality department with all departments at
    Globyz Pharma.
  • Provide support to Quality management during any product Recall.
  • Work with the VP Quality and Regulatory Affairs Director with a focus on process improvements
    in the quality area.
  • Liaison with customers, suppliers, partners and other Globyz Pharma departments

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Qualified Person (QP)

• • • Perform QP duties as per Health Canada regulations and guidance documents.
    • Liaison with supplier of Controlled Drug Substance and the office of Narcotics
    • Maintain Controlled Substance licenses and QP status

2 of 2

• • • Report any theft or missing narcotic units to management and Health Canada
    • Where applicable, prepare application and apply for the import and export permits.
    • Taking care of Controlled drug Safe at Globyz Pharma and ensure the security during handling
      Narcotics and Controlled drugs as per established procedures

Critical Competencies:

• • • Some knowledge in Pharmaceutical Quality Assurance, Quality Compliance and Quality Systems
    • Product disposition upon the quality inspection; Release or Reject.
    • Ability to identify gaps or non-conformances in procedures and documentations upon review.
    • Hand on experience in handling of deviation, CAPA, change controls and customer complaints.
    • Knowledge and experience in processes and continuous improvements
    • Strong interpersonal and communication skills (written and oral)
    • High proficiency with MS Office applications (Excel, Word, PowerPoint), email and software.
    • Active listener and willing to work as a team member.

Decision Making Authority:

• • • Product disposition, to release or reject product lots based on review of the technical
      documentation, regulatory compliance and with the support of quality management.
    • Identification, evaluation of deviations, leading investigations with a focus on problem solving to
      prevent future occurrences and to ensure the release of quality product by Globyz Pharma for
      customer use.
    • Ability to audit GMP activities to ensure GMP Compliance.
    • Ability to Identify the gaps and non-conformances against current regulations and Globyz SOPs.

Education and Experience:

• • • University degree or College diploma in Life sciences
    • Some background in Pharmaceutical products.
    • Some knowledge of Health Canada GMPs and quality regulation during transportation and
      storage of drug products and handling of Controlled drug products.

Please email your resume to info@globyz.com

Business Development Manager, EU

(To be based in EU)

Globyz Pharma specializes in supplying specialty medicines & orphan drugs for rare diseases globally under Managed & Global access Programs.

Globyz Biopharma Services supports Life Sciences, Pharma and Biotech companies with comparator sourcing, packaging, labelling & distribution solutions for their global clinical trials from its state of the art local warehouse & depots across Europe, North America, and Asia.

As part of the team at Globyz, you’ll be improving and saving peoples’ lives by helping customers in finding cures for life threatening diseases. Your contributions will have real-world impact, and you’ll be encouraged in achieving your career goals. This is a high growth, entrepreneurial environment that honours the individual while cultivating a team spirit.

We believe that our team is our strength. Our success is based on the motivation, dedication and performance of our people.

Position Summary:
You will be responsible for taking care of the existing clients and acquiring new clients by providing comparator sourcing subject matter expertise and clinical trial logistics solutions on client projects and requirements.
Meeting these objectives includes the identification of opportunities, the formulation and the conduct of specific sourcing strategies, and the implementation of tactics that primarily result in new sales while building long-term productive customer relationships.

Key Duties & Responsibilities:

Be the subject matter expert on Biosimilar specific trials giving advisory support on sourcing comparators and providing timely and accurate information.

• Provide support in building Globyz’s EU Region capabilities and service offering including clinical supply management , depot and logistics services
• Work with sponsor companies to understand their sourcing, labeling and distribution requirements.
• Help, develop and provide innovative end-to-end drug sourcing solutions and strategies to clients.
• Grow and develop customers according to Annual Sales Plan and gain market share with new customers
• Ensure customer satisfaction by understanding and fulfilling customers’ needs
• Support Marketing in providing market and competition information to be used for client and strategy development.
• Collaborate closely with the global sales team
• Continuously update CRM/ERP system with all relevant data
• Attend/represent Globyz Biopharma Services at trade shows / exhibitions, workshops and seminars

Education & Experience:

• Fluency in English
• 2+ years’ experience in Pharma / clinical trials
• University degree
• Experience in sales /procurement preferred
• Familiarity with drug development and clinical trial packaging supply chain is preferable
• Exposure to commercial/clinical pharmaceutical supply chain is preferable
• Outstanding customer service orientation and responsiveness
• Ability to build relationships. Excellent stakeholder management on all levels
• Ability to communicate efficiently and effectively on all levels. Break down complex communication.
• Action oriented, high energy level, perseverance and drive for results
• Creative and solution-oriented

We offer a competitive salary & a generous employee benefit package with performance based incentives.

If you have a forward-thinking attitude and are ready to go the extra mile with us, we look forward to receiving your application.
Please send your application in pdf format & in English with a covering letter, to info@globyz.com

Director, Business Development, China

(To be based in China)

Globyz Pharma specializes in supplying specialty medicines & orphan drugs for rare diseases globally under Managed & Global access Programs.

Globyz Biopharma Services supports Life Sciences, Pharma and Biotech companies with comparator sourcing, packaging, labelling & distribution solutions for their global clinical trials from its state of the art local warehouse & depots across Europe, North America, and Asia.

As part of the team at Globyz, you’ll be improving and saving peoples’ lives by helping customers in finding cures for life threatening diseases. Your contributions will have real-world impact, and you’ll be encouraged in achieving your career goals. This is a high growth, entrepreneurial environment that honours the individual while cultivating a team spirit.

We believe that our team is our strength. Our success is based on the motivation, dedication and performance of our people.

Position Summary:
You will be responsible for taking care of the existing clients and acquiring new clients by providing comparator sourcing subject matter expertise and clinical trial logistics solutions on client projects and requirements.
Meeting these objectives includes the identification of opportunities, the formulation and the conduct of specific sourcing strategies, and the implementation of tactics that primarily result in new sales while building long-term productive customer relationships.

Key Duties & Responsibilities:

Be the subject matter expert on Biosimilar specific trials giving advisory support on sourcing comparators and providing timely and accurate information.

• Provide support in building Globyz‘s China Region capabilities and service offering including clinical supply management , depot and logistics services
• Work with sponsor companies to understand their sourcing, labeling and distribution requirements.
• Help, develop and provide innovative end-to-end drug sourcing solutions and strategies to clients.
• Grow and develop customers according to Annual Sales Plan and gain market share with new customers
• Ensure customer satisfaction by understanding and fulfilling customers’ needs
• Support Marketing in providing market and competition information to be used for client and strategy development.
• Collaborate closely with the global sales team
• Continuously update CRM/ERP system with all relevant data
• Attend/represent Globyz Biopharma Services at trade shows / exhibitions, workshops and seminars

Education & Experience:

• Fluency in English and Mandarin
• 2+ years’ experience in Pharma / clinical trials
• University degree
• Experience in sales /procurement preferred
• Familiarity with drug development and clinical trial packaging supply chain is preferable
• Exposure to commercial/clinical pharmaceutical supply chain is preferable
• Outstanding customer service orientation and responsiveness
• Ability to build relationships. Excellent stakeholder management on all levels
• Ability to communicate efficiently and effectively on all levels. Break down complex communication
• Action oriented, high energy level, perseverance and drive for results
• Creative and solution-oriented

We offer a competitive salary & a generous employee benefit package with performance based incentives.

If you have a forward-thinking attitude and are ready to go the extra mile with us, we look forward to receiving your application.
Please send your application in pdf format & in English with a covering letter, to info@globyz.com

Account Manager – Biosimilar Trials

Duration: Full time Permanent

GLOBYZ BIOPHARMA SERVICES is specialized in global clinical trial comparators sourcing and supply with expertise in clinical trials logistics, storage, packaging and distribution. With global operations and head offices based in USA & Canada, the company partners with a variety of regional and global pharmaceutical and biotech companies, CROs, and clinical trial packagers around the world. We are fully licensed for the storage and distribution of prescription medications including controlled drugs and we have extensive global network of manufacturers and suppliers, enabling us to access hard to find branded and generic commercial drugs.

As part of the team at Globyz Biopharma Services, you’ll be improving and saving peoples’ lives by helping customers in finding cures for life threatening diseases. Your contributions will have real-world impact, and you’ll be encouraged in achieving your career goals. This is a high growth, entrepreneurial environment that honours the individual while cultivating a team spirit.

Position Summary

The Account Manager – Biosimilar Trials is responsible for taking care of the existing clients and acquiring new clients by providing comparator sourcing subject matter expertise and logistics solutions on client projects and requirements.

Meeting these objectives includes the identification of opportunities, the formulation and the conduct of specific sourcing strategies, and the implementation of tactics that primarily result in new sales while building long-term productive customer relationships.

Key Duties & Responsibilities

• Be the subject matter expert on Biosimilar specific trials giving advisory support on sourcing comparators and providing timely and accurate information.
• Work with sponsor companies of Biosimilar trials to understand their sourcing, labeling and distribution requirements.
• Help, develop and provide innovative end-to-end drug sourcing solutions and strategies to clients meeting revenue objectives
• Grow and develop customers according to Annual Sales Plan and gain market share with new customers
• Ensure customer satisfaction by understanding and fulfilling customers’ needs
• Support Marketing in providing market and competition information to be used for client and strategy development.
• Collaborate closely with the global sales team
• Continuously update CRM/ERP system with all relevant data
• Attend/represent Globyz Biopharma Services at trade shows / exhibitions, workshops and seminars

Skills/Qualification

• Bachelor’s Degree in Science or related field
• Experience in sales /procurement preferred
• Familiarity with drug development and clinical trial packaging supply chain is preferable
• Exposure to commercial/clinical pharmaceutical supply chain is preferable
• Outstanding customer service orientation and responsiveness
• Ability to build relationships. Excellent stakeholder management on all levels
• Ability to communicate efficiently and effectively on all levels. Break down complex communication.
• Action oriented, high energy level, perseverance and drive for results
• Creative and solution-oriented

If interested, please email your resume to info@globyz.com

Apply Now

Digital Marketing Expert

Job Types: Full-time

Location: Mississauga, Canada

About us:

Globyz Biopharma Services is seeking an organized, hardworking, and highly motivated candidate for Digital Marketing. Our Digital Marketing team is looking for a suitable candidate to join us in a generalist capacity. We expect for energetic, creative team players with hands-on experience in digital marketing such as SEO, digital promotion strategy and social media marketing.

Responsibilities include:

• Execution of content marketing campaigns.
• Research and analysis for integrated digital marketing
• Conceptualize, propose and then execute a campaign based on research and company analysis
• Proactively seek new ideas to generate digital marketing programs.
• Advise management team concisely and with meaningful insights
• Manage campaign development and reporting
• Deliver excellent quality work on quick deadlines
• Contribute out-of-the-box ideas and concepts that are brand aligned
• Work with a group of highly motivated, unique, and fun team of experts

Skill Requirements:

• You have excellent interpersonal, team, and written and verbal communication skills
• You are proactive, have pristine organization skills and pay close attention to detail
• You can work under pressure to deliver excellent quality work on quick deadlines
• Creative writing and proofreading skills are an asset
• Experience with social media platforms including Linkedin, Instagram, Facebook, Youtube etc. are an asset

Qualifications:

• Understanding of core digital marketing principles
• Previous digital marketing experience is an asset
• Experience with Google Analytics, Social media Ads, e-mail marketing are plus
• Excellent attention to detail, structured approach to analysis
• Hungry to learn and to contribute

Interested and qualified individuals can apply to info@globyz.com

Apply Now

Logistics & Supply Chain Specialist

JOB TITLE: LOGISTICS & SUPPLY CHAIN SPECIALIST

SCOPE OF THE POSITION:

• Provide logistics support to the team.
• Collaborate with multiple customers, suppliers and internal partners including Sales, Procurement, Warehousing and Transportation to procure, store and ship/deliver products through contracted carriers and follow up right through completion
• Provide shipping quotes, maintaining accurate freight costing and creation of various reports
• Order tracking to making sure all orders is on track and prioritizing orders & deliveries
• Communicating with carriers and external parties to resolve any upcoming issues or delivery requirement
• Actively participating in regularly scheduled/ad hoc communications with customers and suppliers
• Continuously improving areas with inefficiencies and/or low effectiveness
• All other duties as required for Logistics Dept.

THE CANDIDATE:

• University or college degree in a relevant discipline
• Preference to Certified Supply Chain Management Professionals (cSCMP) or Certified Supply Chain Professional (CSCP) or nearing completion of certification
• Supply chain experience preferably within North American Consumer Packaged Goods/Foods /Pharma industry experience)
• Proficient in MS Office – (Excel, Word, PowerPoint etc)
• Excellent communication skills (oral and written)

We encourage all candidates who have the right mix of skills, abilities and a passion for learning and growing to apply.

Please send your resume and cover letter to: sal@globyz.com Referrals is Welcome!!

Apply Now

Warehouse Supervisor

JOB TITLE: WAREHOUSE SUPERVISOR

Location: Globyz Biopharma Services LLC, 2101 Market Street, Suite 3, Boothwyn, PA 19061 USA
Position Type: Full-Time Position

JOB DESCRIPTION

• Manage day to day activities of all warehouse operational functions
• Manage control of incoming/Outgoing shipments
• Performed quality assurance to ensure timely and accurate delivery processes
• Assist with creating and/or revising SOPs as well as setting up distribution protocols
• Responsible for all duties that related to processing and dispatching of shipping requests in accordance with GMPs and SOPs
• Responsibilities included facility Management, Security, and Temperature/Humidity Monitoring on & off Site
• Coordinate with third-party logistics, courier & trucking companies to ensure import / Export shipments are handled properly.
• Candidate with experience in Pharmaceutical wholesale environ will be preferred.

Please forward your inquiries or resume to sal@globyz.com

Apply Now

Business Development Manager

JOB TITLE: BUSINESS DEVELOPMENT MANAGER

Location: New York/New Jersey/Pennsylvania Are
Travel Required: Minimal
Position Type: Permanent or Contract – Full Time Position

Comparator & Clinical Supplies Sourcing

Our sourcing specialists utilize a global network of leading manufacturers and major wholesalers to provide cost-effective access to virtually any product, any quantity, even the most difficult to source items. Supported by our global warehousing and distribution network, Globyz Biopharma Services can also ensure fast delivery practically anywhere in the world.

JOB DESCRIPTION

• New Business Development for Clinical Trials Material /Comparators
• Lead in the development of Clinical Supply Demand Gathering and Supply Plans
• Effectively communicate clinical trial requirements to internal stakeholders and external partners to execute the supply plan
• Manage Vendor relationships where required
• Initiate and see through requests for the manufacture of CTM at the GMP packaging facility and manage trial inventory throughout
• Accurately forecast and track supply chain budgets
• Track and report current clinical supplies activities by study
• Create and finalize packaging/labeling production schedules and identify and resolve any discrepancies/issues
• Track the reconciliation, disposition, and destruction of all clinical supplies materials and
  related communications and reports.

QUALIFICATIONS

• Minimum of 5 years life sciences experience, including a minimum of 3 years experience in labeling, packaging and distribution of clinical trial materials
• Must have experience in the management of labeling, packaging and distribution of materials to clinical sites
• Knowledge of FDA, ICH, GMP, and other regulatory requirements
• Demonstrated knowledge of current pharmaceutical processes, packaging operations and drug development processes
• Knowledge of clinical supply aspects of IND/NDA requirements; ability to present complex issues in oral and written form
• Strong project management abilities.
• Demonstrated ability to contribute successfully in a multi-disciplinary team environment organization.
• Well versed in Windows, MS Office, Word, Excel, Power Point and other related computer software

Apply Now