1453 Jobs

  • Drug Supply Packaging Coordinator (20-00459) – TX – Fort Worth 1 d ago

    The Drug Supply Packaging Coordinator supports secondary packaging and distribution of clinical supplies for US Clinical Development Medical Affairs in Fort Worth, Texas. Additional responsibilities include shipment tracking, drug accountability, processing recycled shippers and copying/filing of GMP documentation.
    Major Activities:
    Responsible for labeling/kitting, distribution and accountability activities in support of the US Pharma portfolio.
    Performing secondary packaging; labeling drug product in different temperature conditions (ambient or 2-8 Celsius)
    Preparing clinical shipments of drug products to be shipped to clinical sites. Shippers can weigh up to 20-25 lbs.
    Receiving, processing and cleaning of reusable shippers that are returned from clinical sites
    Demonstrates an understanding of *** systems, cGMP, and Annex 13 regulatory requirements such that clinical supplies documentation produced and distributed remain compliant throughout the chain of custody.
    Creates, updates, reviews, maintains and archives records and other key documents to provide track and trace evidence for every aspect of the secondary packaging and distribution of investigational product in a cGMP state.
    Accountability for specific record types will be based on job assignments. If label printing is a part of job assignments, demonstrates knowledge of labeling requirements along with the knowledge of printing clinical labels.
    Demonstrates good working knowledge of inventory management best practices. This may be inclusive of any of the following, log books and their correct entry, WIP, quarantine, retention samples, reference samples, released goods, returned and discarded goods

    – Some experience with labeling, packaging and/or shipment of clinical supplies (preferred)
    – Knowledge of cGMP, 21 CFR Part 11, and Annex 13 requirements (preferred)
    – Great attention to detail.
    – Excellent organizational and documentation skills
    – Excellent communication & customer relation skills.
    – Excellent written and spoken English.
    Source: Job Diva – Job Listing

  • USA-Quality Control Analyst II (Manufacturing/Quality) (20-00457) – MA – Northborough 1 d ago

    Perform operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods. Complete routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. Aid in the development of test methods. Conduct data review and preliminary evaluation of results. Solve problems using limited predetermined options such as repeating the assay when parameters are not met to determine the cause, etc. Provide input to the technical composition of operating documentation. Work is closely supervised. Follows standard practices to obtain solutions. Contribute to the completion of routine technical tasks. Failure to achieve results can normally be overcome without serious effect on schedules and programs. Contacts are primarily with immediate supervisor and other personnel in the section or group.

    Responsibilities include:
    Demonstrate proficiency in a task by completing On the Job Training.
    Maintain on-time completion of all training requirements.
    Perform all activities adhering to strict cGMP guidelines.
    Participate in department initiatives to support continuous improvement
    Perform environmental monitoring and clean room activities
    Sample raw materials in accordance with SOPs
    Perform testing and inspection in accordance with SOPs
    Review peer data including data transcription, data calculation and log entries.
    Lab general duties including cleaning, glassware, washing etc.
    Initiate DCRs when assigned.
    Participate in audits.
    Perform PM calibration on lab equipment.
    Conduct Safety and weekly compliance walkthroughs.
    Participate in Lab Investigations and NCMR investigations.
    Adhere to site Quality and Safety Policies.
    Work towards accomplishment of Site Goals.

    Years of Experience: 3 – 6 Years
    Source: Job Diva – Job Listing

  • USA-Quality Control Analyst I (Manufacturing/Quality) (20-00455) – MA – Allston 1 d ago

    Perform operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods. Complete routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. Aid in the development of test methods. Conduct data review and preliminary evaluation of results. Solve problems using limited predetermined options such as repeating the assay when parameters are not met to determine the cause, etc. Provide input to the technical composition of operating documentation. Work is closely supervised. Follows standard practices to obtain solutions. Contribute to the completion of routine technical tasks. Failure to achieve results can normally be overcome without serious effect on schedules and programs. Contacts are primarily with immediate supervisor and other personnel in the section or group.. Years of Experience: 0 – 3 Years
    Source: Job Diva – Job Listing

  • USA-Clinical Data Associate III (Clinical) (20-00454) – NJ – Bridgewater 1 d ago

    MUST Have experience overseeing data management vendor. 
    This will be for a study in start-up and will go on for 2 years.
    Needs to be pro-active, knows the process, what questions to ask, while providing oversight of the vendors/CRO's. 
    5+ years’ experience, know how to dig through the data, deviation protocols, and how to transfer the data files.

    Description:
    Interact both verbally and through written communication with inter-organizational and outside customer contacts as well as with Central and External laboratories, CROs, etc.
    Contribute to the design of protocols. Develop relevant quality standard specifications according to protocol and approved standards (based on industry standards), participate in user acceptance testing.
    Develop protocol specific edit check specifications, participate in user acceptance testing.
    Develop and maintain project- specific Data Management plan throughout the life cycle of the study protocol, which includes CRF annotation, database specifications, edit checks and other pertinent data management documents.
    Provide training for team members in data management procedures.
    Prioritize tasks with respect to pre-determined timelines.
    Provide direction and coordinate data management activities to ensure timely database lock and release of data for interim and final analyses.
    Provide oversight, monitor and track quality of vendor data management deliverables, ensuring audit practices are in place to validate the quality of database content as well as external electronic data transfers.
    Perform metrics on data management processes and guidelines to evaluate efficiency, accuracy, and speed in cleaning clinical study data and locking database for study reporting.
    Ensure data processing activities are performed according to protocol, relevant quality standards and SOPs.
    Participate in hands-on data review and query management as necessary.
     
    Years of Experience: 6 – 9 Years
    Source: Job Diva – Job Listing

  • Software Developer (20-00453) – IN – Carmel 1 d ago

    Software Developer
    MISO R&D is seeking to hire a highly skilled Software Developer to help with the software development aspect of the Advanced Simulation Environment (ASE) project. Primary responsibilities of this role will revolve around building software by writing code, bug-fixing, adaptation of code to new hardware paradigms, and implement software engineering best practices.
     
    Success in this role requires extensive knowledge of programming languages, frameworks, and software engineering. A minimum of a Bachelor's degree in Computer Science is a must.
     
    Hours: Standard 8:00 – 5:00pm  (remote until lockdown is entirely lifted)
    Start Date: 1-July-2020
    Duration: 8-10 months, contractor (will not convert to an FTE; chance for short extension)
    Interview process: Phone screen then in person interviews (in person ideally the week of 6/22)
     
    We' re looking for someone who…

    • Is deeply creative and quick learner of new technology and new domain of knowledge.
    • Is a problem solver with a knack for uncovering elegant solutions
    • Strong Programming and coding experience required; Must be a full-stack developer
    • Has a strong exposure to development in the Cloud and cloud-related technologies

     
    What You Can Expect in This Role:
     

    • As a Software Developer, you may come from a software engineering or design background. Either way, you will work on internal facing tools, platforms, and libraries
    • You'll engage users in conversations to uncover how they do their work, what tools they use, how they understand their work, and how they currently solve their problems. You will work to explore pain points and areas for meaningful improvement. We work through an agile customer oriented approach.
    • You will spend the majority of your time building simulation software, prototypes, data interfaces, presenting data in a visual, interactive format in quick iterations.
    • Since you will be working under the context of Research and Development, you will not be developing 'production-grade' code.

     
    Basic Qualifications:
     

    • Experience (> 5 yrs.) with software development tools and libraries (Python, Go, SQL, Java, VBA, Bash, Tableau, D3, Bitbucket, JIRA, Confluence)
    • Experience (> 5 yrs.) with cloud technologies (K8s, Docker, Ansible)
    • Experience with the SAFE Framework is preferred; (Agile -Scrum is a must)
    • Designing and developing software systems using scientific analysis and mathematical models to predict and measure outcomes and design consequences
    • Making large and/or complex data more accessible, understandable and interactable. The contractor will deliver data in useful and appealing ways to users.
    • Creating working prototypes, simulation software for various business functional components, data retrieval, transformation, and visual information representation
    • Excellent analytical skills
    • Comfortable with approaching users for feedback and quickly pivoting on a new solution design
    • Critical thinking: able to look at numbers, trends, and data; strong attention to detail
    • Story-telling ability & communication skills, both written and oral as they will be working with MISO users.
    • This contractor will work very closely with the Project Lead

     
     
    Monument Intake Call

    • Top Skillsets Looking For
      • This person must be a critical thinker. In this role, they will need to independently create and test new concepts, consider varying options, and determine a best practice.
      • Their developing does not have to be production-grade, but must be highly functional and well written.
      • This person should not be a heads down coder, requiring specific instruction in order to be effective. This position requires an independent thinker, who is excited to create new processes.
      • Python, SQL, Java; prefer that they come in with a certification or a test that the supplier has done to prove technical ability
      • Docker, K8s, Kubernetes, Ansible

     

    Source: Job Diva – Job Listing

  • USA-Financial Analyst II (Professional) (20-00452) – NJ – Bridgewater 1 d ago

    ? Assist the Finance Team to close the books and present monthly results to business partners on a timely basis.
    ? Assist with providing monthly commentary to explain variances between actual results and/or budget/forecasts.
    ? Manage internal control SOX compliance overall and ensuring current and new guidance is adhered to and communicated. Providing support to internal and external auditors.
    ? Prepare and support custom shipments globally in working with global finance team and within the R&D organization in providing guidance to ensure R&D compounds are properly valued and consistent in shipments worldwide.
    ? Support in Reporting of R&D actuals, forecast and comparables for costs, headcount and capital for 5 legal entities.
    ? Provide support in ensuring the accuracy of results and resolutions of disconnects by connecting with the COE (Center of Excellence) and A2R (Account to Report).
    ? Prepare and post journal entries for alliances and temp help accruals. Ensure compliance of temp help with company guidelines and analysis of temp help.
    ? Complete US Government requests pertaining to spend and investments within the R&D organization
    ? Work with the technical accounting team and alliance management in compiling off balance sheet disclosures.

    Years of Experience: 3 – 6 Years
    Source: Job Diva – Job Listing

  • USA-Regulatory Affairs Specialist I (Clinical) (20-00450) – NJ – Bridgewater 1 d ago

    Support the Regulatory/Quality Zone Head in the following:
    • Responding to US RA customer requests
    o Log and track in the customer database
    o Hold sales and RA weekly meeting to track the progress of customer requests
    • Review and publishing of Administrative and Technical amendments to
    the FDA for SAIS Drug Master Files
    o Work closely with the site to ensure document are accurate for
    submissions
    • Respond to FDA Deficiency Letters
    o Hold meeting(s) with the site to discuss the content of the letter if needed
    o Hold meeting(s) with customers affected by the deficiency letter
    o Coordinate with the site timelines to respond to FDA deficiency letter
    o Request publishing, review the response to ensure it is publishing-ready,
    and publish the document to FDA
    • Send and track Information Letters to each Customer
    • Regulatory Intelligence
    o Alert and inform sales managers and BU manager of US governmental
    policies, FDA guidance and trends that may affect our US business

    . Years of Experience: 0 – 3 Years
    Source: Job Diva – Job Listing

  • USA-Quality Control Analyst I (Manufacturing/Quality) (20-00448) – MA – Framingham 1 d ago

    Department Description:
    The Quality Control department supports the Seprafilm (medical device) and Sodium
    Hyaluronate (active pharmaceutical ingredient) GMP operations at the 74/76 NYA
    Manufacturing Facility. The department performs analytical testing on intermediate, inprocess and final product materials using a variety of equipment to include GC, FTIR, UVVIS, and physical property instrumentation.

    Position Summary
    Supports Biosurgery Business by performing in-process, stability and release testing for
    Biosurgery Product lines.
    Core Responsibilities
    Perform Assays in accordance with SOPs for release, stability and in-process samples.
    Review peer data including data transcription, data calculation and log entries.
    Lab general duties including cleaning, glassware, washing etc.
    Initiate DCR when assigned.
    Train on all documents assigned to training plan and complete training as assigned.
    Receive, verify and log incoming samples.
    Participate in audits.
    Perform PM calibration on lab equipment.
    Conduct Safety and weekly compliance walkthroughs.
    Is responsible for adherence to policies, procedures and SOPs
    Participate in Lab Investigations.
    Perform OOS Investigations as Analyst.
    Adhere to site Quality and Safety Policies.
    Work towards accomplishment of Site Goals.
    QC testing of in-process, stability and release samples in a GMP lab
    Support lab operations.
    Participate in lab meetings.
    Perform or Participate in Equipment Qualifications.
    Participate in bringing in new equipment (spec, URS, etc.)
    Early troubleshooting of assay/equipment issues.
    COA Filing and Sample Disposal.
    Coordinator Roles that can be assigned:
    Monthly Log Changes.
    Documentation
    Controls
    Reserves
    Metrology
    Purchasing
    Assay Occasion tracking
    Data backup

    Basic Qualifications:
    Bachelor’s Degree or equivalent in Science.
    0-2 years lab experience.

    Preferred Qualifications:
    Experience in laboratory techniques such as but not limited to pH, GC, UV/VIS and FTIR.

    Special Working Conditions:
    Requires working with hazardous chemicals.

    Requires on site work
    Source: Job Diva – Job Listing

  • USA-Technical Writer II (Manufacturing/Quality) (20-00444) – NJ – Bridgewater 1 d ago

    Duties

    The CMC Regulatory Technical Writer works closely with quality, manufacturing, regulatory, and technical staff from global locations within ***'s industrial network, contract manufacturing organizations (CMOS), and alliance partners to author high-quality Module 2 and 3 CMC regulatory submissions for development and post-approval dossiers in eCTD format. The CMC Regulatory Technical Writer also authors change controls, following ***'s change control procedures.

    The technical writer contributes to various US, EU and rest of world (ROW) registrations. They author and create dossier content from source documentation for registrations, and provide writing support for technical reports. Recommend a table of contents for regulatory submissions. Contribute to regulatory strategy for successful product registration. Assess questions received from health authorities and author responses. Ensure all dossiers are in compliance with ***'s templates, regulatory guidance, and ICH guidance, and maintain up to date knowledge. Maintain the skills required for dossier related software systems.

    Skills

    The candidate must possess substantial Chemistry, Manufacturing and Controls (CMC) and Common Technical Document (CTD) authoring experience. A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. The candidate must have at least 7 years' experience in the industry. Expertise with MS Office, Word, Excel and document management systems such as Veeva or Documentum is mandatory. Working knowledge of cGMP's is desired. Experience with CMC documentation pertinent to various dosage forms is needed.

    This position requires the incumbent to be highly organized, self-motivated, and able to independently manage multiple priorities. The desired candidate will have the capacity to be productive with very little supervision and should enjoy writing. Excellent interpersonal communication skills are required, and the candidate must have previously demonstrated the ability to interact with a multi-disciplinary team. Knowledge of US pharmaceutical regulations is essential. Exposure to non-US regulatory activities is desired, but not mandatory.

    Education

    7 years of experience in the pharmaceutical industry, which includes no less than 4 years of experience with CMC regulatory-related activities. BS/BA or MS, or PhD, from an accredited school in a science/health field (e.g. Biology, Analytical Chemistry, Pharmacy or a related field).
    Source: Job Diva – Job Listing

  • USA-Validation Specialist III (Engineering) (20-00441) – PA – Swiftwater 1 d ago

    Description:
    The candidate will be a member of the team responsible for experimental execution within pilot plant and production areas. The candidate for this position will need to become trained on applicable production operations on the unit operations in the lab as well as general laboratory procedures. Following training, the candidate will be expected to independently execute assigned experiments with minimal direction from laboratory supervision.
     
    Key responsibilities include:
    • Responsible for authoring and reviewing development and validation notebook studies/ protocols/ reports
    • Execution of studies in pilot plant / manufacturing environment
    • Follow good documentation practices to record all activities performed and data generated in production of developmental experiments
    • Follows all procedures put into effect to ensure your safety as well as the safety of others. Participates in safety meetings, reports all safety issues, concerns, incidents and near misses to the team leadership.
    • Identifies production issues and relays them to the laboratory management. Ensures all required paperwork is complete, accurate and done in a timely manner to ensure a quality product.
    • Participation in cross-functional teams, where necessary, to assure correct performance of process operations and working with management to resolve process operations issues.
     
    Preferred Qualification:
    • MS Office
    • EDoc or Geode, with a working knowledge of templates, workflows and approval process
    • LabWare/ LIMS experience preferred
    • Full understanding of GMP Documentation and current GMP standards
    • Good lab / aseptic technique
    • To be able to establish professional working relationships with other support and production areas in order to gather all of the necessary information required.
    • Interact well and professionally with a diverse group of individuals
    • Self-motivated and willing to be proactive in resolving issues
    • Excellent Verbal and written communication skills.
    • Ability to work in a team environment
    • Ability to write and complete deviations in a timely and thorough manner
    • Ability to multitask and prioritize tasks
    • Flexibility of hours during execution to include nights and weekends
     
    Education:
    • Bachelor’s degree in scientific discipline plus 3-6 years of experience in Vaccine, Biologic, or Pharmaceutical manufacturing and/or development.
    Source: Job Diva – Job Listing

  • USA-Laboratory Technician II (Scientific) (20-00440) – MA – Framingham 1 d ago

    Duties:
    Provide scientific support with day-to-day lab activities such as 2D/3D primary mammalian cell culture, ELISA, RT-qPCR, Western blot,
    Luminex/MSD assays and immunofluorescence imaging (80%)
    Provide on-site support to manage the shipping, receiving, labeling, and packing of samples, and test articles, as well as microscopic slides and
    blocks for both GLP and non-GLP in vitro/in vivo studies (10%)
    Provide support in the lab for in vivo studies as needed, including but not limited to necropsy, and documentation (10%)

    Skills:
    Primary mammalian cell culture, basic cell and molecular biology skills
    Experience working in a lab-setting and performing in vitro/in vivo studies
    Familiarity with GLP regulations and compliance
    Willingness to learn other aspects of lab activities

    Keywords:
    Mammalian cell culture, qPCR, ELISA, Western blot, imaging

    Education:
    BS+5 or MS+3 years experience in pharmaceutical industry or academic setting
    Source: Job Diva – Job Listing

  • USA-Quality Control Scientist I (Manufacturing/Quality) (20-00437) – MA – Framingham 1 d ago

    Position Summary
    Quality Control Validation Scientist I is responsible for the qualification activities, following SOPs and regulations including Data Integrity, related to one or more of the following areas: IQ, OQ, PQ and requalification.

    Core Responsibilities
    Perform qualification in a cGMP biotech facility managing multiple complex qualification projects and providing technical assistance to less experienced team members.
    Write, review and approve qualification protocols and reports as well as execute protocol. Resolve protocol discrepancies and deviations.
    Evaluates new technologies platforms for implementation in the QC Laboratories.
    Ensure GMP compliance of all activities performed.
    Represent QC Validation in internal and external audits as required.
    Ensure appropriate facility support and provide technical expertise with regards to equipment.
    Review standard operating procedures.
    Maintain positive relationship and network effectively across sites and organizations.
    Provide project oversight and participate in cross-functional teams.
    Practice safe work habits and adhere to Genzymes safety procedures and guidelines. An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all of our products and services. This includes:
    Perform other additional job related duties as required.
    Adhering to all applicable laws and regulations of the places in which we conduct business, as well as our Company policies and procedures.
    Being honest and treating people with respect and courtesy.
    Constantly striving to make Genzyme a great place to work, and a company respected for the quality of its people and products.
    Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs.
    Skills

    Knowledge of Validation Lifecycle Approach.
    Knowledge of Validation Data Integrity Principals
    Ability to present technical data.
    Ability to work independently on scientific projects.
    Scientific technical writing ability authoring and reviewing SOPs, qualification protocols and technical reports.
    Experience troubleshooting of assay and equipment issues
    Source: Job Diva – Job Listing

  • Consultant Clinical Quality Assurance (CQA), Standards and Training (20-00435) – NJ – Woodcliff Lake 1 d ago

    The Consultant, GCP Quality Assurance will assist the Head of CQA in revising the CQA Standards/SOPs, upskilling auditing practices for CQA staff, develop & deliver training (where applicable).

    Tasks
    1. Perform gap analysis of current CQA Standards and CQA staff skill set
    2. Develop plan for revision of current Processes/ SOPs
    3. Develop roadmap for Skill set training
    4. Revise or create new SOPs
    5. Develop CQA training materials
    6. Deliver training

    Requirements
    Minimum of 5-8 years of Clinical Quality Assurance and auditing experience
    Experience in SOP development
    Experienced trainer
    Experience with inspection management
    Knowledge of ICH GCP, clinical trial methodology, and specific knowledge of applicable regulations/guidance (including 21 CFR Part 11) and ICH Guidelines related to clinical computer systems
    Location: remote
    Source: Job Diva – Job Listing

  • TMF Consultant (20-00434) – NJ – Woodcliff Lake 1 d ago

    Job Summary:
    The role will be responsible for the development of global business strategies related to eTMF.
    This subject matter expert will act as a liaison to the business groups to ensure that strategies and business processes related to TMF are aligned in approach to guarantee inspection readiness
     
    Duties:
    1. Thorough knowledge of the DIA Reference Model, ICH, GCP, and GDP principles
    2. Experience with template development for study specific file plans
    3. Experience in clinical trial document management In accordance with global regulation and ICH/GCP guidelines
    4. Experience with various electronic TMF Systems
    5. Solid expertise with inspections and inspection readiness.
    6. Ensures there is alignment across global TMF management by driving collaboration globally within Company business groups.
    7. Effectively communicate document management and quality issues along with potential solutions to project teams and management.
    8. Provides feedback for correction and resolution to appropriate internal personnel.
    9. Explores ways to standardize and streamline study start-up through close out activities through appropriate document management.
    10. Promotes quality standards and adherence to regulations and ICH guidance for improvement of team performance.
    11. Establish internal and external training standards.
    12. Creates high group engagement metrics across project teams.
     
    Required:
    • Bachelor’s degree is required. Scientific discipline preferred.
    • Min of 10-12 years of experience in pharmaceutical environment; min of 5-7 years’ experience as a TMF expert.
    • Ability to think outside the box and work in faced paced dynamic environment.
    • Must have very strong understanding of clinical development, including Global regulatory requirements (including ICH and GCP guidelines) for the conduct of clinical trials and related regulatory documentation and be able to interpret and make decisions based on the interpretation of such guidelines.
    • Must have very strong knowledge of, and be able to differentiate, all key clinical trial documents (e.g., IBs, ICFs, CRFs, Protocols, regulatory approval documents)
    • In-depth knowledge/understanding of eTMF requirements and technologies
    • Must have strong critical reasoning skills, including the identification and resolution of complex change management
    • Must be proficient in MS Office
    • Shows high level of initiative and has ability to work independently
    • Must have very strong verbal, written and interpersonal communication skills, especially needed to work in and effectively manage a cross-functional team
    • Ability to drive cross-functional projects with conflicting priorities
    • Must be very detail oriented and possess excellent organizational and time management skills
    Source: Job Diva – Job Listing

  • Senior Data Scientist/Programmer (20-00433) – NJ – Woodcliff Lake 1 d ago

    Job Description:

    The Data Operations Group within the Neurology division at Client, Inc. is seeking a Senior Data Scientist/Programmer to drive drug development through predictive modeling of disease and drug response. The Data Scientist will collaborate closely with Biostatisticians in Stat Methodology / Machine learning group to support projects in various stages of development in the Neurology Business Group. The Data Scientist will be part of providing actionable insights that are mission critical data science projects for our business.
    Technical Skills Required:
    Experience with two or more of the following languages
    R, Python, MATLAB
    Experience with data cleansing and processing from SAS server or unstructured data in other sources
    Experience with sophisticated data science methods and tools (such as Python/TensorFlow)
    Advanced data analysis
    Data storytelling
    Visual Analytics

    Qualifications Required:
    Proven track record of developing, deploying, and supporting data analytic tools
    Experience developing front-end interface to statistical models with tools like R/Shiny or others
    Experience managing and coordinating with IT teams to maintain secure and compliant tools and applications
    Experience with developing and deploying cloud-based tools or distributed computing environment using Spark
    Excellent communication and presentation skills required
    Experience in managing different workstreams and coordinating tasks with internal teams and outside consultants

    Educational Qualifications:
    Bachelor of Science or higher
    Source: Job Diva – Job Listing